Objective:To highlight the nephroprotective activity of ethyl acetate extract of dried flowers of Tecomu stans for its protective effects on genlamicin-induced nephrotoxicity in albino rats. Methods:For studying acute toxicity study,single oral dose of 5(KM) mg ethyl acetate floral extract/kg hodv weight was administered to albino rats(five females,five males).Nephrotoxicity was induced in albino rats by intraperitoneal administration of gentamicin 80 mg/kg/day for eight days.Effect of concurrent administration of ethyl acetate floral extract of Tecoma stans at a dose of 100.200 and 300 mg/kg/day given by oral mute was determined using serum creatinine,serum uric acid,blood urea nitrogen and serum urea as indicators of kidney damage.The study groups contained six rats in each group.As nephrotoxicity of gentamicin is known to involve induction of oxidative stress,in vitro antioxidant aclivity and free radical-scavenging activity of this extract was also evaluated.Results:For acute toxicity testing both female and male rats administered with the extract at a dose of 5 000 mg/kg.The results showed no toxicity in terms of general behavior change,mortality,or change in gross appearance of internal organs(LD_(50)>5 000 mg/kg). It was observed that the ethyl acetate floral extract of Tecoma stans significantly protected rat kidneys from gentamicin-induced histopathological changes.Gentamicin-induced glomerular congestion,peritubular and blood vessel congestion,epithelial desquamation,accumulation ol inflamnialoiy cells and necrosis of the kidney cells were found to be reduced in the groups receiving the ethyl acetate floral extract of Tecoma starts along with gentamicin in a dose dependent manner.The floral extract also reduced the gentamicin-induced increase in serum creatinine,serum uric acid,blood urea nitrogen and serum urea levels(P>0.01).Conclusions: The present study indicates a verv important role of reactive oxygen species(BOS) and the relation to renal dysfunction and point to the therapeutic potential of Tecoma stans in gentamicin induced nephrotoxicity. Objective: To highlight the nephroprotective activity of ethyl acetate extract of dried flowers of Tecomu stans for its protective effects on genlamicin-induced nephrotoxicity in albino rats. Methods: For studying acute toxicity study, single oral dose of 5 (KM) mg ethyl acetate floral extract / kg hodv weight was administered to albino rats (five females, five males) .Nephrotoxicity was induced in albino rats by intraperitoneal administration of gentamicin 80 mg / kg / day for eight days. Effect of concurrent administration of ethyl acetate floral extract of Tecoma stans at a dose of 100.200 and 300 mg / kg / day given by oral mute was determined using serum creatinine, serum uric acid, blood urea nitrogen and serum urea as indicators of kidney damage. The study groups contained six rats in each group. nephrotoxicity of gentamicin is known to involve induction of oxidative stress, in vitro antioxidant aclivity and free radical-scavenging activity of this extract was also. Results: For acute toxic ity testing both female and male rats administered with the extract at a dose of 5 000 mg / kg. The results showed no toxicity in terms of general behavior change, mortality, or change in gross appearance of internal organs (LD_ (50)> 5 000 mg / kg). It was observed that the ethyl acetate floral extract of Tecoma stans significantly protected rat kidneys from gentamicin-induced histopathological changes. Gentamicin-induced glomerular congestion, peritubular and blood vessel congestion, epithelial desquamation, accumulation ol inflamnialoiy cells and necrosis of the kidney cells were found to be reduced to the groups receiving the ethyl acetate floral extract of Tecoma starts along with gentamicin in a dose dependent manner. The floral extract also reduced the gentamicin-induced increase in serum creatinine, serum uric acid, blood urea nitrogen and serum urea levels (P> 0.01) .Conclusions: The present study indicates a verv important role of reactive oxygen species (BOS) and the relation to renal dysfunctionn and point to the therapeutic potential of Tecoma stans in gentamicin induced nephrotoxicity.