Browsing by Author "Umaru IJ"
Now showing 1 - 2 of 2
Results Per Page
Sort Options
Item Antidiarheal activity of catechol and ethyl 5, 8,11,14,17 – icosapentanoate-rich fraction of Annona senegalensis stem bark(2022) Ahmed MU; Arise RO; Umaru IJ; Mohammed ABackground and aim Secretory diarrhea is the most common type of diarrhea. This study aimed at exploring the possible mechanism of antisecretory action of Annona senegalensis stem bark and to identify the bioactive compounds. Experimental procedure The ability of three crude extract; aqueous, dichloromethane and hexane stem bark extracts to inhibit castor oil-induced stooling in albino rats were assessed. Bioactivity guided fractionation of the most active extract was done using solvent-solvent partitioning (with hexane, dichloromethane, ethylacetate) and column chromatography. In vitro antioxidant activity of the most active sub-fraction was done using standard methods. The most active sub-fraction (25 mg/kg b. wt.) was administered to castor oil-induced diarrheal rats. Diarrheal rats small intestinal malondialdehyde concentration, antioxidant enzyme, cyclooxygenase II and Na+- K+ ATPase activities were determined using standard procedures. GC-MS analysis was done to identify the chemical compounds in the sub-fraction. Result and conclusion Aqueous extract significantly decreased the number of wet stools. Sub-fraction 1 of ethylacetate fraction of aqueous stem bark extract (EFAS1) showed the highest stool inhibition. The H2O2 scavenging activity of EFAS1 was significantly greater than ascorbic acid. The sub-fraction significantly increased (p < 0.05) the activity of catalase and Na+- K+ ATPase activities but significantly decreased the concentration of malondialdehyde and cyclooxygenase II activity. GC-MS analysis revealed that EFAS1 is rich in catechol, n-hexadecanoic acid and ethyl-5,8,11,14,17-icosapentanoate. The sub-fraction exerts its antisecretory activity by its antioxidative, inhibition of prostaglandin synthesis and stimulation of Na+- K+ ATPase properties due to the presence of catechol, n-hexedecanoic acid and ethyl-5,8,11,14,17-icosapentanoate.Item Identification and biochemical characterization of anti-enteropooling compounds from Annona senegalensis root bark(2022) Ahmed MU; Arise RO; Umaru IJBackground and objectives Annona senegalensis root bark is used in the treatment of diarrhea. This study fractionated Annona senegalensis root bark to identify the anti-enteropooling compounds and explore the possible mechanism of action of the compounds Methods Anti-enteropooling activity of hexane, dichloromethane and aqueous extracts were investigated to determine the most bioactive crude extract. Bioactivity guided fractionation of the most active extract was conducted. The compounds present in the bioactive sub-fraction were identified using GC-MS analysis. The concentration of Na+, Cl− and K+ in the intestinal fluids of rats administered the most active sub-fraction was determined. The effect of the sub-fraction on the small intestine malondialdehyde (MDA) concentration, antioxidant enzymes, Na+ - K + ATPase and cyclooxygenase II activities were evaluated using standard procedures. Results Aqueous root bark extract (AR) significantly decreased the weight and volume of intestinal fluids of castor oil induced diarrheal rats. Sub-fraction 1 of dichloromethane fraction of aqueous root bark extract (DFAR1) decreased the weight and volume of intestinal fluids of castor oil-induced diarrheal rats the most. Androstan-3-one and 3-tetradecen-5-yne were found present in DFAR1. The concentration of Na+ in the intestinal fluid of rats administered DFAR1 significantly decreased when compared with the control. DFAR1 significantly decreased the activities of superoxide dismutase, catalase and cyclooxygenase II. There was no significant difference in MDA concentration and Na+ - K + ATPase activity. Conclusion A. senegalensis root bark is rich in aldosterone derivative (steroid) and 3-tetradecen-5-yne that prevents enteropooling by stimulating Na+ absorption and inhibiting cyclooxygenase activity.