Document Detail

Ferula asafoetida: Traditional uses and pharmacological activity.
Jump to Full Text
MedLine Citation:
PMID:  23055640     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
Ferula asafoetida is herbaceous plant of the umbelliferae family. It is oleo gum resin obtained from the rhizome and root of plant. This spice is used as a digestive aid, in food as a condiment and in pickles. It is used in modern herbalism in the treatment of hysteria, some nervous conditions, bronchitis, asthma and whooping cough. It was at one time employed in the treatment of infantile pneumonia and flatulent colic. The gum resin is antispasmodic, carminative, expectorant, laxative, and sedative. The volatile oil in the gum is eliminated through the lungs, making this an excellent treatment for asthma. The odor of asafoetida is imparted to the breath, secretions, flatus, and gastric eructations. Its properties are antispasmodic, expectorant, stimulant, emmenagogue and vermifuge. Asafoetida has also been used as a sedative. It also thins the blood and lowers blood pressure. It is widely used in India in food and as a medicine in Indian systems of medicine like ayurveda. Asafoetida has been held in great esteem among indigenous medicines, particularly in Unani system from the earliest times.
Authors:
Poonam Mahendra; Shradha Bisht
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Pharmacognosy reviews     Volume:  6     ISSN:  0976-2787     ISO Abbreviation:  Pharmacogn Rev     Publication Date:  2012 Jul 
Date Detail:
Created Date:  2012-10-11     Completed Date:  2012-10-12     Revised Date:  2013-05-30    
Medline Journal Info:
Nlm Unique ID:  101570880     Medline TA:  Pharmacogn Rev     Country:  India    
Other Details:
Languages:  eng     Pagination:  141-6     Citation Subset:  -    
Affiliation:
Department of Pharmacology, School of Pharmacy, Suresh Gyan Vihar University, Jaipur, Rajasthan, India.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Full Text
Journal Information
Journal ID (nlm-ta): Pharmacogn Rev
Journal ID (iso-abbrev): Pharmacogn Rev
Journal ID (publisher-id): PRev
ISSN: 0973-7847
ISSN: 0976-2787
Publisher: Medknow Publications & Media Pvt Ltd, India
Article Information
Copyright: © Pharmacognosy Reviews
open-access:
Received Day: 15 Month: 3 Year: 2011
Revision Received Day: 02 Month: 4 Year: 2011
Accepted Day: 23 Month: 8 Year: 2012
Print publication date: Season: Jul-Dec Year: 2012
Volume: 6 Issue: 12
First Page: 141 Last Page: 146
ID: 3459456
PubMed Id: 23055640
Publisher Id: PRev-6-141
DOI: 10.4103/0973-7847.99948

Ferula asafoetida: Traditional uses and pharmacological activity
Poonam Mahendraaff1
Shradha Bishtaff1
Department of Pharmacology, School of Pharmacy, Suresh Gyan Vihar University, Jaipur, Rajasthan, India
Correspondence: Address for correspondence: Miss. Poonam Mahendra, Pharmacology Division, School Of Pharmacy, Suresh Gyan Vihar University, Jaipur-302004, India. E-mail: poonammahendra84@gmail.com

INTRODUCTION

Plants have been a constant source of drugs and recently, much emphasis has been placed on finding novel therapeutic agents from medicinal plants. Today many people prefer to use medicinal plants rather than chemical drugs. Ferula asafoetida Linn: Asafoetida, the gum resin prized as a condiment in India and Iran, is obtained chiefly from plant Ferula asafoetida. The Latin name ferula means “carrier” or “vehicle”. Asa is a latinized form of Farsi asa “resin”, and Latin foetidus means “smelling, fetid”. In ancient Rome, asafoetida was stored in jars together with pine nuts, which were alone used to flavor delicate dishes. Another method is dissolving asafoetida in hot oil and adding the oil drop by drop to the food. If used with sufficient moderation, asafoetida enhances mushroom and vegetable dishes, but can also be used to give fried or barbecued meat a unique flavor. Ancient texts describe it as hingu and several centuries of its constant use have bestowed upon it the peculiarity of a tempting spice and trusted medicine. Hing is bitter and pungent in taste and light, sharp, unctuous and hot in effect. Ayurvedic texts have categorized hing as deepniya and sanjna-sthapaka (an appetiser and a restorer of consciousness). It is popular household remedies and its components are used for many prescriptions in traditional healing.[1] Asafoetida is used as a flavoring agent and forms a constituent of many spice mixtures. It is used to flavor, curries, meatballs, dal and pickles. The whole plant is used as a fresh vegetable. The herb is also used as an antidote of opium. Given in the same quantity as opium ingested by the patient, it will counteract the effect of the drug.


MYTHS AND HISTORY

As its name suggests, asafoetida has a fetid smell and a nauseating taste; characteristics that also burdened it with the name devil's dung. In the middle Ages, a small piece of the gum was worn around the neck to ward off diseases such as colds and fevers. Whatever effectiveness it had was probably due to the antisocial properties of the amulet rather than any medicinal virtue. Surprisingly, in Persia asafoetida was used as a condiment and called the “food of the gods”. This herb is the major component in the famous Ayurvedic herbal formula Hingashtak, Sanskrit name is hing. In Persia this herb is so highly esteemed as a condiment, it is mixed with almost all their dishes. French gastronomers rub a little asafoetida on hot plates from which they eat beef steaks. The distinctive flavor of Worcestershire sauce is obtained by the addition of this gum. When used with discretion, it adds character to curries, stews, gravies, etc. Skilful manipulation has made asafoetida a useful ingredient in fine perfumes. It is still regarded a valuable medicinal in Europe, Near and far East. As a condiment, it is recommended only to the hearty and the brave. In magic and mythology, asafoetida is used to gain insight and to banish all negative energy, evil spirits and demons. It is used to invoke male gods, especially those of a phallic nature. One myth claims that asafoetida developed from the semen of a god of fertility when it soaked into the earth.


ORIGIN AND DISTRIBUTION

Ferula asafoetida is an herbaceous, monoecious, perennial plant of the UMBELLIFERAE family. Asafoetida is native to central Asia, eastern Iran to Afghanistan, and today it is grown chiefly in Iran and Afghanistan, from where it is exported to the rest of the world. It is not native to India, but has been used in Indian medicine and cookery for ages.

Other Names: Anghuzeh (Farsi); asafétida (Spanish); asafoetida; awei (Chinese); aza(Greek); devil's dung; férule persique or merde dudiable (French); haltit or tyib (Arabic); hing (Hindi); mvuje (Swahili); stinkasant or teufelsdreck (German); stinking gum.

Asafoetida is extracted from the Ferula plants which have massive taproots or carrot-shaped roots, 12.5-15 cm in diameter at the crown when they are 4-5 years old. Just before the plants flower, in March-April, the upper part of the living rhizome root is laid bare and the stem cut off close to the crown. A dome-shaped structure made of twigs and earth covers the exposed surface. A milky juice exudes from the cut surface. After some days, the exudates are scraped off and a fresh slice of the root cut when more latex exudes; sometimes the resin is removed along with the slice. The collection of resin and slicing of the root are repeated until exudation ceases (about 3 months after the first cut). The resin is sometimes collected from successive incisions made at the junction of the stem or rhizome and the taproots.


TRADITIONAL MEDICINAL USES

In Afghanistan hot water extract of the dried gum is taken orally for hysteria and whooping cough and to treat ulcers.[2] Decoction of the plant is taken orally as a vermifuge in China.[3] Hot water extract of the dried root is taken orally as an antispasmodic, a diuretic, a vermifuge and an analgesic in Egypt.[4] Gum is chewed for amenorrhea in Malaysia[5] and as antiepileptic in Morocco.[6] Water extract of the resin in Nepal is taken orally as an anthelmintic[7] and in Saudi Arabia dried gum is used medicinally for whooping cough, asthma, and bronchitis.[8] In Brazil hot water extract of the dried leaf and stem is taken orally by males as an aphrodisiac[9] and oleoresin powder, crushed with the fingertips, is used as a condiment.[10] Fluid extract of the resin is taken orally as an emmenagogue, a stimulating expectorant, an anthelmintic, an aphrodisiac, and a stimulant to the brain and nerves and claimed to be a powerful antispasmodic in United State.[11]

Ferula asafoetida as traditional medicine in India

Asafoetida has been held in great esteem among indigenous medicines from the earliest times in India. It is reputed as a drug which expels wind from the stomach and counteracts any spasmodic disorders. It is also a nervine stimulant, digestive agent and a sedative. A dry Lampyris noctiluca without head is mixed with 200–300 mg of Ferula and taken mornings and evenings for gallstones and kidney stones and potassium nitrate is added to the mixture for old stones.[12] Hot water extract of the dried resin is taken orally as an emmenagogue[13] and hot water extract of the dried gum is taken orally as a carminative, an antispasmodic, and an expectorant in chronic bronchitis.[14] Dried extract with Brassica alba and rock salt is diluted with vinegar and taken orally as an abortifacient.[15] Dried gum resin exudates are eaten to prevent guinea worm disease.[16] Gum resin with salt and the bark juice of Moringa pterygosperma is used externally for stomachaches.[17]


CHEMICAL CONSTITUENT

An analysis of asafoetida shows it to consist of carbohydrates 67.8% per 100 gms, moisture 16.0%, protein 4.0%, fat 1.1%, minerals 7.0% and fiber 4.1%. Its mineral and vitamin contents include substantial calcium besides phosphorus, iron, carotene, riboflavin and niacin. Its calorific value is 297, contains 40-64% resinous material composed of ferulic acid,[18] umbel-liferone,[2, 19] asaresinotannols,[18] farnesiferols A, B, and C[20, 21] etc., about 25% gum composed of glucose, galactose, l-arabinose, rhamnose, and glucuronic acid[18] and volatile oil (3-17%) consisting of disulfides as its major components, notably 2-butyl propenyl disulfide (E- and Z-isomers),[22] with monoterpenes (α- and β-pinene, etc.),[2] free ferulic acid, valeric acid, and traces of vanillin (LAF). The disagreeable odor of the oil is reported to be due mainly to the disulphide C11H20S2.[22, 23] Various chemical constituents responsible for pharmacology has been shown in Table 1.


PHARMACOLOGICAL ACTIVITIES AND CLINICAL TRIALS

Effect of Ferula asafoetida on gastro intestinal tract

The herb is an effective remedy for several diseases of the stomach. It is one of the best remedies available for flatulence and is an essential ingredient for most of the digestive powders. In case of flatulence and distension of the stomach, asafoetida should be dissolved in hot water and a pad of cloth steeped in it may be used for fomenting the abdomen. Colloidal solution, administered orally to rats at a dose of 50 mg/kg, 60 minutes before experiment, produced significant protection against gastric ulcers induced by 2 hours cold-restraint stress, aspirin, and 4 hours pylorus ligation.[24] Gum extract, administered to isolated guinea pig ileum at a dose of 3 mg/mL, produced a decrease of spontaneous contraction to 54 ± 7% of control. Exposure of precontracted ileum by acetylcholine, histamine, and KCl to Ferula gum extract produced a concentration-dependent relaxation. Preincubation with indomethacin, propanolol, atropine and chlorpheniramine before exposure to the gum, did not produce any relaxation.[25] Asafoetida, administered orally to rats at a dose of 2500 mg% for 8 weeks, decreased the levels of phosphatases and sucrase in the small intestine.[26] Powder of the dried entire plant, administered by gastric intubation to adults at a dose of 0.2 g for 1 hour, was active.[27] Asafoetida, administered orally to albino rats at a dose of 250 mg% for 8 weeks, enhanced pancreatic lipase activity, stimulated pancreatic amylase and chymotrypsin. The stimulatory influence was not observed when their intake was restricted to a single oral dose.[28] Asafoetida did not affect the digestibility of protein in sorghum.[29]

Ferula asafoetida and cancer

Ethanol (90%) extract of the dried plant, in cell culture administered at a concentration 0.25 mg/mL, was active on human lymphocytes. The extract was active on Vero cells, effective dose (ED50 0.15 mg/mL; Chinese hamster ovary (CHO) cells, ED50 0.575 mg/mL; and Dalton's lymphoma, ED50 0.6 mg/mL.[30] Water extract of the dried gum, in cell culture at a concentration of 500 μg/mL, produced weak activity on CA-mammarymicroalveolar cells.[31] Water extract of the dried oleoresin, administered by gastric intubation to mice at a dose of 50 mg/animal daily for 5 days, was active on CAEhrlich ascites, 53% increase in life span (ILS). Water extract administered intraperitoneally was inactive on Dalton's lymphoma, 4.8% ILS, and CA-Ehrlich ascites, 5.5% ILS.[32] Dried resin, administered orally to Sprague–Dawley rats at doses of 1.25 and 2.5% w/w of the diet, produced a significant reduction in the multiplicity and size of palpable N-methyl-N-nitrosourea-induced mammary tumors, and a delay in mean latency period of tumor appearance.[33] Oral administration to mice increased the percentage of life span by 52.9%. Intraperitoneal administration did not produce any significant reduction in tumor growth. The extract also inhibited a two-stage chemical carcinogenesis induced by 7,12-dimethylbenzathracene and croton oil on mice skin with significant reduction in papilloma formation.[34] Sodium ferulate, administered to human lymphocytes cell culture, induced apoptosis.[35] Gum, administered to mice at a dose of 40 mg/g of diet, was active. The dose was inactive vs 3′-methyl- 4 dimethylaminoazobenzene-induced carcinogenesis.[36] Water extract of the dried oleoresin, administered externally to mice at a dose of 200 μL/animal, was active vs 7,12-dimethylbenz[a]anthracene and croton oil treatment.[30]

Ferula asafoetida as women's ailments

The herb is considered useful in the treatment of several problems concerning women such as sterility, unwanted abortion, pre-mature labor, unusually painful, difficult and excessive menstruation and leucorrhoea. About 12 centigrams of gum fried in ghee mixed with 120 grams of goat's fresh milk and a tablespoon of honey, should be given thrice daily for a month. It excites the secretion of progesterone hormone. Asafoetida is also useful for women after childbirth. Owing to its antiflatulent and digestive properties, the herb can be taken with beneficial results during the post-delivery period. In southern India, the powder of the herb mixed with rice is given to women after delivery. Methanol extract of the resin, administered orally to Sprague–Dawley rats at a dose of 400 mg/kg daily for 10 days, prevented pregnancy in 80% of the rats. When administered as a polyvinylpyrrolidone 1:2 complex, 100% pregnancy inhibition was observed at this dose. Lower doses of the extract produced a marked reduction in the mean number of implantations. Significant activity was observed in the hexane and chloroform eluents of sulfur-containing extract in an immature rat bioassay, the methanol extract was devoid of any estrogenic activity.[37] A mixture of Embella ribes fruit, Piper longum fruit, borax, Ferula-dried gum, Piper betle, Polianthes tuberosa, and Abrus precatorius, administered orally to female adults at a dose of 0.28 g/person starting from the second day of menstruation twice daily for 20 days, without sexual intercourse during the dosing period, produced the effect for 4 months and the activity was patented for both small and long term effects.[38, 39] Hot water extract of the plant, administered to female rats, was inactive on estrogen of uterus. Extract administered to pregnant rats, was inactive on uterus.[40]

Ferula asafoetida and gene expression

Asafoetida, administered orally to Sprague–Dawley rats at doses of 1.25% and 2.5% w/w, significantly restored the level of antioxidant system, depleted by N-methyl-N-nitrosourea treatment. There was a significant inhibition in lipid peroxidation as measured by thiobarbituric acid-reactive substances in the liver of rats.[33] Ethanol (95%) extract of the dried resin, on agar plate at a concentration of 15 mg/plate, produced weak activity on streptomycin-dependent strains of Salmonella typhimurium TA98. Metabolic activation has no effect on the result.[41] Resin, on agar plate at a concentration of 200 μg/plate, was active on S. typhimurium TA1537 and inactive on S. typhimurium TA1538 and S. typhimurium TA98.[42] Gum, administered by gastric intubation to mice at a dose of 1 g/kg, was active. The results were significant at p less than 0.01 level. A dose of 0.5 g/kg, produced weak activity. Asafoetida, administered orally to mice, produced weak activity in spermatogonia.[43] Water extract of the dried gum, on agar plate at a concentration of 2 mg/plate, was inactive on S. typhimurium TA100 vs aflatoxin B1-induced mutagenesis and a concentration of 10 mg/plate, was inactive on S. typhimurium TA98.[44] Asafoetida, on agar plate, was active on S. typhimurium TA100 and TA1535 microsomal activation-dependent mutagenicity of 2-acetamidofluorene.[45]

Ferula asafoetida and its effect on blood pressure

In one study tincture of the gland, administered intravenously to rabbits, produced significant hypotensive effects.[46] Water extract of the dried gum resin, administered intravenously to dogs at variable doses, shown antihypertensive activity.[47] Gum extract, administered to anesthetized rats at doses of 0.3–2.2 mg/100 g body weight, and significantly reduced the mean arterial blood pressure.[25]

Effect of Ferula asafoetida on blood vessels and blood

Water extract of the dried gum resin, administered to frogs, was active on the vein and shown vasodilatation effect.[47] Tincture of the gland, administered to rabbits, was active on the bladder and intestine and produced significant smooth muscle relaxant effect, which may be helpful in lowering the blood pressure.[46] Water extracts of the gum, administered intravenously to dogs and rats at variable doses, shown anticoagulant activity.[48] Ether extracts of the dried gum and gum resin, administered orally to 10 healthy subjects fed 100 g of butter to produce alimentary hyperlipemia, were actively shown fibrinolytic activity.[49]

Ferula asafoetida and chemoprotective therapy

Dried gum resin, on agar plate, was active on Clostridium perfringens and Clostridium sporogenes.[50] Essential oil of rhizome, on agar plate at a concentration of 400 ppm, was active on Microsporum gypseum and Trichophyton rubrum, and produced weak activity on Trichophyton equinumi.[51] Extract of asafoetida, on agar plate at concentrations of 5–10 mg/ mL, inhibited Aspergillus parasiticus aflatoxin production.[52] Ethanolic (95%) extract of the dried gum on agar plate shown antifungal activity.[53] Oleo-gum resin from roots and stems was active on Trichomonas vaginalis.[54] Asafoetida treatment significantly reduced the levels of cytochrome P450 and b5. There was an enhancement in the activities of glutathione-S-transferase, deoxythymidine- diaphorase, superoxide desmutase, catalase, and reduced glutathione. Asafoetida, administered orally to Sprague–Dawley rats at doses of 1.25% and 2.5% w/w in diet, produced an increase in the development and differentiation of ducts/ductules and lobules and a decrease in terminal end buds as compared to both normal and N-methyl-N-nitrosourea-treated control animals.[33]

Ferula asafoetida and hypersensitivity reactions

Allergenic activity was shown when oleoresin powder, administered externally to adults. Reactions to patch test occurred most commonly in patients who were regularly exposed to the substance, or who already had dermatitis on the fingertips.[10] Ethanolic (95%) extract of the resin, administered orally to two groups of 50 patients with irritable colon, shown anti-inflammatory. Results were significant at P < 0.001 level.[55]

Effect of Ferula asafoetida on lipid profile

Resin, administered to rats fed an atherogenic diet, at a dose of 1.5%, failed to reduce the serum cholesterol levels. Gum, administered to female rats at a concentration of 1% of diet, not shown any antihypercholesterolemic activity.[56] A hot mixture of Nigella sativa, Commiphora myrrha, Ferula asafoetida, Aloe vera, and Boswellia serrata, administered by gastric intubation to rats at a dose of 0.5 g/kg for 7 days, was active vs streptozotocin-induced hyperglycemia.[57]

Hepatoprotective effect of Ferula asafoetida

A mixture of the methanol-insoluble fraction of the dried resin, fresh garlic, curcumin, ellagic acid, butylated hydroxytoluene, and butylated hydroxyanisole, administered by gastric intubation to ducklings at a dose of 10 mg/animal, shown antihepatotoxic activity vs aflatoxin B1-induced hepatotoxicity.[58] Oleoresin, administered to rats at a dose of 250 mg%, shown hepatic oxidase inhibition.[59]

Effect on CNS and heart of Ferula asafoetida

Ethanol extract of the dried gum, administered orally to adults at a dose of 20 mL/person, was active in CNS.[60] Tincture of the gland, administered by perfusion to rabbits, produced weak activity on the heart.[45]

Effect of Ferula asafoetida in blood sugar level

A hot mixture of Nigella sativa, Commiphora myrrha, Ferula asafoetida, Aloe vera, and Boswellia serrata, administered by gastric intubation to rats at a dose of 0.5 g/kg for 7 days, was active vs streptozotocin-induced hyperglycemia.[57] Hot water extract of the dried gum, Nigella sativa, Myrrhis odorata, and Aloe sp. in equal parts, administered by gastric intubation to rats at a dose of 10 mL/kg for 7 days, was active vs streptozotocin-induced hyperglycemia. Results were significant at P < 0.05 level.[61]

Antioxidant activity of Ferula asafoetida

Asafoetida, administered orally to Sprague–Dawley rats at doses of 1.25% and 2.5% w/w, significantly restored the level of antioxidant system, depleted by N-methyl-N-nitrosourea treatment. There was a significant inhibition in lipid peroxidation as measured by thiobarbituric acid-reactive substances in the liver of rats.[33]


TOXIC EFFECT

Methemoglobinemia occurred in a 5-week-old infant after treatment with a gum asafoetida formulation to alleviate colic.[62] Asafoetida may enhance the activity of warfarin.[63] A weak sister chromatid exchange-inducing effect in mouse spermatogonia[43] and clastogenicity in mouse spermatocytes[64] has been documented for asafoetida. Chromosomal damage by asafoetida has been associated with the coumarin constituents.


CONCLUSIONS

Asafoetida is an oleo-gum-resin obtained from the exudates of the roots of the Iranian endemic medicinal plant, F. asafoetida. It is used widely all over the world as a flavoring spice in a variety of foods. Traditionally it is used for the treatment of various diseases, such as asthma, epilepsy, stomach-ache, flatulence, intestinal parasites, weak digestion and influenza. Recent studies including pharmacological and biological have also shown that asafoetida possess several activities, such as antioxidant, antiviral, antifungal, cancer chemopreventive, antidiabetic, antispasmodic, hypotensive and molluscicidal. Asafoetida has great medicinal importance, detailed studies of asafoetida is required prior to clinical trial.


Notes

Source of Support: Nil

Conflict of Interest: None declared.

REFERENCES
1. Eigner D,Scholz D. Ferula assa-foetida and Curcuma longa in traditional medical treatment and diet in NepalJ EthnopharmacolYear: 1999671610616954
2. Mahran GH,El Alfy TS,Ansari SM. A phytochemical study of volatile oil of Afghanian asafetidaBull Fac Pharm Cairo UnivYear: 1973121017
3. Duke JA,Ayensu ES. Medicinal plants of ChinaYear: 19851Algonac, MichiganReference Publications Inc52361
4. Buddrus J,Bauer H,Abu-Mustafa E,Khattab A,Mishaal S,El- Khrisy EA,et al. Foetidin, a sesquiterpenoid coumarin from Ferula assa-foetidaPhytochemistryYear: 19852486970
5. Gimlette JD. A dictionary of Malayan medicineYear: 1939New York, USAOxford University Press
6. Bellakhdar J,Claisse R,Fleuretin J,Younos C. Repertory of standard herbal drugs in the Moroccan PharmacopoeiaJ EthnopharmacolYear: 199135123431809818
7. Bhattarai NK. Folk Anthelmintic drugs of central NepalInt J PharmacolYear: 19923014550
8. Seabrook WB. Adventures in Arabia among the Bedouins, Druses, whirling dervishes and Yezidee devil worshipersYear: 1927New YorkBlue Ribbon Book99105
9. Elisabetsky E,Figueiredo W,Oliveria G. Traditional Amazonian nerve tonics as antidepressant agents: Chaunochiton kappleri: A case studyJ Herbs Spices Med PlantsYear: 1992112562
10. Seetharam KA,Pasricha JS. Condiments and contact dermatitis of the finger-tipsIndian J Dermatol Venerol LeprolYear: 1987533258
11. Anon. Lilly's handbook of pharmacy and therapeuticsYear: 18985th revIndianapolisEli Lilly and Co
12. Tiwar KC,Majumder R,Bhattacharjee S. Folklore medicines from Assam and Arunachal Pradesh (district Tirap)Int J Crude Drug ResYear: 197917617
13. Kamboj VP. A review of Indian medicinal plants with interceptive activityIndian J Med ResYear: 19881988336552844661
14. Subrahmanyan V,Sastry VL,Srinivasan M. AsafoetidaJ Sci Ind Res BYear: 1954133826
15. Venkataraghavan S,Sundareesan TP. A short note on contraceptive in AyurvedaJ Sci Res Pl MedYear: 1981239
16. Joshi P. Herbal drugs used in Guinea worm disease by the tribals of southern Rajasthan (India)Int J PharmacogYear: 199129338
17. John D. One hundred useful raw drugs of the Kani tribes of Trivandrum forest division, Kerala, IndiaInt J Crude Drug ResYear: 1984221739
18. Mahran GH,El-Alfy TS,Ansary HA. A phytochemical study of the gum and resin of Afghanian asafoetidaBull Fac PharmYear: 19751211932
19. Fujita M,Furuya T,Itokawa H. Crude drugs containing coumarins and their derivatives. III. Chromatographic separation and determination of umbelliferone and its homologsYakugaku ZasshiYear: 1958783958
20. Nassar MI. Spectral study of farnesiferol B from Ferula assafoetida LPharmazieYear: 1994495423
21. Caglioti L,Naef H,Arigoni D,Jeger O. Sesquiterpenes and azulenes. CXXVII. The constituents of asafetida. II. Farnesiferol B and CHelv Chim ActaYear: 195942255770
22. Shankaranarayana ML,Raghavan B,Natarajan CP. Odorous compounds of asafetida. VII. Isolation and identifi cationIndian Food PackYear: 1982366576
23. Rajanikanth B,Ravindranath B,Shankaranarayana ML. Volatile polysulphides of asafoetidaPhytochemistryYear: 198423899900
24. Agrawal AK,Rao CV,Sairam K,Joshi VK,Goel RK. Effect of Piper longum Linn, Zingiber officinalis Linn and Ferula species on gastric ulceration and secretion in ratsIndian J Exp BiolYear: 200038994811324171
25. Fatehi M,Farifteh F,Fatehi- Hassanabad Z. Antispasmodic and hypotensive effects of Ferula asafoetida gum extractJ EthnopharmacolYear: 200491321415120456
26. Platel K,Srinivasan K. Influence of dietary spices on their active principles on digestive enzymes of small intestinal mucosa in ratsInt J Food Sci NutrYear: 1996475598616674
27. Desai HG,Kalro RH. Effect of black pepper and asafetida on the DNA content of gastric aspiratesIndian J Med ResYear: 19858132593874826
28. Platel K,Srinivasan K. Influence of dietary spices and their active principles on pancreatic digestive enzymes in albino ratsNahrungYear: 20004442610702999
29. Pradeep KU,Geervani P,Eggum BO. Influence of spices on utilization of sorghum and chickpea proteinPlant Foods Hum NutrYear: 19911269761924191
30. Unnikrishn MC,Kuttan R. Cytotoxicity of extracts of spices to cultured cellsNutr CancerYear: 19881125173217263
31. Sato A. Studies on anti-tumor activity of crude drugs. I. The effects of aqueous extracts of some crude drugs in short-term screening testYakugaku ZasshiYear: 1989109407232810060
32. Unnikrishn MC,Kuttan R. Tumour reducing and anticarcinogenic activity of selected spicesCancer LettYear: 1990518592110862
33. Mallikarjuna GU,Dhanalakshmi S,Raisuddin S,Rao AR. Chemomodulatory influence of Ferula asafoetida on mammary epithelial differentiation, hepatic drug metabolizing enzymes, antioxidant profiles and N-methyl-N-nitrosourea-induced mammary carcinogenesis in ratsBreast Cancer Res TreatYear: 20038111014531492
34. Unnikrishnan MC,Kuttan R. Tumour reducing and anticarcinogenic activity of selected spicesCancer LettYear: 1990518592110862
35. Lu Y,Xu C,Yang Y,Pan H. The effect of antioxidant sodium ferulate on human lymphocytes apoptosis induced by H2O2Zhongguo Yi Xue Ke Xue Yuan Xue BaoYear: 19982044811367733
36. Aruna K,Sivaramakrishnan VM. Anticarcinogenic effect of some Indian plant productsFood Chem ToxicolYear: 19923095361473788
37. Keshr G,Lakshmi V,Singh MM,Kamboj VP. Post-coital antifertility actiivty of Ferula asafoetida extract in female ratsPharmac BiolYear: 1999372738
38. Das PC. Oral contraceptive (longacting)Patent Brit 1,445,599Year: 197611
39. Das PC. Oral contraceptivePatent-Brit-1,025,372Year: 1966
40. Misra MB,Mishra SS,Misra RK. Screening of a few indigenous abortifacientsJ Indian Med AssocYear: 196952535
41. Shashikanth KN,Hosono A. In vitro mutagenicity of tropical spices to streptomycin dependent strains of Salmonella typhimurium TA98Agric Biol ChemYear: 19865029478
42. Siwaswamy SN,Balachandran B,Balanehru S,Sivaramakrishnan VM. Mutagenic activity of south Indian food itemsIndian J Exp BiolYear: 19912973071769715
43. Abraham SK,Kesavan PC. Genotoxicity of garlic, turmeric and asafetida in miceMutat ResYear: 19841368586717474
44. Soni KB,Lahiri M,Chakcradeo P,Bhide SV,Kuttan R. Protective effect of food additives on aflatoxininduced mutagenicity and hepatocarcinogenicityChem LettYear: 199711512933
45. Soudamini KK,Unnikrishnan MC,Sukumaran K,Kuttan R. Mutagenicity and anti-mutagenicity of selected spicesIndian J Physiol PharmacolYear: 199539347538582746
46. Boyd LJ. The pharmacology of the homeopathic drugs.IJ Am Inst HomeopathyYear: 1928217
47. Sarkisyan RG. Effect of Ferula on arterial pressureMeditsinskii Zhurnal UzbekistanaYear: 19691969234
48. Mansurov MM. Effect of Ferula asafoetida on the blood coagulabilityMeditsinskii Zhurnal Uz bekistanaYear: 196719676469
49. Bordia A,Arora SK. The effect of essential oil (active principle) of asafetida on alimentary lipemiaIndian J Med ResYear: 197563707111213769
50. Garg DK,Banerjea AC,Verma J. The role of intestinal Clostridia and the effect of asafetida (Hing) and alcohol in flatulenceIndian J MicrobiolYear: 1980201947
51. Dikshi A,Husain A. Antifungal action of some essential oils against animal pathogensFitoterapiaYear: 1984551716
52. Soni KB,Rajan A,Kuttan R. Reversal of aflatoxin induced liver damage by turmeric and curcuminCancer LettYear: 199266115211394115
53. Thyagaraja N,Hosono A. Effect of spice extract on fungal inhibitionFood Sci Technol (London)Year: 1996292868
54. Ramadan NI,Al Khadrawy FM. The in vitro effect of Assafoetida on Trichomonas vaginalisJ Egypt Soc ParasitolYear: 2003336153014964671
55. Rahlfs VW,Mossinger P. Asafoetida in the treatment of the irritable colon. A double blind studyDtsch Med WochenschrYear: 19791041403365493
56. Kamanna VS,Chandrasekhara N. Effect of garlic (Allium sativum Linn) on serum lipoproteins and lipoprotein cholesterol levels in albino rats rendered hypercholesteremic by feeding cholesterolLipidsYear: 19821748387121209
57. Al-Awadi F,Shoukry M. The lipid lowering effect of an anti-diabetic plant extractActa DiabetolYear: 19882515
58. Soni KB,Rajan A,Kuttan R. Inhibition of aflatoxin-induced liver damage in ducklings by food additivesMycotoxin ResYear: 19939227
59. Sambaiah K,Srinivasan K. Influence of spices and spice principles on hepatic mixed function oxygenase system in ratsIndian J Biochem BiophysYear: 19892625482628260
60. Coleman DE. The effect of certainhomeopathic remedies upon the hearingJ Am Inst HomeopathyYear: 19221527981
61. Al-Awadi FM,Khattar MA,Gumaa KA. On the mechanism of the hypoglycaemic effect of a plant extractDiabetologiaYear: 19852843243899826
62. Kelly KJ,Neu J,Camitta BM,Honig GR. Methemoglobinemia in an infant treated with the folk remedy glycerited asafoetidaPediatricsYear: 19847371796609339
63. Heck AM,DeWitt BA,Lukes AL. Potential interactions between alternative therapies and warfarinAm J Health Syst PharmYear: 2000571221710902065
64. Walia K. Effect of asafoetida (7-hydroxycoumarin) on mouse spermatocytesCytologiaYear: 197338719244783359

Tables
[TableWrap ID: T1] Table 1 

Chemical constituent responsible for pharmacological activity




Article Categories:
  • Review Article

Keywords: Ferula asafoetida, spice, umbelliferae.

Previous Document:  Trianthema portulacastrum Linn. (Bishkhapra).
Next Document:  Nootropic herbs (Medhya Rasayana) in Ayurveda: An update.