Next Article in Journal
Phytochemical Constituents, Health Benefits, and Industrial Applications of Grape Seeds: A Mini-Review
Next Article in Special Issue
The Role of Food Antioxidants, Benefits of Functional Foods, and Influence of Feeding Habits on the Health of the Older Person: An Overview
Previous Article in Journal
A Possible Indicator of Oxidative Damage in Smokers: (13Z)-Lycopene?
Previous Article in Special Issue
Evaluating Modern Techniques for the Extraction and Characterisation of Sunflower (Hellianthus annus L.) Seeds Phenolics
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Antioxidant Activity of Spices and Their Impact on Human Health: A Review

1
International Analytical Center of Zelinsky Institute of Organic Chemistry of Russian, Academy of Science, 119991 Moscow, Russia
2
Department of Research & Development, VDF FutureCeuticals, Inc., Momence, IL 60954, USA
3
Food Science and Human Nutrition, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA
*
Author to whom correspondence should be addressed.
Antioxidants 2017, 6(3), 70; https://doi.org/10.3390/antiox6030070
Submission received: 30 May 2017 / Revised: 14 August 2017 / Accepted: 8 September 2017 / Published: 15 September 2017
(This article belongs to the Special Issue Dietary Antioxidants and Health Promotion)

Abstract

:
Antioxidants are substances that prevent oxidation of other compounds or neutralize free radicals. Spices and herbs are rich sources of antioxidants. They have been used in food and beverages to enhance flavor, aroma and color. Due to their excellent antioxidant activity, spices and herbs have also been used to treat some diseases. In this review article, the chemical composition and antioxidant activity of spices and culinary herbs are presented. The content of flavonoids and total polyphenols in different spices and herbs are summarized. The applications of spices and their impacts on human health are briefly described. The extraction and analytical methods for determination of antioxidant capacity are concisely reviewed.

1. Introduction

Herbs and spices have been used in many different ways. Since the ancient times, spices and culinary herbs have been added to food to enhance flavor and improve their organoleptic properties. Spices and herbs have also been widely used as preservatives and medicine.
Spices and herbs have been extensively studied in different countries because of the high antioxidant activity in certain spices and their beneficial effects on human health [1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22]. As part of our diet, spices and herbs, in addition to fruits and vegetables, could provide us with additional sources of natural antioxidants. Antioxidants from spices are a large group of bioactive compounds which consist of flavonoids, phenolic compounds, sulfur-containing compounds, tannins, alkaloids, phenolic diterpenes, and vitamins [7,8,9,11,12,13,16,21]. These compounds demonstrate different antioxidant activities. For example, flavonoids have the ability to scavenge free radicals and can form complexes with catalytic metal ions rendering them inactive. Studies have shown that spices and herbs such as rosemary, sage, and oregano are excellent sources of antioxidants with their high content of phenolic compounds.
Antioxidants can protect lipids and oils in food against oxidative degradation. When added to food, antioxidants control rancidity development, retard the formation of toxic oxidation products, maintain nutritional quality, and extend the shelf-life of products. Because of safety concerns, synthetic antioxidants are limited to be used as food preservatives. Natural antioxidants obtained from edible materials such as spices and herbs, have been of increasing interest.
Natural antioxidants contained in spices help to reduce oxidative stress. Oxidative stress, which is caused by high concentration of free radicals in cells and tissues, can be induced by various negative factors, such as gamma, UV, and X-ray radiation, psycho-emotional stress, polluted food, adverse environmental conditions, intensive physical exertion, smoking, alcoholism, and drug addiction. Chronic oxidative stress has been reported to lead to a variety of diseases, including cancer, heart related diseases, and the acceleration of aging. Several secondary products of lipid oxidation, such as malondialdehyde and 4-hydroxynonenal, can react with biological components such as proteins, amino acids, and DNA. Malondialdehyde has been shown to be formed both enzymatically and non-enzymatically, and has been implicated in health problems such as mutagenesis and carcinogenesis. Spices and culinary herbs are rich in antioxidants. Therefore, spices could potentially be used as ameliorative or preventive agents for some health issues [5,6,10,13,14,16].
To have a better understanding of the antioxidant activity from spices, we present the bioactive compounds, the content of flavonoids, and the total polyphenols in different spices. The therapeutic effects of various spices for different diseases are summarized. Other applications of spices and herbs are briefly described in this review.

2. Chemical Composition of Spices and Their Antioxidant Activity

The antioxidant activity of spices is related to their chemical composition; primarily to the presence of polyphenolic and other biologically active compounds. Table 1 lists primary antioxidants and the biologically active compounds found in spices and culinary herbs that include flavonoids, phenolic acids, lignans, essential oils, and alkaloids, as summarized from several publications [23,24,25]. These compounds were largely determined by chromatographic methods.
The USDA (U.S. Department of Agriculture) Database contains information of flavonoid contents in spices and culinary herbs as determined by HPLC-UV (High performance liquid chromatography-UV detector) and HPLC-MS (High performance liquid chromatography-mass spectrometry) detection. The highest amounts of flavonoids have been found in parsley, oregano, celery, saffron, dill, fennel, and Tasmanian pepper (Table 2). Consumption of these spices and culinary herbs may contribute a significant portion of the plant antioxidants found in the human diet.
Ten flavonoids with significant quantity have been identified in different spices. The most frequently found compounds were quercetin, luteolin, and kaempferol. The highest flavonoid contents were as follows: apigenin in dried parsley, luteolin in Mexican oregano, luteolin in celery seeds, and cyanidin in Tasmanian pepper. The greatest amount of kaempferol and quercetin was found in capers.
Table 3 shows the most biologically active compounds contained in various spices and their chemical structures. Many of them have been reported to be anti-carcinogenic and their actions have been studied separately. These compounds also have other important therapeutic effects and antioxidant activities. Various research and review articles related to the antioxidant activity of spices have been published during the last decade [12,13,16,17,18,19,20,21,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51].

2.1. Rosmarinic Acid in Spices

Among these biologically active compounds found in spices, rosmarinic acid was the dominant phenolic compound in the six spices of the family Labiatae which contributed significantly to the antioxidant capacity of these spices. Shan et al. [27] investigated the total equivalent antioxidant capacity and phenolic content of 26 common spice extracts from 12 botanical families. In their study, major phenolic compounds were identified and quantified in different spices. Rosmarinic acid was found in mint, sweet basil, oregano, rosemary, sage, and thyme. The spices with the highest content of rosmarinic acid were oregano (2562.7, mg per 100 g of dry weight), sage (2186.1), rosemary (1286.1), mint (1908.5), sweat basil (1086.1), and thyme (681.1) respectively. Vallverdú-Queralt et al. [52] studied the phenolic profile of widely used culinary herbs and spices, which included rosemary, thyme, oregano, cinnamon, cumin and bay. The main phenolic acid in the studied culinary herbs was found to be rosmarinic acid, which varied from 0.39 µg/g dry weight in bay, to 157 µg/g dry weight in rosemary, being the dominant phenolic compound in oregano, thyme and rosemary. The concentrations of rosmarinic acid in rosemary, oregano, cumin, cinnamon, thyme and bay are: 156.90 ± 3.20, 52.02 ± 1.74, 3.29 ± 0.12, 0.73 ± 0.09, 84.04 ± 2.75 and 0.39 ± 0.01 µg/g.
Nagy et al. [53] analyzed the phenolic components in dried spices and found that rosmarinic acid was one of the main constituents in the methanolic extracts of oregano, sage and thyme, which was consistent with other research.
Zheng and Wang [54] investigated antioxidant activity and phenolic compounds in selected herbs. Rosmarinic acid and hydroxycinnamic acid compounds have been demonstrated to possess strong antioxidant activity. Rosmarinic acid was the most abundant phenolic constituents in the sage extracts 117.8 mg/100 g of fresh weight. Oregano extracts also had high contents of rosmarinic acid (124.8–154.6 mg/100 g of fresh weight). Thyme and rosemary were known to have high antioxidant capacities with high contents of rosmarinic acid (91.8 mg/100 g of fresh weight). It was found that certain species of oregano had extremely high total phenolic contents and oxygen radical absorption capacity (ORAC) values as well.

2.2. Flavonoids in Spices

Typically flavonoids and phenolic acids are the main phenolics in spices that possess antioxidant activity. Flavonoids generally occur as glycosylated derivatives with apigenin and luteolin are commonly found in aromatic herbs such as parsley, rosemary, thyme; quercetin and kaempferol in onions.
The antioxidant activity of phenolic compounds is mainly due to their redox propertiessuch as adsorbing and neutralizing free radicals, quenching singlet and triplet oxygen, or decomposing peroxides. In general, flavonoids have higher antioxidant activities against peroxyl radicals than do phenolic acids due to multiple hydroxyl groups.
Research [55] showed that quercetin was the major dietary flavonoid, followed by kaempferol, luteolin, and apigenin in the Netherlands. The greatest dietary source of flavonoids include onions which is 29% of total intake (approximately 23 mg/day expressed as aglycones).
Wojdylo et al. [56] measured antioxidant activity and phenolic compounds in 32 selected herbs. It was found that quercetin, luteolin, apigenin were predominant flavonoids in those herbs in addition to phenolic acids.
Yao et al. [57] studied the flavonoids in food sources for humans and the health aspects of flavonoids. It was indicated that cumin and peppermint were good sources of flavanones (Naringenin, eriodictyol); parsley and thyme are sources of flavones (apigenin, chrysin, luteolin, diosmetin), and onions are sources of flavonols (isorhamnetin, kaempferol, quercetin, myricetin, rutin).
Dimitrios [58] introduced extensive sources of natural antioxidants from fruits, vegetable, seeds, wine, and tea. It was demonstrated that different spices and herbs are important sources of natural phenolic antioxidants: flavones in parsley; carnosic acid, carnosol, rosmarinic acid, rosmanol in rosemary; carnosol, carnosic acid, lateolin, rosmanul, rosmarinic acid in sage; rosmarinic acid, phenolic acids, flavonoids in oregano; thymol, carvacrol, flavonoids, lubeolin in thyme; rosmarinic, carnosol, carvacrol, flavonoids in summer savory and Gingerol and related compounds in Ginger.
Study [54] revealed that Greek mountain oregano, hard sweet marjoram, Mexican oregano and sweet bay had higher total phenolic content in various herbal extracts studied, with total phenolic content 11.8 ± 0.60, 11.65 ± 0.29, 17.51 ± 0.22, and 4.02 ± 0.90 mg GAE/g respectively (Results were expressed as milligrams of gallic acid equivalent (GAE) per gram of fresh weight).
Kähkönen et al. [59] measured the antioxidant activity of different plant extracts spectrometrically according to the Folin–Ciocalteu procedure and found the total phenolic content of bog-rosemary as calculated as GAE was even higher than that of all the vegetables and some fruits studied at the same time.
In a mini review, Embuscado summarized total phenolic content of spices and herbs from different researches [60]: allspice 421.5 µmol gallic acid eq. per gram; basil 122.0 mg per gram; black pepper 3.83 mg per gram; coriander 18.5 µmol gallic acid eq. per gram; cinnamon 157.18 mg per gram; clove 113.19 mg per gram; cumin 49.5 µmol Trolox eq. per gram; fennel 46.1 µmol gallic acid eq. per gram; ginger 3.17 mg per gram; parsley 15.5 mg per gram; thyme 23.24 mg per gram; turmeric 21.17 mg per gram.
Shan et al. [26] found that cloves have the highest amount of flavonoids (366.5 as mg per 100 g), followed by dill (241.2), caraway (171.9), coriander (167.2), oregano (51.3), rosemary (37.8), mint (23.2), basil (21.0), and sage (20.5).
A database [27] that contains data for 425 spices and culinary herbs from 59 countries was produced by a number of manufacturers. The antioxidant content was measured by modified ferric reducing antioxidant power (FRAP) assay. Antioxidants were extracted in water/methanol. Twenty-seven spices had the highest antioxidant content which varied from 100 to 465 mmol per 100 g. Shan et al. [26] showed the total antioxidant capacity of 26 spices from 12 botanical families as determined by ТЕАС. The phenolic content was measured using Folin–Ciocalteu assay. Colves, cinnamon and oregano were the three spices with the highest value. A high correlation (R = 0.9613) was found between the ТЕАС value and the total phenolic content.
It is not a surprising that spices and herbs are at the top of the list of 100 products with the highest antioxidant content [61,62]. Their antioxidant activities are ten times higher than that of fruit and vegetables. The antioxidant capacities of some spices showed a positive correlation with their corresponding total polyphenol concentrations.

3. Methods for Antioxidant Extraction and Determination

3.1. Extraction Techniques for Antioxidant in Spices

Extraction techniques aim to extract the active compounds from spices with certain selectivity and sensitivity. Several well-known methods have been used for extraction of active components from spices, such as liquid-phase extraction (extraction using solvents), solid-phase extraction, and supercritical fluid extraction (extraction using СО2 in its supercritical state) [63].
It was proven that different solvents or solvent mixture applied on the same spice sample can lead to different extraction efficiencies. A list of solvents used for extraction of spices has been provided by AllwynSundarRay et al. [25]. The solvents include methanol, methanol/water mixture (1:1), trichloroacetic acid, acetone, toluene, ethanol, ethyl acetate, and water. Methanol/water (1:1) and ethanol/water (1:1) mixtures are used most frequently. The total contents of flavonoids, polyphenols, and tannins in aqueous and methanolic extracts of cardamon, coriander, and bay leaf were different [50]. The results showed that the content of all these polyphenols in aqueous solutions of coriander was almost twice as much as that in the methanolic solutions. The opposite results were obtained for cardamon and bay leaf with polyphenol content in methanolic extracts significantly higher—2–3 times higher for cardamon and 3–10 times higher for bay leaf.
The extraction efficiency could be affected by the extraction temperature. Hot water extraction (80–100 °C) has been used for measuring antioxidant activity of 13 spices [41]. The extraction lasted 3 h. Antioxidant activity was determined by the 2,2-diphenyl-1-picrylhydrazyl (DPPH) method. However, the measurements may not be appropriate because a significant part of polyphenols could have been oxidized over 3 h at such high temperatures. Ereifej et al. [64] investigated the influence of different extractants (methanol, ethanol and acetone) at different temperatures (20, 40 and 60 °C). It was found that cloves had the highest level of total phenolics using methanol at three different temperature. When ethanol was used as extractant, cloves show the highest level of phenolics at 60 °C. When acetone was used as an extractant at 60 °C, cloves still had the highest levels of total phenolics. The total phenolics of cloves were quite close using methanol and acetone as extractants.
To address the complexity of the extraction characteristics and optimize parameters for solvent extraction of phenolic compounds and antioxidants, response surface methodology by central composite design has been employed to statistically optimize the extraction conditions [65].

3.2. Analytical Methods Applied to Antioxidant Capacities Determination in Spices

A variety of methods have been used to determine antioxidant capacities in spices and herbs. The reported methods include 2,2-azino-bis(3-ehtylbenzothiazoline-6-sulfonic acid (ABTS) assay, DPPH radical scavenging activity, ORAC, ferric reducing antioxidant power (FRAP) and sensitive electrochemical and photochemiluminescent approaches, voltammetric and spectrophotometric methods [65,66,67,68,69,70]. Recently, a rapid approach based on near-infrared spectroscopy was developed for the determination of total polyphenols content and antioxidant activity in a Chinese herb [71]. Lu et al. [72] investigated the antibacterial effects of garlic concentrate by using Fourier Transform Infrared Spectroscopy. Similarly Venetsanou et al. [73] estimated antioxidant activity of different mixed herbal infusions using attenuated total reflectance Fourier transform infrared spectroscopy and chemometrics.
Antioxidant activities and antioxidant capacities of compounds from the same spices could be different depending on the analytical methods used. Antioxidant activity of ethanol and water/ethanol extracts of 13 spices have been evaluated by three different methods [51]. In many cases, water/ethanol extracts contained more antioxidants than ethanol extracts (measurements by ABTS+). When the same extracts were evaluated using photochemiluminescence or cyclic voltammetry, the results obtained for different spices shifted in both directions. Romero et al. [74] studied the antioxidant activities of a set of 17 active components present in different spices and condiment with different methods: (1) spectrophotometric method with DPPH radical scavenging assay and cupric reducing antioxidant capacity (CUPRAC) assay; (2) electrochemical method using either a mercury electrode or a glassy carbon electrode covered with poly-neutral rad and doped with Pt nanoparticles. The electrochemical method saves time for measurement and organic solvents for extraction. The sensitivity of electrochemical method is comparable with those shown by DPPH or CUPRAC.
Antioxidant activities from the same spices measured by different methods could be correlated. Dragland et al. [29] studied antioxidant activity of several dozen spices, culinary and medicinal (Chinese and Japanese) herbs. They reported that the antioxidant activity of these spices differs by as much as three orders of magnitude. Antioxidant activity in their study was determined by an automated FRAP assay. To compare these data to Carlsen et al. [28] using modified version of the FRAP assay, we correlated the two data sets and found their correlation was highly positive with correlation >0.9. A comparative study of antioxidant properties of 30 plant extracts using various methods—DPPH, ABTS, FRAP, superoxide dismutase (SOD), and ORAC assays demonstrated the different correlations among these methods [45]. The total polyphenol contents of cinnamon, cloves, bay leaf, vanilla, lavender and ginger were determined by Folin–Ciocalteu assay. The strongest correlation was found between the FRAP and ABTS assays (0.946), and the weakest was between ABTS and DPPH assays (0.906).
So far no single method will truly reflect the total antioxidant capacity of a particular sample. In order to fully reflect both lipophilic and hydrophilic capacity, elucidate a full profile of antioxidant capacity, and evaluate various reactive oxygen species, a number of methods are required. However, from the routine quality control point of view, it would be more practical to employ fewer, and standardized methods.

4. Effect of Spices on Human Health and Other Applications

Spices have been reported to have various beneficial effects on human health which include anti-sclerotic, antithrombotic, anti-carcinogenic, anti-inflammatory, antiarrhythmic, anti-rheumatic, gastroprotective, and lipid-lowering action. In addition, spices have radioprotective (protects against radiation), anti-allergic, and antimalarial effects. Spices inhibit the oxidation of low-density lipoprotein and protein glycation [75,76,77,78,79].
Many spices are highly potent antiseptics because they have an antibacterial, antimicrobial, and even antiviral effect. A synergistic effect on oral bacteria was observed when cloves were used along with antibiotics [80,81,82,83,84].
Spices and herbs have been used as functional food [85,86,87,88,89]. Table 4 shows various therapeutic effects of spices from different literatures.
The therapeutic effects of certain spices are so significant that they have often been included in non-clinical, clinical, and therapeutic studies. A non-clinical trial of rosemary showed that rosemary could act as a cancer prevention agent. Some clinical and therapeutic trials for evaluation of spices against several diseases have been conducted. Studies show that curcumin possesses anti-inflammatory effects and therapeutic effect in gastrointestinal diseases. It is an inhibitor of low density lipoprotein oxidation and also showed effects against neurodegenerative diseases. Ginger and garlic have extensively therapeutic effects [90,91,114,115,116,117,118,119,120], especially for cardiovascular diseases. These will be reviewed in following section.
Cloves, Nigella, black pepper, garlic, and ginger have been used against cancer [121,122,123]. Aged aqueous-alcoholic extract of garlic was also reported to be potentially effective against certain cancers [124]. Table 5 summarizes anticancer actions of some spices. The following compounds contained in spices have anti-carcinogenic properties: curcumin, apigenin, luteolin, quercetin, thymoquinone, and isothiocyanate.
Some spices play a critical role in the management of heart disease (Table 6) because these spices have been shown to inhibit enzymes involved in lipid synthesis, decrease platelet aggregation, prevent lipid peroxidation, reduce LDL (low-density lipoprotein) levels and increase coronary blood flow.
Spices have been used to preserve food to inhibit or delay lipid oxidation and rancidity in foods. Since ancient times it has been known that spices help preserve many foods. Now the application of spices have become even more broad: extension of cheese shelf-life by adding cinnamon; preservation of vitamin E in sunflower oil by adding different spices; inhibition of omega-3 fatty acid oxidation in vegetable oils by oregano and rosemary as well as sterol oxidation in extra virgin olive oil; extension of meat shelf-life by various spices [145,146,147,148,149].
Due to high antioxidant activity, spices suppress harmful effects of carcinogenic pollutants that may be present in foods and beverages, especially aflatoxins, heterocyclic amines, acrylamide, 1,2-Dimethylhydrazine and cadmium [150,151,152,153,154,155]. Spices can also neutralize the harmful effects of hazardous solvents and motor exhaust emissions from road transport in urban areas [156]. Therefore, it is important and reasonable to encourage people to consume spices regularly in order to protect them from harmful environmental impacts, especially in large, polluted cities.

5. Conclusions

Based on the reviewed literature, we know that spices not only enhance the flavor, aroma, and color of food and beverages, but they can also protect people from acute and chronic diseases, due to their high antioxidant activity. This review presents abundant data on the antioxidant activities of spices and culinary herbs, as well as information related to their content of flavonoids and total polyphenols. Many of the antioxidants contained in spices have significantly high biological activities and are actively used in preclinical, clinical, and therapeutic trials investigating new treatments of diseases. It is possible that new spice-based drugs may be developed. This review also presents a strong body of evidence that spice consumption can reduce or even eliminate the harmful effects on humans from contaminants in foods and from the environment; this is even more important for people living in polluted cities. All of this information will hopefully add to an already high level of interest toward spices and culinary herbs. Spices and herbs should certainly be incorporated as integral parts of healthy, nutritious eating, and as functional food ingredients.

Acknowledgments

Herewith, we thank John Hunter (FutureCeuticals, Inc.) for review and providing valuable advice for editing this manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Baselga-Escudero, L.; Souza-Mello, V.; Pascual-Serrano, A.; Rachid, T.; Voci, A.; Demori, I.; Grasselli, E. Beneficial effects of the Mediterranean spices and aromas on non-alcoholic fatty liver disease. Trends Food Sci. Technol. 2017, 61, 141–159. [Google Scholar] [CrossRef]
  2. Patra, K.; Jana, K.; Mandal, D.P.; Bhattacharjee, S. Evaluation of the antioxidant activity of extracts and active principles of commonly consumed Indian spices. J. Environ. Pathol. Toxicol. Oncol. 2016, 35, 299–315. [Google Scholar] [CrossRef] [PubMed]
  3. Singhal, P.; Singla, N.; Sakhare, D.; Sharma, K.A. A comparative evaluation of in vitro antioxidant activity of some commonly used spices of northern India. Nat. Prod. J. 2017, 7, 131–136. [Google Scholar] [CrossRef]
  4. Ene-Obong, H.; Onuoha, N.; Aburime, L.; Mbah, O. Chemical composition and antioxidant activities of some indigenous spices consumed in Nigeria. Food Chem. 2017. [Google Scholar] [CrossRef] [PubMed]
  5. Bi, X.; Lim, J.; Henry, C.J. Spices in the management of diabetes mellitus. Food Chem. 2017, 217, 281–293. [Google Scholar] [CrossRef] [PubMed]
  6. Serafini, M.; Peluso, I. Functional foods for health: The interrelated antioxidant and anti-inflammatory role of fruits, vegetables, herbs, spices and cocoa in humans. Curr. Pharm. Des. 2016, 22, 6701–6715. [Google Scholar] [CrossRef] [PubMed]
  7. Peter, K.V. Handbook of Herbs and Spices; Woodhead Publishing Limited and CRC Press LLS: Cambridge, UK, 2001; Volume 1. [Google Scholar]
  8. Peter, K.V. Handbook of Herbs and Spices; Woodhead Publishing Limited: Cambridge, UK, 2004; Volume 2. [Google Scholar]
  9. McCormick. The History of Spices. Available online: http://www.mccormickscienceinstitute.com/resources/history-of-spices (accessed on 30 May 2017).
  10. Surh, Y.J. Chemopreventive Phenolic Compounds in Common Spices; Taylor and Francis: New York, NY, USA, 2006. [Google Scholar]
  11. Parthasarathy, V.A.; Chempakam, B.; Zachariah, T.J. Chemistry of Spices; CABI: Oxfordshire, UK, 2008. [Google Scholar]
  12. Charles, D.J. Antioxidant Properties of Spices, Herbs and Other Sources; Springer: New York, NY, USA, 2013; p. 612. [Google Scholar]
  13. Choi, I.S.; Cha, H.S. Physicochemical and antioxidant properties of black garlic. Molecules 2014, 19, 16811–16823. [Google Scholar] [CrossRef] [PubMed]
  14. Samah, N.A.; Mahmood, M.R.; Muhamad, S. The role of nanotechnology application in antioxidant from herbs and spices for improving health and nutrition: A review. Selangor Sci. Technol. Rev. 2014, 1, 17–23. [Google Scholar]
  15. Sobolev, A.P.; Carradori, S.; Capitani, D.; Vista, S.; Trella, A.; Marini, F.; Mannina, L. Saffron samples of different origin. An NMR study of microwave-assisted extracts. Foods 2014, 3, 403–419. [Google Scholar] [CrossRef] [PubMed]
  16. Yesiloglu, Y.; Audin, H.; Kilic, I. In vitro antioxidant activity of various extracts of ginger seed. Asian J. Chem. 2013, 25, 3573–3578. [Google Scholar]
  17. Asha Devi, S.; Umasanker, M.E.; Babu, S. A comparative study of antioxidant properties in common Indian spices. Int. Res. J. Pharm. 2012, 3, 465–468. [Google Scholar]
  18. Panpatil, V.V.; Tattari, S.; Kota, N.; Polasa, K. In vitro evaluation on antioxidant and antimicrobial activity of spice extracts of ginger, turmeric and garlic. J. Pharmacogn. Phytochem. 2013, 2, 143–148. [Google Scholar]
  19. Tchombe, N.L.; Louajri, A.; Benajiba, M.N. Therapeutical effects of Ginger. ISESCO J. Technol. 2012, 8, 64–69. [Google Scholar]
  20. Islam, S.; Nasrin, S.; Khan, M.A.; Hossain, A.S.; Islam, F.; Khandokhar, P.; Mollah, M.N.H.; Rashid, M.; Sadik, G.; Rahman, M.A.A.; et al. Evaluation of antioxidant and anticancer properties of the seed extracts of Syzygium fruticosum Roxb. growing in Rajshahi, Bangladesh. BMC Complement. Altern. Med. 2013, 13, 142. [Google Scholar] [CrossRef] [PubMed]
  21. Srinivasan, K. Antioxidant potential of spices and their active constituents (on line). Crit. Rev. Food Sci. Nutr. 2014, 54, 352–372. [Google Scholar] [CrossRef] [PubMed]
  22. Srinivasan, K. Dietary spices as beneficial modulators of lipid profile in condition of metabolic disorders and disease. Food Funct. 2013, 4, 503–521. [Google Scholar] [CrossRef] [PubMed]
  23. Bhattacharjee, S.; Sengupta, A. Spices in cancer prevention—An overview. Internet J. Nutr. Wellness 2008, 7, 1–16. [Google Scholar]
  24. Kaefer, C.M.; Milner, J.A. The role of herbs and spices in cancer prevention. J. Nutr. Biochem. 2008, 19, 347–354. [Google Scholar] [CrossRef] [PubMed]
  25. AllwynSundarRaj, A.; Aaron, S.; Seinenbalg, S.S.; Tiroutchelvamaa, D.; Ranganathan, T.V. Review on recent trends in isolation of antioxidants from spices and its biological effects of essential oils. J. Eng. Res. Appl. 2014, 4, 75–84. [Google Scholar]
  26. USDA Database for the Flavonoid Content of Selected Foods. Release 3.1 (May 2014). Available online: https://www.ars.usda.gov/ARSUserFiles/80400525/Data/Flav/Flav_R03-1.pdf (accessed on 30 May 2017).
  27. Shan, B.; Cai, Y.Z.; Sun, M.; Corke, H. Antioxidant capacity of 26 extracts of spices and characterization their phenolic components. J. Agric. Food Chem. 2005, 53, 7749–7759. [Google Scholar] [CrossRef] [PubMed]
  28. Carlsen, M.H.; Halvorsen, B.L.; Holte, K.; Bøhn, S.K.; Dragland, S.; Sampson, L.; Willey, C.; Senoo, H.; Umezono, Y.; Sanada, C.; et al. The total antioxidant content of more than 3100 foods, beverages, spices, herbs and supplements used worldwide. Nutr. J. 2010, 9, 3–11. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  29. Dragland, S.; Senoo, H.; Wake, K.; Holte, K.; Blomhoff, R. Several Culinary and medicinal herbs are important sources of dietary antioxidants. J. Nutr. 2003, 133, 1286–1290. [Google Scholar] [PubMed]
  30. Otunola, G.A.; Afolayan, A.J. Evaluation of the polyphenol contents and some antioxidant properties of aqueous extracts of garlic, ginger, cayenne pepper and their mixture. J. Appl. Bot. Food Qual. 2013, 86, 66–70. [Google Scholar]
  31. Gulcin, I. The antioxidant and radical scavenging activities of black pepper (Piper nigrum) seeds. Int. J. Food Sci. Nutr. 2005, 56, 491–499. [Google Scholar] [CrossRef] [PubMed]
  32. Singh, R.; Singh, N.; Saini, B.S.; Rao, H.S. In vitro antioxidant activity of pet ether extract of black pepper. Indian J. Pharmacol. 2008, 40, 147–151. [Google Scholar] [CrossRef] [PubMed]
  33. Jimenez-Alvarez, D.; Giuffrida, F.; Golay, P.A.; Cotting, C.; Lardeau, A.; Keely, B.J. Antioxidant activity of oregano, parsley, and olive mill wastewaters in bulk oils and oil-in-water emulsions enriched in fish oil. J. Agric. Food Chem. 2008, 56, 7151–7159. [Google Scholar] [CrossRef] [PubMed]
  34. Spiridon, I.; Colceru, S.; Anghel, N.; Teaca, C.A.; Bodirlau, R.; Armatu, A. Antioxidant and total phenolic contents of oregano (Origanum vulgare), lavender (Lavandula angus and lemon balm (Melissa officinalis) from Romania. Nat. Prod. Res. 2011, 25, 1657–1661. [Google Scholar] [CrossRef] [PubMed]
  35. Shim, S.M.; Yi, H.L.; Kim, Y.S. Bioaccessibility of flavonoids and total phenolic content in onions and its relationship with antioxidant activity. Int. J. Food Sci. Nutr. 2011, 62, 835–838. [Google Scholar] [CrossRef] [PubMed]
  36. Cazzola, R.; Camerotto, C.; Cestaro, B. Anti-oxidant, anti-glycant, and inhibitory activity against a-amylase and a glucosidase of selected spices and culinary herbs. Int. J. Food Sci. Nutr. 2011, 62, 175–184. [Google Scholar] [CrossRef] [PubMed]
  37. Amira, S.; Dade, M.; Schinella, G.; Rios, J.L. Anti-inflammatory, anti-oxidant, and apoptotic activities of four plant species used in folk medicine in the Mediterranean basin. Pak. J. Pharm. Sci. 2012, 25, 65–72. [Google Scholar] [PubMed]
  38. Mimica-Dukic, N.; Bugarin, D.; Grbovic, S.; Mitic-Culafic, D.; Vukovic-Gacic, B.; Orcic, D.; Jovin, E.; Couladis, M. Essential oil of Myrtus communis L. as a potential antioxidant and anti-mutagenic agents. Molecules 2010, 15, 2759–2770. [Google Scholar] [CrossRef] [PubMed]
  39. Romani, A.; Coinu, R.; Carta, S.; Pinelli, P.; Galardi, C.; Vincieri, F.F.; Franconi, F. Evaluation of antioxidant effect of different extracts of Myrtus communis L. Free Radic. Res. 2004, 38, 97–103. [Google Scholar] [CrossRef] [PubMed]
  40. El-Ghorab, A.H.; Nauman, M.; Anjum, F.M.; Hussain, S.; Nadeem, M.A. Comparative study on chemical composition and antioxidant activity of ginger (Zingiber officinale) and cumin (Cuminum cyminum). J. Agric. Food Chem. 2010, 58, 8231–8233. [Google Scholar] [CrossRef] [PubMed]
  41. Thippeswamy, N.B.; Naidu, A. Antioxidant potency of cumin varieties—Cumin, black cumin and bitter cumin—On antioxidant systems. Eur. Food Res. Technol. 2005, 220, 472–476. [Google Scholar] [CrossRef]
  42. Kim, I.S.; Yang, M.R.; Lee, O.H.; Kang, S.N. Antioxidant activities of hot water extracts from various spices. Int. J. Mol. Sci. 2011, 12, 4120–4131. [Google Scholar] [CrossRef] [PubMed]
  43. Samojlik, I.; Laki, N.; Mimica-Duki, N.; Dakovi-Svajcer, K.; Bozin, B. Antioxidant and hepatoprotective potential of essential oils of coriander (Coriandrum sativum L.) and caraway (Carum carvi L.) (Apiaceae). J. Agric. Food Chem. 2010, 58, 8848–8853. [Google Scholar] [CrossRef] [PubMed]
  44. Hlavackova, H.; Samuelsen, A.B.; Malterud, K.E. Antioxidant activity in extracts from coriander. Food Chem. 2004, 88, 293–297. [Google Scholar]
  45. Dudonné, S.; Vitrac, X.; Coutiere, P.; Woillez, M.; Merillon, J.M. Comparative study of antioxidant properties and total phenolic content of 30 plant extracts of industrial interest using DPPH, ABTS, FRAP, SOD, and ORAC assays. J. Agric. Food Chem. 2009, 57, 1768–1774. [Google Scholar] [CrossRef] [PubMed]
  46. Yao, Y.; Sang, W.; Zhou, M.; Ren, G. Phenolic composition and antioxidant activities of 11 celery cultivars. J. Food Sci. 2010, 75, C9–C13. [Google Scholar] [CrossRef] [PubMed]
  47. Sun, T.; Xu, Z.; Wu, C.T.; Janes, M.; Prinyawiwatkul, W.; No, H.K. Antioxidant activities of different colored sweet bell peppers (Capsicum annuum L.). J. Food Sci. 2007, 72, S98–S102. [Google Scholar] [CrossRef] [PubMed]
  48. Dall’Acqua, S.; Cervellati, R.; Speroni, E.; Costa, S.; Guerra, M.C.; Stella, L.; Greco, E.; Innocenti, G. Phytochemical composition and antioxidant activity of Laurus nobilis L. leaf infusion. J. Med. Food 2009, 12, 869–876. [Google Scholar] [CrossRef] [PubMed]
  49. Ozcan, B.; Esen, M.; Sangun, M.K.; Coleri, A.; Caliskan, M. Effective antibacterial and antioxidant properties of methanolic extract of Laurus nobilis seed oil. J. Environ. Biol. 2010, 31, 637–641. [Google Scholar] [PubMed]
  50. Deepa, G.; Ayesha, S.; Nishta, K.; Thankamani, M. Comparative evaluation of various total antioxidant capacity assays applied to phytochemical compounds of Indian culinary spices. Int. Food Res. J. 2013, 20, 1711–1716. [Google Scholar]
  51. Przyrodzka, M.; Zielinska, D.; Ciesarova, Z.; Kukurova, K.; Zielinski, H. Comparison of methods for evaluation of the antioxidant capacity and phenolic compounds in common spices. LWT Food Sci. Technol. 2014, 58, 321–326. [Google Scholar] [CrossRef]
  52. Vallverdú-Queralt, A.L.; Rejueiro, J.; Martínez-Huélamo, M.; Alvarenga, J.F.R.; Leal, L.N.; Lamuela-Raventos, R.M. A comprehensive study on the phenolic profile of widely used culinary herbs and spices: Rosemary, thyme, oregano, cinnamon, cumin and bay. Food Chem. 2014, 154, 299–307. [Google Scholar] [CrossRef] [PubMed]
  53. Nagy, T.O.; Solar, S.; Sontag, G.; Koenig, J. Identification of phenolic components in dried spices and influence of irradiation. Food Chem. 2011, 128, 530–534. [Google Scholar] [CrossRef] [PubMed]
  54. Zheng, W.; Wang, S.Y. Antioxidant activity and phenolic compounds in selected herbs. J. Agric. Food Chem. 2001, 49, 5165–5170. [Google Scholar] [CrossRef] [PubMed]
  55. Cook, N.C.; Samman, S. Flavonoids-Chemistry, metabolism, cardiopretective effects and dietary sources. J. Nutr. Biochem. 1996, 7, 66–76. [Google Scholar] [CrossRef]
  56. Wojdylo, A.; Oszmiański, J.; Czemerys, R. Antioxidant activity and phenolic compounds in 32 selected herbs. Food Chem. 2007, 105, 940–949. [Google Scholar] [CrossRef]
  57. Yao, L.H.; Jiang, Y.M.; Shi, J.; Tomás-Barberán, F.A.; Datta, N.; Singanusong, R.; Chen, S.S. Flavonoids in food and their health benefits, Flavanones in cumin, peppermint, Flavones in parsley, thyme and Flavonols in onions. Plant Foods Hum. Nutr. 2004, 59, 113–122. [Google Scholar] [CrossRef] [PubMed]
  58. Dinitrios, B. Sources of natural phenolic antioxidants. Trends Food Sci. Technol. 2006, 17, 505–512. [Google Scholar] [CrossRef]
  59. Kähkönen, M.P.; Hopia, A.I.; Vuorela, H.J.; Rauha, J.; Pihlaja, K.; Kujala, T.S.; Heinonen, M. Antioxidant activity of plant extracts containing phenolic compounds. J. Agric. Food Chem. 1999, 47, 3954–3962. [Google Scholar] [CrossRef] [PubMed]
  60. Embuscado, M. Spices and herbs: Natural sources of antioxidants—A mini review. J. Funct. Foods 2015, 18, 811–819. [Google Scholar] [CrossRef]
  61. Jorgustin, K. Top 100 High ORAC Value Antioxidant Foods. Available online: http://modernsurvivalblog.com/health/high-orac-value-antioxidant-foods-top-100/ (accessed on 3 June 2014).
  62. Haytowitz, D.B.; Bhagwat, S. USDA Database for the Oxygen Radical Absorbance Capacity (ORAC) of Selected Foods, Release 2. Available online: http://www.drmarcofranzreb.com/wp-content/uploads/2013/04/ORAC-de-alimentos-2.pdf (accessed on 30 May 2017).
  63. Xu, D.; Li, Y.; Meng, X.; Zhou, T.; Zhou, Y.; Zheng, J.; Zhang, J.; Li, H. Nautral antioxidants in foods and medicinal plants: Extraction, assessment and resources. Int. J. Mol. Sci. 2017, 18, 96. [Google Scholar] [CrossRef] [PubMed]
  64. Ereifej, K.I.; Feng, H.; Rababah, T.M.; Tachtoush, S.H.; Al-U’datt, M.; Gammoh, S.; Al-Rabadi, G.J. Effect of extractant and temperature on phenolic compounds and antioxidant activity of selected spices. Food Nutr. Sci. 2016, 7, 362–370. [Google Scholar] [CrossRef]
  65. Chowdhury, A.; Selvaraj, K.; Bhattacharjee, C.; Chowdhury, R. Optimization of the solvent extraction of phenolics and antioxidants from waste Cauliflower leaves (Brassica oleracea L.) using response surface methodology (RSM). IJBLST 2013, 5, 4–12. [Google Scholar]
  66. Katalinic, V.; Milos, M.; Kulisic, T.; Juki, M. Screening of 70 medicinal plant extracts for antioxidant capacity and total phenols. Food Chem. 2006, 94, 550–557. [Google Scholar] [CrossRef]
  67. Magalhaes, L.M.; Segundo, M.A.; Reis, S.; Lima, J.L.F.C. Methodological aspects about in vitro evaluation of antioxidant properties. Anal. Chim. Acta 2008, 613, 1–19. [Google Scholar] [CrossRef] [PubMed]
  68. Prior, R.L.; Wu, X.; Schaich, K. Standardized methods for the determination of antioxidant capacity and phenolics in foods, and dietary supplements. J. Agric. Food Chem. 2005, 53, 4290–4302. [Google Scholar] [CrossRef] [PubMed]
  69. Zielińska, D.; Wiczkowski, W.; Piskula, M.K. Evaluation of photochemiluminescent, spectrophotometric and cyclic voltammetry methods for the measurement of the antioxidant capacity: The case of roots separated from buckwheat sprouts. Pol. J. Food Nutr. Sci. 2008, 58, 65–72. [Google Scholar]
  70. Pisoschi, A.M.; Pop, A.; Cimpeanu, C.; Predoi, G. Antioxidant capacity determination in plants and plant-derived products: A review. Oxid. Med. Cell. Longev. 2016, 2016, 9130976. [Google Scholar] [CrossRef] [PubMed]
  71. Ma, L.; Zhang, Z.; Zhao, X.; Zhang, S.; Lu, H. The rapid determination of total polyphenols content and antioxidant activity in Dendrobium officinale using near-infrared spectroscopy. Anal. Method 2016, 8, 4584–4589. [Google Scholar] [CrossRef]
  72. Lu, X.; Rasco, B.A.; Jabal, J.M.F.; Aston, D.E.; Lin, M.; Kondel, M.E. Investigating antibacterial effects of garlic (Allium sativum) concentrate and garlic-derived organosulfur compounds on Campylobacter jejuni by using fourier transform infrared spectroscopy, raman spectroscopy, and electron microscopy. Appl. Environ. Microbiol. 2011, 77, 5257–5269. [Google Scholar] [CrossRef] [PubMed]
  73. Venetsanou, A.; Anastasaki, E.; Gardeli, C.; Tarantilis, P.A.; Pappas, C.S. Estimation of antioxidant activity of different mixed herbal infusions using attenuated total reflectance Fourier transform infrared spectroscopy and chemometrics. Emir. J. Food Agric. 2017, 29, 149–155. [Google Scholar] [CrossRef]
  74. Romero, M.P.R.; Brito, R.E.; Palma, A.; Montoya, M.R.; Mellado, J.M.R.; Rodríguez-Amaro, R. An electrochemical method for the determination of antioxidant capacities applied to components of spices and condiments. J. Electrochem. Soc. 2017, 164, B97–B102. [Google Scholar] [CrossRef]
  75. Hlavackova Assayed, M.E. Radioprotective effects of black seed (Nigella sativa) oil against hemopoietic damage and immunosuppression in gamma-irradiated rats. Immunopharmacol. Immunotoxicol. 2010, 32, 284–296. [Google Scholar] [CrossRef] [PubMed]
  76. Castellan, M.L.; Perrella, A.; Conti, F.; Salini, V.; Tete, S.; Madhappan, B.; Vecchiet, J.; De Lutiis, M.A.; Caraffa, A.; Cerulli, G. Role of quercetin (a natural herbal compound) in allergy and inflammation. J. Biol. Regul. Homeost. Agents 2006, 20, 47–52. [Google Scholar]
  77. El Babili, F.; Bouajila, J.; Souchard, J.P.; Bertrand, C.; Bellvert, F.; Fouraste, I.; Moulis, C.; Valentin, A. Oregano: Chemical analysis and evaluation of its antimalarial, antioxidant, and cyto-toxic activities. J. Food Sci. 2011, 76, C512–C518. [Google Scholar] [CrossRef] [PubMed]
  78. Naidu, A.K.; Thippeswamy, N.B. Inhibition of human low density lipoprotein oxidation by active principles from spices. Mol. Cell. Biochem. 2002, 229, 19–23. [Google Scholar] [CrossRef] [PubMed]
  79. Dearlove, R.P.; Greenspan, P.; Hartle, D.K.; Swanson, R.B.; Hargrove, J.L. Inhibition of protein glycation by extracts of culinary herbs and spices. J. Med. Food 2008, 11, 275–281. [Google Scholar] [CrossRef] [PubMed]
  80. Islam, R.; Khan, M.H. Antibacterial activity of natural spices on multiple drug resistant Escherichia coli isolated from drinking water, Bangladesh. Ann. Clin. Microbiol. Antimicrob. 2011, 10, 10. [Google Scholar]
  81. Devi, K.P.; Nisha, S.A.; Sakthivel, R.; Pandian, S.K. Eugenol (an essential oil of clove) acts as an antibacterial agent against Salmonella typhi by disrupting the cellular membrane. J. Ethnopharmacol. 2010, 130, 107–115. [Google Scholar] [CrossRef] [PubMed]
  82. Hlavackova, D.; Toroglu, S. Studies on antimicrobial activities of solvent extracts of different spices. J. Environ. Biol. 2011, 32, 251–256. [Google Scholar]
  83. Ailahverdiyev, A.; Duran, N.; Ozguven, M.; Koltas, S. Antiviral activity of the volatile oils of Melissa officinalis L. against Herpes simplex virus type-2. Phytomedicine 2004, 11, 657–661. [Google Scholar] [CrossRef] [PubMed]
  84. Moon, S.E.; Kim, H.Y.; Cha, J.D. Synergistic effect between clove oil and its major compounds and antibiotics against oral bacteria. Arch. Oral Biol. 2011, 56, 907–916. [Google Scholar] [CrossRef] [PubMed]
  85. Gruenwald, J.; Freder, J.; Armbruester, N. Cinnamon and health. Crit. Rev. Food Sci. Nutr. 2010, 50, 822–834. [Google Scholar] [CrossRef] [PubMed]
  86. Butt, M.S.; Sultan, M.T.; Butt, M.S.; Igbal, J. Garlic: Nature’s protection against physiological threats. Crit. Rev. Food Sci. Nutr. 2009, 49, 538–551. [Google Scholar] [CrossRef] [PubMed]
  87. Butt, M.S.; Sultan, M.T. Nigella sativa-reduces the risk of various maladies. Crit. Rev. Food Sci. Nutr. 2010, 50, 654–655. [Google Scholar] [CrossRef] [PubMed]
  88. Stajner, D.; Canadanovic-Brunet, J.; Pavlovic, A. Allium species. Phytother. Res. 2008, 22, 113–117. [Google Scholar] [PubMed]
  89. Vinda-Martos, M.; Ruiz-Navajos, Y.; Fernandes-Lopes, J.; Perez-Alvarez, J.A. Spices as functional foods. Crit. Rev. Food Sci. Nutr. 2011, 51, 13–28. [Google Scholar] [CrossRef] [PubMed]
  90. Gorinstein, S.; Leontowicz, H.; Leontowicz, M.; Namiesnik, J.; Najman, K.; Drzewiecki, J.; Cvikrova, M.; Martincova, O.; Katrich, E.; Trakhtenberg, S. Comparison of the main bioactive compounds and antioxidant activities in garlic and white and red onions after treatment protocols. J. Agric. Food Chem. 2008, 56, 4418–4426. [Google Scholar] [CrossRef] [PubMed]
  91. Gorinstein, S.; Leontowicz, H.; Leontowicz, M.; Jastrzebski, Z.; Najman, K.; Tashma, Z.; Katrich, E.; Heo, B.G.; Cho, J.Y.; Park, Y.J.; et al. The influence of raw and processed garlic and onions on plasma classical and non-classical atherosclerosis indices: Investigations in vitro and in vivo. Phytother. Res. 2010, 24, 706–714. [Google Scholar] [CrossRef] [PubMed]
  92. Rastogi, S.; Mohan Pandey, M.; Kumar Singh Rawat, A. Spices: Therapeutic potential in cardiovascular health. Curr. Pharm. Des. 2017, 23, 989–998. [Google Scholar] [CrossRef] [PubMed]
  93. Hwang, I.K.; Lee, C.H.; Yoo, K.Y.; Choi, J.H.; Park, O.K.; Lim, S.S.; Kang, I.J.; Kwon, D.Y.; Park, J.; Yi, J.S.; et al. Neuroprotective effects of onion extract and quercetin against ischemic neuronal damage in the gerbil hippocampus. J. Med. Food 2009, 12, 990–995. [Google Scholar] [CrossRef] [PubMed]
  94. Mills, E.; Koren, G. From type 2 diabetes to antioxidant activity: A systematic review of the safety and efficacy of common and cassia cinnamon bark. Can. J. Physiol. Pharmacol. 2007, 85, 837–847. [Google Scholar]
  95. Khan, A.; Zaman, G.; Anderson, R.A. Bay leaves improve glucose and lipid profile of people with type 2 diabetes. J. Clin. Biochem. Nutr. 2009, 44, 52–56. [Google Scholar] [CrossRef] [PubMed]
  96. Mehmood, M.H.; Gilani, A. Pharmacological basis for the medicinal use of black pepper and piperine in gastrointestinal disorders. J. Med. Food 2010, 13, 1086–1096. [Google Scholar] [CrossRef] [PubMed]
  97. Speroni, E.; Cervellati, R.; Dall’Acqua, S.; Guerra, M.C.; Greco, E.; Govoni, P.; Innocenti, G. Gastroprotective effect and antioxidant properties of different Laurus nobilis L. leaf extracts. J. Med. Food 2011, 14, 499–504. [Google Scholar] [CrossRef] [PubMed]
  98. Edwards, R.L.; Lyon, T.; Litwin, S.E.; Rabovsky, A.; Symons, J.D.; Jalili, T. Quercetin reduces blood pressure in hypertensive subjects. J. Nutr. 2007, 137, 2405–2411. [Google Scholar] [PubMed]
  99. Davis, P.A.; Yokoyama, W. Cinnamon intake lowers fasting blood glucose: Meta-analysis. J. Med. Food 2011, 14, 884–889. [Google Scholar] [CrossRef] [PubMed]
  100. Mallikarjuna, K.; Sahitya Chetan, P.; Sathyavelu Reddy, K.; Rajendra, W. Ethanol toxicity: Rehabilitation of hepatic antioxidant defense system with dietary ginger. Fitoterapia 2008, 79, 174–178. [Google Scholar] [CrossRef] [PubMed]
  101. Beric, T.; Nikolic, B.; Stanojevic, J.; Vukovic-Gacic, B.; Knezevic-Vukcevic, J. Protective effect of basil (Ocimum basilicum L.) against oxidative DNA damage and mutagenesis. Food Chem. Toxicol. 2008, 46, 724–732. [Google Scholar] [CrossRef] [PubMed]
  102. Alappat, L.; Awad, A.B. Curcumin and obesity: Evidence and mechanisms. Nutr. Rev. 2010, 68, 729–738. [Google Scholar] [CrossRef] [PubMed]
  103. Karmakar, S.; Choudhury, M.; Das, A.S.; Maiti, A.; Majumdar, S.; Mitra, C. Clove (Syzygium aromaticum Linn) extract rich in eugenol and eugenol derivatives shows bone-preserving efficacy. Nat. Prod. Res. 2012, 26, 500–509. [Google Scholar] [CrossRef] [PubMed]
  104. Kaviarasan, S.; Vijagalakshmi, K.; Anuradha, C.V. Polyphenol-rich extract of fenugreek seeds protect erythrocytes from oxidative damage. Plant Foods Hum. Nutr. 2004, 59, 143–147. [Google Scholar] [CrossRef] [PubMed]
  105. Majdalawieh, A.F.; Carr, R.I. In vitro investigation of the potential immunomodulatory and anti-cancer activities of black pepper (Piper nigrum) and cardamom (Elettaria cardamomum). J. Med. Food 2010, 13, 371–381. [Google Scholar] [CrossRef] [PubMed]
  106. Salem, M.L. Immunomodulatory and therapeutic properties of Nigella Sativa L. seed. Int. Immunopharmacol. 2005, 5, 1749–1770. [Google Scholar] [CrossRef] [PubMed]
  107. Elbarbry, F.; Gazarin, S.; Shoker, A. The protective effect of thymoquinone, an anti-oxidant and anti-inflammatory agent, against renal injury: A review. Saudi J. Kidney Dis. Transpl. 2009, 20, 741–752. [Google Scholar]
  108. Mahmoud, M.F.; Diaai, A.A.; Ahmed, F. Evaluation of the efficacy of ginger, Arabic gum and Boswellia in acute and chronic renal failure. Ren. Fail. 2012, 34, 73–82. [Google Scholar] [CrossRef] [PubMed]
  109. Hlavackova Singh, P.K.; Kaur, I.P. Synbiotic (probiotic and ginger extract) loaded floating beads: A novel therapeutic option in an experimental paradigm of gastric ulcer. J. Pharm. Pharmacol. 2012, 64, 207–217. [Google Scholar] [CrossRef] [PubMed]
  110. Alex, A.F.; Spitznas, M.; Tittel, A.P.; Kurts, C.; Eter, N. Inhibitory effect of epigallocatechin gallate (EGCG), resveratrol, and curcumin on proliferation of human retinal pigment epithelial cells in vitro. Curr. Eye Res. 2010, 35, 1021–1033. [Google Scholar] [CrossRef] [PubMed]
  111. Atsumi, T.; Tonosaki, K. Smelling lavender and rosemary increases free radical scavenging activity and decreases cortisol level in saliva. Psychiatry Res. 2007, 150, 89–96. [Google Scholar] [CrossRef] [PubMed]
  112. Shati, A.A.; Elsaid, F.G. Effects of water extracts of thyme (Thymus vulgaris) and ginger (Zingiber officinale Roscoe) on alcohol abuse. Food Chem. Toxicol. 2009, 47, 1945–1949. [Google Scholar] [CrossRef] [PubMed]
  113. Geoghegan, F.; Wong, R.W.; Rabie, A.B. Inhibitory effect of quercetin on periodontal pathogens in vitro. Phytother. Res. 2010, 24, 817–820. [Google Scholar] [PubMed]
  114. Nyo, S.N.T.; Williams, D.B.; Head, R.J. Rosemary and cancer prevention-preclinical perspectives. Crit. Rev. Food Sci. Nutr. 2011, 51, 946–954. [Google Scholar]
  115. Basnet, P.; Skalko-Basnet, N. Curcumin: An anti-inflammatory molecule from a curry spice on the path to cancer treatment. Molecules 2011, 16, 4567–4598. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  116. Goel, A.; Kunnumakkara, A.B.; Aggarwal, B.B. Curcumin as curecumin-from kitchen to clinic. Biochem. Pharmacol. 2008, 75, 787–809. [Google Scholar] [CrossRef] [PubMed]
  117. Rajasekaran, S.A. Therapeutical potential of curcumin in gastrointerestinal deaseases. World J. Gastrointest. Pathophysiol. 2011, 2, 1–14. [Google Scholar] [CrossRef] [PubMed]
  118. Aggarwal, B.B.; Harikumar, K.B. Potential therapeutic effects of curcumin, the anti-inflammatory agent, against neurodegenerative, cardiovascular, pulmonary, metabolic, autoimmune and neoplastic diseases. Int. J. Biochem. Cell Biol. 2009, 41, 40–59. [Google Scholar] [CrossRef] [PubMed]
  119. Al-Suhaimi, E.A.; Al-Riziza, N.A.; Al-Essa, R.A. Physiological and therapeutical roles of ginger and turmeric on endocrine functions. Am. J. Chin. Med. 2011, 39, 215–231. [Google Scholar] [CrossRef] [PubMed]
  120. Srinivasan, K. Ginger rhizomes (Zingiber officinale): A spice with multiple health beneficial potentials. FarmaNutition 2017, 5, 18–28. [Google Scholar] [CrossRef]
  121. Randhawa, M.A.; Alghamdi, M.S. Anticancer activity of Nigella sativa (black seed)—A review. Am. J. Chim. Med. 2011, 39, 1075–1091. [Google Scholar] [CrossRef] [PubMed]
  122. Shukla, Y.; Kolra, N. Cancer chemoprevention with garlic and its constituents. Cancer Lett. 2007, 247, 167–181. [Google Scholar] [CrossRef] [PubMed]
  123. Kundu, J.K.; Na, H.K.; Surth, Y.J. Ginger-derived phenolic substance with cancer preventive and therapentic potential. Forum Nutr. 2009, 61, 182–192. [Google Scholar] [PubMed]
  124. Aguilera, P.; Chanez-Cardenas, M.E.; Ortiz-Plata, A.; León-Aparicio, D.; Espinoza-Rojo, M.; Villeda-Hernández, J.; Sánchez-García, A.; Maldonado, P.D. Aged garlic extract delays the appearance of infarct, an effect likely conditioned by the cellular antioxidant systems. Phytomedicine 2010, 17, 241–247. [Google Scholar] [CrossRef] [PubMed]
  125. Villegas, I.; Sanches-Fidalgo, S.; de la Lastra, A. New mechanisms and therapeutic potential of curcumin for colorectal cancer. Mol. Nutr. Food Res. 2008, 52, 1040–1061. [Google Scholar] [CrossRef] [PubMed]
  126. Wilken, R.; Veena, M.S.; Wang, M.B.; Srivatson, E.S. Curcumin: A review of anticancer properties and therapeutic activity in head and neck squamores cell carcinoma. Mol. Cancer 2011, 10, 12. [Google Scholar] [CrossRef] [PubMed]
  127. Amin, A.; Hamza, A.A.; Bajbouj, K.; Ashraf, S.S.; Daoud, S. Saffron: A potential candidate for a novel anticancer drug against hepatocellular carcinoma. Hepatology 2011, 54, 857–867. [Google Scholar] [CrossRef] [PubMed]
  128. Aung, H.H.; Wang, C.Z.; Ni, M.; Fishbein, A.; Mehendale, S.R.; Xie, J.T.; Shoyama, C.Y.; Yuan, C.S. Crocin from Crocus sativus possesses significant anti-proliferation effects on human colorectal cancer cells. Exp. Oncol. 2007, 29, 175–180. [Google Scholar] [PubMed]
  129. Das, I.; Das, S.; Saha, T. Saffron suppresses oxidative stress in DMBA-induced skin carcinoma-a histopathological study. Acta Histochem. 2010, 112, 317–327. [Google Scholar] [CrossRef] [PubMed]
  130. Kim, S.H.; Bommareddy, A.; Singh, S.V. Garlic constituent diallyl trisulfide suppresses x-linked inhibitor of apoptosis protein in prostate cancer cells in culture and in vivo. Cancer Prev. Res. 2011, 4, 897–906. [Google Scholar] [CrossRef] [PubMed]
  131. Zhou, Y.; Zhuang, W.; Hu, W.; Liu, G.J.; Wu, T.X.; Wu, X.T. Consumption of large amounts of Allium Vegetables reduces risk for gastric cancer in a meta-analysis. Gastroenterology 2011, 141, 80–89. [Google Scholar] [CrossRef] [PubMed]
  132. Dorant, E.; van den Brandt, P.A.; Goldbohm, R.A.; Sturmans, F. Consumption of onions and a reduced risk of stomach carcinoma. Gastroenterology 1996, 110, 12–20. [Google Scholar] [CrossRef] [PubMed]
  133. Angelo, L.S.; Kurzrock, R. Turmeric and green tea: A recipe for the treatment of beta-chronic lymphocytic leukemia. Clin. Cancer Res. 2009, 15, 1123–1125. [Google Scholar] [CrossRef] [PubMed]
  134. Kim, H.Y.; Yokozawa, T.; Cho, E.J.; Cheigh, H.S.; Choi, J.S.; Chung, H.Y. In vitro and in vivo antioxidant effects of mustard leaf. Phytother. Res. 2003, 17, 465–471. [Google Scholar] [PubMed]
  135. Bhattacharya, A.; Li, Y.; Wade, K.L.; Paonessa, J.D.; Fahey, J.W.; Zhang, Y. Allyl isothiocyanate rich mustard seed powder inhibits bladder cancer growth and muscle invasion. Carciogenesis 2010, 31, 2105–2110. [Google Scholar] [CrossRef] [PubMed]
  136. Panza, E.; Tersigni, M.; Iorizzi, M.; Zollo, F.; De Marino, S.; Festa, C.; Napolitano, M.; Castello, G.; Lalenti, A.; Lanaro, A. Lauroside B-a megastigmane glycoside from Laurus nobilis (bay laurel) leaves, induces apoptosis in human melanoma cell lines by inhibitory NF-κB activation. J. Nat. Prod. 2011, 74, 225–233. [Google Scholar] [CrossRef] [PubMed]
  137. Yuan, H.; Zhu, M.; Guo, W.; Jin, L.; Chen, W.; Brunk, U.T.; Zhao, M. Mustard seeds attenuate azoxymethane-induced colon carcinogenesis. Redox. Rep. 2011, 16, 38–44. [Google Scholar] [CrossRef] [PubMed]
  138. Stavinoha, R.C.; Vattem, D.A. Potential neuroprotective effects of cinnamon. Int. J. Appl. Res. Nat. Prod. 2015, 8, 24–46. [Google Scholar]
  139. Wang, Y.S. Pharmacology and Applications of Chinese Materia Medica; Peoples Health Publishers: Beijing, China, 1983. [Google Scholar]
  140. Vasanthi, H.R.; Rarameswari, R.P. Indian spices for healthy heart—An overview. Curr. Cardiol. Rev. 2010, 6, 274–279. [Google Scholar] [CrossRef] [PubMed]
  141. Bordia, A.; Verma, S.K.; Srivastava, K.C. Effect of ginger (Zingiber officinale Roscoe) and fenugreek (Trigonella foenumgraecum L.) on blood lipids, blood sugar and platelet aggregation in patients with coronary artery disease. Prostaglandins Leukot. Essent. Fatty Acids 1997, 56, 379–384. [Google Scholar] [CrossRef]
  142. Rahman, K. Historical perspective on garlic and cardiovascular disease. J. Nutr. 2001, 131, 977–979. [Google Scholar]
  143. Kleijnen, J.; Knipschild, P.; Terriet, G. Garlic onions and cardiovascular risk factors. A review of the evidence from human experiments with emphasis on commercially available preparations. Br. J. Clin. Pharmacol. 1989, 28, 535–544. [Google Scholar] [CrossRef] [PubMed]
  144. Wani, S.A.; Kumar, P. Fenugreek: A review on its nutraceuticals properties and utilization in various food products. J. Saudi Soc. Agric. Sci. 2016. [Google Scholar] [CrossRef]
  145. Shan, B.; Cai, Y.Z.; Brooks, J.D.; Corke, H. Potential application of spices and herb extracts as natural preservatives in cheese. J. Med. Food 2011, 14, 284–290. [Google Scholar] [CrossRef] [PubMed]
  146. Beddows, C.G.; Jagait, C.; Kelly, M.J. Preservation of alpha-tocopherol in sunflower oil by herbs and spices. Int. J. Food Sci. Nutr. 2000, 51, 327–339. [Google Scholar] [PubMed]
  147. Bhale, S.D.; Xu, Z.; Prinyawiwatkul, W.; King, J.M.; Godber, J.S. Oregano and rosemary extracts inhibit oxidation of long-chain n-3 fatty acids in menhaden oil. J. Food Sci. 2007, 72, C504–C508. [Google Scholar] [CrossRef] [PubMed]
  148. D’Evoli, L.; Huikko, L.; Lampi, A.M.; Lucarini, M.; Lombardi-Boccia, G.; Nicoli, S.; Piironen, V. Influence of rosemary (Rosmarinus officinalis, L.) on plant sterol oxidation in extra virgin olive oil. Mol. Nutr. Food Res. 2006, 50, 818–823. [Google Scholar] [CrossRef] [PubMed]
  149. Colindres, P.; Brewer, M.S. Oxidative stability of cooked, frozen, reheated beef patties: Effect of antioxidants. J. Sci. Food Agric. 2011, 91, 963–968. [Google Scholar] [CrossRef] [PubMed]
  150. Nayak, S.; Sashidnar, R.B. Metabolic intervention of aflatoxin B1 toxicity by curcumin. J. Ethnopharmacol. 2010, 127, 641–644. [Google Scholar] [CrossRef] [PubMed]
  151. Renzulli, C.; Galvano, F.; Pierdomenico, L.; Speroni, E.; Guerra, M.C. Effects of rosmarinic acid against aflatoxin Bl and ochratoxin-A-induced cell damage in a human hepatoma cell line (Hep G2). J. Appl. Toxicol. 2004, 24, 289–296. [Google Scholar] [CrossRef] [PubMed]
  152. Puangsombat, K.; Smith, J.S. Inhibition of heterocyclic amine formation in beef patties by ethanolic extracts of rosemary. J. Food Sci. 2010, 75, T40–T47. [Google Scholar] [CrossRef] [PubMed]
  153. Cao, J.; Liu, Y.; Jia, L.; Jiang, L.P.; Geng, C.Y.; Yao, X.F.; Kong, Y.; Jiang, B.N.; Zhong, L.F. Curcumin attenuates acrylamide-induced cytotoxicity and genotoxicity in HepG2 cells by ROS scavenging. J. Agric. Food Chem. 2008, 56, 12059–12063. [Google Scholar] [CrossRef] [PubMed]
  154. Srihari, T.; Sengottuvelan, M.; Nalini, N. Dose-dependent effect of oregano (Origanum vulgare L.) on lipid peroxidation and antioxidant status in 1,2-dimethylhydrazine-induced ran carcinogenesis. J. Pharm. Pharmacol. 2008, 60, 787–794. [Google Scholar] [CrossRef] [PubMed]
  155. Ige, S.F.; Salawu, E.O.; Olaleye, S.B.; Adeeyo, O.A.; Badmus, J.; Adeleke, A.A. Onion (Allium cepa) extract prevents cadmium induced renal dysfunction. Indian J. Nephrol. 2009, 19, 140–144. [Google Scholar] [PubMed]
  156. Izawa, H.; Kohara, M.; Aizawa, K.; Suganuma, H.; Inakuma, T.; Watanabe, G.; Taya, K.; Sagai, M. Alleviative effects of quercetin and onion on male reproductive toxicity induced by diesel exhaust particles. Biosci. Biotechnol. Biochem. 2008, 72, 1235–1241. [Google Scholar] [CrossRef] [PubMed]
Table 1. Chemical composition of spices (seasonings) and culinary herbs [23,24,25].
Table 1. Chemical composition of spices (seasonings) and culinary herbs [23,24,25].
Spices and HerbsImportant Chemical Constituents
ClovesEugenol, isoeugenol, acetyleugenol, sesquiterpene, pinene, vanillin, gallic acid, flavonoids, phenolic acids
CinnamonEugenol, limonene, terpineol, catechins, proanthocyanidins, tannins, linalool, safrole, pinene, methyleugenol, benzaldehyde
CardamonLimonene, 1,8-cineole, terpinolene, myrcene, caffeic acid, quercetin, kaempferol, luteolin, pelargonidin
CorianderLinalool, borneol, geraniol, terpineol, cumene, pinene, terpinene, quercetin, kaempferol, caffeic, ferulic, n-coumaric and vanillic acids, rutin, tocopherols, pyrogallol
SaffronCrocins (water soluble carotenoids), safranal, flavonoids, gallic, caffeic, ferulic, n-catechuic, syringic, salicylic, and vanillic acids
TurmericCurcumins, essential oils, eugenol, carotene, ascorbic acid, caffeic, p-coumaric, protocatechuic, syringic, vanillic acid
GingerGingerol, turmeric, paradol, geraniol, geranial, borneol, linalool, camphene, zingerol, zingiberon
AniseCamphene, pinene, linalool, trans-, cis-anetholes, eugenol, acetanisole, rutin, luteolin-7-glucoside, apigenin-7-glucoside, isoorientin
CarawayMonoterpenes, sesquiterpene, aromatic aldehydes, terpene esters, terpenol, terpenal, terpenon, limonene, safranal, kaempferol, quercetin, tannins, caffeic, ferulic, p-coumaric, and chlorogenic acids
FenugreekSesquiterpenes, aromatic aldehydes, terpenes
Black pepperPiperine, pinene, camphene, limonene, terpenes, piperidine, isoquercetin, sarmentine
OreganoApigenin, quercetin, luteolin, myricetin, diosmetin, eriodictyol, carvacrol, thymol, rosmarinic, caffeic, p-coumaric, protocatechuic acid
BasilApigenin, catechins, quercetin, rutin, kaempferol, anthocyanins, eugenol, limonene, terpinene, carvacrol, geraniol, menthol, safrole, tannins, ursolic, p-coumaric, rosmarinic acids
Bay leaf1,8-cineole, cinnamtannin
DillQuercetin, kaempferol, myricetin, catechins, isorhamnetin, carvone, limonene
GarlicAllicin, diallyl sulfide, diallyl disulfide, diallyl trisulfide, allyl isothiocyanate, S-allyl cysteine
HorseradishPhenyl methyl isothiocyanate, allyl isothiocyanate, sinigrin, asparagine
AllspiceEugenol, gallic acid, pimentol, quercetin
MarjoramLimonene, pinene, terpinene, p-cumene, apigenin, ferulic, sinapinic, caffeic, syringic, rosmarinic, 4-hydroxybenzoic, vanillic acids
MustardAllyl isothiocyanate, carotene, isorhamnetin, isorhamnetin-7-O-glucoside, kaempferol glucoside
FennelflowerPinene, p-cumene, thymoquinone, thymohydroquinone, thymol, carvacrol, nigellicine, nigellidine, hederin
OnionQuercetin, apigenin, dipyridyl disulfide, rutin, quercetin-4-glucoside
ParsleyApigenin, luteolin, kaempferol, myricetin, quercetin, caffeic acid
Red pepperCapsaicin, tocopherol, lutein, carotene, capsanthin, quercetin, ascorbic acid
PeppermintMenthol, menthone, limonene, isomenthone, eriocitrin, hesperidin, apigenin, luteolin, rutin, carotenes, tocopherols, caffeic, rosmarinic, chlorogenic acid
RosemaryCarnosol, rosmanol, geraniol, pinene, limonene, apigenin, naringin, luteolin, rosmarinic, vanillic, ursolic, caffeic acids
SageGeraniol, pinene, limonene, carnosol, saponin, catechins, apigenin, luteolin, rosmarinic, carnosine, vanillic, caffeic acids
NutmegCatechins, lignans, myricetin, orgentin, caffeic acid
MyrtleAnthocyanins, pinene, limonene, gallic and ellagic acids, myrtocommulone, myricetin-3-O-galactoside, myricetin-3-O-rhamnoside
LavenderLimonene, quercetin, apigenin, kaempferol glucoside, ferulic, rosmarinic, caffeic, p-coumaric acid
Table 2. Flavonoid content in spices from the USDA (U.S. Department of Agriculture) database on flavonoids content of selected foods, release 3.1 (2014) [26].
Table 2. Flavonoid content in spices from the USDA (U.S. Department of Agriculture) database on flavonoids content of selected foods, release 3.1 (2014) [26].
NameFlavonoid Content (mg per 100 g)Total Flavonoid Content (mg per 100 g)
ParsleyApigenin 4503.5, isorhamnetin 331.2, luteolin 19.74854.5
Mexican oreganoLuteolin 1028.7, naringenin 372.0, eriodictyol 85.3, quercetin 42.0, apigenin 17.71550.79
Celery seedsLuteolin 762.4, apigenin 78.65841.05
CapersKaempferol 259.19, quercetin 233.84493.03
SaffronKaempferol 205.48205.48
DillQuercetin 55.15, isorhamnetin 43.50, kaempferol 13.33, myricetin 0.70112.68
ThymeLuteolin 45.25, apigenin 2.5047.75
FennelQuercetin 48.80, myricetin 19.80, isorhamnetin 9.30, kaempferol 6.50, luteolin 0.1084.50
Coriander, leavesQuercetin 52.9052.90
WormwoodQuercetin 10.0, kaempferol 11.0, isorhamnetin 5.0, luteolin 1.027.0
RosemaryNaringenin 24.86, luteolin 2.0, apigenin 0.5527.41
GingerKaempferol 33.6033.60
MustardKaempferol 38.20, quercetin 8.80, isorhamnetin 16.2062.90
SageLuteolin 16.70, apigenin 1.2017.90
Red onionQuercetin 20.30, isorhamnetin 4.58, delphinidin 4.28, cyanidin 3.19, peonidin 2.07, kaempferol 0.65, apigenin 0.2435.31
Chile pepperQuercetin 14.7014.70
Yellow pepperQuercetin 50.63, luteolin 6.9357.56
Tasmanian pepperCyanidin 752.68752.68
GarlicQuercetin 1.74, myricetin 1.61, kaempferol 0.263.61
Table 3. The major biologically active compounds found in spices and herbs.
Table 3. The major biologically active compounds found in spices and herbs.
SpicesActive SubstanceFormula
GingerGingerol Antioxidants 06 00070 i001
RosemaryRosmarinic acid Antioxidants 06 00070 i002
OnionQuercetin Antioxidants 06 00070 i003
TurmericCurcumin Antioxidants 06 00070 i004
ClovesEugenol Antioxidants 06 00070 i005
FennelflowerThymoquinone Antioxidants 06 00070 i006
Black pepperPiperine Antioxidants 06 00070 i007
GarlicAllicin, S-allyl cysteine Antioxidants 06 00070 i008
Red pepperCapsaicin Antioxidants 06 00070 i009
ParsleyApigenin Antioxidants 06 00070 i010
Oregano, celery (seeds)Luteolin Antioxidants 06 00070 i011
CapersKaempferol Antioxidants 06 00070 i012
Tasmanian pepperCyanidin Antioxidants 06 00070 i013
SaffronCrocetin, crocin Antioxidants 06 00070 i014
Table 4. Reported therapeutic effects of spices in different diseases.
Table 4. Reported therapeutic effects of spices in different diseases.
DiseasesSpicesReferences
Cardiovascular diseases, including heart attackGarlic, turmeric, ginger[90,91,92]
neurodegenerative diseasesMint, onion[93]
Antidiabetic actionCinnamon, bay leaf, wormwood, fenugreek, mustard, pomegranate[94,95]
Gastrointestinal diseasesBlack pepper, bay leaf[96,97]
HypertensionCardamon, cinnamon[98,99]
Hepatic diseasesCaraway, cardamon[43,100]
Endocrine diseasesGinger, turmeric[87]
Against DNA oxidationBasil[101]
ObesitySaffron, turmeric[102]
Bone diseasesCloves[103]
Protection against oxidative damage to red blood cellsFenugreek, garlic[104]
Immunomodulatory actionTurmeric[105,106]
Renal diseasesGarlic, fennelflower, ginger[107,108]
Antiulcer actionGinger[109]
Pigment cell growth inhibitionTurmeric[110]
Reduction of cortisol level in salivaLavender, rosemary[111]
Against alcohol abuseThyme, ginger[112]
Against gum diseaseLicorice[113]
Table 5. Spices against cancer.
Table 5. Spices against cancer.
SpicesCancer TypeReferences
TurmericRectal cancer, oral cancer, leukemia, carcinoma of the head and neck[125,126]
SaffronSkin carcinoma, rectal cancer, hepatic carcinoma[127,128,129]
GarlicProstate cancer, colon cancer[130,131]
OnionGastric carcinoma[132]
TurmericLeukemia[133]
MustardRectal carcinoma, bladder cancer[134,135]
Bay leafInhibits melanoma cell growth[136]
Mustard (seeds)Rectal carcinoma, bladder cancer[137]
Table 6. Major bioactive compounds of spices with potential beneficial effects for the management of CVD (Cardiovascular disease).
Table 6. Major bioactive compounds of spices with potential beneficial effects for the management of CVD (Cardiovascular disease).
SpicesMajor Bioactive CompoundsPotential Beneficial EffectsPotential Mechanism for Anti-CVD CharacteristicsReferences
CinnamonProcyanidinAntioxidantIncrease coronary blood flow[85,99]
CinnamaldehydeAntimicrobial potentialProvoke pituitrin induced reduction of blood flow[138,139,140]
Reduce peripheral vascular resistance
Increase cardiac contractile force
GingerGingerolAntioxidantReduction in platelet aggregation[19,140,141]
ShogaolAnti-inflammatoryReduce LDL cholesterol levels
ZerumboneReduce LDL atherogenic modifications
Reduction in the oxidative response of macrophages
GarlicAllicinAntioxidantInhibit enzymes involved in lipid synthesis[140,141,142]
Decrease platelet aggregation
Prevent lipid peroxidation of oxidized erythrocytes
Increase antioxidant status
Inhibit angiotensin-converting enzyme
TurmericCurcuminAntioxidantReduce platelet aggregation[140]
CapsaicinAnti-inflammatoryDecrease triglycerides
Reduce thromboxane
Decrease serum cholesterol
Decrease cardiomyocytic apoptosis
OnionPolyphenolsAntioxidantReduce platelet aggregation[143]
FlavonoidsReduce cholestrol level
FlavonolsEnhance blood fibrinolytic activity
Red pepperCurcuminAntioxidantHypotriglyceridemic[22]
CapsaicinAnti-inflammatoryReduce cholestrol in blood and liver
FenugreekRhaponticinAntioxidantLymphatic cleansing[141,142,143,144]
IsovitexinAnticarcinogenicDecrease blood pressure
Hypoglycermic effect

Share and Cite

MDPI and ACS Style

Yashin, A.; Yashin, Y.; Xia, X.; Nemzer, B. Antioxidant Activity of Spices and Their Impact on Human Health: A Review. Antioxidants 2017, 6, 70. https://doi.org/10.3390/antiox6030070

AMA Style

Yashin A, Yashin Y, Xia X, Nemzer B. Antioxidant Activity of Spices and Their Impact on Human Health: A Review. Antioxidants. 2017; 6(3):70. https://doi.org/10.3390/antiox6030070

Chicago/Turabian Style

Yashin, Alexander, Yakov Yashin, Xiaoyan Xia, and Boris Nemzer. 2017. "Antioxidant Activity of Spices and Their Impact on Human Health: A Review" Antioxidants 6, no. 3: 70. https://doi.org/10.3390/antiox6030070

APA Style

Yashin, A., Yashin, Y., Xia, X., & Nemzer, B. (2017). Antioxidant Activity of Spices and Their Impact on Human Health: A Review. Antioxidants, 6(3), 70. https://doi.org/10.3390/antiox6030070

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