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Medical Journal of Mashad University of Medical Sciences. 2007; 49 (94): 357-366
in Persian | IMEMR | ID: emr-100035

ABSTRACT

Captopril and Allopurinol have protective effect against renal warm ischemia with different mechanisms. The aime of this study was to evaluate this protective effect against induced 1 hour warm ischemia in dog's kidneys. This experimental study was done in the year 2006. We performed the operation on 15 healthy dogs. During these procedures both kidneys were clamped for 1 hour, then left kidney was removed for pathologic evaluation and right kidney remained insitue for functional assessment. Five random dogs received 1 [mg/kg]d[day] Captopril orally before and after surgery [captopril group]; another five dogs received 10 [mg/kg]/day Allopurinol orally before and after surgery [allopurinol group]. Five dogs of control group received no drugs. Serum urea and creatinine were measured preoperatively and on postoperative days of 1, 3, 5, 10 and 16 in all groups. Serum levels of urea and creatinine elevated in all groups but in Captopril group maximum levels of urea and creatinine were significantly lower than control [P<0.05]. In Allopurinol group the maximum rise of creatinine was significantly lower in comparison to control group [p< 0.05], but the maximum levels of urea in this group had no significant difference when compared with control values [p< 0.05]. There was no significant difference in pathologic changes in the three groups. One hour warm ischemia results in ATN so it is not safe for dog's kidneys. Althogh Captopril and Allopurinol do not prevent ATN after one hour warm ischemia; they can reduce its severity and improve renal function after warm ischemia


Subject(s)
Animals , Allopurinol , Captopril , Dogs , Kidney Tubular Necrosis, Acute/drug therapy , Kidney Tubular Necrosis, Acute/prevention & control
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