Next Article in Journal
Death-Associated Protein Kinase 1 Phosphorylation in Neuronal Cell Death and Neurodegenerative Disease
Next Article in Special Issue
Modulation of the Negative Affective Dimension of Pain: Focus on Selected Neuropeptidergic System Contributions
Previous Article in Journal
Magnesium Deficiency Induced Global Transcriptome Change in Citrus sinensis Leaves Revealed by RNA-Seq
Previous Article in Special Issue
Metabotropic Glutamate Receptor 5 and 8 Modulate the Ameliorative Effect of Ultramicronized Palmitoylethanolamide on Cognitive Decline Associated with Neuropathic Pain
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 20
Issue 13
10.3390/ijms20133130
ijms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Chronic Pain: Structural and Functional Changes in Brain Structures and Associated Negative Affective States

by
Seoyon Yang
1 and
Min Cheol Chang
2,*
1
Department of Rehabilitation Medicine, Ewha Woman’s University Seoul Hospital, School of Medicine, Ewha Woman’s University, Seoul 07804, Korea
2
Department of Rehabilitation Medicine, College of Medicine, Yeungnam University, Daegu 42415, Korea
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2019, 20(13), 3130; https://doi.org/10.3390/ijms20133130
Submission received: 28 May 2019 / Revised: 21 June 2019 / Accepted: 25 June 2019 / Published: 26 June 2019
(This article belongs to the Special Issue Chronic Pain: Spinal and Sovraspinal Neuroinflammation and Associated Negative Affective States)
Browse Figure
Versions Notes

Abstract

:
Chronic pain is a condition in which pain progresses from an acute to chronic state and persists beyond the healing process. Chronic pain impairs function and decreases patients’ quality of life. In recent years, efforts have been made to deepen our understanding of chronic pain and to develop better treatments to alleviate chronic pain. In this review, we summarize the results of previous studies, focusing on the mechanisms underlying chronic pain development and the identification of neural areas related to chronic pain. We review the association between chronic pain and negative affective states. Further, we describe the structural and functional changes in brain structures that accompany the chronification of pain and discuss various neurotransmitter families involved. Our review aims to provide guidance for the development of future therapeutic approaches that could be used in the management of chronic pain.

1. Introduction

Pain is a serious and common global medical problem that can cause long-term disability [1,2]. The perception of pain is underpinned by the transduction of mechanical, thermal, and chemical sensory inputs into the subjective awareness of pain [3]. Chronic pain is a condition in which pain progresses from an acute to chronic state, persisting beyond the healing process [4]. As the experience of chronic pain is associated with activity in multiple networks in the central nervous system (CNS), chronic pain is considered a CNS disorder [5]. As a result of multi-network activation in the CNS, chronic pain comprises multiple components, including sensory, emotional, cognitive, and behavioral elements [6].
Patients who suffer from painful conditions may demonstrate various clinical outcomes. In most cases, pain-inducing conditions resolve over time, as the body goes through the normal healing process. In a subset of cases, pain progresses into a chronic condition in which pain persists for many years [3]. In recent years, numerous clinical and animal studies have investigated the mechanisms underlying chronic pain to elucidate its cellular and molecular mechanisms. Understanding the mechanisms of development of chronic pain will guide the search for novel therapeutic options for chronic pain. The primary goal of this review is to explore the mechanisms of development of chronic pain. We review the current knowledge of neural areas related to chronic pain, the relationship between chronic pain and negative affective states, structural and functional changes that occur in brain structures during the development of chronic pain, and various neurotransmitter systems involved in the chronification of pain.

2. Pain Pathways and Mechanisms of Chronic Pain

Pain can be classified into three major types: Nociceptive, inflammatory, and neuropathic pain. Nociceptive pain is the response of sensory systems to actual or potentially harmful stimuli detected by nociceptors around the body. Inflammatory pain is associated with tissue damage and the resulting inflammatory process, which may lead to responses such as hyperalgesia, allodynia, and sympathetically maintained pain [7]. Neuropathic pain is a localized sensation of unpleasant discomfort caused by damage or disease in the peripheral and/or central nervous system that persists after a primary lesion or dysfunction. Neuropathic pain may be associated with allodynia, which refers to pain sensitization to stimuli that do not normally provoke pain (non-painful stimulation) [7]. Hyperalgesia refers to an abnormally increased sensitivity to pain, which is associated with hypersensitivity to stimuli. Primary hyperalgesia occurs directly in damaged tissues, whereas secondary hyperalgesia occurs in areas surrounding damaged tissues due to pain-related mediators binding to receptors around the injury site, causing sensitization of adjacent uninjured tissues to mechanical stimuli [7].
Pain pathways comprise a complex sensory system, which is activated to provide protective responses to noxious stimuli. Input regarding noxious stimuli is transmitted from nociceptors by primary afferent Aδ and C fibers. These fibers have cell bodies located in the dorsal root ganglion and synapse with neurons in the spinal dorsal horn. Various neurotransmitters such as glutamate, calcitonin gene-related peptide (CGRP), and substance P are released as part of signal transduction [8,9,10,11]. Primary nociceptive afferents synapse onto neurons in the Rexed laminae I and II and make connections with neurons located deeper in the dorsal horn, which play a role in signaling the presence, location, and intensity of pain [12]. Projection neurons from the dorsal horn decussate at the ventral commissure and ascend in the lateral spinothalamic tract to the ventral posterolateral nuclei of the thalamus. Finally, the information is transmitted to the somatosensory cortex and periaqueductal gray matter (PAG) [9,13]. Nociceptive information is transmitted to brain areas involved in memory and affective aspects of pain, such as the amygdala, hypothalamus, PAG, and nucleus accumbens (NAc) through the spinoreticular and spinomesencephalic tracts [9,14]. These brain regions, including the somatosensory cortex, PAG, amygdala, hypothalamus, and NAc, are associated with supraspinal responses of pain pathways [15,16,17,18]. Descending pain modulatory systems involve the PAG and rostral ventral medulla (RVM). The RVM is the major output node in the descending modulation of nociception. It receives input from the PAG and sends diffuse bilateral projections to the dorsal horn, terminating at multiple levels [19]. The ascending and descending pain pathways are summarized in Figure 1.
Peripheral injury activates both neuronal and glial cells, and subsequent neuron-glia interactions influence pain hypersensitivity [20]. Glia are nonneuronal cells that support and protect neurons in both the central and peripheral nervous systems. Glia comprise microglia, astrocytes, oligodendroctyes, and radial cells [21]. The development of pain is affected by glial cells, which release neurotransmitters and molecules involved in pain pathways. Glial cells initiate a series of signaling cascades that regulate pain processing at the spinal and supraspinal levels. Glial cells also release inflammatory cytokines and chemokines which may facilitate pain transmission through coupling to neuronal glutamate receptors. Bidirectional neuron–glia interactions affect processing, expression, and transmission of pain and play a critical role in the development and maintenance of pain [21].
Central sensitization is triggered by increased nociceptive input caused by injury or inflammation and is an outcome of physiological plasticity and long-lasting changes in the CNS [22]. Increases in primary afferent fiber responses, as well as increased spontaneous activity and excitability of dorsal horn neurons and receptive field areas, are associated with central sensitization [22,23]. The mechanism of central sensitization involves glutamate signaling via postsynaptic N-methyl-D-aspartate (NMDA) receptors. Activation of NMDA receptors results in the opening of ion channels and calcium influx. This calcium flow plays a critical role in synaptic plasticity in both excitatory and inhibitory synapses. Synaptic plasticity can sensitize the central nociceptive system, resulting in pain hypersensitivity and persistent pain [24].

3. Pain and Negative Affective States

Brain structures, including the primary somatosensory cortex, secondary somatosensory cortex, anterior cingulate cortex (ACC), prefrontal cortex (PFC), insular cortex, amygdala, thalamus, cerebellum, and PAG, have been identified as regions associated with the perception of pain [15,16,17,18]. The ventral tegmental area (VTA) and NAc, structures comprising the mesolimbic reward circuit, are involved in chronic pain. The prefrontal region and limbic system (ACC, amygdala, VTA, and NAc) are associated with affective aspects of pain and regulate emotional and motivational responses [16,17,25]. These brain regions are not activated separately; they are functionally connected and contribute in a combined fashion to pain processing. Changes in emotional and motivational cues can affect the intensity and degree of pain experience [26].
Several studies have investigated the brain areas associated with emotional aspects of pain. Baliki et al. showed that patients with persistent back pain had greater functional connectivity between the medial PFC (mPFC) and NAc [27]. Since the mPFC and NAc are involved in emotion, motivation, and reward-related behaviors, this suggests that the processing of pain perception can be influenced by changes in these functional connections. Hashmi et al. also suggested that regions involved in processing emotions, such as the mPFC and amygdala, are associated with the chronification of pain [28]. Changes in emotion, motivation, and reward-related circuits of the brain (which encode emotional features of pain) may cause disorders associated with emotion in chronic pain conditions.
A number of neuroimaging studies have demonstrated that morphological changes in corticolimbic structures and emotional systems are associated with persistent pain. Patients with persistent subacute back pain show a reduction in gray matter density in the insular cortex, primary somatosensory cortex, motor cortex, and NAc [27]. The transition of brain activity from the insular cortex, ACC, thalamus, and basal ganglia to the mPFC and amygdala (structures associated with emotion-related circuitry) manifests in patients with persistent subacute back pain [28]. Furthermore, patients with chronic pain conditions show reductions in gray matter volume in the hippocampus and amygdala. Given the functions of these two regions, this reduction suggests that chronic pain may be correlated with emotional and cognitive changes [29,30]. In summary, functional and structural changes in the corticolimbic system and corticolimbic interactions in patients with chronic pain can contribute to emotional and cognitive problems [31].
To date, several studies have demonstrated the high comorbidity of affective disorders in patients with chronic pain. Many patients with chronic pain also have severe depression. Patients with chronic pain-induced depression have poorer prognosis than those with chronic pain alone [32]. Chronic pain and depression share similar changes in neuroplasticity and involve overlapping neurobiological mechanisms; monoamine neurotransmitters such as serotonin, dopamine, and norepinephrine are decreased in both chronic pain and depression patients [33,34]. Additionally, brain regions involved in pain pathways, such as the prefrontal cortex, hippocampus, and amygdala, are similar to those involved in mood disorders [33,35].
As pain develops into a chronic condition, negative emotional states may be accompanied by other emotional disorders such as anxiety, anhedonia, cognitive deficits, sleep disturbances, and suicide [15,36]. The prevalence of suicidal ideation and suicide attempts is noticeably higher in patients with chronic pain than in control patients [37]. A recent review indicated that chronic pain itself is an important independent risk factor for suicidality regardless of type and concluded that depressive symptoms, anger problems, and harmful habits are general risk factors for suicidality in patients with chronic pain [38].
Several animal studies have demonstrated the negative affective disorders associated with pain. A study using a rat model with a chronic constriction injury reported that long-term pain led to an anxiety-like profile, increased responses to aversion, and impairments in cognitive tasks [39]. Wu et al. reported that negative effects including pain aversion and anxiety were associated with hyperalgesia but that the manifestations of negative effects may occur over different time courses, suggesting that therapy should be targeted based on the different stages of pain and its comorbidities [40].
Chronic pain and various affective disorders are often managed poorly [41,42]. Understanding the affective aspects related to chronic pain may facilitate the development of novel therapies for more effective management.

4. Pain and Long-Term Functional Changes in Corticolimbic Structures

The corticolimbic system is a mediator of chronic pain and plays an important role in the development, maintenance, and amplification of chronic pain [3,43]. Pain chronification is accompanied by spatiotemporal reorganization of brain activity, with a transition from sensory regions to emotional and limbic regions of the brain [13]. Structural and functional plasticity in the corticolimbic circuitry accompanies the transition from acute to chronic pain. When nociceptive signals persist, the corticolimbic circuitry stays activated. Through the interactions with the prefrontal cortical circuitry, nociceptive state progresses to a more emotional state. The persistent activation of the corticolimbic circuitry brings functional and anatomic alterations to the cortex, resulting in pain chronification [44]. Corticolimbic structures that are associated with pain and their long-term functional changes are described below (Table 1).

4.1. Prefrontal Cortex

The mPFC is an important region for top-down cognitive control over emotion-driven behaviors [31]. The mPFC is a critical region involved in emotional and cognitive processing in chronic pain [45]. The prelimbic and infralimbic mPFCs receive inputs from brain regions including the basolateral amygdala (BLA), hippocampus, thalamus, and contralateral mPFC and send excitatory projections to the amygdala [31]. Chronic pain is considered to develop as a result of the persistence of pain memory and inability to erase pain memory after injury [43]. Considering its importance in extinction of fear behaviors, impaired mPFC activation could lead to a failure in the elimination of subcortically driven fear behaviors, thereby resulting in pain chronification [31]. Preclinical evidence suggests that mPFC function is associated with pain states, based on electrophysiology studies in anesthetized rats showing a reduction in evoked and background activity in the mPFC in acute arthritis pain [46,47]. A decrease in mPFC volume has also been observed in patients with chronic pain [45].

4.2. Anterior Cingulate Cortex

The ACC is associated with affective and motivational aspects of pain [48,49,50,51]. The ACC is involved in the processing and modulation of pain. Nociceptive inputs are sent from the medial thalamus to ACC and combined with motivation and affective information received from other areas of the brain, such as the insular cortex, mPFC, and BLA [16,49,52,53,54]. The ACC then generates affective and motivational pain responses through its projections to the amygdala, NAc, and mPFC [49,52,53,54,55]. Additionally, the interactions of the ACC with pain neurocircuitry in the PAG have been reported, which accounts for the activation of the ACC and PAG in the presence of noxious stimuli [16]. The activation of ACC-PFC-PAG circuity and increased activity in the ACC is associated with negative emotions [16,56].

4.3. Amygdala

The amygdala is associated with emotions and affective disorders [50,51,57]. Studies have reported activation of the amygdala in pain states, suggesting that the amygdala plays an important role in emotional affective aspects of pain [3,50,51,52,58,59]. The amygdala receives cortical and thalamic inputs, and the lateral/basolateral (LA/BLA) complex of the amygdala adds emotional and affective context to sensory information [50,51,52]. This information is then sent to the central nucleus of the amygdala, which comprises γ-aminobutyric aid (GABA)-ergic neurons and regulates fear and pain [50,51,52]. Preclinical studies have demonstrated that neuronal excitability is increased in the central nucleus of the amygdala in neuropathic pain [60,61].

4.4. Hippocampus

The hippocampus is part of the limbic system, which plays an important role in declarative and episodic memory [62]. The hippocampus possesses extensive nerve fiber connectivity with other brain regions involved in emotion and cognition [31,63]. It regulates the hypothalamic–pituitary–adrenal axis, which makes it vulnerable to neuropsychiatric disorders such as stress and depression [63]. Volumetric changes in the hippocampus are associated with increased risk of depressive disorders, and decreased hippocampal volumes in patients with depression have been reported [63,64].
Changes in the hippocampus have been reported in chronic pain conditions. Hippocampal neurogenesis contributes to learning and memory and may trigger the development of chronic pain. The upregulation of hippocampal neurogenesis resulted in the prolongation of persistent pain [65]. Chronic pain is generally accompanied by cognitive deficits and aversive emotional states, including depression and anxiety disorders. Functional and structural changes in the hippocampus, such as decreased hippocampal neurogenesis, are closely associated with memory deficits and aversive affective states in patients with chronic pain [31,65].

4.5. Nucleus Accumbens

The NAc is a forebrain structure that integrates cortical and affective information and assigns motivation and value for the selection of appropriate behavioral responses [43,54,55,66,67,68,69]. The NAc participates in emotional learning, evaluation of reward signals, and encoding of salience for pain [70]. Changes in NAc circuitry and connectivity are risk factors for pain chronification. A brain-imaging study reported that changes in NAc circuitry were predictive of the transition to chronicity in patients with back pain [71,72]. The transition to chronic pain is influenced by NAc plasticity.

4.6. Periaqueductal Gray Matter

The PAG is located in the brain stem and is divided into three subregions: ventrolateral, lateral, and dorsolateral [73]. The PAG plays an important role in both the ascending and descending modulation of nociception and regulates other autonomic and emotional behaviors [74]. It projects to the rostroventral medulla, which sends descending inhibitory and excitatory fibers to the dorsal horn of the spinal cord [75]. The PAG integrates information received from higher centers of the brain and receives ascending nociceptive input from the dorsal horn. The PAG regulates the processing of nociceptive information in the dorsal horn of the spinal cord and plays a critical role in the descending modulation of pain [7].

5. The Role of Neurotransmitters in Chronic Pain

Neurotransmitters are chemical substances that mediate transmission of impulses across the synapse. The transmission of neuronal signals across the synapse is initiated with the release of neurotransmitters from the presynaptic neuron. Neurotransmitters are released into the synaptic cleft and bind to neurotransmitter receptors on postsynaptic neurons. Neurotransmitters can be classified based on their function (excitatory or inhibitory), molecular size (small molecules, including amino acids and monoamines, or large molecules, including peptides), or type (inflammatory mediators, including prostaglandin E2, adenosine triphosphate, adenosine, histamine, glutamate, and nitric oxide (NO), or non-inflammatory mediators, including GABA, CGRP, peptides, glycine, and cannabinoids) [7]. The binding of neurotransmitters to their receptors on postsynaptic neurons influences pain transmission in either an inhibitory or excitatory way. Glial cells, such as microglia and astrocytes, release various neurotransmitters that contribute to the development and maintenance of chronic pain by activating or deactivating nociceptive neurons in the CNS [76,77,78].

5.1. Neuropeptides

Neuropeptides are a family of neurotransmitters that are relatively large molecules from a structural perspective. Neuropeptides constitute a diverse group of signaling molecules that are widely distributed in primary sensory neurons in the dorsal root ganglion of the spinal cord and also in the brain. Neuropeptides play various roles in the formation, transmission, modulation, and perception of different types of pain. Neuropeptides that affect pain sensitivity by modifying the activity of glial cells have been recently reported, including proopiomelanocortin (POMC)-derived peptides, neuropeptide Y, vasoactive intestinal peptide (VIP), pituitary adenylate cyclase-activating polypeptide (PACAP), somatostatin, cortistatin, tachykinins, CGRP, adrenomedullin, and ghrelin [77,79,80]. These neuropeptides bind to specific receptors expressed on microglial cells and influence pain processes, including neuroinflammation, neurodegeneration, and neuromodulation.

5.2. Glutamate

Glutamate is an excitatory neurotransmitter which plays an important role in neuronal activation. Glutamate mediates synaptic transmission of sensations such as pain and itchiness. Glutamate also participates in the generation of long-term plastic changes in the cortex and is a key player in central sensitization [11,81]. Glutamate receptors are involved in neurotransmission and plasticity at the level of the spinal cord. Once pain signals are transmitted, glutamate plays a critical role in the storage and generation of long-term memories [82]. Glutamate receptors comprise ionotropic and metabotropic subtypes. Alterations in these receptors increase synaptic strength and neuronal excitability [83]. Ionotropic glutamate receptors form an ion channel pore, which is activated when glutamate binds to the receptor, whereas metabotropic glutamate receptors indirectly activate ion channels through signaling cascades involving G proteins [81].
The ionotropic glutamate receptors include N-methyl-d-aspartate (NMDA), α-amino-3-hydroxy-5-methyl-r-isoxazoleproprionic acid (AMPA), and kainite (KA) receptors. NMDA receptors contribute to the initiation of long-term plasticity such as long-term potentiation [84], while AMPA receptors are involved in synaptic transmission and plasticity [85]. NMDA and AMPA receptors are both involved in the development of chronic pain and depression [33,86,87]. KA receptors are involved in sensory transmission at higher intensities and regulate synaptic transmission presynaptically [81]. Increased activity in the excitatory system and attenuation of the inhibitory system by glutamate induce central hyperalgesia, leading to persistent pain.

5.3. Gamma-Aminobutyric Acid (GABA)

GABA is an inhibitory neurotransmitter in the CNS that reduces neuronal excitability and regulates muscle tone. GABA is involved in pain modulation by regulating the transmission of nociceptive signals through the activation of GABA receptors located on primary afferent terminals and in the dorsal horn [88]. Stimulation of GABA receptors leads to that inhibition of voltage-gated calcium channel activity and inhibits the release of other neurotransmitters, such as glutamate, substance P, and CGRP [89]. In neuropathic and chronic inflammatory pain conditions, GABAergic inhibitory control is decreased, leading to increased excitation and central sensitization [82].

5.4. Neurotrophic Factors

Neurotrophic factors are molecules that regulate the growth of neurons and contribute to the proliferation of nociceptive axons and terminals in peripheral tissues, which may result in persistent pain conditions [90]. Among these factors, nerve growth factors (NGFs), a neurotrophin subfamily of growth factors, play a role in the development and modulation of persistent pain [91,92]. NGF is a neurotrophic factor or neuropeptide which is released locally by fibroblasts at the site of injury [7]. The binding of NGF to receptors on peripheral nociceptors triggers rapid sensitization of the nociceptive response [10,93]. NGF signaling also induces pain by promoting the sprouting of nociceptive fibers in peripheral tissues, which causes hyperinnervation [91]. Preclinical studies have reported that anti-NGF treatments can reduce markers of peripheral and central sensitization, can reverse hyper-innervation of peripheral tissues, and can mitigate pain-related behaviors [94,95,96].
Interleukin-6 (IL-6), another neurotrophic factor, is an important mediator in pain processing [91]. Following nerve injury, IL-6 is released and its levels are increased. IL-6 is involved in the development of pain and CNS sensitization [97,98]. It promotes and mediates various inflammatory pain conditions [99].
Inhibition of neurotrophic factors with the goal of developing medications to better manage chronic pain is an active area of investigation. Potential harmful effects of neurotrophic factor inhibitors in the treatment of chronic pain warrant further research.

5.5. Nitric Oxide

NO is a freely diffusible, soluble gas with a half-life of seconds [100]. NO is synthesized by nitric oxide synthase (NOS) and is primarily regulated by the expression and activity of NOS [100]. There are three different NOS isoforms: neuronal NOS (nNOS), inducible NOS (iNOS), and endothelial NOS (eNOS) [101]. Among these, nNOS is the major source of NO involved in pain processing, which occurs in the dorsal horn of the spinal cord. The number and density of nNOS in dorsal horn neurons are increased during the inflammatory process of pain induced by proinflammatory agents [101,102,103]. During neuropathic pain, nNOS expression is upregulated in the dorsal root ganglion (DRG) which leads to an increase in the number of nNOS-positive DRG neurons [101,104]. Therefore, nNOS seems to be involved in the processing of persistent inflammatory and neuropathic pain in the spinal cord. NO induces cyclic guanosine monophosphate formation in cells of the nociceptive system and activates downstream targets. While evidence suggests that the production of NO can reduce pain through its antinociceptive effects, the inhibition of NO can also reduce inflammatory and neuropathic pain [101]. Focusing on specific NO-dependent signaling mechanisms is necessary when targeting NO for the treatment of pain.

5.6. Opioid Peptides

Opioid peptides are a family of neuropeptides that bind to opioid receptors, including μ, δ, and κ receptor subtypes [105]. Opioid receptors are abundantly distributed in both primary afferent neurons and dendrites of postsynaptic neurons. Enkephalin and dynorphin are two endogenous opioid peptides that inhibit the release of excitatory neurotransmitters from afferent terminals and reduce neuronal excitability, resulting in decreased pain sensation [7]. Changes in the capacity of brain regions to respond to endogenous or exogenous opioids are related to decreased opioid receptor expression, which may underscore the lack of efficacy of opioids in chronic pain. Reduced opioid receptor availability, reflecting decreased receptor expression, contributes to the development of chronic pain [106].

5.7. Endocannabinoids

Cannabinoids are a class of neurotransmitters present in pain signal transduction pathways. After injury, neural and nonneural cells release arachidonic acid derivatives known as endocannabinoids [107]. Endocannabinoids regulate neural conduction of pain signals by attenuating sensitization and inflammation via the activation of cannabinoid receptors type 1 and type 2 (CB1 and CB2), which are located at peripheral, spinal, or supraspinal sites [108]. CB receptors modulate neuroimmune interactions and inflammatory hyperalgesia. Cannabinoids inhibit the release of presynaptic neurotransmitters and neuropeptides, modulate postsynaptic neuronal excitability, activate descending inhibitory pathways, and reduce neuro-inflammatory signaling [109,110].
Cannabis has been used throughout the world for centuries, both legally and illegally [111]. Although cannabis is usually not the first drug of choice for patients with acute pain, several studies have reported that the use of cannabinoids is significantly associated with a reduction in pain and may be an effective approach for pain management [112,113]. Long-term studies evaluating treatment effects of exogenous cannabinoids should take into consideration the efficacy, therapeutic window, dose-dependent effects, and side effects to provide support for the use of cannabinoids in pain treatment [109].

5.8. Leptin and Orexin

Leptin is a peptide produced by adipose tissue. The concentration of leptin is regulated by nutritional state. Leptin expression is increased following food intake and suppresses appetite, whereas leptin expression is decreased with fasting. Although leptin is known to be involved in the modulation of pain signals, its role in the pathogenesis of neuropathic pain is controversial. Studies using a rat model reported that leptin induced interleukin-1β production and enhanced production of pronociceptive mediators such as cyclooxygenase-2, iNOS, and matrix metalloprotrease-9, linking adipokines to the development of neuropathic pain [114,115]. However, another study reported that acute leptin administration after injury prevented the development of thermal hyperalgesia and mechanical allodynia and reduced inflammatory mediators [116]. The role of leptin should be clarified in future studies.
In addition, orexin-A and B (also known as hypocretin-1 and-2) are neuropeptides involved in the modulation of nociception. Orexin signaling in some spinal and supra-spinal sites regulates descending pain modulatory circuitry. The involvement of the orexinergic system in pain modulation suggests that orexins may be potential therapeutic targets for chronic pain treatment [117].

5.9. Melatonin

Melatonin is a hormone produced from tryptophan in the pineal gland. It is involved in the control of circadian rhythms and associated physiological responses such as sleep, anxiety, and pain [118]. The development of chronic pain syndromes is associated with the desynchronization of circadian and biological rhythms. The mechanisms underlying the analgesic effects of melatonin include the involvement of β-endorphins, GABA receptors, opioid 1-receptors, and the NO-arginine pathway [119]. Melatonin promotes anti-analgesic effects by interacting with opioidergic, benzodiazepinergic, muscarinic, nicotinic, serotonergic, and α1 and α2-adrenergic receptors [120]. Treatment with melatonin may improve conditions such as migraine, fibromyalgia, irritable bowel syndrome, preoperative anxiety, and postoperative pain [118].

6. Treatment of Chronic Pain

The prevention and treatment of chronic pain may be achievable with pharmacological and/or psychological interventions. Despite the progress made in understanding how chronic pain occurs, the development of effective drugs capable of controlling chronic pain remains a challenge. Pharmacological agents commonly used in primary care settings include gabapentin and pregabalin, which decrease calcium-mediated release of glutamate and other neurotransmitters. NMDA receptor antagonists (such as dextromethorphan and ketamine) and antidepressants (such as serotonin and norepinephrine reuptake inhibitors and tricyclic antidepressants) are also effective in the management of chronic pain conditions [13]. Other pharmacological interventions targeting a variety of ion channels, neurotransmitters, and receptors are under investigation for prevention or reversal of the reorganization of chronic pain pathways [13,121,122].
Psychological interventions for chronic pain include operant behavioral therapy, cognitive behavioral therapy, and motivational interviewing [123,124]. These approaches focus on factors that influence chronic pain, such as failure to obliterate pain responses and maladaptive learned responses. Other approaches include strategies related to maladaptive brain plasticity, such as imagery, mirror training, and virtual reality. These novel treatments aim to reverse the distorted sensory input and motor output, and to restore correct information by enhancing a coherent body image in patients with chronic pain [13,125].
Repetitive transcranial magnetic stimulation (rTMS) is a noninvasive brain stimulation technique used to reduce chronic pain by directly altering brain activity by electrical stimulation [13]. rTMS targeting the primary motor cortex reduces pain by triggering activity in descending inhibitory pathways to the dorsal horn. Additionally, rTMS is thought to exert antinociceptive effects by altering neuronal activity in the PAG matter related to pain processing. rTMS also influences the endogenous opioid system, which can control chronic pain [126,127].
Integrative strategies such as exercise, yoga, and nutrition have been suggested to have analgesic effects [128]. During and after exercise, different endogenous systems are activated and various neurotransmitters that modulate pain perception are released, resulting in increased levels of endogenous opioids, nitric oxide, serotonin, anti-inflammatory cytokines, brain-derived neurotrophic factor, and endocannabinoids [129]. The practice of yoga postures increases brain GABA levels, improves mood, and decreases anxiety [130]. Nutrition is also important for the treatment of painful and inflammatory conditions. Anti-inflammatory diets can prevent many chronic diseases that are associated with pain; nutritional interventions such as gluten- or grain-free diets or the elimination of nightshade vegetables from the diet may help to alleviate chronic pain conditions [131].
For effective treatment of chronic pain, various therapeutic approaches described above should be used in combination. However, despite the application of several therapeutic methods, some patients will experience persistent pain, which affects quality of life. To address this persistent need, efforts to identify novel therapeutic targets should be continued. Additionally, further research on the modulation of synaptic plasticity and the identification of novel neurotransmitter targets for the management of refractory chronic pain are warranted.

7. Discussion

Chronic pain is a critical medical problem worldwide, characterized by a high prevalence and significant cost. If pain becomes chronic, it can significantly reduce quality of life and cause depression, suicide, insomnia, impaired cognitive function, and other deleterious effects [15,32,36]. In order to develop appropriate therapeutic targets for chronic pain, it is important to understand factors that affect the transition of acute pain to chronic pain and the mechanisms underlying the development of chronic pain. In addition, the reasons underpinning the high comorbidity between chronic pain and negative affective states should be investigated to identify appropriate treatments.
This review provides an overview of existing knowledge on the mechanisms underlying the development of chronic pain and neural areas related to chronic pain. The development of chronic pain is associated with synaptic plasticity and changes in the CNS and various neural areas that modulate pain. Chronic pain entails structural and functional changes in corticolimbic brain regions such as the prefrontal cortex, ACC, amygdala, hippocampus, NAc, and PAC. Changes related to chronic pain can induce negative affective states such as depression, anger, and anxiety, underpinned by common neuroplasticity changes in chronic pain and negative affective states [32,38]. It is important to note that the transmission of pain signals across the synapse involves various neurotransmitters released by glial cells, such as neuropeptides, glutamate, GABA, and neurotrophic factors, which play an important role in the development of chronic pain.
We acknowledge that we have not addressed all the factors influencing the shift from acute to chronic pain and changes in areas related to pain. Pain has several important dimensions, including sensory, emotional, and cognitive dimensions. The sensory dimension of pain involves how we perceive pain signals and the amount of pain we recognize. The emotional dimension of pain indicates how we feel about experiencing pain. The cognitive dimension of pain entails how we interpret pain and how we respond to pain stimuli. In the future, correlations or interactions among these dimensions of pain should be elucidated. Future studies should investigate factors that trigger pain chronification to provide insight into how acute pain becomes chronic.

8. Conclusions

Chronic pain is one of the most intractable clinical problems faced by clinicians and can be physically and emotionally debilitating. Combinations of treatments are currently used for treating chronic pain, but a subset of patients experience persistent non-endurable pain. Therefore, deeper understanding of the mechanisms and key factors involved in pain chronification is necessary to identify novel therapeutic targets for developing better treatments for chronic pain.

Author Contributions

Conceptualization, M.C.C. and S.Y.; methodology, S.Y.; investigation, M.C.C. and S.Y.; writing—original draft preparation, M.C.C. and S.Y.; writing—review and editing, S.Y.; supervision, M.C.C.

Funding

This research was supported by Dr.Ahn’s Rehabilitation Clinic (grant number: 219C000425).

Conflicts of Interest

The authors declare no conflict of interest. The funder had no role in the design of the study; in the collection, analyses, or interpretating of data; in the writing of the manuscript, or in the decision to publish the results.

Abbreviations

CNS central nervous system
CGRPcalcitonin gene-related peptide
PAGperiaqueductal gray matter
NAcnucleus accumbens
RVMrostral ventromedial medulla
NMDAN-methyl-D-aspartate
ACCanterior cingulate cortex
PFCprefrontal cortex
VTAventral tegmental area
mPFCmedial prefrontal cortex
LA/BLAlateral/basolateral complex of the amygdala
GABAgamma-aminobutyric aid
NOnitric oxide
POMCproopiomelanocortin
VIPvasoactive intestinal peptide
PACAPpituitary adenylate cyclase-activating polypeptide
AMPAα-amino-3-hydroxy-5-methyl-r-isoxazoleproprionic acid
KAkainite
NGFnerve growth factor
IL-6interleukin-6
NOSnitric oxide synthase
nNOSneuronal nitric oxide synthase
iNOSinducible nitric oxide synthase
eNOSendothelial nitric oxide synthase
CB1/CB2cannabinoid receptors type 1 and type 2
rTMSrepetitive transcranial magnetic stimulation

References

  1. Tsang, A.; Von Korff, M.; Lee, S.; Alonso, J.; Karam, E.; Angermeyer, M.C.; Borges, G.L.; Bromet, E.J.; Demytteneare, K.; de Girolamo, G.; et al. Common chronic pain conditions in developed and developing countries: Gender and age differences and comorbidity with depression-anxiety disorders. J. Pain 2008, 9, 883–891. [Google Scholar] [CrossRef] [PubMed]
  2. GBD 2015 Disease and Injury Incidence and Prevalence Collaborators. Global, regional, and national incidence, prevalence, and years lived with disability for 310 diseases and injuries, 1990–2015: A systematic analysis for the Global Burden of Disease Study 2015. Lancet 2016, 388, 1545–1602.
  3. Vachon-Presseau, E.; Centeno, M.V.; Ren, W.; Berger, S.E.; Tetreault, P.; Ghantous, M.; Baria, A.; Farmer, M.; Baliki, M.N.; Schnitzer, T.J.; et al. The Emotional Brain as a Predictor and Amplifier of Chronic Pain. J. Dent. Res. 2016, 95, 605–612. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Treede, R.D.; Rief, W.; Barke, A.; Aziz, Q.; Bennett, M.I.; Benoliel, R.; Cohen, M.; Evers, S.; Finnerup, N.B.; First, M.B.; et al. A classification of chronic pain for ICD-11. Pain 2015, 156, 1003–1007. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Tracey, I.; Bushnell, M.C. How neuroimaging studies have challenged us to rethink: Is chronic pain a disease? J. Pain 2009, 10, 1113–1120. [Google Scholar] [CrossRef] [PubMed]
  6. Seminowicz, D.A.; Moayedi, M. The Dorsolateral Prefrontal Cortex in Acute and Chronic Pain. J. Pain 2017, 18, 1027–1035. [Google Scholar] [CrossRef] [PubMed]
  7. Yam, M.F.; Loh, Y.C.; Tan, C.S.; Khadijah Adam, S.; Abdul Manan, N.; Basir, R. General Pathways of Pain Sensation and the Major Neurotransmitters Involved in Pain Regulation. Int. J. Mol. Sci. 2018, 19. [Google Scholar] [CrossRef] [PubMed]
  8. Reddi, D.; Curran, N.; Stephens, R. An introduction to pain pathways and mechanisms. Br. J. Hosp. Med. (Lond.) 2013, 74, C188–C191. [Google Scholar] [CrossRef]
  9. Bourne, S.; Machado, A.G.; Nagel, S.J. Basic anatomy and physiology of pain pathways. Neurosurg. Clin. N. Am. 2014, 25, 629–638. [Google Scholar] [CrossRef]
  10. Dubin, A.E.; Patapoutian, A. Nociceptors: The sensors of the pain pathway. J. Clin. Investig. 2010, 120, 3760–3772. [Google Scholar] [CrossRef]
  11. Zhuo, M. Cortical excitation and chronic pain. Trends Neurosci. 2008, 31, 199–207. [Google Scholar] [CrossRef] [PubMed]
  12. Cata, J.P.; Weng, H.R.; Chen, J.H.; Dougherty, P.M. Altered discharges of spinal wide dynamic range neurons and down-regulation of glutamate transporter expression in rats with paclitaxel-induced hyperalgesia. Neuroscience 2006, 138, 329–338. [Google Scholar] [CrossRef] [PubMed]
  13. McCarberg, B.; Peppin, J. Pain Pathways and Nervous System Plasticity: Learning and Memory in Pain. Pain Med. 2019. [Google Scholar] [CrossRef] [PubMed]
  14. Price, D.D. Psychological and neural mechanisms of the affective dimension of pain. Science 2000, 288, 1769–1772. [Google Scholar] [CrossRef] [PubMed]
  15. Apkarian, A.V.; Bushnell, M.C.; Treede, R.D.; Zubieta, J.K. Human brain mechanisms of pain perception and regulation in health and disease. Eur. J. Pain 2005, 9, 463–484. [Google Scholar] [CrossRef] [PubMed]
  16. Bushnell, M.C.; Ceko, M.; Low, L.A. Cognitive and emotional control of pain and its disruption in chronic pain. Nat. Rev. Neurosci. 2013, 14, 502–511. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Leknes, S.; Tracey, I. A common neurobiology for pain and pleasure. Nat. Rev. Neurosci. 2008, 9, 314–320. [Google Scholar] [CrossRef]
  18. Liang, M.; Mouraux, A.; Hu, L.; Iannetti, G.D. Primary sensory cortices contain distinguishable spatial patterns of activity for each sense. Nat. Commun. 2013, 4, 1979. [Google Scholar] [CrossRef]
  19. Chen, Q.; Heinricher, M.M. Descending Control Mechanisms and Chronic Pain. Curr. Rheumatol. Rep. 2019, 21, 13. [Google Scholar] [CrossRef]
  20. Ren, K.; Dubner, R. Neuron-glia crosstalk gets serious: Role in pain hypersensitivity. Curr. Opin. Anaesthesiol. 2008, 21, 570–579. [Google Scholar] [CrossRef]
  21. Tiwari, V.; Guan, Y.; Raja, S.N. Modulating the delicate glial-neuronal interactions in neuropathic pain: Promises and potential caveats. Neurosci. Biobehav. Rev. 2014, 45, 19–27. [Google Scholar] [CrossRef] [PubMed]
  22. Kuner, R. Central mechanisms of pathological pain. Nat. Med. 2010, 16, 1258–1266. [Google Scholar] [CrossRef] [PubMed]
  23. Yaksh, T.L.; Woller, S.A.; Ramachandran, R.; Sorkin, L.S. The search for novel analgesics: Targets and mechanisms. F1000prime Rep. 2015, 7, 56. [Google Scholar] [CrossRef] [PubMed]
  24. Latremoliere, A.; Woolf, C.J. Central sensitization: A generator of pain hypersensitivity by central neural plasticity. J. Pain 2009, 10, 895–926. [Google Scholar] [CrossRef] [PubMed]
  25. Becker, S.; Gandhi, W.; Schweinhardt, P. Cerebral interactions of pain and reward and their relevance for chronic pain. Neurosci. Lett. 2012, 520, 182–187. [Google Scholar] [CrossRef] [PubMed]
  26. Navratilova, E.; Morimura, K.; Xie, J.Y.; Atcherley, C.W.; Ossipov, M.H.; Porreca, F. Positive emotions and brain reward circuits in chronic pain. J. Comp. Neurol. 2016, 524, 1646–1652. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Baliki, M.N.; Petre, B.; Torbey, S.; Herrmann, K.M.; Huang, L.; Schnitzer, T.J.; Fields, H.L.; Apkarian, A.V. Corticostriatal functional connectivity predicts transition to chronic back pain. Nat. Neurosci. 2012, 15, 1117–1119. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Hashmi, J.A.; Baliki, M.N.; Huang, L.; Baria, A.T.; Torbey, S.; Hermann, K.M.; Schnitzer, T.J.; Apkarian, A.V. Shape shifting pain: Chronification of back pain shifts brain representation from nociceptive to emotional circuits. Brain 2013, 136, 2751–2768. [Google Scholar] [CrossRef]
  29. Mutso, A.A.; Radzicki, D.; Baliki, M.N.; Huang, L.; Banisadr, G.; Centeno, M.V.; Radulovic, J.; Martina, M.; Miller, R.J.; Apkarian, A.V. Abnormalities in hippocampal functioning with persistent pain. J. Neurosci. 2012, 32, 5747–5756. [Google Scholar] [CrossRef]
  30. Schmidt-Wilcke, T.; Ganssbauer, S.; Neuner, T.; Bogdahn, U.; May, A. Subtle grey matter changes between migraine patients and healthy controls. Cephalalgia 2008, 28, 1–4. [Google Scholar] [CrossRef]
  31. Thompson, J.M.; Neugebauer, V. Cortico-limbic pain mechanisms. Neurosci. Lett. 2019. [Google Scholar] [CrossRef] [PubMed]
  32. Bair, M.J.; Robinson, R.L.; Katon, W.; Kroenke, K. Depression and pain comorbidity: A literature review. Arch. Intern. Med. 2003, 163, 2433–2445. [Google Scholar] [CrossRef] [PubMed]
  33. Sheng, J.; Liu, S.; Wang, Y.; Cui, R.; Zhang, X. The Link between Depression and Chronic Pain: Neural Mechanisms in the Brain. Neural Plast. 2017, 2017, 9724371. [Google Scholar] [CrossRef] [PubMed]
  34. Haase, J.; Brown, E. Integrating the monoamine, neurotrophin and cytokine hypotheses of depression—A central role for the serotonin transporter? Pharmacol. Ther. 2015, 147, 1–11. [Google Scholar] [CrossRef] [PubMed]
  35. Meerwijk, E.L.; Ford, J.M.; Weiss, S.J. Brain regions associated with psychological pain: Implications for a neural network and its relationship to physical pain. Brain Imaging Behav. 2013, 7, 1–14. [Google Scholar] [CrossRef] [PubMed]
  36. Elman, I.; Borsook, D.; Volkow, N.D. Pain and suicidality: Insights from reward and addiction neuroscience. Prog. Neurobiol. 2013, 109, 1–27. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Fishbain, D.A.; Lewis, J.E.; Gao, J. The pain suicidality association: A narrative review. Pain Med. 2014, 15, 1835–1849. [Google Scholar] [CrossRef]
  38. Racine, M. Chronic pain and suicide risk: A comprehensive review. Prog. Neuro-Psychopharmacol. Biol. Psychiatry 2018, 87, 269–280. [Google Scholar] [CrossRef]
  39. Llorca-Torralba, M.; Suarez-Pereira, I.; Bravo, L.; Camarena-Delgado, C.; Garcia-Partida, J.A.; Mico, J.A.; Berrocoso, E. Chemogenetic Silencing of the Locus Coeruleus-Basolateral Amygdala Pathway Abolishes Pain-Induced Anxiety and Enhanced Aversive Learning in Rats. Biol. Psychiatry 2019, 85, 1021–1035. [Google Scholar] [CrossRef]
  40. Wu, Y.; Yao, X.; Jiang, Y.; He, X.; Shao, X.; Du, J.; Shen, Z.; He, Q.; Fang, J. Pain aversion and anxiety-like behavior occur at different times during the course of chronic inflammatory pain in rats. J. Pain Res. 2017, 10, 2585–2593. [Google Scholar] [CrossRef]
  41. Finnerup, N.B.; Sindrup, S.H.; Jensen, T.S. The evidence for pharmacological treatment of neuropathic pain. Pain 2010, 150, 573–581. [Google Scholar] [CrossRef] [PubMed]
  42. Backonja, M.M.; Irving, G.; Argoff, C. Rational multidrug therapy in the treatment of neuropathic pain. Curr. Pain Headache Rep. 2006, 10, 34–38. [Google Scholar] [CrossRef] [PubMed]
  43. Apkarian, A.V.; Baliki, M.N.; Geha, P.Y. Towards a theory of chronic pain. Prog. Neurobiol. 2009, 87, 81–97. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Mansour, A.R.; Farmer, M.A.; Baliki, M.N.; Apkarian, A.V. Chronic pain: The role of learning and brain plasticity. Restor. Neurol. Neurosci. 2014, 32, 129–139. [Google Scholar] [PubMed] [Green Version]
  45. Kang, D.; McAuley, J.H.; Kassem, M.S.; Gatt, J.M.; Gustin, S.M. What does the grey matter decrease in the medial prefrontal cortex reflect in people with chronic pain? Eur. J. Pain 2019, 23, 203–219. [Google Scholar] [CrossRef] [PubMed]
  46. Ji, G.; Neugebauer, V. CB1 augments mGluR5 function in medial prefrontal cortical neurons to inhibit amygdala hyperactivity in an arthritis pain model. Eur. J. Neurosci. 2014, 39, 455–466. [Google Scholar] [CrossRef]
  47. Ji, G.; Sun, H.; Fu, Y.; Li, Z.; Pais-Vieira, M.; Galhardo, V.; Neugebauer, V. Cognitive impairment in pain through amygdala-driven prefrontal cortical deactivation. J. Neurosci. 2010, 30, 5451–5464. [Google Scholar] [CrossRef]
  48. Becerra, L.; Navratilova, E.; Porreca, F.; Borsook, D. Analogous responses in the nucleus accumbens and cingulate cortex to pain onset (aversion) and offset (relief) in rats and humans. J. Neurophysiol. 2013, 110, 1221–1226. [Google Scholar] [CrossRef] [Green Version]
  49. Navratilova, E.; Atcherley, C.W.; Porreca, F. Brain Circuits Encoding Reward from Pain Relief. Trends Neurosci. 2015, 38, 741–750. [Google Scholar] [CrossRef] [Green Version]
  50. Neugebauer, V. Amygdala pain mechanisms. Handb. Exp. Pharmacol. 2015, 227, 261–284. [Google Scholar]
  51. Neugebauer, V.; Galhardo, V.; Maione, S.; Mackey, S.C. Forebrain pain mechanisms. Brain Res. Rev. 2009, 60, 226–242. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Thompson, J.M.; Neugebauer, V. Amygdala Plasticity and Pain. Pain Res. Manag. 2017, 2017, 8296501. [Google Scholar] [CrossRef] [PubMed]
  53. Williams, D.J.; Crossman, A.R.; Slater, P. The efferent projections of the nucleus accumbens in the rat. Brain Res. 1977, 130, 217–227. [Google Scholar] [CrossRef]
  54. Baliki, M.N.; Apkarian, A.V. Nociception, Pain, Negative Moods, and Behavior Selection. Neuron 2015, 87, 474–491. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Baliki, M.N.; Chialvo, D.R.; Geha, P.Y.; Levy, R.M.; Harden, R.N.; Parrish, T.B.; Apkarian, A.V. Chronic pain and the emotional brain: Specific brain activity associated with spontaneous fluctuations of intensity of chronic back pain. J. Neurosci. 2006, 26, 12165–12173. [Google Scholar] [CrossRef] [PubMed]
  56. Villemure, C.; Bushnell, M.C. Mood influences supraspinal pain processing separately from attention. J. Neurosci. 2009, 29, 705–715. [Google Scholar] [CrossRef] [PubMed]
  57. Kato, F.; Sugimura, Y.K.; Takahashi, Y. Pain-Associated Neural Plasticity in the Parabrachial to Central Amygdala Circuit: Pain Changes the Brain, and the Brain Changes the Pain. Adv. Exp. Med. Biol. 2018, 1099, 157–166. [Google Scholar] [PubMed]
  58. Simons, L.E.; Moulton, E.A.; Linnman, C.; Carpino, E.; Becerra, L.; Borsook, D. The human amygdala and pain: Evidence from neuroimaging. Hum. Brain Mapp. 2014, 35, 527–538. [Google Scholar] [CrossRef]
  59. Simons, L.E.; Pielech, M.; Erpelding, N.; Linnman, C.; Moulton, E.; Sava, S.; Lebel, A.; Serrano, P.; Sethna, N.; Berde, C.; et al. The responsive amygdala: Treatment-induced alterations in functional connectivity in pediatric complex regional pain syndrome. Pain 2014, 155, 1727–1742. [Google Scholar] [CrossRef] [Green Version]
  60. Ikeda, R.; Takahashi, Y.; Inoue, K.; Kato, F. NMDA receptor-independent synaptic plasticity in the central amygdala in the rat model of neuropathic pain. Pain 2007, 127, 161–172. [Google Scholar] [CrossRef]
  61. Nakao, A.; Takahashi, Y.; Nagase, M.; Ikeda, R.; Kato, F. Role of capsaicin-sensitive C-fiber afferents in neuropathic pain-induced synaptic potentiation in the nociceptive amygdala. Mol. Pain 2012, 8, 51. [Google Scholar] [CrossRef] [PubMed]
  62. Eichenbaum, H. Memory: Organization and Control. Annu. Rev. Psychol. 2017, 68, 19–45. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  63. Liu, W.; Ge, T.; Leng, Y.; Pan, Z.; Fan, J.; Yang, W.; Cui, R. The Role of Neural Plasticity in Depression: From Hippocampus to Prefrontal Cortex. Neural Plast. 2017, 2017, 6871089. [Google Scholar] [CrossRef] [PubMed]
  64. Chan, S.W.; Harmer, C.J.; Norbury, R.; O’Sullivan, U.; Goodwin, G.M.; Portella, M.J. Hippocampal volume in vulnerability and resilience to depression. J. Affect. Disord. 2016, 189, 199–202. [Google Scholar] [CrossRef] [PubMed]
  65. Apkarian, A.V.; Mutso, A.A.; Centeno, M.V.; Kan, L.; Wu, M.; Levinstein, M.; Banisadr, G.; Gobeske, K.T.; Miller, R.J.; Radulovic, J.; et al. Role of adult hippocampal neurogenesis in persistent pain. Pain 2016, 157, 418–428. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. Apkarian, A.V. Pain perception in relation to emotional learning. Curr. Opin. Neurobiol. 2008, 18, 464–468. [Google Scholar] [CrossRef] [Green Version]
  67. Floresco, S.B. The nucleus accumbens: An interface between cognition, emotion, and action. Annu. Rev. Psychol. 2015, 66, 25–52. [Google Scholar] [CrossRef]
  68. Ito, R.; Hayen, A. Opposing roles of nucleus accumbens core and shell dopamine in the modulation of limbic information processing. J. Neurosci. 2011, 31, 6001–6007. [Google Scholar] [CrossRef]
  69. Salgado, S.; Kaplitt, M.G. The Nucleus Accumbens: A Comprehensive Review. Stereotact. Funct. Neurosurg. 2015, 93, 75–93. [Google Scholar] [CrossRef]
  70. Chang, P.C.; Pollema-Mays, S.L.; Centeno, M.V.; Procissi, D.; Contini, M.; Baria, A.T.; Martina, M.; Apkarian, A.V. Role of nucleus accumbens in neuropathic pain: Linked multi-scale evidence in the rat transitioning to neuropathic pain. Pain 2014, 155, 1128–1139. [Google Scholar] [CrossRef] [Green Version]
  71. Apkarian, A.V.; Baliki, M.N.; Farmer, M.A. Predicting transition to chronic pain. Curr. Opin. Neurol. 2013, 26, 360–367. [Google Scholar] [CrossRef] [PubMed]
  72. Vachon-Presseau, E.; Tetreault, P.; Petre, B.; Huang, L.; Berger, S.E.; Torbey, S.; Baria, A.T.; Mansour, A.R.; Hashmi, J.A.; Griffith, J.W.; et al. Corticolimbic anatomical characteristics predetermine risk for chronic pain. Brain 2016, 139, 1958–1970. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  73. Hemington, K.S.; Coulombe, M.A. The periaqueductal gray and descending pain modulation: Why should we study them and what role do they play in chronic pain? J. Neurophysiol. 2015, 114, 2080–2083. [Google Scholar] [CrossRef] [PubMed]
  74. Holstege, G. The periaqueductal gray controls brainstem emotional motor systems including respiration. Prog. Brain Res. 2014, 209, 379–405. [Google Scholar] [PubMed]
  75. Millan, M.J. Descending control of pain. Prog. Neurobiol. 2002, 66, 355–474. [Google Scholar] [CrossRef]
  76. Ji, R.R.; Suter, M.R. p38 MAPK, microglial signaling, and neuropathic pain. Mol. Pain 2007, 3, 33. [Google Scholar] [CrossRef]
  77. Carniglia, L.; Ramirez, D.; Durand, D.; Saba, J.; Turati, J.; Caruso, C.; Scimonelli, T.N.; Lasaga, M. Neuropeptides and Microglial Activation in Inflammation, Pain, and Neurodegenerative Diseases. Mediat. Inflamm. 2017, 2017, 5048616. [Google Scholar] [CrossRef] [PubMed]
  78. Ji, R.R.; Berta, T.; Nedergaard, M. Glia and pain: Is chronic pain a gliopathy? Pain 2013, 154, S10–S28. [Google Scholar] [CrossRef] [PubMed]
  79. Diaz-delCastillo, M.; Woldbye, D.P.D.; Heegaard, A.M. Neuropeptide Y and its Involvement in Chronic Pain. Neuroscience 2018, 387, 162–169. [Google Scholar] [CrossRef] [Green Version]
  80. Zieglgansberger, W. Substance P and pain chronicity. Cell Tissue Res. 2019, 375, 227–241. [Google Scholar] [CrossRef]
  81. Zhuo, M. Ionotropic glutamate receptors contribute to pain transmission and chronic pain. Neuropharmacology 2017, 112, 228–234. [Google Scholar] [CrossRef] [PubMed]
  82. Malcangio, M. GABAB receptors and pain. Neuropharmacology 2018, 136, 102–105. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  83. Sheng, N.; Bemben, M.A.; Diaz-Alonso, J.; Tao, W.; Shi, Y.S.; Nicoll, R.A. LTP requires postsynaptic PDZ-domain interactions with glutamate receptor/auxiliary protein complexes. Proc. Natl. Acad. Sci. USA 2018, 115, 3948–3953. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  84. Collingridge, G.L.; Bliss, T.V. Memories of NMDA receptors and LTP. Trends Neurosci. 1995, 18, 54–56. [Google Scholar] [CrossRef]
  85. Anggono, V.; Huganir, R.L. Regulation of AMPA receptor trafficking and synaptic plasticity. Curr. Opin. Neurobiol. 2012, 22, 461–469. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  86. Yao, L.; Zhou, Q. Enhancing NMDA Receptor Function: Recent Progress on Allosteric Modulators. Neural. Plast. 2017, 2017, 2875904. [Google Scholar] [CrossRef] [PubMed]
  87. Zanos, P.; Moaddel, R.; Morris, P.J.; Georgiou, P.; Fischell, J.; Elmer, G.I.; Alkondon, M.; Yuan, P.; Pribut, H.J.; Singh, N.S.; et al. NMDAR inhibition-independent antidepressant actions of ketamine metabolites. Nature 2016, 533, 481–486. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  88. Calver, A.R.; Medhurst, A.D.; Robbins, M.J.; Charles, K.J.; Evans, M.L.; Harrison, D.C.; Stammers, M.; Hughes, S.A.; Hervieu, G.; Couve, A.; et al. The expression of GABA(B1) and GABA(B2) receptor subunits in the cNS differs from that in peripheral tissues. Neuroscience 2000, 100, 155–170. [Google Scholar] [CrossRef]
  89. Bowery, N.G. GABAB receptor: A site of therapeutic benefit. Curr. Opin. Pharmacol. 2006, 6, 37–43. [Google Scholar] [CrossRef]
  90. Skaper, S.D. Neurotrophic Factors: An Overview. Methods Mol. Biol. 2018, 1727, 1–17. [Google Scholar]
  91. Kelleher, J.H.; Tewari, D.; McMahon, S.B. Neurotrophic factors and their inhibitors in chronic pain treatment. Neurobiol. Dis. 2017, 97, 127–138. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  92. Bjurstrom, M.F.; Giron, S.E.; Griffis, C.A. Cerebrospinal Fluid Cytokines and Neurotrophic Factors in Human Chronic Pain Populations: A Comprehensive Review. Pain Pract. 2016, 16, 183–203. [Google Scholar] [CrossRef] [PubMed]
  93. Patapoutian, A.; Tate, S.; Woolf, C.J. Transient receptor potential channels: Targeting pain at the source. Nat. Rev. Drug Discov. 2009, 8, 55–68. [Google Scholar] [CrossRef]
  94. Jimenez-Andrade, J.M.; Ghilardi, J.R.; Castaneda-Corral, G.; Kuskowski, M.A.; Mantyh, P.W. Preventive or late administration of anti-NGF therapy attenuates tumor-induced nerve sprouting, neuroma formation, and cancer pain. Pain 2011, 152, 2564–2574. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  95. McCaffrey, G.; Thompson, M.L.; Majuta, L.; Fealk, M.N.; Chartier, S.; Longo, G.; Mantyh, P.W. NGF blockade at early times during bone cancer development attenuates bone destruction and increases limb use. Cancer Res. 2014, 74, 7014–7023. [Google Scholar] [CrossRef] [PubMed]
  96. Sevcik, M.A.; Ghilardi, J.R.; Peters, C.M.; Lindsay, T.H.; Halvorson, K.G.; Jonas, B.M.; Kubota, K.; Kuskowski, M.A.; Boustany, L.; Shelton, D.L.; et al. Anti-NGF therapy profoundly reduces bone cancer pain and the accompanying increase in markers of peripheral and central sensitization. Pain 2005, 115, 128–141. [Google Scholar] [CrossRef]
  97. Moalem, G.; Tracey, D.J. Immune and inflammatory mechanisms in neuropathic pain. Brain Res. Rev. 2006, 51, 240–264. [Google Scholar] [CrossRef]
  98. Scholz, J.; Woolf, C.J. The neuropathic pain triad: Neurons, immune cells and glia. Nat. Neurosci. 2007, 10, 1361–1368. [Google Scholar] [CrossRef]
  99. De Jongh, R.F.; Vissers, K.C.; Meert, T.F.; Booij, L.H.; De Deyne, C.S.; Heylen, R.J. The role of interleukin-6 in nociception and pain. Anesth. Analg. 2003, 96, 1096–1103, table of contents. [Google Scholar] [CrossRef]
  100. Chen, S.R.; Jin, X.G.; Pan, H.L. Endogenous nitric oxide inhibits spinal NMDA receptor activity and pain hypersensitivity induced by nerve injury. Neuropharmacology 2017, 125, 156–165. [Google Scholar] [CrossRef]
  101. Schmidtko, A. Nitric oxide-mediated pain processing in the spinal cord. Handb. Exp. Pharmacol. 2015, 227, 103–117. [Google Scholar] [PubMed]
  102. Chu, Y.C.; Guan, Y.; Skinner, J.; Raja, S.N.; Johns, R.A.; Tao, Y.X. Effect of genetic knockout or pharmacologic inhibition of neuronal nitric oxide synthase on complete Freund’s adjuvant-induced persistent pain. Pain 2005, 119, 113–123. [Google Scholar] [CrossRef] [PubMed]
  103. Maihofner, C.; Euchenhofer, C.; Tegeder, I.; Beck, K.F.; Pfeilschifter, J.; Geisslinger, G. Regulation and immunhistochemical localization of nitric oxide synthases and soluble guanylyl cyclase in mouse spinal cord following nociceptive stimulation. Neurosci. Lett. 2000, 290, 71–75. [Google Scholar] [CrossRef]
  104. Guan, Y.; Yaster, M.; Raja, S.N.; Tao, Y.X. Genetic knockout and pharmacologic inhibition of neuronal nitric oxide synthase attenuate nerve injury-induced mechanical hypersensitivity in mice. Mol. Pain 2007, 3, 29. [Google Scholar] [CrossRef] [PubMed]
  105. Azzam, A.A.H.; McDonald, J.; Lambert, D.G. Hot topics in opioid pharmacology: Mixed and biased opioids. Br. J. Anaesth. 2019, 122, e136–e145. [Google Scholar] [CrossRef] [PubMed]
  106. Brown, C.A.; Matthews, J.; Fairclough, M.; McMahon, A.; Barnett, E.; Al-Kaysi, A.; El-Deredy, W.; Jones, A.K. Striatal opioid receptor availability is related to acute and chronic pain perception in arthritis: Does opioid adaptation increase resilience to chronic pain? Pain 2015, 156, 2267–2275. [Google Scholar] [CrossRef] [PubMed]
  107. Piomelli, D.; Sasso, O. Peripheral gating of pain signals by endogenous lipid mediators. Nat. Neurosci. 2014, 17, 164–174. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  108. Rice, A.S. Cannabinoids and pain. Curr. Opin. Investig. Drugs. 2001, 2, 399–414. [Google Scholar]
  109. Jimenez, X.F. Cannabis for chronic pain: Not a simple solution. Clevel. Clin. J. Med. 2018, 85, 950–952. [Google Scholar] [CrossRef]
  110. Starowicz, K.; Finn, D.P. Cannabinoids and Pain: Sites and Mechanisms of Action. In Advances in Pharmacology; Academic Press: Cambridge, MA, USA, 2017; Volume 80, pp. 437–475. [Google Scholar]
  111. Hill, K.P.; Palastro, M.D.; Johnson, B.; Ditre, J.W. Cannabis and Pain: A Clinical Review. Cannabis Cannabinoid Res. 2017, 2, 96–104. [Google Scholar] [CrossRef] [Green Version]
  112. Hill, K.P. Medical Marijuana for Treatment of Chronic Pain and Other Medical and Psychiatric Problems: A Clinical Review. JAMA 2015, 313, 2474–2483. [Google Scholar] [CrossRef] [PubMed]
  113. Whiting, P.F.; Wolff, R.F.; Deshpande, S.; Di Nisio, M.; Duffy, S.; Hernandez, A.V.; Keurentjes, J.C.; Lang, S.; Misso, K.; Ryder, S.; et al. Cannabinoids for Medical Use: A Systematic Review and Meta-analysis. JAMA 2015, 313, 2456–2473. [Google Scholar] [CrossRef] [PubMed]
  114. Lim, G.; Wang, S.; Zhang, Y.; Tian, Y.; Mao, J. Spinal leptin contributes to the pathogenesis of neuropathic pain in rodents. J. Clin. Investig. 2009, 119, 295–304. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  115. Maeda, T.; Kiguchi, N.; Kobayashi, Y.; Ikuta, T.; Ozaki, M.; Kishioka, S. Leptin derived from adipocytes in injured peripheral nerves facilitates development of neuropathic pain via macrophage stimulation. Proc. Natl. Acad. Sci. USA 2009, 106, 13076–13081. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  116. Fernandez-Martos, C.M.; Gonzalez, P.; Rodriguez, F.J. Acute leptin treatment enhances functional recovery after spinal cord injury. PLoS ONE 2012, 7, e35594. [Google Scholar] [CrossRef]
  117. Pourreza, P.; Babapour, V.; Haghparast, A. Role of dorsal hippocampal orexin-1 receptors in modulation of antinociception induced by chemical stimulation of the lateral hypothalamus. Physiol. Behav. 2018, 185, 79–86. [Google Scholar] [CrossRef] [PubMed]
  118. Chen, W.W.; Zhang, X.; Huang, W.J. Pain control by melatonin: Physiological and pharmacological effects. Exp. Ther. Med. 2016, 12, 1963–1968. [Google Scholar] [CrossRef]
  119. Marseglia, L.; D’Angelo, G.; Manti, S.; Aversa, S.; Arrigo, T.; Reiter, R.J.; Gitto, E. Analgesic, anxiolytic and anaesthetic effects of melatonin: New potential uses in pediatrics. Int. J. Mol. Sci. 2015, 16, 1209–1220. [Google Scholar] [CrossRef]
  120. Srinivasan, V.; Lauterbach, E.C.; Ho, K.Y.; Acuna-Castroviejo, D.; Zakaria, R.; Brzezinski, A. Melatonin in antinociception: Its therapeutic applications. Curr. Neuropharmacol. 2012, 10, 167–178. [Google Scholar] [CrossRef]
  121. Salat, K.; Kowalczyk, P.; Gryzlo, B.; Jakubowska, A.; Kulig, K. New investigational drugs for the treatment of neuropathic pain. Expert Opin. Investig. Drugs 2014, 23, 1093–1104. [Google Scholar] [CrossRef]
  122. Schaible, H.G. Emerging concepts of pain therapy based on neuronal mechanisms. Handb. Exp. Pharmacol. 2015, 227, 1–14. [Google Scholar] [PubMed]
  123. Molton, I.R.; Graham, C.; Stoelb, B.L.; Jensen, M.P. Current psychological approaches to the management of chronic pain. Curr. Opin. Anaesthesiol. 2007, 20, 485–489. [Google Scholar] [CrossRef] [PubMed]
  124. Osborne, T.L.; Raichle, K.A.; Jensen, M.P. Psychologic interventions for chronic pain. Phys. Med. Rehabil. Clin. N. Am. 2006, 17, 415–433. [Google Scholar] [CrossRef] [PubMed]
  125. Mouraux, D.; Brassinne, E.; Sobczak, S.; Nonclercq, A.; Warzee, N.; Sizer, P.S.; Tuna, T.; Penelle, B. 3D augmented reality mirror visual feedback therapy applied to the treatment of persistent, unilateral upper extremity neuropathic pain: A preliminary study. J. Man. Manip. Ther. 2017, 25, 137–143. [Google Scholar] [CrossRef] [PubMed]
  126. Hsu, J.H.; Daskalakis, Z.J.; Blumberger, D.M. An Update on Repetitive Transcranial Magnetic Stimulation for the Treatment of Co-morbid Pain and Depressive Symptoms. Curr. Pain Headache Rep. 2018, 22, 51. [Google Scholar] [CrossRef] [PubMed]
  127. Choi, G.S.; Kwak, S.G.; Lee, H.D.; Chang, M.C. Effect of high-frequency repetitive transcranial magnetic stimulation on chronic central pain after mild traumatic brain injury: A pilot study. J. Rehabil. Med. 2018, 50, 246–252. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  128. Bonakdar, R.A. Integrative Pain Management. Med. Clin. N. Am. 2017, 101, 987–1004. [Google Scholar] [CrossRef] [PubMed]
  129. Da Silva Santos, R.; Galdino, G. Endogenous systems involved in exercise-induced analgesia. J. Physiol. Pharmacol. 2018, 69, 3–13. [Google Scholar] [PubMed]
  130. Streeter, C.C.; Whitfield, T.H.; Owen, L.; Rein, T.; Karri, S.K.; Yakhkind, A.; Perlmutter, R.; Prescot, A.; Renshaw, P.F.; Ciraulo, D.A.; et al. Effects of yoga versus walking on mood, anxiety, and brain GABA levels: A randomized controlled MRS study. J. Altern. Complement. Med. 2010, 16, 1145–1152. [Google Scholar] [CrossRef]
  131. Tick, H. Nutrition and pain. Phys. Med. Rehabil. Clin. N. Am. 2015, 26, 309–320. [Google Scholar] [CrossRef]
Ijms 20 03130 g001 550
Figure 1. Ascending pathway (red line): A nerve pathway that projects upwards from the spinal cord to the brain carrying sensory information from the body to the brain. Pain signals ascend from the spinal dorsal horn to the rostral ventral medulla (RVM) and periaqueductal grey matter (PAG). Pain signals are then transmitted to the thalamus, where they are sent to higher brain centers, such as the primary and secondary somatosensory cortices (S1/S2), prefrontal cortex (PFC), anterior cortex (ACC), amygdala (AMG), and nucleus accumbens (NAc). Descending pathway (blue line): A nerve pathway that descends down the spinal cord and has a role in the modulation of pain, involving important areas of the brainstem such as the RVM, PAG, and locus coeruleus (LC).
Figure 1. Ascending pathway (red line): A nerve pathway that projects upwards from the spinal cord to the brain carrying sensory information from the body to the brain. Pain signals ascend from the spinal dorsal horn to the rostral ventral medulla (RVM) and periaqueductal grey matter (PAG). Pain signals are then transmitted to the thalamus, where they are sent to higher brain centers, such as the primary and secondary somatosensory cortices (S1/S2), prefrontal cortex (PFC), anterior cortex (ACC), amygdala (AMG), and nucleus accumbens (NAc). Descending pathway (blue line): A nerve pathway that descends down the spinal cord and has a role in the modulation of pain, involving important areas of the brainstem such as the RVM, PAG, and locus coeruleus (LC).
Ijms 20 03130 g001
Table
Table 1. Corticolimbic structures associated with chronic pain.
Table 1. Corticolimbic structures associated with chronic pain.
Brain StructuresLocationFunction
Medial prefrontal cortexLocated in the frontal lobeDecision making, self-control, regulation of emotion, processing of risk and fear, and regulation of amygdala activity
AmygdalaLocated in the frontal portion of the temporal lobe, close to the hippocampus Memory modulation, decision-making, reward, and emotional responses
Periaqeuductal grayLocated around the cerebral aqueduct within the tegmentum of the midbrainAutonomic function, motivated behavior, behavioral responses to threatening stimuli, and primary control center for descending pain modulation
Anterior cingulate cortexLocated in the frontal part of the cingulate cortexAutonomic functions, attention allocation, reward anticipation, decision-making, ethics and morality, impulse control, emotion, and registration of physical pain
HippocampusLocated in the medial temporal lobeConsolidation of memories, emotion, navigation, spatial orientation, and learning
Nucleus accumbensLocated in the basal forebrain Cognitive processing of motivation, aversion, reward, reinforcement learning, and significant role in addiction

Share and Cite

MDPI and ACS Style

Yang, S.; Chang, M.C. Chronic Pain: Structural and Functional Changes in Brain Structures and Associated Negative Affective States. Int. J. Mol. Sci. 2019, 20, 3130. https://doi.org/10.3390/ijms20133130

AMA Style

Yang S, Chang MC. Chronic Pain: Structural and Functional Changes in Brain Structures and Associated Negative Affective States. International Journal of Molecular Sciences. 2019; 20(13):3130. https://doi.org/10.3390/ijms20133130

Chicago/Turabian Style

Yang, Seoyon, and Min Cheol Chang. 2019. "Chronic Pain: Structural and Functional Changes in Brain Structures and Associated Negative Affective States" International Journal of Molecular Sciences 20, no. 13: 3130. https://doi.org/10.3390/ijms20133130

APA Style

Yang, S., & Chang, M. C. (2019). Chronic Pain: Structural and Functional Changes in Brain Structures and Associated Negative Affective States. International Journal of Molecular Sciences, 20(13), 3130. https://doi.org/10.3390/ijms20133130

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop