Key result
Neither captopril nor losartan potassium significantly ameliorated the histological or biochemical features of partial bladder outlet obstruction in rats compared to untreated controls.
Why the study?
Does captopril or losartan ameliorate histological or biochemical features of partial bladder outlet obstruction in rats?
Does captopril or losartan ameliorate histological or biochemical features of partial bladder outlet obstruction in rats?
In a rat model of partial bladder outlet obstruction, neither ACE inhibition nor ARB therapy significantly ameliorated obstructive histological or biochemical changes.
Does not support renin-angiotensin blockade for bladder outlet obstruction; leaves open efficacy in other models or species.
PURPOSE: Others have demonstrated that inhibition of angiotensin II production partially ameliorates obstructive changes in the neonatal rabbit bladder. We examined the effect of angiotensin II converting enzyme inhibition and receptor antagonism on the obstructed rat bladder. MATERIALS AND METHODS: Three groups of animals were investigated. Partial bladder neck obstruction was created in 23 rats by placing a 2-zero silk ligature around the vesicourethral junction. Eight rats were given untreated tap water, 9 were given water supplemented with 50 mg./kg. of the angiotensin-converting enzyme inhibitor captopril and 6 were given water with 30 mg./kg. of the angiotensin II subtype AT1 receptor antagonist losartan potassium. Eight unobstructed rats served as controls. After 2 weeks of partial outlet obstruction the animals were sacrificed and bladders were harvested. Routine histological evaluation and assays for total protein, deoxyribonucleic acid and collagen content were performed. RESULTS: Histological evaluation revealed that administration of captopril or losartan potassium resulted in a mild decrease in the degree of obstructive bladder changes. Biochemically neither captopril nor losartan potassium caused a significant decrease in the amount of total deoxyribonucleic acid, protein or collagen content per bladder compared to untreated obstructed bladders. CONCLUSIONS: In contrast to previous studies in neonatal rabbits, neither captopril nor losartan potassium significantly ameliorated the histological or biochemical features of partial bladder outlet obstruction in the rat. Further investigation is necessary into species specific differences to understand better the role that angiotensin II may have in mediating the bladder changes of experimentally induced obstruction.
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Palmer et al. (1997) studied Partial bladder neck obstruction (n=31). Captopril or Losartan potassium vs. Untreated tap water was evaluated on Histological evaluation and total deoxyribonucleic acid, protein, and collagen content per bladder. Neither captopril nor losartan potassium significantly ameliorated the histological or biochemical features of partial bladder outlet obstruction in rats compared to untreated controls.
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