Why the study?
Does prepubertal treatment with candesartan cilexetil attenuate hypertension and renal damage in Dahl salt-sensitive rats on a high-salt diet?
Does prepubertal treatment with candesartan cilexetil attenuate hypertension and renal damage in Dahl salt-sensitive rats on a high-salt diet?
Prepubertal treatment with an angiotensin receptor blocker provides sustained renoprotection and blood pressure attenuation in a low-renin rat model of salt-sensitive hypertension.
Prepubertal ARB may confer lasting protection in salt-sensitive rat models; hypothesis-generating and should not yet inform clinical practice.
Recently, we have shown that treatment of stroke-prone spontaneously hypertensive rats with angiotensin inhibitors for a limited time-window before puberty results in an attenuation of hypertensive nephrosclerosis in later life. The aim of this study was to examine the applicability of this therapeutic paradigm to a low-renin model. Dahl salt-sensitive (Dahl-S) rats were fed a high-salt diet from age 6 weeks. Some rats were treated with the angiotensin receptor blocker (ARB) candesartan cilexetil (2 mg/kg/d) from weaning to puberty (age 3-10 weeks), whereas other rats were treated continuously until overt renal damage was seen (age 3-16 weeks). Dahl-S rats on a high salt diet had increased blood pressure (207 +/- 3 vs. 125 +/- 2 mm Hg), proteinuria, and glomerular/vascular histological changes. The prepubertal treatment with ARB resulted in a continued suppression of blood pressure (153 +/- 2 mm Hg) at 16 weeks. Both proteinuria and renal histological changes were significantly (p < 0.05) attenuated, but not completely prevented by the treatment. No significant differences in plasma renin activity, renin mRNA, or AT1/AT2 mRNA were seen between groups. These results suggest that prepubertal treatment affords sustained renoprotection, even in an animal model with a suppressed renin-angiotensin system, and support the notion that appropriate prepubertal intervention may lead to a partial attenuation in the susceptibility to inherited renal diseases.
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Nakaya et al. (2002) studied this question.
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