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The Brain as a Manager of Central and Peripheral Functions in Health and Disease

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Neurobiology".

Deadline for manuscript submissions: 31 March 2025 | Viewed by 6281

Special Issue Editor


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Guest Editor
1. Faculty of Psychology, National Research University “Higher School of Economy”, Moscow, Russia
2. Institute of Developmental Biology of the Russian Academy of Sciences, Moscow, Russia
Interests: developmental neurobiology; neuroendocrinology; neurodegenerative diseases; Parkinson’s disease; preclinical diagnosis; preventive neuroprotective therapy
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Special Issue Information

Dear Colleagues, 

I am pleased to invite you to contribute to this Special Issue of IJMS titled: “The Brain as a Manager of Central and Peripheral Functions in Health and Disease”. The brain plays a key role in the regulation of the development of the body and the brain (autoregulation) and central and peripheral functions in adulthood. These regulations are controlled by chemical signals—classical, neurotransmitters, neuropeptides, and amino acids. They are involved in synaptic or volume neurotransmission in the brain and neuroendocrine regulation when delivered to body fluids (CSF, blood). The role of brain-derived chemical signals during the so-called critical period of morphogenesis (the perinatal period) is fundamentally different compared to their role in adulthood. Indeed, in the perinatal period, before the closure of the blood–brain barrier, chemical signals exert an irreversible morphogenetic effect on differentiating target cells in the brain and peripheral organs. Impaired brain function during this period leads to the development of congenital neurological, mental, and neuroendocrine diseases. Data on the molecular mechanisms of brain diseases obtained using experimental models and pathological material are of particular importance since they can be applied to the development of new diagnostic and therapeutic technologies for patients.

Thus, this Special Issue of IJMS titled “The Brain as a Manager of Central and Peripheral Functions in Health and Disease” invites a wide range of studies on the molecular mechanisms of brain function in relation to ontogenesis, adulthood, health, and disease. Reviews, original papers, and new technological developments are welcome. Notably, according to Google Scholar Metrics 2024, IJMS ranks 22nd among the top 100 journals and 7th in the Life Sciences and Earth Sciences category.

Prof. Dr. Michael Ugrumov
Guest Editor

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Keywords

  • brain
  • animals
  • humans
  • cells
  • neural regulation
  • neuroendocrine regulation
  • synaptic neurotransmission
  • volume neurotransmission
  • ontogenesis
  • blood–brain barrier
  • brain diseases
  • neurological diseases
  • mental diseases
  • congenital diseases
  • modeling of brain pathology

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Published Papers (2 papers)

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Research

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17 pages, 4701 KiB  
Article
Compensatory Processes in Striatal Neurons Expressing the Tyrosine Hydroxylase Gene in Transgenic Mice in a Model of Parkinson’s Disease
by Dmitry Troshev, Alyona Bannikova, Victor Blokhin, Ekaterina Pavlova, Anna Kolacheva and Michael Ugrumov
Int. J. Mol. Sci. 2023, 24(22), 16245; https://doi.org/10.3390/ijms242216245 - 13 Nov 2023
Cited by 5 | Viewed by 1954
Abstract
The mammalian striatum is known to contain non-dopaminergic neurons that express dopamine (DA)-synthesizing enzymes and produce DA, responsible for the regulation of motor function. This study assessed the expression of DA-synthesizing enzymes in striatal neurons and their role in DA synthesis in transgenic [...] Read more.
The mammalian striatum is known to contain non-dopaminergic neurons that express dopamine (DA)-synthesizing enzymes and produce DA, responsible for the regulation of motor function. This study assessed the expression of DA-synthesizing enzymes in striatal neurons and their role in DA synthesis in transgenic mice expressing the green fluorescent protein (GFP) gene under the tyrosine hydroxylase (TH) gene promoter in a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) model of Parkinson’s disease (PD). We showed that, in Parkinsonian animals, the number of neurons expressing the TH gene increased by 1.9 times compared with the control (0.9% NaCl), which indicates a compensatory response to the DAergic denervation of the striatum. This assumption is supported by a 2.5-fold increase in the expression of genes for TH and transcription factor Nurr1 and a 1.45-fold increase in the expression of the large amino acid transporter 1 gene. It is noteworthy that, in Parkinsonian mice, in contrast to the controls, DA-synthesizing enzymes were found not only in nerve fibers but also in neuronal cell bodies. Indeed, TH or TH and aromatic L-amino acid decarboxylase (AADC) were detected in GFP-positive neurons, and AADC was detected in GFP-negative neurons. These neurons were shown to synthesize DA, and this synthesis is compensatorily increased in Parkinsonian mice. The above data open the prospect of improving the treatment of PD by maintaining DA homeostasis in the striatum. Full article
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Review

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36 pages, 1930 KiB  
Review
The Involvement of Neuroinflammation in the Onset and Progression of Parkinson’s Disease
by Anamaria Jurcau, Felicia Liana Andronie-Cioara, Delia Carmen Nistor-Cseppento, Nicoleta Pascalau, Marius Rus, Elisabeta Vasca and Maria Carolina Jurcau
Int. J. Mol. Sci. 2023, 24(19), 14582; https://doi.org/10.3390/ijms241914582 - 26 Sep 2023
Cited by 21 | Viewed by 3537
Abstract
Parkinson’s disease is a neurodegenerative disease exhibiting the fastest growth in incidence in recent years. As with most neurodegenerative diseases, the pathophysiology is incompletely elucidated, but compelling evidence implicates inflammation, both in the central nervous system and in the periphery, in the initiation [...] Read more.
Parkinson’s disease is a neurodegenerative disease exhibiting the fastest growth in incidence in recent years. As with most neurodegenerative diseases, the pathophysiology is incompletely elucidated, but compelling evidence implicates inflammation, both in the central nervous system and in the periphery, in the initiation and progression of the disease, although it is not yet clear what triggers this inflammatory response and where it begins. Gut dysbiosis seems to be a likely candidate for the initiation of the systemic inflammation. The therapies in current use provide only symptomatic relief, but do not interfere with the disease progression. Nonetheless, animal models have shown promising results with therapies that target various vicious neuroinflammatory cascades. Translating these therapeutic strategies into clinical trials is still in its infancy, and a series of issues, such as the exact timing, identifying biomarkers able to identify Parkinson’s disease in early and pre-symptomatic stages, or the proper indications of genetic testing in the population at large, will need to be settled in future guidelines. Full article
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