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Published on: July 3, 2013
Impact of Total or Afferent Renal-Nerve Denervation on Cardiovascular and Renal Function in Sprague Dawley Rats Fed
Sharif Hasan Siddiqui1, Dragana Komnenov1, Afoluso Olayonwa1
1Department of Physiology, School of Medicine, Wayne State University, 540 E. Canfield, Detroit, MI 48201, USA.
Abstract:
Background: Combined high fructose and high sodium diet (FHS) is linked to elevated blood pressure (BP), heightened sympathetic activity, and cardiovascular and renal dysfunction. Total-renal denervation is effective in lowering BP in some hypertension models. Objectives: The present studies tested whether selective afferent (A-RDNx) or total-renal denervation (T-RDNx) ameliorates FHS cardiovascular and renal function. Methods: Male and female Sprague Dawley rats were fed 20% glucose and 0.4% Na chow for one week then assigned to one of four groups: 20% glucose plus 0.4% Na sham-operation (G-Sham) or 20% fructose plus 4% Na with either sham-operation (F-Sham), A-RDNx, or T-RDNx for ~21 days. Telemetric BP and heart rate, echocardiography, pulse-wave velocity (PWV), and renal function were assessed. Results: T-RDNx reduced FHS-induced high BP in both sexes. LVEF did not differ, but global longitudinal strain showed hypercontractility in male F-Sham, which normalized with A-RDNx or T-RDNx. Increased LV perivascular fibrosis in F-Sham rats of both sexes was prevented by A-RDNx or T-RDNx. T-RDNx improved elevated PWV, endothelium-independent vasodilation by myography, and aortic oxidative stress in male F-Sham aortas. High plasma renin activity in male F-Sham decreased with T-RDNx to levels similar to G-Sham rats. Serum creatinine, urine albumin:creatinine ratio, and mesangial hypercellularity in F-Sham male rats decreased with A-RDNx or T-RDNx. Renal function was unchanged in female F-Sham; T-RDNx decreased albuminuria. Conclusions: Renal-sympathetic nerves play a crucial role in elevated BP, cardiac dysfunction, vascular stiffness, and renal impairment associated with FHS diet, particularly in male rats, and implicates a complex interplay with BP, the renin-angiotensin system, and oxidative stress.
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