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Reactive oxygen species in rostral ventrolateral medulla modulate cardiac sympathetic afferent reflex in rats
Author(s) -
Zhong M.K.,
Gao J.,
Zhang F.,
Xu B.,
Fan Z.D.,
Wang W.,
Zhu G.Q.
Publication year - 2009
Publication title -
acta physiologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.591
H-Index - 116
eISSN - 1748-1716
pISSN - 1748-1708
DOI - 10.1111/j.1748-1716.2009.02026.x
Subject(s) - rostral ventrolateral medulla , microinjection , apocynin , medicine , chemistry , superoxide , endocrinology , reflex , superoxide dismutase , angiotensin ii , medulla oblongata , nadph oxidase , oxidative stress , central nervous system , blood pressure , biochemistry , enzyme
Aim: The aim of the present study was to investigate whether reactive oxygen species (ROS) in rostral ventrolateral medulla (RVLM) modulate cardiac sympathetic afferent reflex (CSAR) and the enhanced CSAR response caused by microinjection of angiotensin II (Ang II) into the paraventricular nucleus (PVN). Methods: Under urethane and α‐chloralose anaesthesia, renal sympathetic nerve activity (RSNA) and mean arterial pressure (MAP) were recorded in sinoaortic‐denervated and cervical‐vagotomized rats. The CSAR was evaluated by the RSNA response to epicardial application of capsaicin (1.0 nmol). Results: Bilateral RVLM microinjection of tempol (a superoxide anion scavenger) or polyethylene glycol‐superoxide dismutase (PEG‐SOD, an analogue of endogenous superoxide dismutase) attenuated the CSAR, but did not cause significant change in baseline RSNA and MAP. NAD(P)H oxidase inhibitors apocynin or phenylarsine oxide (PAO) also showed similar effects, but SOD inhibitor diethyldithio‐carbamic acid (DETC) enhanced the CSAR and baseline RSNA, and increased the baseline MAP. Bilateral PVN microinjection of Ang II (0.3 nmol) enhanced the CSAR and increased RSNA and MAP, which was inhibited by the pre‐treatment with RVLM administration of tempol, PEG‐SOD, apocynin or PAO. The pre‐treatment with DETC in the RVLM only showed a tendency in potentiating the CSAR response of Ang II in the PVN, but significantly potentiated the RSNA and MAP responses of Ang II. Conclusion: These results suggest that the NAD(P)H oxidase‐derived ROS in the RVLM modulate the CSAR. The ROS in the RVLM is necessary for the enhanced CSAR response caused by Ang II in the PVN.