B Vrushabendra Swamy, K Jayaveera, K Ravindra Reddy, T Bharathi
diarrhea, memc, methanol extract
B Vrushabendra Swamy, K Jayaveera, K Ravindra Reddy, T Bharathi. Anti-diarrhoeal activity of fruit extract of Momordica cymbalaria Hook. F.. The Internet Journal of Nutrition and Wellness. 2007 Volume 5 Number 2.
A study was undertaken to evaluate the effect of methanolic extract of the fruit of
Diarrhoea has long been recognized as one of the most important health problem in the developing countries1. World Wide distribution of diarrhea accounts for more than 5-8 millions deaths each year in infants and small children's less than 5 years. According to WHO estimation for the year 1998, there were about 7.1 million deaths due to diarrhea2. Secretory diarrhoea is most dangerous symptom of gastrointestinal problems3 and is associated with excessive defecation and stool outputs. The stool being of abnormally loose consistency4. The World Health Organization has constituted a Diarrhoeal Disease Control program (CDD), which includes studies of traditional medicinal practices, together with the evaluation of health educational and prevention approaches5.
24× 15mm attenuated at the apex and with the base narrowed into the curved peduncle, which is fleshy, dark green and ribbed. The seeds are 4.6 mm long, ovoid shaped, smooth and shiny. Flowering occurs during October; fruits are harvested from November to January. The yield of each plant is 1.25 to 1.5kg. The tender fruits closely resemble those of a small variety of bitter gourd Athalakkai is used as a vegetable by the rural people of South Tamil Nadu and North Karnataka, India6 The phytochemicals reported in this plants are tannins, alkaloids, phenols, proteins, amino acids7, Vitamin C, carbohydrate and ß-Carotene6. The fruits of this plant reported anti diabetic and antihyperlipedimic activities (Kameswararao et al., 2003). The tubers were reported as antiovulatory activity8.
Furthermore, literature survey of
Materials And Methods
The fruits of Momordica cymbalaria Hook F. was collected in November 2006 from the Bellary, Karnataka, India. The fruit material was taxonomically identified by the Regional Research Institute, Karnataka, India, and the Voucher specimen RRI/BNG/DSRU/F53/2006-07. The fruits were dried under shade with occasional shifting and then powdered with a mechanical grinder and stored in an airtight container.
Preparation of extract
The powder obtained was subjected to successive soxhlet extraction with the solvents with increasing order of polarity i.e. Pet. Ether (60-80 ), Chloroform (59.5-61.5 ), Methanol (64.5-65.5 ) and water. Yield 3.29, 6.19, 11.70, and 15.71% respectively.
A preliminary phytochemical screening of all extracts carried out as described by Khandelwal K.L 9
Albino rats (Wistar) weighing 150-200g and albino mice weighing 20-25g of either sex were used in this study. They were procured from Sri Venkateshwara Enterprises, Bangalore. The animals were acclimatized for one week under laboratory conditions. They were housed in polypropylene cages and maintained at 27 C 2 C under 12 hrs dark / light cycle. They were fed with standard rat feed (Gold Mohr Lipton India Ltd.) and water
Acute oral toxicity studies
The acute oral toxicity was performed according to OPPTS following up and down procedure. Colony bred female albino rats Wistar strain (150-200gm) were maintained under controlled animal house condition with access to food and water
Castor oil induced diarrhoea
The doses of MEMC were selected on a trial basis and administered orally (200, 400 & 600mg/kg body weight) by gavage to three groups of animals. The fourth group received diphenoxylate (5mg/kg body weight) orally and the fifth group received neither drug nor extract but 2% v/v aqueous Tween 80 (1 ml) only and served as a control. After 60 min of drug treatment, each animal was administered 1ml of castor oil orally by gavage and observed for defecation up to 4hrs after castor oil administration. Characteristic diarrheal droppings were noted in the transparent plastic dishes placed beneath the individual perforated rat cages. The mean number of wet feces was calculated from the diarrhoeal droppings in the transplant plastic dishes10, 11.
PGE induced enteropooling
For this evaluation, rats of same stock as above were deprived of food and water for 18hrs prior to the experiment. Five groups of six animals were used, which were placed in five perforated cages. The first three groups of rats were treated with MEMC (200, 400 & 600mg/kg body weight, p.o) while the fourth and fifth group received 1ml of 5% v/v ethanol in normal saline (i.p). The fourth group was then administered 1ml of normal saline and used as control. Immediately afterwards, each rat was treated with PGE2 (100µg/kg body weight in 5% v/v ethanol in normal saline) administered orally. All the rats were sacrificed under mild anesthesia after 30min. The entire length of intestine from the pylorus to the caecum was dissected out, and its contents were collected and measured12.
Gastrointestinal motility test
In this method rate were tasted for 18hrs and placed in five metal cages, six in each. Each animal was given 1ml of charcoal meal (3% deactivated charcoal in normal saline). The first three groups of animals were administered MEMC orally (200, 400 & 600 mg/kg body weight) immediately after the charcoal meal treatment. The fourth group received atropine (0.1mg/kg body weight, i.p) as standard for comparison. The fifth group was treated with normal saline as control. 30min after administration of the charcoal meal, animals of each individual group were killed and the movement of charcoal from pylorus to caecum was measured. The charcoal movement in the intestine was expressed as percentage12.
For all the above experiments results were expressed as mean ±sem. statistical significance tests were performed using the students‘t' test and p-values (graph pad software) were calculated by comparison with control groups.
Preliminary phytochemical studies revealed the presence of tannins, alkoloids, phenols, proteins, aminoacids, flavanoids, triterpenoids, sterols, Vitamins. The MEMC found to be non toxic up to 5000 mg/kg.
Inhibition of castor oil induced diarrhoea
The extract (MEMC) inhibited the frequency of defecation significantly, like standard drug (diphenoxylate) as compared to control (2% aqueous tween 80 treated). The wetness of fecal material also reduced by both the standard and extract (MEMC). The results are shown in Table – 1.
PGE2 induced a significant increase in the fluid volume of the rat as compared to control animals receiving only ethanol in normal saline. The extract (MEMC) significantly inhibited PGE2 induced enteropooling in rats at almost all doses used (Table – 2).
Effect on gastrointestinal motility
The extract (MEMC) decreased propulsion of charcoal meal through the gastrointestinal tract significantly with respect to the control group. The effect was comparable to the standard drug. The results are shown in Table – 3.
In developing countries a quarter of infant and childhood mortality is related to the diarrhea13. The highest mortality rates have been reported to be in children less than five years of age. During the past decade oral dehydration therapy has reduced mortality from acute diarrheal disease, where as chronic diarrhea remains a life-threatening problem in those regions in which malnutrition is common co-existing and complication factors number of factors, such as infective, immunological and nutritional has been involved in the perpetuation of the diarrheal syndrome14. Many plants conveniently available in India are used in traditional folklore medicine for the treatment of diarrhea and dysentery of the indigenous plants used,
The MEMC exhibited significant anti-diarrheal activity against castor oil induced diarrhea in rats. The extract had a similar activity as diphenoxylate, when tested at 200, 400 & 600mg/kg and statistically significant reduction in the frequency of defecation and the wetness of the fecal droppings when compared to untreated control rats.
It is widely known that castor oil or its active component ricinoleic acid induces permeability changes in mucosal fluid and electrolyte transport that result in hyper secretory response of diarrhea19, 20. The experimental studies in rat's demonstrated a significant increase in the portal venous PGE2 concentration following oral administration of castor oil21. The recinoleic acid from castor oil results in irritation and inflammation of the intestinal mucosa, leading to release of prostaglandins, which stimulate motility and secretion22. Inhibitors of prostaglandin biosynthesis delayed castor oil induced diarrhea10.
The MEMC significantly inhibited the PGE2 induced intestinal fluid accumulation (enteropooling). It has been shown that E type of prostaglandin cause diarrhoea in experimental animals as well as human beings23. Their mechanism has been associated with dual effects on gastrointestinal motility as well as on water and electrolyte transport24. PGE2 also inhibit the absorption of glucose a major stimulus to intestinal adsorption of water and electrolytes25. These observations tend to suggest that MEMC reduced diarrhea by inhibiting PGE2 induced intestinal accumulation of fluid.
The MEMC appears to act on all parts of the intestine. Thus it reduced the intestinal propulsive movement in the charcoal meal treated model. The MEMC showed activity similar to that of atropine. Previous study shows that activated charcoal avidly absorbs drugs and chemicals on the surface of the charcoal particles there by preventing absorption26. Thus gastrointestinal motility test with activated charcoal was carried out to find out the effect of MEMC on peristalsis movement. The results shows that the MEMC suppressed the propulsion of charcoal meal thereby increased the absorption of water and electrolytes.
Previous reports have demonstrated the antidiarrhoeal activity of tannins27, flavanoids28, alkaloids29, sterols and terpenes30 containing plant extracts. The phytochemical analysis of the extract showed presence of tannins, alkaloids, sterols, terpenes and flavanoids. These constituents may responsible for the antidiarrhoeal activity.
All authors are grateful to our honorable founder secretary Mr. C. Basavaraja, Rural college of Pharmacy, Devanahalli, Bangalore, for providing facilities to carryout this project.
Srinivasa Institute of Pharmaceutical Sciences, Sri Chowdeswari Nagar, Peddasetty Palli, Proddadur, Kadapa (Dist), Andhra Pradesh, India 516 361 email@example.com, firstname.lastname@example.org Mobile: 00 91 9959661915