| Literature DB >> 35043421 |
Bina Gidwani1, Ruchi Bhattacharya1, Shiv Shankar Shukla1, Ravindra Kumar Pandey1.
Abstract
Spices are natural plant products enriched with the history of being used as herbal medicine for prevention of diseases. India is also known as the 'Land of Spices'. Out of 109 spices recognized by the International Organization for Standardization (ISO) more than 52-60 spice crops are grown in India. The major spices exported by India are turmeric, cumin, coriander, fenugreek, peppers, etc. The Indian spices are divided into three era viz. early period, middle age and early modern period. Spices are used in beverages, liquors, and pharmaceutical, cosmetic and perfumery products. The major issue with spices is their handling and storage. This review article mainly focuses on two aspects: at the outset the handling and storage of the spices is an essential factor as spices are available in different forms like raw, processed, fresh, whole dried, or pre-ground dried. Therefore, the need of processing, packaging, storage and handling of the spices is important as the deterioration of spices can lead to the loss of therapeutic activity. Furthermore, many herbal constituents have the capability to enhance the bioavailability of drugs. Therefore, an attempt has been made to throw a light on the bioenhancer activity and therapeutic activity along with their mechanism of action of some Indian spices which are regularly used for cooking purpose on a daily basis to enhance the taste of food. The spices suggested by ministry of AYUSH which is relevant to its medicinal and biological property in treatment and prevention from COVID-19 are discussed.Entities:
Keywords: COVID-19; Indian spices; bioenhancer activity; handling; storage; therapeutic activity
Mesh:
Year: 2022 PMID: 35043421 PMCID: PMC9015280 DOI: 10.1002/jsfa.11771
Source DB: PubMed Journal: J Sci Food Agric ISSN: 0022-5142 Impact factor: 4.125
Figure 1(A) Classification of bioenhancers. (B) Flow chart of processing of spices.
Material for specific packaging and storage of raw herbs
| Serial number | Part of plant and category | Packing material |
|---|---|---|
| 1. | Woody in nature like stem, bark, etc. | Gunny bags and woven sacks |
| 2. | Fleshy in nature like fruit, rhizomes, etc. | High gauge high‐density high molecular (HDHM) bags, woven sac with Low density (LD) liner, wooden box |
| 3. | Soft in nature like creepers, leaves, etc. | High gauge HDHM bags, woven sac with LD liner, high gauge polyethylene bags |
| 4. | Flowers, anthers, stigma, petals, seeds, etc. | Corrugated box with polypropylene, woven sack, high‐density poly ethylene (HDPE) container, fibers boards drums |
| 5. | Herbal extracts and compounds | Air tight HDPE containers, corrugated box with polyethylene, woven sack and fiber boards drum with polyethylene bags |
| 6. | Volatile content | Air tight HDPE containers, Air tight carboys, card board box with polyethylene liners |
List of some reported therapeutic activity of spices and their constituents
| Species name (part used) | Scientific name | Activity | Mechanism of action | Reference |
|---|---|---|---|---|
| Black pepper (fruits) |
| Gastrointestinal stimulatory activity | The anti‐spasmodic activity of black pepper and piperine is mediated through activation of opioid receptor along with Ca2+ channel blocking (CCB) effect. |
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| Antibacterial activity | Bactericidal action of pepper appears by alteration of cell membrane permeability result in leakage of intracellular material might cause cell death. |
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| Antihistamic activity | The inhibition of histamine release from the mast cells plays an important role in the mechanism of anti‐allergic effect against type I allergy. |
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| Analgesic and anti‐inflammatory activity | Piperine possesses inhibition of prostaglandin synthesis and release. |
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| Antidepressant | Inhibit monoamine oxidase activity, increase monoamine neurotransmitter levels, and thus produce antidepressant‐like activity in various mouse models of behavioral despair. |
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| Anti‐asthamatic activity | H‐1 receptor antagonism |
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| Blood pressure lowering | Piperine mediates spasmolytic effect through calcium antagonism. |
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| Antidiabetic activity | Enhancement of glucose utilization, so blood glucose levels were significantly decreased in glucose. |
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| Hypolipidemic activity | Clearance of lipids from circulation may be due to reactivation of lipolytic enzymes. |
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| Anticancer activity | Cytotoxic analysis revealed a dose‐dependent response with maximum cellular inhibition |
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| Cardamom (seed pods) |
| Skin disorders (non‐melanoma skin cancer) | Cardamom contains copper and manganese that are required for the activation of superoxide dismutase (SOD) enzyme, which in turn helps in the decrease in the process of lipid peroxidation. Thus, play anticarcinogenic role in preventing the progression of skin carcinogenesis in mice. |
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| Anticonvulsant activity | Cardamom extract increase the level of γ‐aminobutyric acid (GABA) in the blood serum and shows the anticonvulsant activity |
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| Blood pressure lowering activity | Cardamom produced a dose‐dependent fall in the arterial blood pressure. Partial blockade of hypotensive responses with atropine indicate that cardamom lowers blood pressure due to the presence of cholinergic and an additional (Ca2+ antagonist) components, as identified in the gut preparations. Blood pressure is the product of peripheral resistance and cardiac output. |
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| Diuresis | The diuretic effect of cardamom was confirmed, when it caused significant increase in the urine volume (diuresis) in rats, like furosemide, a standard diuretic. Cardamom also enhanced the urinary excretion of Na+ and K+, similar to that caused by furosemide. |
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| Antioxidant activity | The extract showed protection against hydrogen peroxide (H2O2) induced DNA damage and inhibited 2,2'‐azobis(2‐amidinopropane) dihydrochloride (AAPH) induced protein oxidation and lipid peroxidation. Cardamom also exhibited antioxidant effects. |
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| Anti‐inflammatory and analgesic | Cardamom extract administration to rats at 50 and 100 mg kg−1 inhibited carrageenan‐induced paw edema, and down‐regulated cytokines such as COX‐2, IL‐6, and TNF‐α and inhibited i‐NOS mediated nitric oxide (NO) generation. |
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| Gastro‐ protective activity | A crude methanolic extract (TM), essential oil (EO), petroleum ether soluble (PS) and insoluble (PI) fractions of methanolic extract, were studied in rats at doses of 100–500, 12.5–50, 12.5–150 and 450 mg kg−1, respectively for their ability to inhibit the gastric lesions induced by asprin, ethanol and pylorous ligature. In addition their effects on wall mucus and gastric acid output were recorded. All fractions (TM, EO, PS and PI) significantly inhibited gastric lesions |
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| Asthma | The cardamom extract was then studied in isolated tracheal tissues, to elucidate the possible mode of bronchodilator action, where crude extract of cardamom caused relaxation of both carbachol and K+‐induced contractions, like verapamil, a Ca2+ antagonist. |
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| Insecticidal activity | The volatile oil from cardamom acts as a potential grain protectant by killing various life stages of the stored product insects attacking wheat, e.g. |
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| Action: Moreover, it also prevented eggs treated with the oil from developing to the adult stage. Cardamom oil dramatically suppressed egg hatching and larval survival of | ||||
| Cinnamon (bark) |
| Anti‐microbial activity |
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| Anti‐diabetic activity | The effect of cinnamon extract on glycosylated hemoglobin A1c and fasting blood glucose levels in patients with type 2 diabetes was analyzed. A total of 66 patients with type 2 diabetes were recruited and randomly divided into three groups: placebo and low‐dose and high‐dose supplementation with cinnamon extract at 120 and 360 mg d−1, respectively. |
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| Both hemoglobin A1c and fasting blood glucose levels were significantly reduced in patients in the low‐ and high‐dose groups, whereas they were not changed in the placebo group. Thus, significantly improving blood glucose in patients with type 2 diabetes. | ||||
| Cinnamon (bark) | Antioxidant activity | The volatile oil was screened for its potential as an antioxidant by using |
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| Immuno‐modulatory activity | Cinnamon at high dose increases both cell mediated and humoral immunity and at low dose shows effect only on humoral immunity. Cinnamaldehyde is reported to inhibit lymphocyte proliferation and NF‐κ B stimulation. The results of the present study shows that cinnamon is a possible immune system booster. |
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| Wound healing activity | The ethanol extract of the bark of |
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| Clove (flower buds) | Syzygium aromaticum | Antioxidant activity | The antioxidant potential of clove is evaluated against copper induced lipid peroxidant, 2,2‐diphenyl‐1‐picrylhydrazy (DPPH) free radical scavenging capability of methanol extract of clove is examined. The clove exhibited a concentration dependent antioxidant activity. Furthermore, 56% of DPPH free radicals were scavenged with extract equivalent to 100 μg clove. |
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| Antibacterial activity | Antibacterial susceptibility assay shows promising evidence for the antibacterial effect of clove methanolic and ethanolic extract against three foods associated with |
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| Anti‐inflammatory activity | The current study clearly demonstrated anti‐inflammatory effect of clove essential oil |
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| Hair growth enhancer | Formulation containing clove oil was clinically evaluated on rats back compared with minoxidil standard lotion as a positive control and distilled water as a negative control. The selected formulation was demonstrated to condition hair with grooming and enhanced hair growth with longer lag time compared with minoxidil but after one week the hair growth accelerated. |
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| Anti‐cancer activity | Significant reduction in the number of proliferating cells and an increased number of apoptotic cells was noted in these blood pressure‐induced lung lesions following clove treatment. |
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Coriander (dried seeds) |
| Antioxidant activity | Three different bioassays were used, namely scavenging of the DPPH radical method, inhibition of 15‐lipoxygenase (15‐LO) and inhibition of Fe2+ induced porcine brain phospholipid peroxidation. Coriander leaves showed stronger antioxidant activity than the seeds, and in both parts of coriander, the ethyl acetate extract contributed to the strongest activity. |
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| Anti‐diabetic activity | Coriander incorporated into the diet (62.5 g kg−1) and drinking water (2.5 g L−1, prepared by 15 min decoction) reduced hyperglycaemia of streptozotocin‐diabetic mice. Insulin secretion by hyperpolarized B‐cells (16.7 mm‐glucose, 25 mm‐KCl) was further enhanced by the presence of extract. |
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| Anti‐bacterial activity | Coriander oil exhibited bactericidal activity against almost all bacteria tested, due to membrane permeability with the exception of |
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Star anise (fruit) |
| Anticancer activity | Diseases induced by free radicals and nicotine can be cured by star anise because it has anticarcinogenic agents. The anticancer action is because of flavonoids, resveratrol and curcumin. They additionally have exhibited remedial potential, including cell‐defensive anti‐inflammatory, and DNA protective properties. This spice also has positive effect on DNA damage, which can be a trigger for cancer, as well as on cancer cell migration. |
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| Insecticidal activity | Insecticidal activity of star anise, the direct contact methods were applied against fruit flies ( |
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| Anti‐inflammatory activity | Star anise anti‐inflammatory action was identified in mice by xylene‐induced auricle edema. The star anise extracts of 10 and 20 mg rough drugs mL−1, clearly decreased the contractility of mice intestinal smooth muscles in 15 min under the effect of acetylcholine and barium chloride. Therefore, it is concluded that aqueous extract of star anise has analgesic and anti‐inflammatory effects on mice intestinal smooth muscles. |
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| Anti‐fungal activity | The anti‐fungal activity of star anise was tested against |
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| Fenugreek (leaves and seeds) |
| Anti‐inflammatory and anti‐arthritic activity | Anti‐inflammatory activity was noted with linolenic acid in various acute models involving carrageenan, prostaglanin E2, leukotrienes, and arachidonic acid‐induced inflammation signifying its ability to inhibit both cyclooxygenase and lipoxygenase pathways. Petroleum ether extract of fenugreek seeds show anti‐inflammatory and anti‐arthritic activities in all the models tested. |
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| Fenugreek seed extract attenuated hyperglycaemia was investigated |
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| The seed extract exhibit scavenging of hydroxyl radical (OH‐) and inhibition of H2O2 induced lipid peroxidation in rat liver. The result shows that the extract of fenugreek seed contains antioxidant property. |
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| The effect of fenugreek seeds (Trigonella foenum graecum) compared to omeprazole was studied on ethanol‐induced gastric ulcer. The soluble gel fraction derived from the seeds was more effective than omeprazole in preventing lesion formation. |
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| Turmeric (rhizomes) |
| Anti‐ulcer activity | An ethanol extract of turmeric was studied in rats for its ability to inhibit gastric secretion and to protect gastroduodenal mucosa against the injuries caused by pyloric ligation. An oral dose of 500 mg kg−1 of the extract produced significant anti‐ulcerogenic activity in rats subjected to pyloruic ligation. |
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| Anti‐fungal activity | In the experimental animals, turmeric oil (dilution 1:80) was applied by dermal application on the seventh day following dermatophytosis induction with |
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| Antioxidant, anti‐inflammatory activity | Turmeric oil was found to have |
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Figure 2(A) Mechanism of action of black pepper as bioenhancer. (B) Mechanism of action for bioenhancer activity of cardamom. (C) Mechanism of action for bioenhancer activity of cinnamon. (D) Mechanism of action for bioenhancer activity of clove. (E) Mechanism of action of turmeric as bioenhancer.
Reported bioenhancer activity of some constituents of herbal spices
| Herbal spices with drug | Bioenhancement activity | Reference |
|---|---|---|
| Piperine and resveratrol | Bioenhancer activity was studied on mice and the study demonstrated significant improvement in bioavailability of resveratrol. |
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| Piperine and curcumin | The pharmacokinetic of curcumin with piperine was studied on animal and human volunteers. Piperine inhibit the hepatic and intestinal glucuronidation, thus extend the bioavailability of curcumin in both rat and human with no adverse effect. |
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| Piperine and aflatoxin B1 | 10 mg dose of piperine enhance bioavailability of aflatoxin B1 in rat tissue |
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| Cardamom and piroxicam | The penetration index of piroxicam after 1 h pretreatment with 10% cardamom oil was about 340.9‐fold higher than that of non‐pretreatment |
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| Cardamom and indomethacin, diclofanac and piroxicam | The penetration index of piroxicam was extremely increased by 1% cardamom oil about 81.9‐fold compared with that of indomethacin or diclofanac. |
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| Cinnamon and saquinavir | It enhances bioavailability of saquinavir. |
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| Clove oil and carvedilol | It enhances bioavailability of carvedilol. |
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| Curcumin with celiprolol and midazolam | Curcumin suppresses drug metabolizing enzyme CYP3A4 in liver and increase AUC and Cmax of celiprolol and midazolam. |
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Recent patents of some bioenhancers
| Name of bioenhancer | Patent number | Assignee | Date | Title |
|---|---|---|---|---|
| Piperine | US5744161A | Sabinsa Corporation | 4 April 1998 | Use of piperine as a bioavailability enhancer |
| Piperine | USOO5536506A | Sabinsa Corporation | 16 July 1996 | Use of piperine to increase the boavailability of nutritional compounds |
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| WO2003049753A1 | Council of Scientific and Industrial Research | 19 June 2003 | Bioavailability enhancing activity of |
| Cuminum Cyminum | WO2003075685A2 | Council of Scientific and Industrial Research | 18 September 2003 | Bioavailability/bioefficacy enhancing activity of cuminum cyminum and extracts and fractions thereof |
| Fenugreek | US7338675B2 | TSI Group Ltd Hong Kong | 4 March 2008 | Fenugreek seed bio‐active compositions and methods for extracting same |
| Fenugreek | WO2005084323A2 | Technical Sourcing International, Inc. | 15 September 2005 | Compositions of bio‐active compounds from fenugreek seed and methods for producing same |
| Star anise | CN105713732B | Shandong Agricultural University | 17 March 2020 | Extraction method of star anise oil |
Mechanism of action of curcumin on virus replication process
| Process | Mechanism of action | Reference |
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| Viral attachment/penetration | Curcumin could alter the surface protein structure in viruses and block the entry of viruses to the cell. In addition, the positively charged curcumin on the surface is subjected to electrostatic interactions with porcine epidemic diarrhea virus |
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| Viral replication |
The effects of curcumin on negative‐strand RNA synthesis by using PEDV as a coronavirus model. They demonstrated that curcumin could inhibit PEDV at the replication step. This evidence supports the potential role of curcumin as a promising antiviral agent. The effect of curcumin on viral replication, by quantification of the number of spike proteins present in cultures of Vero E6 cells infected with SARS‐CoV. Their result demonstrated that the inhibitory effect of curcumin in half maximal concentration (EC50) values was higher than 10 μmol L−1 on SARS‐CoV replication. |
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| Potential inhibitory effect of curcumin on viral protease | The drugs that are at present tried for the management of COVID‐19 are protease inhibitors that primarily act on the main protease curcumin that may have the potential to inhibit the COVID‐19 infection by molecular docking. Curcumin showed relatively low binding energies and inhibition constants. They suggested that curcumin could have a potential inhibitory effect on COVID‐19 and could potentially act as a therapeutic agent. |
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| Potential effect of curcumin on interferons |
Interferons play an essential role in the defense against coronavirus infection. These viruses could hinder the induction of interferon in humans. All types of interferons play a role in preventing viral infections. Treatment with cationic carbon dots based on curcumin can suppress PEDV model of coronavirus reproduction by stimulating the production of interferon‐stimulating genes (ISGs) and the cytokines (IL8 and IL6) of Vero cells by triggering the innate immunity of the host. |
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