PMID- 31161612 OWN - NLM STAT- MEDLINE DCOM- 20200720 LR - 20200720 IS - 1469-445X (Electronic) IS - 0958-0670 (Linking) VI - 104 IP - 9 DP - 2019 Sep TI - Selective denervation of the aortic and carotid baroreceptors in rats. PG - 1335-1342 LID - 10.1113/EP087764 [doi] AB - NEW FINDINGS: What is the central question of this study? The traditional surgical approach for sino-aortic denervation in rats leads to simultaneous carotid baroreceptor and chemoreceptor deactivation, which does not permit their individual study in different situations. What is the main finding and its importance? We have described a new surgical approach capable of selective denervation of the arterial (aortic and carotid) baroreceptors, keeping the carotid bodies (chemoreceptors) intact. It is understood that this technique might be a useful tool for investigating the relative role of the baro- and chemoreceptors in several physiological and pathophysiological conditions. ABSTRACT: Studies have demonstrated that the traditional surgical approach for sino-aortic denervation in rats leads to simultaneous carotid baroreceptor and chemoreceptor deactivation. The present study reports a new surgical approach to denervate the aortic and the carotid baroreceptors selectively, keeping the carotid bodies (peripheral chemoreceptors) intact. Wistar rats were subjected to specific aortic and carotid baroreceptor denervation (BAROS-X) or sham surgery (SHAM). Baroreflex activation was achieved by i.v. administration of phenylephrine, whereas peripheral chemoreflex activation was produced by i.v. administration of potassium cyanide. The SHAM and BAROS-X rats displayed significant hypertensive responses to phenylephrine administration. However, the reflex bradycardia following the hypertensive response caused by phenylephrine was remarkable in SHAM, but not significant in the BAROS-X animals, confirming the efficacy of the surgical procedure to abolish the baroreflex. In addition, the baroreflex activation elicited by phenylephrine increased carotid sinus nerve activity only in SHAM, but not in the BAROS-X animals, providing support to the notion that the baroreceptor afferents were absent. Instead, the classical peripheral chemoreflex hypertensive and bradycardic responses to potassium cyanide were similar in both groups, suggesting that the carotid body chemoreceptors were preserved after BAROS-X. In summary, we describe a new surgical approach in which only the baroreceptors are eliminated, while the carotid chemoreceptors are preserved. Therefore, it is understood that this procedure is potentially a useful tool for examining the relative roles of the arterial baroreceptors versus the chemoreceptors in several pathophysiological conditions, for instance, arterial hypertension and heart failure. CI - (c) 2019 The Authors. Experimental Physiology (c) 2019 The Physiological Society. FAU - Castania, Jaci A AU - Castania JA AD - Department of Physiology, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, Sao Paulo, Brazil. FAU - Katayama, Pedro L AU - Katayama PL AUID- ORCID: 0000-0001-5641-7305 AD - Department of Physiology, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, Sao Paulo, Brazil. FAU - Brognara, Fernanda AU - Brognara F AUID- ORCID: 0000-0002-5042-1319 AD - Department of Physiology, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, Sao Paulo, Brazil. FAU - Moraes, Davi J A AU - Moraes DJA AD - Department of Physiology, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, Sao Paulo, Brazil. FAU - Sabino, Joao Paulo J AU - Sabino JPJ AD - Department of Biophysics and Physiology, Federal University of Piaui, Teresina, Piaui, Brazil. FAU - Salgado, Helio C AU - Salgado HC AD - Department of Physiology, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, Sao Paulo, Brazil. LA - eng GR - #2013/20549-7/Sao Paulo Research Foundation/International GR - #2013/10484-5/Sao Paulo Research Foundation/International GR - #2015/18511-7/Sao Paulo Research Foundation/International GR - #2017/05163-6/Sao Paulo Research Foundation/International GR - #475715/2012-8/National Council for Scientific and Technological Development/International PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20190707 PL - England TA - Exp Physiol JT - Experimental physiology JID - 9002940 RN - 1WS297W6MV (Phenylephrine) SB - IM MH - Animals MH - Aorta/drug effects/physiology/*surgery MH - Arteries/drug effects/*surgery MH - Baroreflex/drug effects/physiology MH - Blood Pressure/drug effects/physiology MH - Carotid Body/drug effects/physiology/*surgery MH - Chemoreceptor Cells/drug effects/physiology MH - Denervation/methods MH - Heart Rate/drug effects/physiology MH - Hypertension/physiopathology MH - Male MH - Phenylephrine/pharmacology MH - Pressoreceptors/drug effects/physiology MH - Rats MH - Rats, Wistar OTO - NOTNLM OT - autonomic nervous system OT - baroreflex OT - haemodynamics OT - phenylephrine EDAT- 2019/06/05 06:00 MHDA- 2020/07/21 06:00 CRDT- 2019/06/05 06:00 PHST- 2019/03/29 00:00 [received] PHST- 2019/06/03 00:00 [accepted] PHST- 2019/06/05 06:00 [pubmed] PHST- 2020/07/21 06:00 [medline] PHST- 2019/06/05 06:00 [entrez] AID - 10.1113/EP087764 [doi] PST - ppublish SO - Exp Physiol. 2019 Sep;104(9):1335-1342. doi: 10.1113/EP087764. Epub 2019 Jul 7.