OBJECTIVE:To elucidate potential antioxidant,antidiarrheal,cytotoxic,and antibacterial activities of the ethanol extract of Alocasia indica Schott tuber in different experimental models established in vitro and in vivo.METHODS:In vitro antioxidant activity was evaluated by 2,2-diphenyl-1-picrylhydrazyl(DPPH)radical-scavenging assay.Phenolic content was estimated by using Folin-Ciocalteu’s reagent while reducing ability was measured by ferric reducing power assay.In vivo antidiarrheal studies were carried out in mice,and the activity was evaluated in castor oil and magnesium sulfateinduced diarrhea.Disk diffusion assay was utilized to determine antibacterial activity against a number of pathogenic bacterial strains.Acute toxicity test was carried out to measure the safe doses for the extract.RESULTS:In DPPH radical-scavenging assay,the extract exhibited strong radical-scavenging activity with the 50%inhibitory concentration value of 42.66μg/mL.Total phenolic content was found to be 542.26 mg gallic acid equivalent per 100 g of dried tuber extract,whereas flavonoid content was found to be 4.30 mg quercetin equivalent/g of dried tuber extract.In reducing power assay,the extract showed strong reducing power in a concentration-dependent manner.The extract significantly(P<0.01)enhanced the latent period and decreased defecation in both castor oil-and magnesium sulfate-induced diarrhea.The extract also lessened gastrointestinal motility in mice.Potential antibacterial activity was exhibited by the extract against all the tested bacterial strains in disk diffusion assay.The 50%lethal concentration against brine shrimp nauplii was 81.09μg/mL.CONCLUSION:The results demonstrated that the ethanol extract of A.indica has potential antioxidant,antidiarrheal,cytotoxic,and antibacterial activity. OBJECTIVE: To elucidate potential antioxidant, antidiarrheal, cytotoxic, and antibacterial activities of the ethanol extract of Alocasia indica Schott tuber in different experimental models established in vitro and in vivo. METHODS: In vitro antioxidant activity was evaluated by 2,2-diphenyl-1 -picrylhydrazyl (DPPH) radical-scavenging assay. Phenolic content was estimated by using Folin-Ciocalteu’s reagent while reducing ability was measured by ferric reducing power assay. In vivo antidiarrheal studies were carried out in mice, and the activity was evaluated in castor oil and magnesium sulfateinduced diarrhea. Disk diffusion assay was utilized to determine antibacterial activity against a number of pathogenic bacterial strains. Acute toxicity test was carried to measure the safe doses for the extract .RESULTS: In DPPH radical-scavenging assay, the extract showed strong radical -scavenging activity with the 50% inhibitory concentration value of 42.66 μg / mL. Total phenolic content was found to be 5 42.26 mg gallic acid equivalent per 100 g of dried tuber extract, flav flavoid content was found to be 4.30 mg quercetin equivalent / g of dried tuber extract. Reducing power assay, the extract showed strong reducing power in a concentration-dependent manner. extract the latent period and reduced defecation in both castor oil-and magnesium sulfate-induced diarrhea. The extract also lessened gastrointestinal motility in mice. Potential antibacterial activity was exhibited by the extract against all the tested bacterial strains in disk diffusion assay. The 50% lethal concentration against brine shrimp nauplii was 81.09 μg / mL. CONCLUSION: The results demonstrated that the ethanol extract of A.indica has potential antioxidant, antidiarrheal, cytotoxic, and antibacterial activity.