Literature DB >> 23521912

Exercise training lowers the enhanced tonically active glutamatergic input to the rostral ventrolateral medulla in hypertensive rats.

Yan-Ping Zha1, Yang-Kai Wang, Yu Deng, Ru-Wen Zhang, Xing Tan, Wen-Jun Yuan, Xiao-Ming Deng, Wei-Zhong Wang.   

Abstract

AIMS: It is well known that low-intensity exercise training (ExT) is beneficial to cardiovascular dysfunction in hypertension. The tonically active glutamatergic input to the rostral ventrolateral medulla (RVLM), a key region for control of blood pressure and sympathetic tone, has been demonstrated to be increased in hypertensive rats. The aim of this study was to determine the effect of ExT on the increased glutamatergic input to the RVLM in spontaneously hypertensive rat (SHR).
METHODS: Normotensive rats Wistar-Kyoto (WKY) and SHR were treadmill trained or remained sedentary (Sed) for 12 weeks and classed into four groups (WKY-Sed, WKY-ExT, SHR-Sed, and SHR-ExT). The release of glutamate in the RVLM and its contribution to cardiovascular activity were determined in WKY and SHR after treatment of ExT.
RESULTS: Blood pressure and sympathetic tone were significantly reduced in SHR after treatment with ExT. Bilateral microinjection of the glutamate receptor antagonist kynurenic acid (2.7 nmol in 100 nL) into the RVLM significantly decreased resting blood pressure, heart rate, and renal sympathetic nerve activity in SHR-Sed but not in WKY groups (WKY-Sed and WKY-ExT). However, the degree of reduction in these cardiovascular parameters evoked by KYN was significantly blunted in SHR-ExT compared with SHR-Sed group. The concentration of glutamate and the protein expression of vesicular glutamate transporter 2 in the RVLM were significantly increased in SHR-Sed compared with WKY-Sed, whereas they were reduced after treatment with ExT.
CONCLUSION: Our findings suggest that ExT attenuates the enhancement in the tonically acting glutamatergic input to the RVLM of hypertensive rats, thereby reducing the sympathetic hyperactivity and blood pressure.
© 2013 Blackwell Publishing Ltd.

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Year:  2013        PMID: 23521912      PMCID: PMC6493496          DOI: 10.1111/cns.12065

Source DB:  PubMed          Journal:  CNS Neurosci Ther        ISSN: 1755-5930            Impact factor:   5.243


  13 in total

1.  The phosphoinositide-3 kinase signaling is involved in neuroinflammation in hypertensive rats.

Authors:  Xing Tan; Pei-Lei Jiao; Yang-Kai Wang; Zhao-Tang Wu; Xiao-Rong Zeng; Miao-Ling Li; Wei-Zhong Wang
Journal:  CNS Neurosci Ther       Date:  2017-02-12       Impact factor: 5.243

Review 2.  Modulation of angiotensin II signaling following exercise training in heart failure.

Authors:  Irving H Zucker; Harold D Schultz; Kaushik P Patel; Hanjun Wang
Journal:  Am J Physiol Heart Circ Physiol       Date:  2015-02-13       Impact factor: 4.733

3.  Overexpression of angiotensin-converting enzyme 2 attenuates tonically active glutamatergic input to the rostral ventrolateral medulla in hypertensive rats.

Authors:  Yang-Kai Wang; Du Shen; Qiang Hao; Qiang Yu; Zhao-Tang Wu; Yu Deng; Yan-Fang Chen; Wen-Jun Yuan; Qi-Kuan Hu; Ding-Feng Su; Wei-Zhong Wang
Journal:  Am J Physiol Heart Circ Physiol       Date:  2014-05-16       Impact factor: 4.733

4.  Metabolic syndrome emerges after artificial selection for low baroreflex sensitivity.

Authors:  Li-Li Zhang; Ying Zhang; Yan-Qiong Cheng; Jing-Ming Zhang; Hong-Qi Liu; Wei-Zhong Wang; Jawahar L Mehta; Zhi-Gang Xiong; Ding-Feng Su; Ai-Jun Liu
Journal:  CNS Neurosci Ther       Date:  2018-07-01       Impact factor: 5.243

Review 5.  (In)activity-related neuroplasticity in brainstem control of sympathetic outflow: unraveling underlying molecular, cellular, and anatomical mechanisms.

Authors:  Nicholas A Mischel; Madhan Subramanian; Maryetta D Dombrowski; Ida J Llewellyn-Smith; Patrick J Mueller
Journal:  Am J Physiol Heart Circ Physiol       Date:  2015-05-08       Impact factor: 4.733

6.  Neuroplasticity in N-methyl-d-aspartic acid receptor signaling in subregions of the rat rostral ventrolateral medulla following sedentary versus physically active conditions.

Authors:  Bozena E Fyk-Kolodziej; Farhad Ghoddoussi; Patrick J Mueller
Journal:  J Comp Neurol       Date:  2021-01-06       Impact factor: 3.028

7.  Exercise training attenuates renovascular hypertension partly via RAS- ROS- glutamate pathway in the hypothalamic paraventricular nucleus.

Authors:  Yan Zhang; Xiao-Jing Yu; Wen-Sheng Chen; Hong-Li Gao; Kai-Li Liu; Xiao-Lian Shi; Xiao-Yan Fan; Lin-Lin Jia; Wei Cui; Guo-Qing Zhu; Jin-Jun Liu; Yu-Ming Kang
Journal:  Sci Rep       Date:  2016-11-24       Impact factor: 4.379

8.  Exercise Training Improves the Altered Renin-Angiotensin System in the Rostral Ventrolateral Medulla of Hypertensive Rats.

Authors:  Chang-zhen Ren; Ya-hong Yang; Jia-cen Sun; Zhao-tang Wu; Ru-wen Zhang; Du Shen; Yang-kai Wang
Journal:  Oxid Med Cell Longev       Date:  2016-01-05       Impact factor: 6.543

9.  An Ultra-High Field Magnetic Resonance Spectroscopy Study of Post Exercise Lactate, Glutamate and Glutamine Change in the Human Brain.

Authors:  Andrea Dennis; Adam G Thomas; Nancy B Rawlings; Jamie Near; Thomas E Nichols; Stuart Clare; Heidi Johansen-Berg; Charlotte J Stagg
Journal:  Front Physiol       Date:  2015-12-17       Impact factor: 4.566

10.  Overexpression of ß-Arrestin1 in the Rostral Ventrolateral Medulla Downregulates Angiotensin Receptor and Lowers Blood Pressure in Hypertension.

Authors:  Jia-Cen Sun; Bing Liu; Ru-Wen Zhang; Pei-Lei Jiao; Xing Tan; Yang-Kai Wang; Wei-Zhong Wang
Journal:  Front Physiol       Date:  2018-03-28       Impact factor: 4.566

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