Why the study?
Does valsartan administration induce proliferative changes in renal arteriolar walls more frequently in juvenile compared to adult spontaneous hypertensive rats?
Does valsartan administration induce proliferative changes in renal arteriolar walls more frequently in juvenile compared to adult spontaneous hypertensive rats?
Valsartan administration induces unusual proliferative changes and increased renin expression in renal afferent arterioles more frequently in juvenile than adult hypertensive rats, suggesting potential age-dependent renal risks.
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May indicate greater ARB-related renal arteriolar risk in juvenile hypertensive models; hypothesis-generating for age-specific effects in humans.
INTRODUCTION: Our previous study of angiotensin II receptor blocker (ARB) administration in rats induced unusual proliferative changes of smooth muscle cells in renal arteriolar walls. The present study examined if the incidence of the changes depended on the rats' age, and how long it would take to find changes. MATERIALS AND METHODS: Six-week-old (juvenile spontaneous hypertensive rats (SHRs)+ARB group, n=15) and 20-week-old (adult SHRs+ARB group, n=10) male SHRs were fed a standard diet (0.4% NaCl) containing valsartan (10 mg/kg/day; Novartis Co.). Fifteen age-matched SHRs were studied as controls. After 4, 8, and 12 weeks, the rat kidneys were examined under light and electron microscopes and through immunohistochemical studies. RESULTS: Extremely concentric proliferative changes in afferent arteriolar walls were frequently observed in the juvenile SHR+ARB group compared to the adult SHR+ARB group (48.7±6.8% vs 19.3±6.9%; p=0.0307) at the 12(th) week. Increased renin expression and arteriolar changes were found from the 4(th) week in the juvenile SHR+ARB group. CONCLUSION: This study indicates that ARB administration induces unusual proliferative changes and a marked renin-producing cell increase in afferent arterioles more frequently in juveniles than adult rats. It is suggested that the treatment of ARB in juveniles might have a higher risk of changes in renal afferent arterioles.
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Nagai et al. (2013) studied this question.
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