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|Year : 2006 | Volume
| Issue : 2 | Page : 95--99
Exploring Indian medicinal plants for antiulcer activity
P Dharmani, Gautam Palit
Division of Pharmacology, Central Drug Research Institute, Lucknow - 226 001, India
Division of Pharmacology, Central Drug Research Institute, Lucknow - 226 001
Peptic ulcer disease (PUD) is a serious gastrointestinal disorder that requires a well targeted therapeutic strategy. A number of drugs including proton pump inhibitors and H2 receptor antagonists are available for the treatment of peptic ulcer, but clinical evaluation of these drugs has shown incidence of relapses, side effects, and drug interactions. This has been the rationale for the development of new antiulcer drugs and the search for novel molecules has been extended to herbal drugs that offer better protection and decreased relapse. Drugs of plant origin are gaining popularity and are being investigated for a number of disorders, including peptic ulcer. The present article reviews the antiulcerogenic and ulcer healing property of Ocimum sanctum , Allophylus serratus , Desmodium gagenticum, Azadirachta indica , Hemidesmus racemosus , Asparagus racemosus, and Musa sapientum. We have highlighted some of the important plants reported for their anti-ulcer and ulcer healing properties, in our laboratory and elsewhere during the last few years. Ayurvedic knowledge supported by modern science is necessary to isolate, characterise, and standardise the active constituents from herbal sources for antiulcer activity.
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Dharmani P, Palit G. Exploring Indian medicinal plants for antiulcer activity.Indian J Pharmacol 2006;38:95-99
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Dharmani P, Palit G. Exploring Indian medicinal plants for antiulcer activity. Indian J Pharmacol [serial online] 2006 [cited 2021 Nov 29 ];38:95-99
Available from: https://www.ijp-online.com/text.asp?2006/38/2/95/24613
Peptic ulcer disease (PUD) encompassing gastric and duodenal ulcer is the most prevalent gastrointestinal disorder. The pathophysiology of PUD involves an imbalance between offensive (acid, pepsin, and H. pylori) and defensive factors (mucin, prostaglandin, bicarbonate, nitric oxide and growth factors). An estimated 15,000 deaths occur each year as a consequence of PUD. In India, PUD is common. In the Indian Pharmaceutical industry, antacids and antiulcer drugs share 6.2 billion rupees and occupy 4.3% of the market share. Today, there are two main approaches for treating peptic ulcer. The first deals with reducing the production of gastric acid and the second with re-enforcing gastric mucosal protection.,
Recently, there has been a rapid progress in the understanding of the pathogenesis of peptic ulcer. Most of the studies focus on newer and better drug therapy. These have been made possible largely by the availability of the proton pump inhibitors, histamine receptor blockers, drugs affecting the mucosal barrier and prostaglandin analog. However, the clinical evaluation of these drugs showed development of tolerance and incidence of relapses and side effects that make their efficacy arguable. This has been the rationale for the development of new antiulcer drugs, which includes herbal drugs. Indian Medicinal plants and their derivatives have been an invaluable source of therapeutic agents to treat various disorders including PUD. An indigenous drug possessing fewer side effects is the major thrust area of the present day research, aiming for a better and safer approach for the management of PUD. Several plant species like Allophylus serratus , Desmodium gangeticum , Ocimum sanctum , Hemidesmus indicus , Emblica officinalis , Convovulus pluricaulis , Bidens pilosa and Asparagus recemosus have shown encouraging findings.
This review summarises the features of some of these plants reported to possess antiulcer and ulcer healing properties. Although extensive research has been conducted in this area, recent studies with significant findings involving Ocimum sanctum, Allophylus serratus , Desmodium gagenticum, Azadirachta indica , Hemidesmus indicus , Asparagus racemosus and Musa sapientum are emphasised here.
Ocimum sanctum Linn. (Tulsi)
Ocimum sanctum (OS), popularly known as Tulsi in Hindi, is a sacred plant that belongs to the family Labiatae . OS contains a number of chemical constituents that interact in a complex way to elicit their pharmacodynamic responses. OS is highly effective in a wide spectrum of diseases and reported to possess anticarcinogenic, anthelmintic, antiseptic, antirheumatic, antistress, and antibacterial properties.,, Clinical trails have reported the usefulness of OS in heart diseases and diabetes. OS also possess antiinflammatory and immunomodulatory properties, attributed to its potential to inhibit cyclooxygenase and lymphokines.
Previous studies have reported significant antiulcer activity by different parts of OS., Singh and Majumdar (1999) while working with fixed oil of OS showed that OS had potent antiulcer effect against ulcer induced by aspirin, indomethacin, histamine, serotonin, alcohol, reserpine and stress. They suggested that the strong antiulcer effect of OS was possibly due to the inhibition of 5- lipooxygenase in aspirin, indomethacin, and alcohol induced ulcer models. In histamine, reserpine, and stress induced ulcer models, the antiulcer effect was due to its antihistaminic, anticholinergic, and antisecretory properties, respectively. They concluded that OS was a potent antiulcer and antiinflammatory agent. The findings strengthen the view that a drug that possesses both antiinflammatory and antiulcer activity would be an additional benefit as most of the antiinflammatory drugs used today are ulcerogenic. Our research extended the findings of Singh and Majumdar (1999) further by evaluating ulcer healing properties of OS. We studied the ethanolic extract of leaves of OS in gastric ulcer induced by cold restraint (CRU), alcohol (AL), aspirin (ASP), and pyloric ligation (PL) model in rats, and histamine (HST) induced duodenal ulcer model in guinea pigs, for its antiulcer activity. In addition, healing effect of OS was examined in acetic acid (AA) induced chronic gastric ulcer model. It was found that the ethanolic extract of OS not only reduced acid secretion, but also potentially elevated the mucoprotective effect. Another important finding of our study was the dose dependent manner of OS activity, where 100 mg/kg body weight was found to be the most effective dose. However, the most important finding of our study was the effectiveness of OS extract in all the five models, indicating that OS extract exhibited antiulcerogenic activity through different mechanisms. Another possibility is the presence of more than one active component in OS extracts, which are effective against various ulcer induction mechanisms.
Ulcer healing is a complex process that involves combination of wound retraction and re-epithelialization. It also involves other factors, such as, growth factors and angiogenesis. OS significantly reduced the size of ulcer after 10 days of treatment. Furthermore, after 20 days of treatment, complete regeneration of the mucosal glandular structure was seen through histological studies of ulcer base. The ulcer healing property of OS seems to be based on its mucoprotective activity and its antisecretory effect. The ulcer base may have healed quickly because the basic fibroblast growth factor was protected from acid, which is considered to be chiefly responsible for epithelial regeneration.
Overall, our results fortify the ethnopharmacolgical importance of OS as an antiulcer and ulcer healing agent. Furthermore, OS and its active constituents may emerge as potent therapeutic agents against PUD. However, more experimentation and detailed molecular analysis of active constituents of OS is required for a definite conclusion.
Allophylus serratus Kurz
Allophylus serratus Kurz (Synonym Allophylus cobbe Raeuschel; Allophylus edulis Radlk), is one of the largest genus of family Sapindaceae and carries a strong ethnopharmacological background. The plant is used in Ayurveda, to treat problems like inflammation, elephantiasis, oedma, and fracture of bones. It is also used in several gastrointestinal disorders including dyspepsia, anorexia, and diarrhoea.,
Pharmacognostic studies and phytochemical screening of Allophylus serratus (AS) showed the presence of various chemical compounds in different parts of AS plant. Leaves of the plant contain β-sitosterol. They also contain phenacetamide, a chemical known for its antiulcer activity. A edulis has also been reported to contain two flavonoid glycosides that are effective against ulcer.,
We have studied the antiulcerogenic potential of AS by analysing the ethanolic extract of its dried, powdered leaves against different ulcer models. We have supported the finding further by studying biochemical parameters like free and total acidity, peptic activity, and mucin secretion. AS showed a substantial and significant protection against gastric ulcers in all the models.
Reduction in acid output and peptic activity and increase in mucin secretion were the major mechanisms behind the protection shown in the PL model. Reduced acid output was the major reason in the CRU model, while the tremendous increase of mucus content and a possible increase in prostaglandin level could be the protective mechanism in the AL and the ASP models.
Therefore, AS can be effectively used as an antiulcer drug. However, further insight into the precise mechanism of action is essential to exploit the complete potency of AS.
Desmodium gangeticum DC (Leguminosae), popularly known as "Shaparni" in Hindi, is a well-known Indian medicinal plant. It is of great therapeutic value in treating diseases such as, typhoid, piles, inflammation, asthma, bronchitis, and dysentry. The root is prescribed in combination with other drugs for the treatment of snakebite and scorpion sting. This cure is mentioned in the Shrangdharasamhita and the Charakasamhita by Sushruta.
While studying the ethanolic extract of DG for its antiulcerogenic potential in four-induction models, namely CRU, ASP, PL and AL we observed that a dose of 200 mg/kg was most effective in all the models. Efficacy of DG in the CRU model may be due to its antioxidant activity. This is in agreement with some earlier reports about the antioxidant activity of DG, which suggests the free radical scavenging effect of DG. Such activities may also be responsible for the antiulcer effect of DG. The reduced acid output measured after pyloric ligation, indicates the effect of the extract's protective mechanism on gastric mucosa, causing an inhibition of gastric secretion. The cytoprotective ability was depicted by increased mucin secretion in the AL and the ASP induced ulcer models.
Unlike OS and AS, antiulcerogenic efficacy of DG is mainly due to its better cytoprotective effect in comparison with its antisecretory effect. It is well documented, that natural drugs augment the defensive factors and although slow in activity, are more reliable and safer. Therefore, the use of DG alone or in combination with other drugs requires serious consideration.
Azadirachta indica A. Juss, commonly known as "Neem," has been extensively used in India as an ayurvedic medicine for the treatment of various diseases, such as, leprosy, intestinal helminthiasis, and respiratory disorders in children.,,,
Bandyopadhyay et al. have reported the gastroprotective property of dried bark extract of Azadirachta indica (AI) in the mercaptomethylimidazole, PL, CRU, indomethacin, AL, and HST induced ulcer models. It acts mainly by inhibiting acid secretion and blocking oxidative damage of the gastric mucosa. Inhibition of acid secretion was confirmed by inhibition of H+K+ATPase activity, while blockade of oxidative damage of gastric mucosa was evident from blocking of lipid peroxidation and scavenging of endogenous hydroxyl radical (OH.). Furthermore, they compared the bark extract with known antiulcer drugs, ranitidine and omeprazole in the PL and the stress ulcer models and found that the extract was almost equipotent to the standard drugs. The bark extract exhibited more antioxidant activity than a variety of known antioxidants. Garg et al ., have also reported an antiulcer effect of neem leaf extract and the prevention of mucus depletion and mast cell degranulation as possible mechanism.
A phenolic glycoside has been isolated by Bandyopadhyay et al ., as an active constituent, whose characterisation and mechanism are under investigation. Therefore, Azadirachta indica offers another option for a safer and an effective antiulcer drug .
Hemidesmus indicus var. indicus (family Asclepiadaceae), is a widely distributed medicinal plant in India. It has been used in various diseases and disorders, such as, antinociceptive, antidiarrhoeal, renoprotective, antiathero-genic, and skin carcinogenesis.,,,,, Jain and Singh have reported that Hemidesmus indicus (HI) is employed in traditional medicine for gastric ailments.
Anoop and Jagdeesan have recently studied the aqueous ethanolic extract of HI and have reported that the doses of 300 and 450 mg/kg are effective in the PL, cysteamine, and aspirin induced ulcer models in rats. The antiulcerogenic effect of HI was mainly because of its high mucoprotective activity, depicted by a selective increase in prostaglandin content.
Hemidesmus indicus , therefore, provides another alternative for ulcer treatment. It aims at enhancing the defensive factors so that the normal balance between offensive and defensive factors is achieved.
Asparagus racemosus (AR), belonging to the family Liliaceae, is a well-known ayurvedic rasayana. AR is reported to be antidiarrhoeal, antibacterial, antilithiatic and antiulcer. ,,,
Sairam et al ., have reported antiulcerogenic activity of methanolic extract of fresh roots of AR in the CRU, AL, ASP, and PL induced gastric ulcer models and cysteamine induced duodenal ulcer model. AR was found to be effective in the CRU, AL, and cysteamine induced ulcer models, but was ineffective in PL and ASP models. The plant did not show any significant effect on acid and peptic activity, but it increased mucin secretion tremendously, suggesting cytoprotective property as the possible mechanism. The plant did not show any effect on acid secretion. However, its effect in the CRU model, apart from its effect on defensive mucosal factors, was attributed to its adaptogenic activity, This defensive system showed protection in the PL induced model. In the ASP model, both local and systemic effects produced ulcers. It may be possible that AR was not able to overcome all the factors that play a role in ulcerogenesis. Along with the above-mentioned properties, AR was also reported to have antioxidant effect., Apart from finding AR to be antiulcerogenic, authors found that it accelerated gastric ulcer healing in 10 days of treatment.
Overall, AR has shown gastroduodenal ulcer protecting and gastric ulcer healing effects, which are mainly due to increase in mucosal defensive factors.
Several other plant species that have utility in ulcer therapy have also been reported in the literature. Some of these plants like Musa sapientum and Zingiber officinale have been reviewed extensively by Goel and Sairam. These herbal plants along with other plants reportedly possessing antiulcerogenic property are summarised in [Table 1]. Some of these herbal drugs have been chemically characterized, and the entities involved in the activity have been isolated.
According to the old hypothesis, acid secretion was thought to be the sole cause of ulcer formation and reduction in acid secretion was thought to be the major approach towards therapy. However, in the light of recent evidences this concept has changed. Now, treatment of ulcer mainly targets the potentiation of the defensive system along with lowering of acid secretion.
Chemical substances derived from plants have been used to treat human diseases since the dawn of medicine. Roughly 50% of new chemical entities introduced during the past two decades are from natural products. Recent technological advances have renewed interest in natural products in drug discovery. Therefore, efforts should be directed towards isolation and characterisation of the active principles and elucidation of the relationship between structure and activity. Furthermore, detailed analysis of the active constituents of natural drugs should be directed towards clinical relevance. Standardisation is indispensable to maintain reproducible quality in biological evaluation. Although the clinical efficacy of these preparations is reported by traditional practices, they have not been scientifically validated.
Ayurveda, the oldest medicinal system in the world, provides leads to find therapeutically useful compounds from plants. Therefore, ayurvedic knowledge supported by modern science is necessary to isolate, characterise, and standardise the active constituents from herbal source. This combination of traditional and modern knowledge can produce better antiulcer drugs with fewer side effects. Herbs are widely available in India and other countries. The wide spectrum makes them attractive candidates for further research.
|1||Valle DL. Peptic ulcer diseases and related disorders. In: Braunwald E, Fauci AS, Kasper DL, Hauser SL, Longo DL, Jameson JL, editors. Harrison's principles of internal medicine. 16th ed. New York: McGraw-Hill; 2005. p. 1746-62.|
|2||Hoogerwerf WA, Pasricha PJ. Agents used for control of gastric acidity and treatment of peptic ulcers and gastroesophageal reflux disease. In: Hardman JG, Limbird LE, Goodman Gilaman A, editors. Goodman and Gilman The Pharmacological Basis of Therapeutics. 10th ed. New York: Mc Graw-Hill; 2001. p. 1005-19.|
|3||Manonmani S, Viswanathan VP, Subramanian S, Govindasamy S. Biochemical studies on the antiulcerogenic activity of cauvery 100, an ayurvedic formulation in experimental ulcers. Indian J Pharmacol 1995;27:101-5.|
|4||Koehn FE, Carter GT. The evolving role of natural products in drug discovery. Nature Rev Drug Discov 2005;4:206-20.|
|5||Dharmani P, Mishra PK, Maurya R, Chauhan VS, Palit G. Allophylus serratus : a plant with potential anti-ulcerogenic activity. J Ethnopharmacol 2005;99:361-6.|
|6||Dharmani P, Mishra PK, Maurya R, Chauhan VS, Palit G. Desmodium gangeticum : A plant with potent anti-ulcer effect. Indian J Exp Biol 2005;43: 517-21.|
|7||Dharmani P, Kuchibhotla VK, Maurya R, Srivastava S, Sharma S, Palit G. Evaluation of anti-ulcerogenic and ulcer healing properties of Ocimum sanctum Linn. J Ethnopharmacol 2004;93:197-206.|
|8||Anoop A, Jegadeesan M. Biochemical studies on the anti-ulcerogenic potential of Hemidesmus indicus R.Br. var. indicus. J Ethnopharmacol 2003;84:149-56.|
|9||Sairam K, Rao CV, Babu MD, Kumar VK, Agarwal VK, Goel RK. Antiulcerogenic effect of ethanolic extract of Emblica officinalis : An experimental study. J Ethnopharmacol 2002;82:1-9.|
|10||Sairam K, Rao CV, Goel RK. Effect of Convolvulus pluricaulis Chois on gastric ulceration and secretion in rats. Indian J Exp Biol 2001;39:350-4.|
|11||Alvarez A, Pomar F, Sevilla MA, Montero MJ. Gastric antisecretory and antiulcer activities of an ethanolic extract of Bidens pilosa L. var. radiata Schult. Bip. J Ethnopharmacol 1999;67:333-40.|
|12||Sairam K, Priyambada S, Aryya NC, Goel RK. Gastroduodenal ulcer protective activity of Asparagus racemosus : an experimental, biochemical and histological study. J Ethnopharmacol 2003;86:1-10.|
|13||Godhwani S, Godhwani JL, Vyas DS. Ocimum sanctum : An experimental study evaluating its anti-inflammatory, analgesic and antipyretic activity in animals. J Ethnopharmacol 1987;21:153-63.|
|14||Singh S, Majumdar DK. Evaluation of the gastric antiulcer activity of fixed oil of Ocimum sanctum (Holy Basil). J Ethnopharmacol 1999;65:13-9.|
|15||Bhargava KP, Singh N. Anti-stress activity of Ocimum sanctum Linn. Indian J Med Res 1 981;73:443-51.|
|16||Sood S, Narang D, Dinda AK, Maulik SK. Chronic oral administration of Ocimum sanctum Linn. augments cardiac endogenous antioxidants and prevents isoproterenol-induced myocardial necrosis in rats . J Pharm Pharmacol 2005;57:127-33.|
|17||Rai V, Mani UV, Iyer UM. Effect of Ocimum sanctum leaf powder on blood lipoproteins, glycated protein and total amino acids in patients with non-insulin-dependent diabetes mellitus. J Nutr Environ Med 1997;7:113-8.|
|18||Mediratta PK, Sharma KK, Singh S. Evaluation of immunomodulatory potential of Ocimum sanctum seed oil and its possible mechanism of action. J Ethnopharmacol 2002;80:15-20.|
|19||Mandal S, Das DN, De Kamala, Ray K, Roy G, Chaudhari SB, et al . Ocimum sanctum Linn- a study on gastric ulceration and gastric secretion in rats. Indian J Physiol Pharmacol 1993;37:91-2.|
|20||Perini RF, Ma L, Wallace JL. Mucosal repair and COX-2 inhibition. Current Pharma Design 2003;9:2207-11.|
|21||Gupta AK, Tandon N. Reviews on Indian Medicinal Plants. Vol 2. New Delhi: Indian Council of Medical Research; 2004.|
|22||Agrawal VS. Drug plants of India. Ludhiana, India: Kalyani publishers; 1997.|
|23||Rastogi RP, Mehrotra BN. Compendium of Indian Medicinal Plants. Vol 4. New Delhi: Publication and Information Directorate; 1995.|
|24||Rastogi RP, Mehrotra BN. Compendium of Indian Medicinal Plants. Vol 1. New Delhi: Publication and Information Directorate; 1990.|
|25||Rastogi RP, Mehrotra BN. Compendium of Indian Medicinal Plants. Vol 3. , New Delhi: Publication and Information Directorate;1993.|
|26||Avasthi BK, Tewari JD. Chemical investigation of Desmodium gangeticum II chemical constitution of the lactane. J Am Pharma Assoc 1955;44:628-9.|
|27||Yadava RN, Tripathi P. A novel flavone glycoside from the stem of Desmodium gangeticum . Fitoterapia 1998;69:443-4.|
|28||Maxwell AG, Masato Y, Yoko A. Free radical scavenging action of the medicinal herbs from Ghana: Thanningia Sanguinea on experimentally- induced liver injuries. Gen Pharmacol 1999;32:661-7.|
|29||Goel RK, Govinda Das D, Sanyal AK. Effect of vegetabl banana powder on changes induced by ulcerogenic agents on dissolved mucosubstances in gastric juice. Indian J Gastroenterol 1985;4:249-51.|
|30||Ketkar AY, Ketkar CM. Various uses of Neem product: Medicinal uses including pharmacology in Asia. In: Schmutterer H, editor. The Neem Tree. Weinheim: Federal Republic of Germany; 1995.|
|31||Sengupta P, Chowdhuri SN, Khastagir HN. Terpenoids and related compounds-I Contituents of the trunk bark of Melia azadirachta Linn. and the structure of the ketophenol, nimbiol . Tetrahedron 1960;10:45-54.|
|32||VanDer Nat JM, Klerx J, Van Dijk H, De Silva KT, Labadie RP. Immunomodulatory activity of an aqueous extract of Azadirachta indica stem bark. J Ethnopharmacol 1987;19:125-31.|
|33||Sengupta P, Chowdhuri SN, Khastagir HN. Terpenoids and related compounds-I Contituents of the trunk bark of Melia azadirachta Linn. and the structure of the ketophenol, nimbiol. Tetrahedron 1960;10:45-54.|
|34||Bandyopadhyay U, Biswas K, Chatterjee R, Bandyopahyay D, Chattopadhyay I, Ganguly CK, et al . Gastroprotective effect of Neem ( Azadirachta indica ) bark extract: Possible involvement of H+K+ ATPase inhibition and scavenging of hydroxyl radical. Life Sci 2002;71:2845-65.|
|35||Garg GP, Nigam SS, Ogle CW. The gastric antiulcer effects of the leaves of the neem tree. Planta Medica 1993;59:215-7.|
|36||Nadkarni AN. Indian Materia Medica. Vol. 1. India: Popular Book Depot, Bombay; 1989.|
|37||Verma PR, Joharapurkar AA, Chatpalliwar VA, Asnani AJ. Antinociceptive activity of alcoholic extract of Hemidesmus indicus R. Br. in mice. J Ethnopharmacol 2005;102:298-301.|
|38||Das S, Prakash R, Devaraj SN. Antidiarrhoeal effects of methanolic root extract of Hemidesmus indicus (Indian sarsaparilla)-an in vitro and in vivo study. Indian J Exp Biol 2003;41:363-6.|
|39||Kotnis MS, Patel P, Menon SN, Sane RT. Renoprotective effect of Hemidesmus indicus , a herbal drug used in gentamicin-induced renal toxicity. Nephrology 2004;9:142-52. |
|40||Mary NK, Babu BH, Padikkala J. Antiatherogenic effect of Caps HT2, a herbal Ayurvedic medicine formulation. Phytomedicine 2003;10:474-82.|
|41||Sultana S, Alam A, Khan N, Sharma S. Inhibition of cutaneous oxidative stress and two-stage skin carcinogenesis by Hemidesmus indicus (L.) in Swiss albino mice. Indian J Exp Biol 2003;41:1416-23.|
|42||Jain SP, Singh SC. Ethno-Medico-Botanical survey of Ambikapur district, MP. Fourth international congress of ethnobiology. NBRI. Lucknow, India. 1994.|
|43||Venkatesan N, Thiyagarajan V, Narayanan S, Arul A, Raja S, Kumar SG, et al . Anti-diarrhoeal potential of Asparagus racemosus wild root extracts in laboratory animals. J Pharm Pharm Sci 2005;8:39-46. |
|44||Mandal SC, Nandy A, Pal M, Saha BP. Evaluation of antibacterial activity of Asparagus racemosus willd. root. Phytother Res 2000;14:118-9.|
|45||Christina AJ, Ashok K, Packialakshmi M, Tobin GC, Preethi J, Murugesh N. Antilithiatic effect of Asparagus racemosus willd on ethylene glycol-induced lithiasis in male albino Wistar rats. Methods Find Exp Clin Pharmacol 2005;27:633-8. |
|46||Bhatnagar M, Sisodia SS, Bhatnagar R. Antiulcer and antioxidant activity of Asparagus racemosus willd and Withania somnifera dunal in rats. Ann N Y Acad Sci 2005;1056:261-78.|
|47||Rege NN, Thatte UM, Dahanukar SA. Adaptogenic properties of six rasayana herbs used in Ayurvedic medicine. Phytother Res 1999;13:275-91.|
|48||Wiboonpun N, Phuwapraisirisan P, Tip-pyang S. Identification of antioxidant compound from Asparagus racemosus . Phytother Res 2004;18:771-3.|
|49||Kamat JP, Boloor KK, Devasagayam TP, Venkatachalam SR. Antioxidant properties of Asparagus racemosus against damage induced by gamma-radiation in rat liver mitochondria. J Ethnopharmacol 2000;71:425-35. |
|50||Goel RK, Sairam K. Anti-ulcer drugs from indigenous sources with emphasis on Musa sapientum , Tamrabhasma , Asparagus racemosus and Zingiber officinale . Indian J Pharmacol 2002;34:100-10.|
|51||Gupta M, Mazumder UK, Manikandan L, Bhattacharya S, Senthikumar GP, Suresh R. Anti-ulcer activity of ethanol extract of Terminalia pallida Brandis in swiss albino rats. J Ethnopharmacol 2005;97:405-8.|
|52||Sairam K, Rao CV, Goel RK. Effect of Centella asiatica Linn on physical and chemical factors induced gastric ulceration and secretion in rats. Indian J Exp Biol 2001;39;137-42.|
|53||Rao CV, Sairam K, Goel RK. Experimental evaluation of Bacopa monniera on rat gastric ulceration and secretion. Indian J Physiol Pharmacol 2000;44:435-41.|
|54||Sanyal AK, Gupta KK, Chowdhury NK. Banana and experimental peptic ulcer. J Pharm Pharmacol 1963;15:283-4.|