Key result
Transient prepubertal exposure to an ARB or MR-ant significantly suppressed the later development of diabetic nephropathy in spontaneously hypertensive rats.
Why the study?
Does transient prepubertal exposure to ARB, MR-ant, or vasodilator prevent the development of diabetic nephropathy in spontaneously hypertensive rats?
Does transient prepubertal exposure to ARB, MR-ant, or vasodilator prevent the development of diabetic nephropathy in spontaneously hypertensive rats?
Transient prepubertal exposure to ARB or MR-ant confers protection against the later development of diabetic nephropathy in spontaneously hypertensive rats through blood pressure-independent mechanisms.
Answers are grounded in this paper and cite their sources.
Does not support clinical use of prepubertal ARB or MR-ant; leaves open developmental windows for diabetic nephropathy prevention in hypertensive models.
BACKGROUND/AIMS: We have previously shown that treatment of spontaneously hypertensive rats (SHR) with an angiotensin receptor blocker (ARB) during the 'critical period' from age 3 to 10 weeks confers protection against L-NAME-induced renal injury later in life. The aim of this study was to examine the effects of transient prepubertal exposure to ARB on the development of nephropathy in streptozotocin-induced diabetic SHR and to compare the results with other antihypertensive agents including a mineralocorticoid receptor antagonist (MR-ant). METHODS: Male SHR (n = 43) were transiently treated with candesartan (ARB), potassium canreonate (the active metabolite of the MR-ant spironolactone) or hydralazine (vasodilator) between 3 and 10 weeks of age with untreated rats serving as controls. An additional group was treated continuously with candesartan throughout the study. Rats were injected with streptozotocin to induce diabetes at age 16 weeks and followed until age 8 months. RESULTS: Diabetic control rats showed signs of diabetic nephropathy including albuminuria and mesangial expansion. These changes were significantly suppressed in rats exposed to ARB or MR-ant. Systolic blood pressure was significantly reduced compared to controls in the ARB (transient) and ARB (sustained) groups, but not in the MR-ant or vasodilator groups. CONCLUSION: Transient prepubertal exposure to ARB or MR-ant, but not vasodilator, confers protection against the later development of diabetic nephropathy and involves blood pressure-independent protective mechanisms.
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Ishiguro et al. (2008) studied Diabetic nephropathy (n=43). Candesartan (ARB) or potassium canreonate (MR-ant) vs. Untreated controls and hydralazine (vasodilator) was evaluated on Signs of diabetic nephropathy including albuminuria and mesangial expansion. Transient prepubertal exposure to an ARB or MR-ant significantly suppressed the later development of diabetic nephropathy in spontaneously hypertensive rats.
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