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PVN Blockade of p44/42 MAPK Pathway Attenuates Salt-induced Hypertension through Modulating Neurotransmitters and Attenuating Oxidative Stress

The imbalance of neurotransmitters and excessive oxidative stress responses contribute to the pathogenesis of hypertension. In this study, we determined whether blockade of p44/42 MAPK pathway in the hypothalamic paraventricular nucleus (PVN) ameliorates the development of hypertension through modul...

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Autores principales: Gao, Hong-Li, Yu, Xiao-Jing, Liu, Kai-Li, Shi, Xiao-Lian, Qi, Jie, Chen, Yan-Mei, Zhang, Yan, Bai, Juan, Yi, Qiu-Yue, Feng, Zhi-Peng, Chen, Wen-Sheng, Cui, Wei, Liu, Jin-Jun, Zhu, Guo-Qing, Kang, Yu-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320530/
https://www.ncbi.nlm.nih.gov/pubmed/28225041
http://dx.doi.org/10.1038/srep43038
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author Gao, Hong-Li
Yu, Xiao-Jing
Liu, Kai-Li
Shi, Xiao-Lian
Qi, Jie
Chen, Yan-Mei
Zhang, Yan
Bai, Juan
Yi, Qiu-Yue
Feng, Zhi-Peng
Chen, Wen-Sheng
Cui, Wei
Liu, Jin-Jun
Zhu, Guo-Qing
Kang, Yu-Ming
author_facet Gao, Hong-Li
Yu, Xiao-Jing
Liu, Kai-Li
Shi, Xiao-Lian
Qi, Jie
Chen, Yan-Mei
Zhang, Yan
Bai, Juan
Yi, Qiu-Yue
Feng, Zhi-Peng
Chen, Wen-Sheng
Cui, Wei
Liu, Jin-Jun
Zhu, Guo-Qing
Kang, Yu-Ming
author_sort Gao, Hong-Li
collection PubMed
description The imbalance of neurotransmitters and excessive oxidative stress responses contribute to the pathogenesis of hypertension. In this study, we determined whether blockade of p44/42 MAPK pathway in the hypothalamic paraventricular nucleus (PVN) ameliorates the development of hypertension through modulating neurotransmitters and attenuating oxidative stress. Dahl salt-sensitive (S) rats received a high-salt diet (HS, 8% NaCl) or a normal-salt diet (NS, 0.3% NaCl) for 6 weeks and were treated with bilateral PVN infusion of PD-98059 (0.025 μg/h), a p44/42 MAPK inhibitor, or vehicle via osmotic minipump. HS resulted in higher mean arterial pressure (MAP) and Fra-like (Fra-LI) activity, and plasma and PVN levels of norepinephrine (NE), tyrosine hydroxylase (TH), NOX2 and NOX4, lower PVN levels of gamma-aminobutyric acid (GABA), copper/zinc superoxide dismutase (Cu/Zn-SOD) and the 67-kDa isoform of glutamate decarboxylase (GAD67), as compared with NS group. PD-98059 infusion reduced NE, TH, NOX2 and NOX4 in the PVN, and induced Cu/Zn-SOD and GAD67 in the PVN. It suggests that PVN blockade of p44/42 MAPK attenuates hypertension through modulating neurotransmitters and attenuating oxidative stress.
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spelling pubmed-53205302017-03-01 PVN Blockade of p44/42 MAPK Pathway Attenuates Salt-induced Hypertension through Modulating Neurotransmitters and Attenuating Oxidative Stress Gao, Hong-Li Yu, Xiao-Jing Liu, Kai-Li Shi, Xiao-Lian Qi, Jie Chen, Yan-Mei Zhang, Yan Bai, Juan Yi, Qiu-Yue Feng, Zhi-Peng Chen, Wen-Sheng Cui, Wei Liu, Jin-Jun Zhu, Guo-Qing Kang, Yu-Ming Sci Rep Article The imbalance of neurotransmitters and excessive oxidative stress responses contribute to the pathogenesis of hypertension. In this study, we determined whether blockade of p44/42 MAPK pathway in the hypothalamic paraventricular nucleus (PVN) ameliorates the development of hypertension through modulating neurotransmitters and attenuating oxidative stress. Dahl salt-sensitive (S) rats received a high-salt diet (HS, 8% NaCl) or a normal-salt diet (NS, 0.3% NaCl) for 6 weeks and were treated with bilateral PVN infusion of PD-98059 (0.025 μg/h), a p44/42 MAPK inhibitor, or vehicle via osmotic minipump. HS resulted in higher mean arterial pressure (MAP) and Fra-like (Fra-LI) activity, and plasma and PVN levels of norepinephrine (NE), tyrosine hydroxylase (TH), NOX2 and NOX4, lower PVN levels of gamma-aminobutyric acid (GABA), copper/zinc superoxide dismutase (Cu/Zn-SOD) and the 67-kDa isoform of glutamate decarboxylase (GAD67), as compared with NS group. PD-98059 infusion reduced NE, TH, NOX2 and NOX4 in the PVN, and induced Cu/Zn-SOD and GAD67 in the PVN. It suggests that PVN blockade of p44/42 MAPK attenuates hypertension through modulating neurotransmitters and attenuating oxidative stress. Nature Publishing Group 2017-02-22 /pmc/articles/PMC5320530/ /pubmed/28225041 http://dx.doi.org/10.1038/srep43038 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Gao, Hong-Li
Yu, Xiao-Jing
Liu, Kai-Li
Shi, Xiao-Lian
Qi, Jie
Chen, Yan-Mei
Zhang, Yan
Bai, Juan
Yi, Qiu-Yue
Feng, Zhi-Peng
Chen, Wen-Sheng
Cui, Wei
Liu, Jin-Jun
Zhu, Guo-Qing
Kang, Yu-Ming
PVN Blockade of p44/42 MAPK Pathway Attenuates Salt-induced Hypertension through Modulating Neurotransmitters and Attenuating Oxidative Stress
title PVN Blockade of p44/42 MAPK Pathway Attenuates Salt-induced Hypertension through Modulating Neurotransmitters and Attenuating Oxidative Stress
title_full PVN Blockade of p44/42 MAPK Pathway Attenuates Salt-induced Hypertension through Modulating Neurotransmitters and Attenuating Oxidative Stress
title_fullStr PVN Blockade of p44/42 MAPK Pathway Attenuates Salt-induced Hypertension through Modulating Neurotransmitters and Attenuating Oxidative Stress
title_full_unstemmed PVN Blockade of p44/42 MAPK Pathway Attenuates Salt-induced Hypertension through Modulating Neurotransmitters and Attenuating Oxidative Stress
title_short PVN Blockade of p44/42 MAPK Pathway Attenuates Salt-induced Hypertension through Modulating Neurotransmitters and Attenuating Oxidative Stress
title_sort pvn blockade of p44/42 mapk pathway attenuates salt-induced hypertension through modulating neurotransmitters and attenuating oxidative stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320530/
https://www.ncbi.nlm.nih.gov/pubmed/28225041
http://dx.doi.org/10.1038/srep43038
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