Open access peer-reviewed chapter

Spices-Reservoir of Health Benefits

Written By

Cheryl Sachdeva and Naveen Kumar Kaushik

Submitted: 24 January 2021 Reviewed: 07 February 2021 Published: 02 March 2021

DOI: 10.5772/intechopen.96471

From the Edited Volume

Natural Medicinal Plants

Edited by Hany A. El-Shemy

Chapter metrics overview

399 Chapter Downloads

View Full Metrics

Abstract

Spices contribute to the quality, nutritive value, and flavor of food. Since ancient times, they hold a great medicinal value. Their antimicrobial, antiviral, antibacterial, anti-inflammatory, and other numerous properties have made them a potent source of therapeutic agents. Phytochemical analysis revealed presence of active constituents such as eugenol, curcumin, carotenoids in clove, turmeric, saffron respectively that explains the efficacious nature of these spices. Owing to their easy availability and consumption, it is advised to make spices daily part of our diet though in balanced amount as sometimes excess usage bear few consequences. Evaluating multiple benefits offered by these as immunity boosters especially in times of pandemic and incorporating them in our routine diet would improve disease management strategies. This chapter discusses the reservoir of activities exhibited by few spices along with the components responsible for these activities. Here, we also discussed their negative effects if at all.

Keywords

  • curcumin
  • spices
  • antiviral
  • clove
  • immune booster

1. Introduction

Spices are plant-derived substances and play a crucial role in cooking. They are responsible for bringing out complex and rich flavors of food with their color, taste, aroma and making a cuisine distinct and popular. Without them kitchen looks empty and food gives a feeling of Stone Age. But do these spices just provide aroma or piquancy to food? Or is there any underlying advantage behind their regular consumption with food. Moreover, their usage depends upon habitat, time, and weather conditions. It is evident from both traditional as well as modern literature that vast medicinal properties offered by the spices makes them legendary and a vital part of daily diet. Pharmacological and molecular studies revealed that oils and alkaloids produced by most of the spices possess antimicrobial, anti-parasitic, immune booster, antioxidant and other important biological properties [1, 2, 3, 4]. Their antioxidant and bactericidal activities prevents rancidity thereby increasing storage life of food [5]. Turmeric, with curcumin as principle ingredient, has been quite extensively used in the treatment of disorders such as amenorrhea, inflammation, hepatitis, arthritis [6, 7]. Clove, cinnamon, are rich source of antioxidants exhibiting wide range of pharmacological effects [8].

As spices are rich in immunity boosting ingredients, their daily consumption would lead to development of long-lasting immune protection and might maintain safe drug bullets at a certain basal level in blood stream to tackle the infection. Since the outbreak of COVID-19, the first line of defense is body’s immune system. Therefore, regular usage of spices not only enhances the body’s immunity to fight against the infection but also provides a prophylactic therapy to prevent and minimize the chances of infection. Out of wide variety of spices, pharmaco-potential of some of them has been discussed here.

Advertisement

2. Turmeric

Turmeric (rhizome of Curcuma longa L.), native to Tropical South Asia, is used as a condiment, food preservative and a traditional remedy for various diseases. This spice of Zingiberaceae family is widely cultivated in tropics and is known by different names such as Haldi, bhadra, pitika, mehagni, terre merite etc. To date various compounds of turmeric have been identified such as monoterpenes, sesquiterpenes, curcuminoids, alkaloids, sterols. Among these, most abundant is curcumin (77%) which is responsible for characteristic yellow color of turmeric and exhibits a wide spectrum of biological effects viz. antidiabetic, antimicrobial, anti-inflammatory, etc. (Figure 1) [9].

Figure 1.

Biological properties and chemical constituents of Turmeric.

Anti-inflammatory and antioxidant effects of curcumin have proved to be beneficial against neurological diseases. Curcumin has the ability to bind amyloid β (Aβ) inhibiting fibrils formation [10] and, also enhance its cellular uptake [11], circumvent plaque deposition [12] thereby preventing Alzheimer’s disease. Furthermore, curcumin is capable of decreasing Aβ serum levels and attenuating inflammation in Alzheimer’s disease mouse models [13] along with rescuing altered neuritic morphology around Aβ plaques [14]. Additionally, studies have shown that curcumin decreased Huntington protein aggregation [15], suppressed cell death relieving disease symptoms [16]; modulated accumulation of α-synuclein which is the prime reason for Parkinson’s disease [17]. It has been reported that intravenous and oral administration of curcumin modulates dopamine related damage, induces microglial activation, and improves locomotion [18]. Curcumin has, further, shown to increase docosahexaenoic acid (DHA) levels [19]; improve learning and mental ability in scopolamine induced amnesia in mice [20]. Moreover, numerous other compounds with potent antioxidant activity have also been isolated from turmeric [21].

Curcumin has been known to downregulate production of inflammatory cytokines such as MCP- 1, TNF α, IL6, IL-1β both in vitro and in vivo [22, 23, 24]. However, recent study have suggested that efficacy to reduce levels of pro-inflammatory cytokines is enhanced on administering liposomal curcumin [25]. Studies have reported upregulation of heme oxygenase-1 reducing oxidative stress and providing protection against acute vascular inflammation in vitro as well as in vivo [26, 27].

Anti-rheumatic effects of curcumin have also been reported as curcumin decreased β3 and β7 integrins expression (adhesion molecules) ultimately decreasing joint inflammation; downregulated expression of chemokines, pro-inflammatory cytokines and growth-related oncogene/keratinocyte chemoattractant [28]. Further, randomized trials have also shown the efficacy of oral administration of curcumin in treatment of Rheumatoid Arthritis [29, 30].

Curcumin is effective in the management of virus infections as it inhibited Zika and Chikungunya virus at a concentration of 5 μM (IC50 = 1.9 and 3.89 μM respectively) [31], herpes simplex virus [32] and dengue virus [33]. Further, it inhibited human immunodeficiency virus (HIV) integrase and protease suggesting its protective effects against AIDS [34, 35]. The pandemic, COVID-19 related mortality is mainly due to acute respiratory distress syndrome with extensive cytokine storm. It has been reported that curcumin upregulates peroxisome proliferator-activated receptor-γ induction leading to inhibition of nuclear factor-κB (NFkb) signaling eventually decreasing cytokine storm [36] which suggests that curcumin might ameliorate COVID associated symptoms. Bioinformatic analysis have further shown ability of curcumin to interact with ACE2 receptor [37] and main protease [38] thereby fighting against COVID-19.

Curcumin displays antiparasitic and anti-cancer effects too. At a dose of 5 μM, it altered P. falciparum microtubules leading to reduction of 70–90% of parasitemia (IC50 = 50 μM) [39] and further at 100 mg/kg showed 80–90% decrease in P. berghei parasitemia [40]. Curcumin, in synergistic effect with Mitomycin C (5 μmol/L) arrested growth of MCF 7 breast cancer cell lines at G0/G1 phase of the cell cycle at a concentration of 40 μmol/L [41], decreased sensitivity of NFκB in human pancreatic cells lines BxPC-3, Capan-1, Capan-2, ASPC-1, and HS766-T (73–95% inhibition) [42], induced apoptosis [43]; inhibited cyclo-oxygenase 2 (COX 2- its overexpression leads to carcinogenesis) production in HT-29 colon cancer cell lines [44]. This prompts the requirement of detailed investigation to understand the potential of curcumin in cancer biology. Apart from curcumin, non-curcuminoids have also been reported to exhibit potential anticancer activities too [45].

Regardless of its demonstrated efficacy, purified curcumin has also been reported as pan assay interference compounds (PAINS) that show activity by interfering with assay readouts [46]. Curcumin exhibits PAIN properties such as fluorescence interference [47], aggregation [48], metal chelation [49], redox reactivity [50]. It is a highly unstable compound as it degrades rapidly in alkaline solutions [51]. Another drawback of curcumin is its poor bioavailability, however, number of formulations of curcumin with enhanced bioavailability and absorption are now available such as BioPerine-20x [52], BCM-95CG [52], Longvida-67x [53], Meriva-29x [54]. Furthermore, it is advised, traditionally, to consume turmeric powder with warm milk and ghee (Milk fat) as it is believed that this combination boosts immunity, purifies blood, beats everyday fatigue and anxiety, relieves cold and cough, which all are requirement to fight against COVID-19. Moreover, this combination might also enhance bioavailability of curcumin due to the constituents of milk and ghee such as casein, fats, iodine, phosphorus, calcium, vitamins etc.

Advertisement

3. Cinnamon

Cinnamon has a sweet, warm taste and is derived from dried central part of bark of Cinnamomum zeylanicum Blume (family Lauraceae). It is native to the Caribbean, South America, and Southeast Asia and is used throughout the world for its astounding properties such as anti-inflammatory, antidiabetic, antimicrobial, anticarcinogenic effects (Figure 2) [55]. Biochemical investigation of cinnamon revealed presence of camphor, linalool, cinnamaldehyde (major constituent), terpinen-4-ol, 1,8-cineole, α-cadiene, safrole, α-cadinol, germacrene D, γ-muurolene, α- terpineol, eugenol, 1,6-octadien-3-ol, 3,7-dimethyl,1-phenyl-propanr-2,2-diol diethanoate, etc. [56].

Figure 2.

Biological properties of Cinnamon.

Cinnamon has been reported to exhibit antioxidant effects. In vitro studies showed free radical scavenging activity of methanolic extracts of cinnamon against 2,20 -azinobis- 3-ethylbenzothiazoline-6-sulphonic acid (ABTS) radical and Diphenylpicrylhydrazyl (DPPH) radical cations [57]. Intake of 100 mg/30 ml of cinnamon tea for 2 weeks showed reduction in the levels of 2-thiobarbituric acid reactive substances (TBARS) in plasma by 38% and increase in total antioxidant power 21% in a clinical study [58].

Antidiabetic and cholesterol lowering effects of aqueous extracts of cinnamon (AEC) have also been reported where it reduced fasting glucose levels (at 250 mg) from 1.14 mg/ml to 1.02 mg/ml in patients with impaired fasting glucose [59]; at a dose of 500 mg/kg for two months decreased glucose levels (p < 0.005) along with increasing in insulin sensitivity [60] and at 200 mg/kg reduced levels of LDL cholesterol, triglycerides and total cholesterol and increased levels of HDL-cholesterol in diabetic rats and hyper-lipidemic albino rabbits [61]. Further, decline in gastric acid secretion by 60% and reduction in gastric hemorrhagic lesions in rats was observed on pre-treatment with 250 mg/kg and 500 mg/kg of AEC [62].

Peterson et al., reported cinnamon as a potent anti-alzheimer agent as AEC inhibited tau aggregation (aggregation destabilizes microtubules causing Alzheimer’s disease) [63].

In addition, cinnamon possesses antimicrobial and anticancer activities. Ethanolic extracts of cinnamon exhibited anti-microbial properties against Listeria monocytogenes (MIC 0.4 mg/ml other MICs) [64]. Further, essential oil of cinnamon also showed inhibitory effects against Candida albicans (MIC 7.81 μl/ml) [65]; nosocomial P. aeruginosa isolate (MIC- 1.9 μl/ml) [66]; Anopheles tessellatus (LD50: 0.33 μg/mL) and Culex quinquefasciatus (LD50: 0.66 μg/mL) [67]. Furthermore, AEC inhibited vascular endothelial growth factor (VEGF) and induced growth of vessels in aortic ring of rat ex vivo at a dose of 25 and 50 μg/ml suppressing angiogenesis [68]. Constituents of cinnamon essential oil, trans-cinnamaldehyde and its analogue - 4-hydroxy-3-methoxy-trans-cinnamaldehyde are effective inhibitors of bacterial acetyl-CoA carboxylase [69].

Cinnamon is considered as a strong immunity booster. At a dosage of 10 mg/kg, it significantly increased serum immunoglobulin levels whereas at 100 mg/kg dosage, along with boosting humoral immunity, cinnamon increased antibody titer and phagocytic index too thereby increasing cell-mediated immunity [70]. Cinnamon reportedly exhibits immunomodulatory properties as well. Studies have suggested that cinnamon decreased fibrotic symptoms and pro-inflammatory cytokines on treatment with 4.5 ml/kg dose [71] and 0.8 g/kg dose for 12 weeks [72] respectively in colitis infected mice models. Suppression of pro-inflammatory cytokines such as TNF-a, IL-1b, and IL-6 along with inhibition of nitric oxide secretion were also observed in BV 2 microglial cells on treatment with 50 μg/ml of ethanolic cinnamon extract [73]. Further, cinnamon bark is capable of decreasing in IFN-γ levels, enhancing of IL2 secretion thereby inhibiting cell death [74]. Studies have also suggested that cinnamaldehyde inhibits PI3K, NF-B activation and PDK1 thereby regulating monocyte\macrophage-mediated immune responses [74].

Recent bioinformatic analysis showed the possible effectiveness of molecules isolated from cinnamon against COVID-19 [75]. The ability to reduce pro-inflammatory cytokines and strong in silico investigation suggests the probable potential of cinnamon in fight against COVID-19.

Though cinnamon exhibits a wide range of health benefits, it is important to keep a check on the quantity of cinnamon consumed. A large amount can cause a dramatic drop in the blood sugar levels. In addition, high levels of cinnamon can cause rapid increase in heart rate, liver toxicity [76, 77].

Advertisement

4. Fennel

Fennel (seeds of Foeniculum vulgare Mill), originally cultivated in Mediterranean region, is used throughout the world for its licorice-like flavor. Belonging to class Magnoliopsida and family Apiaceae, fennel is known by different names such as suanf, sweet fennel, florence fennel, finocchio and is a concentrated source of minerals. This perennial herb is long loved for its culinary use. The essential oil of fennel constitutes anethole, estragole as major components and limonene, fenchone and others as minor components (Figure 3) [78, 79].

Figure 3.

Biological properties and chemical constituent of Fennel.

Fennel has been used for a long time for medicinal purposes (Figure 3) [80, 81]. It is a potent antioxidant agent. Essential oil of fennel seeds (FS) showed 45.05% DPPH radical scavenging activity along with 48.80–70.35% inhibition of peroxidation [81]. Ethanol and water extracts of FS (100 μg/ml) inhibited peroxidation in linoleic acid system by 77.5 and 99.1% respectively [82]. Parejo et al., isolated phenolic compounds from fennel viz. rosmarinic acid, kaempferol-3- O-glucoside, eriodictyol-7-Orutinoside, caffeoylquinic acid, quercetin-3-O-galactoside and observed decrease in absorbance of DPPH by 50% (IC50 in μg/mL = 1.17, 8.21, 24.78, 3.82, 7.52 respectively) [83].

Further, essential oil from fennel fruit showed inhibitory effects on growth of Paenibacillus larvae (MIC = 250 μg/ml) [84] and mycelial growth of S. sclerotiorum(MIC = 0.2 μg/ml) [85]. Similar inhibitory effects were observed against C. quinquefasciatus (LC50 = 70.85); A. gambiae (LC50 = 44.74) [86] and larvae of C. pipiens (90% inhibition at 60 mg/L) [87]. Hexane extracts of FS showed potent inhibitory effects against E. coli (MIC = 12.5 μg/mL), S. typhi (MIC =15 μg/mL), S. aureus (MIC = 10 μg/mL) [88].

Recent study reported that 300 μg/μl FS ethanolic extract inhibited Influenza virus H5N1 by 82.8% [89]. Moreover, Alazadeh et al., showed that oral administration of FS extract in capsular form ameliorated knee ostroarthritis [90]. In addition, methanol extract of FS showed significant anticancer potential against liver cancer cell line Hepg-2 (IC50 = 27.96 μg/mL) and breast cancer cell line MCF-7 (IC50 = 15.78 μg/mL) [80]. Özbek et al., 2003 studied hepatoprotective effects of fennel and observed that a dose of 0.4 ml/kg of fennel oil showed significant protective role against liver fibrosis (CCl4 induced) in rats [91].

It is safe to consume fennel and since it provides protection against flu, cough, it is advised to take fennel with warm milk.

Advertisement

5. Clove

Clove [Syzygium aromaticum (L.) Merr. & L.M. Perry] is one of the most valuable spices of family Myrtaceae and is a native of Indonesia, albeit found all around the globe. Major bioactive component of clove is eugenol. Other components include phenolic acids such as gallic acid, gallic acid derivatives, caffeic acids, salicylic acids; flavonoids such as quercetin, kaempferol (Figure 4) [92].

Figure 4.

Chemical constituents and biological properties of Clove.

Traditionally used to prevent nausea, enhance blood circulation and liver function, clove is commonly applied for toothache relief and has been long known as a medicine for numerous ailments (Figure 4). Miyazawa & Hisama, isolated dehydrodieugenol and trans-coniferyl aldehyde from ethyl acetate extract of clove bud and observed significant activity of both, at a concentration of 0.6 μmol/mL and 1.2 μmol/ml respectively, against mutagens 4-nitroquinolin 1-oxide and N-methyl-N′-nitro-N-nitrosoguanidine [93]. Furthermore, eugenol and eugenol acetate extracted from aroma extract of clove buds inhibited 99% of hexanal oxidation [94].

Eugenol also exhibits remarkable antimicrobial, antiparasitic, antiviral activities. Essential oil of clove has reportedly inhibited growth of S. aureus, H. influenzae (MIC = .0125 ml/ml each), K. pneumoniae (MIC = .050 ml/ml) [95], C. albicans (MIC = 2.5 μg/ml), L. monocytogenes (MIC = 5 μg/ml), Y. enterocolitica (MIC = 2.5 μg/ml) [96]. It has been reported that clove decreases ergosterol (cell membrane component) inhibiting growth of C. albicans (MIC = 0.64 μg/ml) [97]. Methanol extract, ether soluble fraction (ES), ethyl acetate soluble fraction (EAS) and acetone soluble fraction (AS) of clove buds showed inhibitory effects on Bacillus cereus (MIC =250 μg/disc each). Further, EAS and AS also inhibited Micrococcus luteus and Shigella dysenteriae respectively (MIC = 62.5 μg/disc each) [98]. In addition, antiparasitic effects were reported by Bagavan et al., who observed growth inhibition of chloroquine resistant P. falciparum on treatment with ethyl acetate and methanol extracts of clove (IC50 = 13 μg/ml and 6.25 μg/ml respectively) [99]. Hypoglycemic effects of clove have also been identified. Methanol extract of clove activated AMP-activated protein kinase (AMPK) pathway, a regulator of cellular energy homeostasis thereby regulating glucose metabolism [100]. A recent report has pointed out that it relieves insulin resistance [101].

Consumption of clove is safe, and it offers numerous benefits, however, studies have shown that clove oil increases clotting time [102] which might increases the risk of bleeding in case of bleeding disorders.

Advertisement

6. Cardamom

Cardamom [Elettaria cardamomum (L.) Maton, also known as “Queen of Spices”] is an aromatic spice commonly used as a flavoring agent. This perennial herb belongs to Zingiberaceae family. It is native to Western Ghats of Southern India and widely cultivated in countries such as Sri Lanka, North America, Guatemala, New Guinea, and Thailand. Essential oil of cardamom constitutes α- terpinyl acetate, 1,8-cineole, linalool, limonene, eugenol, safrole (Figure 5a) [103, 104].

Figure 5.

(a) Chemical constituents of Cardamom; (b) Biological properties of Cardamom.

Cardamom is a valuable in relieving against ischemic heart disease. It showed protective effects against cardiac dysfunction associated with oxidative stress. A dose of 100 and 200 mg/kg of cardamom extract showed cardioprotective effects in albino rats who were induced with myocardial infarction due to isoproterenol [105]. Further, cardamom-oil maintained cholesterol homeostasis by potentially reducing cholesterol levels in hypercholesterolemic conditions and restoring atherogenicity index [106]. In addition, a dose of 1.5 g of cardamom powder for 12 weeks (two times a day) decreased the blood pressure in hypertensive individuals by 19 mmHg in systolic and 12 mmHg in diastolic BP [107].

Cardamom is an effective immunomodulatory agent due to its anti-inflammatory effects. It is capable of downregulating pro-inflammatory cytokines (Figure 5b) [108]; suppressing T helper (TH)1 cytokine release and enhancing T helper (TH)2 cytokine release [109]. Methanol and petroleum ether extract of cardamom reduced 70% and 50% lesions in ethanol-induced ulcer mice model at 500 mg/kg and 100 mg/kg respectively exhibiting gastroprotective effects [110]. A constituent of cardamom, cardamonin inhibited the formation of new cancer stem cells in case of breast cancer by effectively suppressing the up-regulation of IL-8 and, MCP-1 cytokines and activation of NF-κB pathway [111]. Antibacterial effects of cardamom has also been demonstrated [108, 112].

Recently, its efficacy against toxic effects of uranium has been reported. Uranium increases sodium and calcium ion levels, decreases and phosphate ion levels, inhibits Na+/K+ ATPase increasing the influx of into the neurons, and thereby damaging central nervous system. Aqueous extracts of cardamom (250 mg/kg) significantly increased the levels of phosphate and potassium ions and decreased the levels of calcium and sodium ions in albino rats administered with uranyl acetate dehydrate (40 mg/kg) [113]. Furthermore, protective effects against neurological disorders have also been reported as oral administration with 100 and 200 mg/kg of cardamom oil improved behavioral patterns, inhibited amyloid-β expression, declined in oxidative stress and inhibited of acetylcholinesterase in Wister rats [114, 115].

Advertisement

7. Red chili

Out of the wide variety of species under genus Capsicum like frutescens, pubscens, baccatum etc., dried fruits of Capsicum annum L. are the most commonly used spice of Solanaceae family. Commonly known as red chili, lal mirch, this plant is native to Central and South America and is cultivated in many parts of the world such as India, China. Biochemical analysis of red chili led to the identification of capsaicinoids (capsaicin, dihydrocapsaincin) (Figure 6), antioxidant vitamins (ascorbic acid, vitamin E), carotenoids (β - carotene, β cryptoxanthine) and several organic acids and minerals [116, 117]. Red chili has a phenolic substance, capsaicin responsible for its pungent smell and irritant properties. Capsaicin excites nociceptors that induce pain along with rise in temperature giving a sensation of heat (pungency). As spicy is not one of the five basic tastes viz. sweet, sour, bitter, umami and salty, heat produced by capsaicin is considered as taste of red chili.

Figure 6.

Biological properties and chemical constituent of Red Chili.

Capsaicin also exhibits anti-inflammatory properties [118]. It showed protective effects against gastric mucosal injury (ethanol-induced) in rats [119]. Capsaicin treatment ameliorated lipid peroxidation, inhibited myeloperoxidase activity in gastric lesions (ethanol induced) in rats [120].

Dried red chili powder (1% w/v) showed inhibitory effects against Listeria monocytogenes [121]. Tropical application of capsaicin (0.075%) reduced fat accumulation in mesenteric and epididymal adipose tissue by increasing expression of adipokines [122]. It was also found that a dose of 200 mg/kg of capsaicin decreases plasma triglyceride levels and fasting glucose in obese mouse model kept on high fat diet [123].

Earlier studies suggested the risk of oral cavity [124] and stomach [125] cancer on consumption of red chili, however, recent reports suggested that consumption of red chili is safe and does not increase risks of cancer [126]. Numerous reports have suggested protective effects of capsaicin against cancer. Capsaicin showed inhibitory effects on the growth of human KB cancer cells by promoting apoptosis at a concentration of 200–250 μM [127]. Further, capsaicin led to the formation of reactive oxidative species through mitochondria (at a dose of 150 μM) causing loss in mitochondrial membrane potential in BxPC-3 and AsPC-1, human pancreatic cancer cell lines [128]; inhibited activation of NF-kB and AP-1, transcription factors responsible for cellular proliferation and malignant formation, in mice model [129]. In addition, capsaicin inhibited growth of MCF breast cancer cell lines by causing cell cycle arrest at S phase and induced poly(ADP-ribose) polymerase-1 (PARP-1) cleavage (apoptosis is marked by the cleavage of PARP-1) by activating caspase-7 which is involved in apoptosis (Figure 6) [130]. Capsaicin and cisplatin, in a synergistic manner, arrested the growth of SNU-668, human gastric cell line at G1/S phase [131].

Advertisement

8. Black cumin

Seeds of Nigella sativa L., an annual flowering plant of Ranunculaceae family, have been of extensive use as a spice. Commonly known as black cumin, it is native to South and Southwest Asia and has diverse medicinal applications. Phytochemical analysis of black cumin seeds has showed presence of thymoquinone (TQ), para-cymene, and carvone, linoleic acid, oleic acid, palmitic acid, and stearic acid (Figure 7) [132].

Figure 7.

Chemical constituents of Black Cumin.

Black cumin has been reported to exhibit anti-inflammatory properties. Intra-peritoneal injection black cumin essential oil reduced inhibited carrageenan-induced paw oedema in rats thereby relieving inflammation [133]. Aqueous extracts of black cumin up-regulated the secretion of T-helper 2 cells and suppressed the secretion of pro-inflammatory cytokines viz. IL-6, TNFα, and NO [109]. Furthermore, black El-Mahmoudy et al., isolated TQ from essential oil of black cumin seeds and showed that TQ reduced nitrite accumulation and decreased inducible nitric oxide synthase levels (responsible for NO production) in rat peritoneal macrophages suggesting anti-inflammatory and cytoprotective effects of black cumin [134]. Methanol extract of seeds of black cumin (1 mg/ml) protected erythrocytes against protein degradation and loss of deformability induced due to peroxide [135] and has proved to stimulate innate humoral immune responses [136]. Proteins purified from black cumin exhibit potent antioxidant activities [137]. Furthermore, neuroprotective effects of black cumin have also been reported [138].

In addition, black cumin exhibits anti-bacterial, anti-viral, anti-helminthic effects. Black cumin seed oil (BSO) showed protective effects against murine cytomegalovirus (MCMV) that targets liver and spleen. Treatment with BSO showed approximately 38% and 20% decrease in viral load in liver and spleen respectively in MCMV infected mice [139]. Decrease in the number of S. mansoni worms in liver and eggs in both liver and intestine of mice has been observed after treatment with black cumin oil at a dose of 2.5 ml/kg and 5 ml/kg [140]. TQ has proved to be an effective bactericidal agent as it inhibited growth of Staphylococcus aureus (BIC50 = 22 μg/ml) [141], Salmonella typhii [142] Streptococcus mutans [143]. Further, black cumin inhibited the P. yoelii parasitemia by 94% [144].

Black cumin has protective effects against diabetes. Black cumin seeds (BCS) led to the decrease in elevated levels of glucose with increase in GSH levels and further inhibited liver damage induced by lipid peroxidation in diabetic rabbits [145]. In addition, improvement of glucose homeostasis in patients with type 2 diabetes on administration of black cumin (2 g/day for 3 months) with hypoglycemic drugs have also been reported [146].

Furthermore, aqueous extracts of black cumin significantly up-regulated cytotoxic activity of natural killer cells against YAC-1 tumor cells [109]. Oral administration of TQ at a dose of 0.01% suppressed benzo(a)pyrene induced forestomach tumor in mice by 70% [147] exhibiting anti-tumor effects.

Minor toxicological effects have also been reported, however, numerous studies demonstrated diverse therapeutic effects of black cumin and TQ and have supported its safe consumption [132].

Advertisement

9. Conclusion

Spices are rich source of bioactive components with innumerable beneficial attributes that have been verified and accepted by modern world in the past few decades. These are nowadays considered as a crucial & natural component of our daily diet. Consumption of spices aids in combating diseases when they are at their peak, for instance, best remedy for stomach infections are fennel seeds; turmeric is the tonic for fever-related diseases. Antimicrobial activities of spices make them valuable in hot climates as they prevent food spoilage. Although they lower the risk of various diseases such as diabetes, cancer, etc., there are some contradictions about their use. Despite all the pleiotropic effects offered by the spices, further evaluation about their mechanism of action is mandated to validate their clinical effects and their amount of consumption.

Advertisement

Conflict of interest

The authors declare no conflict of interest.

References

  1. 1. Baratta MT, Dorman HJD, Deans SG, Figueiredo AC, Barroso JG, Ruberto G. Antimicrobial and antioxidant properties of some commercial essential oils. Flavour Fragr J. 1998;13. DOI:3.0.CO;2-T
  2. 2. Mohamad RH, El-Bastawesy AM, Abdel-Monem MG, Noor AM, Al-Mehdar HAR, Sharawy SM, et al. Antioxidant and anticarcinogenic effects of methanolic extract and volatile oil of fennel seeds (Foeniculum vulgare). J Med Food. 2011;14:986-1001
  3. 3. Dolati M, Rezaei K, Vanak ZP, Movahed S. Study of the Effects of Essential Oils of Cumin, Savory and Cardamom as Natural Antioxidants on the Flavor and Oxidative Stability of Soybean Oil During the Storage. J Essent Oil Bear Plants. 2016;19:176-84. DOI:10.1080/0972060X.2014.935030
  4. 4. Sharma V, Singh P, Rani A. Antimicrobial Activity of Trigonella foenum-graecum L . ( Fenugreek ) Keywords : Eur J Exp Biol. 2017;7:1-4
  5. 5. Teneva D, Denkova Z, Goranov B, Denkova R, Kostov G, Atanasova T, et al. Chemical composition and antimicrobial activity of essential oils from black pepper , cumin , coriander and cardamom against Against Some Pathogenic Microorganisms [2016]. Acta Univ Cibiniensis Ser E FOOD Technol. 2016;XX
  6. 6. Aggarwal BB, Surh Y-J, Shishodia S. The Molecular Targets and Therapeutic Uses of Curcumin in Health and Disease. 2014
  7. 7. Aggarwal B. Curcumin : The Indian solid gold. 2015
  8. 8. Özcan MM, Arslan D. Antioxidant effect of essential oils of rosemary, clove and cinnamon on hazelnut and poppy oils. Food Chem. 2011;129:171-4. DOI:http://dx.doi.org/10.1016/j.foodchem.2011.01.055
  9. 9. Wickenberg J, Ingemansson SL, Hlebowicz J. Effects of Curcuma longa (turmeric) on postprandial plasma glucose and insulin in healthy subjects. Nutr J. 2010;9:43. DOI:10.1186/1475-2891-9-43
  10. 10. Ono K, Hasegawa K, Naiki H, Yamada M. Curcumin has potent anti-amyloidogenic effects for Alzheimer’s ?-amyloid fibrils in vitro. J Neurosci Res. 2004;75:742-50. DOI:10.1002/jnr.20025
  11. 11. Zhang L, Fiala M, Cashman J, Sayre J, Espinosa A, Mahanian M, et al. Curcuminoids enhance amyloid-β uptake by macrophages of Alzheimer’s disease patients. J Alzheimer’s Dis. 2006;10:1-7. DOI:10.3233/JAD-2006-10101
  12. 12. Kim H, Park B-S, Lee K-G, Choi CY, Jang SS, Kim Y-H, et al. Effects of Naturally Occurring Compounds on Fibril Formation and Oxidative Stress of β-Amyloid. J Agric Food Chem. 2005;53:8537-41. DOI:10.1021/jf051985c
  13. 13. Wang Y-J, Thomas P, Zhong J-H, Bi F-F, Kosaraju S, Pollard A, et al. Consumption of Grape Seed Extract Prevents Amyloid-β Deposition and Attenuates Inflammation in Brain of an Alzheimer’s Disease Mouse. Neurotox Res. 2009;15:3-14. DOI:10.1007/s12640-009-9000-x
  14. 14. Garcia-Alloza M, Borrelli LA, Rozkalne A, Hyman BT, Bacskai BJ. Curcumin labels amyloid pathology in vivo , disrupts existing plaques, and partially restores distorted neurites in an Alzheimer mouse model. J Neurochem. 2007;102:1095-104. DOI:10.1111/j.1471-4159.2007.04613.x
  15. 15. Hickey MA, Zhu C, Medvedeva V, Lerner RP, Patassini S, Franich NR, et al. Improvement of neuropathology and transcriptional deficits in CAG 140 knock-in mice supports a beneficial effect of dietary curcumin in Huntington’s disease. Mol Neurodegener. 2012;7:12. DOI:10.1186/1750-1326-7-12
  16. 16. Chongtham A, Agrawal N. Curcumin modulates cell death and is protective in Huntington’s disease model. Sci Rep. 2016;6:18736. DOI:10.1038/srep18736
  17. 17. Sharma N, Nehru B. Curcumin affords neuroprotection and inhibits α-synuclein aggregation in lipopolysaccharide-induced Parkinson’s disease model. Inflammopharmacology. 2018;26:349-60. DOI:10.1007/s10787-017-0402-8
  18. 18. Tripanichkul W, Jaroensuppaperch E. Curcumin Protects Nigrostriatal Dopaminergic Neurons and Reduces Glial Activation in 6-Hydroxydopamine Hemiparkinsonian Mice Model. Int J Neurosci. 2012;122:263-70. DOI:10.3109/00207454.2011.648760
  19. 19. Sugasini D, Lokesh BR. Curcumin and linseed oil co-delivered in phospholipid nanoemulsions enhances the levels of docosahexaenoic acid in serum and tissue lipids of rats. Prostaglandins, Leukot Essent Fat Acids. 2017;119:45-52. DOI:10.1016/j.plefa.2017.03.007
  20. 20. Khalid A, Shakeel R, Justin S, Iqbal G, Shah SAA, Zahid S, et al. Pharmacological Effects of Turmeric on Learning, Memory and Expression of Muscarinic Receptor Genes (M1, M3 and M5) in Stress-induced Mouse Model. Curr Drug Targets. 2017;18. DOI:10.2174/1389450118666170315120627
  21. 21. Akter J, Hossain MA, Takara K, Islam MZ, Hou D-X. Antioxidant activity of different species and varieties of turmeric (Curcuma spp): Isolation of active compounds. Comp Biochem Physiol Part C Toxicol Pharmacol. 2019;215:9-17. DOI:10.1016/j.cbpc.2018.09.002
  22. 22. Jain SK, Rains J, Croad J, Larson B, Jones K. Curcumin Supplementation Lowers TNF-α, IL-6, IL-8, and MCP-1 Secretion in High Glucose-Treated Cultured Monocytes and Blood Levels of TNF-α, IL-6, MCP-1, Glucose, and Glycosylated Hemoglobin in Diabetic Rats. Antioxid Redox Signal. 2009;11:241-9. DOI:10.1089/ars.2008.2140
  23. 23. Aggarwal BB, Gupta SC, Sung B. Curcumin: an orally bioavailable blocker of TNF and other pro-inflammatory biomarkers. Br J Pharmacol. 2013;169:1672-92. DOI:10.1111/bph.12131
  24. 24. Park S, Lee LR, Seo JH, Kang S. Curcumin and tetrahydrocurcumin both prevent osteoarthritis symptoms and decrease the expressions of pro-inflammatory cytokines in estrogen-deficient rats. Genes Nutr. 2016;11:2. DOI:10.1186/s12263-016-0520-4
  25. 25. Bulboacă AE, Boarescu PM, Bolboacă SD, Blidaru M, Feștilă D, Dogaru G, et al. Comparative Effect Of Curcumin Versus Liposomal Curcumin On Systemic Pro-Inflammatory Cytokines Profile, MCP-1 And RANTES In Experimental Diabetes Mellitus. Int J Nanomedicine. 2019;14:8961-72
  26. 26. Xiao Y, Xia J, Wu S, Lv Z, Huang S, Huang H, et al. Curcumin Inhibits Acute Vascular Inflammation through the Activation of Heme Oxygenase-1. Oxid Med Cell Longev. 2018;2018:1-12. DOI:10.1155/2018/3295807
  27. 27. Motterlini R, Foresti R, Bassi R, Green CJ. Curcumin, an antioxidant and anti-inflammatory agent, induces heme oxygenase-1 and protects endothelial cells against oxidative stress. Free Radic Biol Med. 2000;28:1303-12. DOI:10.1016/S0891-5849(00)00294-X
  28. 28. Funk JL, Oyarzo JN, Frye JB, Chen G, Lantz RC, Jolad SD, et al. Turmeric Extracts Containing Curcuminoids Prevent Experimental Rheumatoid Arthritis. J Nat Prod. 2006;69:351-5. DOI:10.1021/np050327j
  29. 29. Chandran B, Goel A. A Randomized, Pilot Study to Assess the Efficacy and Safety of Curcumin in Patients with Active Rheumatoid Arthritis. Phyther Res. 2012;26:1719-25. DOI:10.1002/ptr.4639
  30. 30. Amalraj A, Varma K, Jacob J, Divya C, Kunnumakkara AB, Stohs SJ, et al. A Novel Highly Bioavailable Curcumin Formulation Improves Symptoms and Diagnostic Indicators in Rheumatoid Arthritis Patients: A Randomized, Double-Blind, Placebo-Controlled, Two-Dose, Three-Arm, and Parallel-Group Study. J Med Food. 2017;20:1022-30. DOI:10.1089/jmf.2017.3930
  31. 31. Mounce BC, Cesaro T, Carrau L, Vallet T, Vignuzzi M. Curcumin inhibits Zika and chikungunya virus infection by inhibiting cell binding. Antiviral Res. 2017;142:148-57. DOI:10.1016/j.antiviral.2017.03.014
  32. 32. Zhu L, Ding X, Zhang D, Yuan C, Wang J, Ndegwa E, et al. Curcumin inhibits bovine herpesvirus type 1 entry into MDBK cells. Acta Virol. 2015;59:221-7. DOI:10.4149/av_2015_03_221
  33. 33. Padilla-S L, Rodríguez A, Gonzales MM, Gallego-G JC, Castaño-O JC. Inhibitory effects of curcumin on dengue virus type 2-infected cells in vitro. Arch Virol. 2014;159:573-9. DOI:10.1007/s00705-013-1849-6
  34. 34. Vajragupta O, Boonchoong P, Morris GM, Olson AJ. Active site binding modes of curcumin in HIV-1 protease and integrase. Bioorg Med Chem Lett. 2005;15:3364-8. DOI:10.1016/j.bmcl.2005.05.032
  35. 35. Prasad S, Tyagi AK. Curcumin and its analogues: A potential natural compound against HIV infection and AIDS. Food Funct. 2015;6:3412-3419
  36. 36. Jacob A, Wu R, Zhou M, Wang P. Mechanism of the Anti-inflammatory Effect of Curcumin: PPAR- γ Activation. PPAR Res. 2007;2007:1-5. DOI:10.1155/2007/89369
  37. 37. Shanmugarajan D, P. P, Kumar BRP, Suresh B. Curcumin to inhibit binding of spike glycoprotein to ACE2 receptors: computational modelling, simulations, and ADMET studies to explore curcuminoids against novel SARS-CoV-2 targets. RSC Adv. 2020;10:31385-99. DOI:10.1039/D0RA03167D
  38. 38. Rajagopal K, Varakumar P, Baliwada A, Byran G. Activity of phytochemical constituents of Curcuma longa (turmeric) and Andrographis paniculata against coronavirus (COVID-19): an in silico approach. Futur J Pharm Sci. 2020;6:104. DOI:10.1186/s43094-020-00126-x
  39. 39. Chakrabarti R, Rawat PS, Cooke BM, Coppel RL, Patankar S. Cellular Effects of Curcumin on Plasmodium falciparum Include Disruption of Microtubules. Bejon P, editor. PLoS One. 2013;8:e57302. DOI:10.1371/journal.pone.0057302
  40. 40. Reddy RC, Vatsala PG, Keshamouni VG, Padmanaban G, Rangarajan PN. Curcumin for malaria therapy. Biochem Biophys Res Commun. 2005;326:472-4. DOI:10.1016/j.bbrc.2004.11.051
  41. 41. Zhou Q , Wang X, Liu X, Zhang H, Lu Y, Su S. Curcumin enhanced antiproliferative effect of mitomycin C in human breast cancer MCF-7 cells in vitro and in vivo. Acta Pharmacol Sin. 2011;32:1402-10. DOI:10.1038/aps.2011.97
  42. 42. Li L, Aggarwal BB, Shishodia S, Abbruzzese J, Kurzrock R. Nuclear factor-kappaB and IkappaB kinase are constitutively active in human pancreatic cells, and their down-regulation by curcumin (diferuloylmethane) is associated with the suppression of proliferation and the induction of apoptosis. Cancer. 2004;101:2351-62. DOI:10.1002/cncr.20605
  43. 43. Yuliani S, Widyarini S, Mustofa, Partadiredja G. Turmeric extract inhibits apoptosis of hippocampal neurons of trimethyltin-exposed rats. Bratisl Lek Listy. 2017;118:142-8
  44. 44. Goel A, Boland CR, Chauhan DP. Specific inhibition of cyclooxygenase-2 (COX-2) expression by dietary curcumin in HT-29 human colon cancer cells. Cancer Lett. 2001;172:111-8. DOI:10.1016/S0304-3835(01)00655-3
  45. 45. Nair A, Amalraj A, Jacob J, Kunnumakkara AB, Gopi S. Non-Curcuminoids from Turmeric and Their Potential in Cancer Therapy and Anticancer Drug Delivery Formulations. Biomolecules. 2019;9:13. DOI:10.3390/biom9010013
  46. 46. Nelson KM, Dahlin JL, Bisson J, Graham J, Pauli GF, Walters MA. The Essential Medicinal Chemistry of Curcumin. J Med Chem. 2017;60:1620-37. DOI:10.1021/acs.jmedchem.6b00975
  47. 47. Priyadarsini KI. Photophysics, photochemistry and photobiology of curcumin: Studies from organic solutions, bio-mimetics and living cells. J Photochem Photobiol C Photochem Rev. 2009;10:81-95. DOI:10.1016/j.jphotochemrev.2009.05.001
  48. 48. Duan D, Doak AK, Nedyalkova L, Shoichet BK. Colloidal Aggregation and the in Vitro Activity of Traditional Chinese Medicines. ACS Chem Biol. 2015;10:978-88. DOI:10.1021/cb5009487
  49. 49. Chin D, Huebbe P, Frank J, Rimbach G, Pallauf K. Curcumin may impair iron status when fed to mice for six months. Redox Biol. 2014;2:563-9. DOI:10.1016/j.redox.2014.01.018
  50. 50. Schneider C, Gordon ON, Edwards RL, Luis PB. Degradation of Curcumin: From Mechanism to Biological Implications. J Agric Food Chem. 2015;63:7606-14. DOI:10.1021/acs.jafc.5b00244
  51. 51. Kharat M, Du Z, Zhang G, McClements DJ. Physical and Chemical Stability of Curcumin in Aqueous Solutions and Emulsions: Impact of pH, Temperature, and Molecular Environment. J Agric Food Chem. 2017;65:1525-32. DOI:10.1021/acs.jafc.6b04815
  52. 52. Antony B, Merina B, Iyer V, Judy N, Lennertz K, Joyal S. A pilot cross-over study to evaluate human oral bioavailability of BCM-95 ® CG (Biocurcumax TM ), a novel bioenhanced preparation of curcumin. Indian J Pharm Sci. 2008;70:445. DOI:10.4103/0250-474X.44591
  53. 53. Gota VS, Maru GB, Soni TG, Gandhi TR, Kochar N, Agarwal MG. Safety and Pharmacokinetics of a Solid Lipid Curcumin Particle Formulation in Osteosarcoma Patients and Healthy Volunteers. J Agric Food Chem. 2010;58:2095-9. DOI:10.1021/jf9024807
  54. 54. Pia A. Management of chronic anterior uveitis relapses: efficacy of oral phospholipidic curcumin treatment. Long-term follow-up. Clin Ophthalmol. 2010;1201. DOI:10.2147/OPTH.S13271
  55. 55. Rao PV, Gan SH. Cinnamon: A Multifaceted Medicinal Plant. Evidence-Based Complement Altern Med. 2014;2014:1-12. DOI:10.1155/2014/642942
  56. 56. Jantan I, Ling YE, Romli S, Ayop N, Ahmad AS. A Comparative Study of the Constituents of the Essential Oils of Three Cinnamomum Species from Malaysia. J Essent Oil Res. 2003;15:387-91. DOI:10.1080/10412905.2003.9698618
  57. 57. Mathew S, Abraham TE. Studies on the antioxidant activities of cinnamon (Cinnamomum verum) bark extracts, through various in vitro models. Food Chem. 2006;94:520-8. DOI:10.1016/j.foodchem.2004.11.043
  58. 58. Ranjbar A, Ghasmeinezhad S, Zamani H, Malekirad AA, Baiaty A, Mohammadirad A, et al. Antioxidative stress potential of Cinnamomum zeylanicum in humans: a comparative cross-sectional clinical study. Therapy. 2006;3:113-7. DOI:10.2217/14750708.3.1.113
  59. 59. Roussel A-M, Hininger I, Benaraba R, Ziegenfuss TN, Anderson RA. Antioxidant Effects of a Cinnamon Extract in People with Impaired Fasting Glucose That Are Overweight or Obese. J Am Coll Nutr. 2009;28:16-21. DOI:10.1080/07315724.2009.10719756
  60. 60. Anderson RA, Zhan Z, Luo R, Guo X, Guo Q , Zhou J, et al. Cinnamon extract lowers glucose, insulin and cholesterol in people with elevated serum glucose. J Tradit Complement Med. 2016;6:332-6. DOI:10.1016/j.jtcme.2015.03.005
  61. 61. Hassan S, Barthwal R, Nair M, Haque S. Aqueous Bark Extract of Cinnamomum zeylanicum: A Potential Therapeutic Agent for Streptozotocin- Induced Type 1 Diabetes Mellitus (T1DM) Rats. Trop J Pharm Res. 2012;11. DOI:10.4314/tjpr.v11i3.12
  62. 62. Alqasoumi S. Anti-secretagogue and antiulcer effects of Cinnamon Cinnamomum zeylanicum in rats. J Pharmacogn Phyther. 2012;4:53-61. DOI:10.5897/JPP12.023
  63. 63. Peterson DW, George RC, Scaramozzino F, LaPointe NE, Anderson RA, Graves DJ, et al. Cinnamon Extract Inhibits Tau Aggregation Associated with Alzheimer’s Disease In Vitro. J Alzheimer’s Dis. 2009;17:585-97. DOI:10.3233/JAD-2009-1083
  64. 64. Bayoub K, Baibai T, Mountassif D, Retmane A, Abdelaziz S. Antibacterial activities of the crude ethanol extracts of medicinal plants against Listeria monocytogenes and some other pathogenic strains. African J Biotechnol. 2010;9:4251-8
  65. 65. Sharma M, Bhatia A. Inactivation of Candidia albicans in culture media by eight spices native to Indian subcontinent. Int J Pharm Sci Rev Res. 2012;16:125-9
  66. 66. Kaskatepe B, Kiymaci ME, Suzuk S, Erdem SA, Cesur S, Yildiz S. Antibacterial effects of cinnamon oil against carbapenem resistant nosocomial Acinetobacter baumannii and Pseudomonas aeruginosa isolates. Ind Crops Prod. 2016;81:191-4. DOI:10.1016/j.indcrop.2015.11.058
  67. 67. Samarasekera R, Kalhari KS, Weerasinghe IS. Mosquitocidal Activity of Leaf and Bark Essential Oils of Ceylon Cinnamomum zeylanicum. J Essent Oil Res. 2005;17:301-3. DOI:10.1080/10412905.2005.9698909
  68. 68. Kim E-C, Kim HJ, Kim T-J. Water extract of Cinnamomum cassia suppresses angiogenesis through inhibition of VEGF receptor 2 phosphorylation. Biosci Biotechnol Biochem. 2015;79:617-24. DOI:10.1080/09168451.2014.993917
  69. 69. Meades G, Henken R, Waldrop G, Rahman M, Gilman S, Kamatou G, et al. Constituents of Cinnamon Inhibit Bacterial Acetyl CoA Carboxylase. Planta Med. 2010;76:1570-5. DOI:10.1055/s-0030-1249778
  70. 70. Niphade SR, Asad M, Chandrakala GK, Toppo E, Deshmukh P. Immunomodulatory activity of Cinnamomum zeylanicum bark. Pharm Biol. 2009;47:1168-73. DOI:10.3109/13880200903019234
  71. 71. Hagenlocher Y, Satzinger S, Civelek M, Feilhauer K, Köninger J, Bischoff SC, et al. Cinnamon reduces inflammatory response in intestinal fibroblasts in vitro and in colitis in vivo leading to decreased fibrosis. Mol Nutr food Res. 2017;
  72. 72. Hagenlocher Y, Hösel A, Bischoff S, Lorentz A. Cinnamon extract reduces symptoms, inflammatory mediators and mast cell markers in murine IL-10−/− colitis. J Nutr Biochem. 2016;30:85-92
  73. 73. Ho S-C, Chang K-S, Chang P-W. Inhibition of neuroinflammation by cinnamon and its main components. Food Chem. 2013;138:2275-82. DOI:http://dx.doi.org/10.1016/j.foodchem.2012.12.020
  74. 74. Kim BH, Lee YG, Lee J, Lee JY, Cho JY. Regulatory effect of cinnamaldehyde on monocyte/macrophage-mediated inflammatory responses. Mediators Inflamm. 2010;2010
  75. 75. Prasanth DSNBK, Murahari M, Chandramohan V, Panda SP, Atmakuri LR, Guntupalli C. In silico identification of potential inhibitors from Cinnamon against main protease and spike glycoprotein of SARS CoV-2. J Biomol Struct Dyn. 2020;1-15. DOI:10.1080/07391102.2020.1779129
  76. 76. Kawatra P, Rajagopalan R. Cinnamon: Mystic powers of a minute ingredient. Pharmacognosy Res. 2015;7:1. DOI:10.4103/0974-8490.157990
  77. 77. Shinde P, Patil P, Bairagi V. Herbs In Pregnancy And Lactation: A Review Appraisal. Int J Pharm Sci Res. 2012;3:3001-6
  78. 78. García-Jiménez N, Péerez-Alonso MJ, Velasco-Negueruela A. Chemical Composition of Fennel Oil, Foeniculum vulgare Miller, from Spain. J Essent Oil Res. 2000;12:159-62. DOI:10.1080/10412905.2000.9699487
  79. 79. Diao W-R, Hu Q-P, Zhang H, Xu J-G. Chemical composition, antibacterial activity and mechanism of action of essential oil from seeds of fennel (Foeniculum vulgare Mill.). Food Control. 2014;35:109-16. DOI:10.1016/j.foodcont.2013.06.056
  80. 80. Mohamad RH, El-Bastawesy AM, Abdel-Monem MG, Noor AM, Al-Mehdar HAR, Sharawy SM, et al. Antioxidant and Anticarcinogenic Effects of Methanolic Extract and Volatile Oil of Fennel Seeds ( Foeniculum vulgare ). J Med Food. 2011;14:986-1001. DOI:10.1089/jmf.2008.0255
  81. 81. Anwar F, Ali M, Hussain AI, Shahid M. Antioxidant and antimicrobial activities of essential oil and extracts of fennel ( Foeniculum vulgare Mill.) seeds from Pakistan. Flavour Fragr J. 2009;24:170-6. DOI:10.1002/ffj.1929
  82. 82. Oktay M, Gülçin İ, Küfrevioğlu Öİ. Determination of in vitro antioxidant activity of fennel (Foeniculum vulgare) seed extracts. LWT - Food Sci Technol. 2003;36:263-71. DOI:10.1016/S0023-6438(02)00226-8
  83. 83. Parejo I, Viladomat F, Bastida J, Schmeda-Hirschmann G, Burillo J, Codina C. Bioguided Isolation and Identification of the Nonvolatile Antioxidant Compounds from Fennel ( Foeniculum vulgare Mill.) Waste. J Agric Food Chem. 2004;52:1890-7. DOI:10.1021/jf030717g
  84. 84. Gende LB, Maggi MD, Fritz R, Eguaras MJ, Bailac PN, Ponzi MI. Antimicrobial Activity of Pimpinella anisum and Foeniculum vulgare Essential Oils Against Paenibacillus larvae. J Essent Oil Res. 2009;21:91-3. DOI:10.1080/10412905.2009.9700120
  85. 85. Soylu S, Yigitbas H, Soylu EM, Kurt Ş. Antifungal effects of essential oils from oregano and fennel on Sclerotinia sclerotiorum. J Appl Microbiol. 2007;103:1021-30. DOI:10.1111/j.1365-2672.2007.03310.x
  86. 86. Runyoro D, Ngassapa O, Innocent E, Sangeda R, Lukuba T. Larvicidal activity of essential oils from spices sold at Kariakoo market in Dar es Salaam, Tanzania, against Anopheles gambiae Giles ss and Culex quinquefasciatus Say. J Complement Med Drug Discov. 2016;6:1. DOI:10.5455/spatula.20160613034220
  87. 87. Zoubiri S, Baaliouamer A, Seba N, Chamouni N. Chemical composition and larvicidal activity of Algerian Foeniculum vulgare seed essential oil. Arab J Chem. 2014;7:480-5. DOI:10.1016/j.arabjc.2010.11.006
  88. 88. Roby MHH, Sarhan MA, Selim KA-H, Khalel KI. Antioxidant and antimicrobial activities of essential oil and extracts of fennel (Foeniculum vulgare L.) and chamomile (Matricaria chamomilla L.). Ind Crops Prod. 2013;44:437-45. DOI:10.1016/j.indcrop.2012.10.012
  89. 89. Dorra N, El-Berrawy M, Sallam S, Mahmoud R. Evaluation of Antiviral and Antioxidant Activity of Selected Herbal Extracts. J High Inst Public Heal. 2019;49:36-40. DOI: 10.21608/jhiph.2019.29464
  90. 90. Alazadeh M, Azadbakht M, Niksolat F, Asgarirad H, Moosazadeh M, Ahmadi A, et al. Effect of sweet fennel seed extract capsule on knee pain in women with knee osteoarthritis. Complement Ther Clin Pract. 2020;40:101219. DOI:https://doi.org/10.1016/j.ctcp.2020.101219
  91. 91. Özbek H, Uğraş S, Dülger H, Bayram İ, Tuncer İ, Öztürk G, et al. Hepatoprotective effect of Foeniculum vulgare essential oil. Fitoterapia. 2003;74:317-9. DOI:10.1016/S0367-326X(03)00028-5
  92. 92. Shan B, Cai YZ, Sun M, Corke H. Antioxidant Capacity of 26 Spice Extracts and Characterization of Their Phenolic Constituents. J Agric Food Chem. 2005;53:7749-59. DOI:10.1021/jf051513y
  93. 93. Miyazawa M, Hisama M. Antimutagenic Activity of Phenylpropanoids from Clove ( Syzygium aromaticum ). J Agric Food Chem. 2003;51:6413-22. DOI:10.1021/jf030247q
  94. 94. Lee K-G, Shibamoto T. Antioxidant property of aroma extract isolated from clove buds [Syzygium aromaticum (L.) Merr. et Perry]. Food Chem. 2001;74:443-8. DOI:10.1016/S0308-8146(01)00161-3
  95. 95. Fabio A, Cermelli C, Fabio G, Nicoletti P, Quaglio P. Screening of the antibacterial effects of a variety of essential oils on microorganisms responsible for respiratory infections. Phyther Res. 2007;21:374-7. DOI:10.1002/ptr.1968
  96. 96. Trajano VN, Lima E de O, Souza EL de, Travassos AER. Inhibitory effect of the essential oil from Eugenia caryophyllata Thumb leaves on coalho cheese contaminating microorganisms. Ciência e Tecnol Aliment. 2010;30:1001-6. DOI:10.1590/S0101-20612010000400025
  97. 97. Pinto E, Vale-Silva L, Cavaleiro C, Salgueiro L. Antifungal activity of the clove essential oil from Syzygium aromaticum on Candida, Aspergillus and dermatophyte species. J Med Microbiol. 2009;58:1454-62. DOI:10.1099/jmm.0.010538-0
  98. 98. Never Zekeya, Francis Shahada MC. In vitro Antibacterial and Antifungal Activity of Tanzanian Bersama abyssinica. Int J Sci Res. 2014;3:1150-4
  99. 99. Bagavan A, Rahuman AA, Kaushik NK, Sahal D. In vitro antimalarial activity of medicinal plant extracts against Plasmodium falciparum. Parasitol Res. 2011;108:15-22. DOI:10.1007/s00436-010-2034-4
  100. 100. Tu Z, Moss-Pierce T, Ford P, Jiang TA. Syzygium aromaticum L. (Clove) Extract Regulates Energy Metabolism in Myocytes. J Med Food. 2014;17:1003-10. DOI:10.1089/jmf.2013.0175
  101. 101. Ghaffar S, Afridi SK, Aftab MF, Murtaza M, Hafizur RM, Sara S, et al. Clove and Its Active Compound Attenuate Free Fatty Acid-Mediated Insulin Resistance in Skeletal Muscle Cells and in Mice. J Med Food. 2017;20:335-44. DOI:10.1089/jmf.2016.3835
  102. 102. Chegu K, Mounika K, Rajeswari M, Vanibala N, Sujatha P, Sridurga P, et al. In Vitro Study Of The Anticoagulant Activity Of Some Plant Extracts. WORLD J Pharm Pharm Sci. 2018;7:904-13
  103. 103. Singh G, Kiran S, Marimuthu P, Isidorov V, Vinogorova V. Antioxidant and antimicrobial activities of essential oil and various oleoresins Ofelettaria cardamomum (seeds and pods). J Sci Food Agric. 2008;88:280-9. DOI:10.1002/jsfa.3087
  104. 104. Ashokkumar K, Murugan M, Dhanya MK, Warkentin TD. Botany, traditional uses, phytochemistry and biological activities of cardamom [Elettaria cardamomum (L.) Maton] – A critical review. J Ethnopharmacol. 2020;246:112244. DOI:10.1016/j.jep.2019.112244
  105. 105. Goyal S, Sharma C, Mahajan U, Patil C, Agrawal Y, Kumari S, et al. Protective Effects of Cardamom in Isoproterenol-Induced Myocardial Infarction in Rats. Int J Mol Sci. 2015;16:27457-69. DOI:10.3390/ijms161126040
  106. 106. Nagashree S, Archana KK, Srinivas P, Srinivasan K, Sowbhagya HB. Anti-hypercholesterolemic influence of the spice cardamom ( Elettaria cardamomum ) in experimental rats. J Sci Food Agric. 2017;97:3204-10. DOI:10.1002/jsfa.8165
  107. 107. Verma SK, Jain V, Katewa SS. Blood pressure lowering, fibrinolysis enhancing and antioxidant activities of Cardamom (Elettaria cardamomum). Indian J Biochem Biophys. 2009;46:503-6
  108. 108. Souissi M, Azelmat J, Chaieb K, Grenier D. Antibacterial and anti-inflammatory activities of cardamom (Elettaria cardamomum) extracts: Potential therapeutic benefits for periodontal infections. Anaerobe. 2020;61:102089. DOI:10.1016/j.anaerobe.2019.102089
  109. 109. Majdalawieh AF, Carr RI. In Vitro Investigation of the Potential Immunomodulatory and Anti-Cancer Activities of Black Pepper ( Piper nigrum ) and Cardamom ( Elettaria cardamomum ). J Med Food. 2010;13:371-81. DOI:10.1089/jmf.2009.1131
  110. 110. Jamal A, Javed K, Aslam M, Jafri MA. Gastroprotective effect of cardamom, Elettaria cardamomum Maton. fruits in rats. J Ethnopharmacol. 2006;103:149-53. DOI:10.1016/j.jep.2005.07.016
  111. 111. Jia D, Tan Y, Liu H, Ooi S, Li L, Wright K, et al. Cardamonin reduces chemotherapy-enriched breast cancer stem-like cells in vitro and in vivo. Oncotarget. 2016;7:771-85. DOI:10.18632/oncotarget.5819
  112. 112. Kaushik P, Goyal P, Chauhan A, Chauhan G. In Vitro Evaluation of Antibacterial Potential of Dry FruitExtracts of Elettaria cardamomum Maton (Chhoti Elaichi). Iran J Pharm Res IJPR. 2010;9:287-92
  113. 113. Abdel-Rahman M, Rezk MM, Kader SA. The role of cardamom on the hazardous effects of depleted uranium in cerebellum and midbrain of albino rats. Toxicol Environ Health Sci. 2017;9:64-73. DOI:10.1007/s13530-017-0305-5
  114. 114. Auti ST, Kulkarni YA. Neuroprotective Effect of Cardamom Oil Against Aluminum Induced Neurotoxicity in Rats. Front Neurol. 2019;10:399. DOI:10.3389/fneur.2019.00399
  115. 115. Abu-Taweel GM. Effects of Perinatal Cardamom Exposure on Social Behavior, Anxiety, Locomotor Activity, Blood Biochemical Parameters and Brain Acetylcholinesterase of Mice Offspring. Curr Pharm Biotechnol. 2020;21:1316-24. DOI:10.2174/1389201021666191216160546
  116. 116. Marín A, Ferreres F, Tomás-Barberán FA, Gil MI. Characterization and Quantitation of Antioxidant Constituents of Sweet Pepper ( Capsicum annuum L.). J Agric Food Chem. 2004;52:3861-9. DOI:10.1021/jf0497915
  117. 117. Materska M, Perucka I. Antioxidant Activity of the Main Phenolic Compounds Isolated from Hot Pepper Fruit ( Capsicum annuum L.). J Agric Food Chem. 2005;53:1750-6. DOI:10.1021/jf035331k
  118. 118. Kim C-S, Kawada T, Kim B-S, Han I-S, Choe S-Y, Kurata T, et al. Capsaicin exhibits anti-inflammatory property by inhibiting IkB-a degradation in LPS-stimulated peritoneal macrophages. Cell Signal. 2003;15:299-306. DOI:10.1016/S0898-6568(02)00086-4
  119. 119. Kang JY, Teng CH, Wee A, Chen FC. Effect of capsaicin and chilli on ethanol induced gastric mucosal injury in the rat. Gut. 1995;36:664-9. DOI:10.1136/gut.36.5.664
  120. 120. Park J-S, Choi M-A, Kim B-S, Han I-S, Kurata T, Yu R. Capsaicin protects against ethanol-induced oxidative injury in the gastric mucosa of rats. Life Sci. 2000;67:3087-93. DOI:10.1016/S0024-3205(00)00890-0
  121. 121. Leuschner RGK, Ielsch V. Antimicrobial effects of garlic, clove and red hot chilli on Listeria monocytogenes in broth model systems and soft cheese. Int J Food Sci Nutr. 2003;54:127-33. DOI:10.1080/0963748031000084070
  122. 122. Lee G-R, Shin MK, Yoon D-J, Kim A-R, Yu R, Park N-H, et al. Topical Application of Capsaicin Reduces Visceral Adipose Fat by Affecting Adipokine Levels in High-Fat Diet-Induced Obese Mice. Obesity. 2013;21:115-22. DOI:10.1038/oby.2012.166
  123. 123. Kang J-H, Tsuyoshi G, Le Ngoc H, Kim H-M, Tu TH, Noh H-J, et al. Dietary Capsaicin Attenuates Metabolic Dysregulation in Genetically Obese Diabetic Mice. J Med Food. 2011;14:310-5. DOI:10.1089/jmf.2010.1367
  124. 124. Notani PN, Jayant K. Role of diet in upper aerodigestive tract cancers. Nutr Cancer. 1987;10:103-13. DOI:10.1080/01635588709513945
  125. 125. Archer VE, Jones DW. Capsaicin pepper, cancer and ethnicity. Med Hypotheses. 2002;59:450-7. DOI:10.1016/S0306-9877(02)00152-4
  126. 126. Yang Y, Zhang J, Weiss NS, Guo L, Zhang L, Jiang Y, et al. The consumption of chili peppers and the risk of colorectal cancer: a matched case-control study. World J Surg Oncol. 2019;17:71. DOI:10.1186/s12957-019-1615-7
  127. 127. Lin C-H, Lu W-C, Wang C-W, Chan Y-C, Chen M-K. Capsaicin induces cell cycle arrest and apoptosis in human KB cancer cells. BMC Complement Altern Med. 2013;13:46. DOI:10.1186/1472-6882-13-46
  128. 128. Pramanik KC, Boreddy SR, Srivastava SK. Role of Mitochondrial Electron Transport Chain Complexes in Capsaicin Mediated Oxidative Stress Leading to Apoptosis in Pancreatic Cancer Cells. Polymenis M, editor. PLoS One. 2011;6:e20151. DOI:10.1371/journal.pone.0020151
  129. 129. Han SS, Keum Y-S, Seo H-J, Chun K-S, Lee SS, Surh Y-J. Capsaicin suppresses phorbol ester-induced activation of NF-κB/Rel and AP-1 transcription factors in mouse epidermis. Cancer Lett. 2001;164:119-26. DOI:10.1016/S0304-3835(01)00378-0
  130. 130. Chang H, Chen S, Chien S, Kuo S, Tsai H, Chen D. Capsaicin may induce breast cancer cell death through apoptosis-inducing factor involving mitochondrial dysfunction. Hum Exp Toxicol. 2011;30:1657-65. DOI:10.1177/0960327110396530
  131. 131. Huh H-C, Lee S-Y, Lee S-K, Park NH, Han I-S. Capsaicin Induces Apoptosis of Cisplatin-Resistant Stomach Cancer Cells by Causing Degradation of Cisplatin-Inducible Aurora-A Protein. Nutr Cancer. 2011;63:1095-103. DOI:10.1080/01635581.2011.607548
  132. 132. Yimer EM, Tuem KB, Karim A, Ur-Rehman N, Anwar F. nigella sativa L. (Black Cumin): A Promising Natural Remedy for Wide Range of Illnesses. Evidence-Based Complement Altern Med. 2019;2019:1-16. DOI:10.1155/2019/1528635
  133. 133. Hajhashemi V, Ghannadi A, Jafarabadi H. Black cumin seed essential oil, as a potent analgesic and antiinflammatory drug. Phyther Res. 2004;18:195-9. DOI:10.1002/ptr.1390
  134. 134. El-Mahmoudy A, Matsuyama H, Borgan M., Shimizu Y, El-Sayed M., Minamoto N, et al. Thymoquinone suppresses expression of inducible nitric oxide synthase in rat macrophages. Int Immunopharmacol. 2002;2:1603-11. DOI:10.1016/S1567-5769(02)00139-X
  135. 135. Suboh SM, Bilto YY, Aburjai TA. Protective effects of selected medicinal plants against protein degradation, lipid peroxidation and deformability loss of oxidatively stressed human erythrocytes. Phyther Res. 2004;18:280-4. DOI:10.1002/ptr.1380
  136. 136. Celik Altunoglu Y, Bilen S, Ulu F, Biswas G. Immune responses to methanolic extract of black cumin ( Nigella sativa ) in rainbow trout ( Oncorhynchus mykiss ). Fish Shellfish Immunol. 2017;67:103-9. DOI:10.1016/j.fsi.2017.06.002
  137. 137. Trigui I, Zarai Z, Chevance S, Cheikh-Rouhou S, Attia H, Ayadi MA. Physicochemical properties, antioxidant activity and in vitro gastrointestinal digestion of purified proteins from black cumin seeds. Int J Biol Macromol. 2019;126:454-65. DOI:10.1016/j.ijbiomac.2018.12.198
  138. 138. Sahak MKA, Kabir N, Abbas G, Draman S, Hashim NH, Hasan Adli DS. The Role of Nigella sativa and Its Active Constituents in Learning and Memory. Evidence-Based Complement Altern Med. 2016;2016:1-6. DOI:10.1155/2016/6075679
  139. 139. Salem ML, Hossain MS. Protective effect of black seed oil from Nigella sativa against murine cytomegalovirus infection. Int J Immunopharmacol. 2000;22:729-40. DOI:10.1016/S0192-0561(00)00036-9
  140. 140. Mahmoud M., El-Abhar H., Saleh S. The effect of Nigella sativaoil against the liver damage induced by Schistosoma mansoni infection in mice. J Ethnopharmacol. 2002;79:1-11. DOI:10.1016/S0378-8741(01)00310-5
  141. 141. Chaieb K, Kouidhi B, Jrah H, Mahdouani K, Bakhrouf A. Antibacterial activity of Thymoquinone, an active principle of Nigella sativa and its potency to prevent bacterial biofilm formation. BMC Complement Altern Med. 2011;11:29. DOI:10.1186/1472-6882-11-29
  142. 142. Utami AT, Pratomo B, Noorhamdani. Study of Antimicrobial Activity of Black Cumin Seeds (Nigella sativa L.) Against Salmonella typhi In Vitro. J Med Surg Pathol. 2016;01. DOI:10.4172/2472-4971.1000127
  143. 143. Rostinawati T, Karipaya S, Iskandar Y. Antibacterial Activity of Ethanol Extract of Nigella sativa L. Seed Against Streptococcus mutans. IOP Conf Ser Earth Environ Sci. 2019;334:012050. DOI:10.1088/1755-1315/334/1/012050
  144. 144. Okeola VO, Adaramoye OA, Nneji CM, Falade CO, Farombi EO, Ademowo OG. Antimalarial and antioxidant activities of methanolic extract of Nigella sativa seeds (black cumin) in mice infected with Plasmodium yoelli nigeriensis. Parasitol Res. 2011;108:1507-12. DOI:10.1007/s00436-010-2204-4
  145. 145. Meral I, Yener Z, Kahraman T, Mert N. Effect of Nigella sativa on Glucose Concentration, Lipid Peroxidation, Anti-Oxidant Defence System and Liver Damage in Experimentally-Induced Diabetic Rabbits. J Vet Med Ser A. 2001;48:593-9. DOI:10.1046/j.1439-0442.2001.00393.x
  146. 146. Kaatabi H, Bamosa AO, Badar A, Al-Elq A, Abou-Hozaifa B, Lebda F, et al. Nigella sativa Improves Glycemic Control and Ameliorates Oxidative Stress in Patients with Type 2 Diabetes Mellitus: Placebo Controlled Participant Blinded Clinical Trial. Ye J, editor. PLoS One. 2015;10:e0113486. DOI:10.1371/journal.pone.0113486
  147. 147. Badary OA, AI-Shabanah OA, Nagi MN, AI-Rikabi AC, Elmazar MMA. Inhibition of benzo(a)pyrene-induced forestomach carcinogenesis in mice by thymoquinone. Eur J Cancer Prev. 1999;8:435-40. DOI:10.1097/00008469-199910000-00009

Written By

Cheryl Sachdeva and Naveen Kumar Kaushik

Submitted: 24 January 2021 Reviewed: 07 February 2021 Published: 02 March 2021