Abstract

In the spontaneously hypertensive (SH) rat, hyperoxic inactivation of the carotid body (CB) produces a rapid and pronounced fall in both arterial pressure and renal sympathetic nerve activity (RSA). Here we show that CB de-afferentation through carotid sinus nerve denervation (CSD) reduces the overactive sympathetic activity in SH rats, providing an effective antihypertensive treatment. We demonstrate that CSD lowers RSA chronically and that this is accompanied by a depressor response in SH but not normotensive rats. The drop in blood pressure is not dependent on renal nerve integrity but mechanistically accompanied by a resetting of the RSA-baroreflex function curve, sensitization of the cardiac baroreflex, changes in renal excretory function and reduced T-lymphocyte infiltration. We further show that combined with renal denervation, CSD remains effective, producing a summative response indicative of an independent mechanism. Our findings indicate that CB de-afferentation is an effective means for robust and sustained sympathoinhibition, which could translate to patients with neurogenic hypertension.

Highlights

  • In the spontaneously hypertensive (SH) rat, hyperoxic inactivation of the carotid body (CB) produces a rapid and pronounced fall in both arterial pressure and renal sympathetic nerve activity (RSA)

  • Given the current clinical interest and application of renal denervation (RD) in the treatment of drug-resistant hypertension[25,26,27,28,29], we have characterized the interaction between carotid sinus nerve denervation (CSD) and RD in combination to establish the type of interaction: summative, occlusive or facilitatory

  • Unlike Wistar rats, we find that the CB of the SH rat has resting tone driving hypertension, which is not dependent on renal nerves, depresses both the cardiac and sympathetic vasomotor baroreflex and attenuates the adaptive immune response

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Summary

Introduction

In the spontaneously hypertensive (SH) rat, hyperoxic inactivation of the carotid body (CB) produces a rapid and pronounced fall in both arterial pressure and renal sympathetic nerve activity (RSA). We found that in spontaneously hypertensive (SH) rats, carotid sinus nerve denervation (CSD) lowered arterial pressure by B17 mm Hg, and that this was well maintained and tolerated[11] These data are comparable to those in human hypertensive patients where inactivation of the CB with 100% oxygen reduced both arterial pressure and sympathetic activity[24], supporting a causal role for peripheral chemoreceptors in the aetiology of neurogenic hypertension. Unlike Wistar rats, we find that the CB of the SH rat has resting tone driving hypertension, which is not dependent on renal nerves, depresses both the cardiac and sympathetic vasomotor baroreflex and attenuates the adaptive immune response We hypothesize that these findings may translate to patients with neurogenic hypertension

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