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PVN 阻断 p44/42 MAPK 通路通过调节神经递质和减轻氧化应激减轻盐诱导的高血压。

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

机构信息

Department of Physiology and Pathophysiology, Xi'an Jiaotong University School of Basic Medical Sciences, Key Laboratory of Environment and Genes Related to Diseases (Xi'an Jiaotong University), Ministry of Education, Xi'an 710061, China.

Department of Pharmacology, Xi'an Jiaotong University School of Basic Medical Sciences, Xi'an 710061, China.

出版信息

Sci Rep. 2017 Feb 22;7:43038. doi: 10.1038/srep43038.

DOI:10.1038/srep43038
PMID:28225041
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5320530/
Abstract

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.

摘要

神经递质失衡和氧化应激反应过度导致高血压的发病机制。在这项研究中,我们确定了阻断下丘脑室旁核 (PVN) 中的 p44/42 MAPK 通路是否通过调节神经递质和减轻氧化应激来改善高血压的发展。Dahl 盐敏感 (S) 大鼠接受高盐饮食 (HS,8% NaCl) 或正常盐饮食 (NS,0.3% NaCl) 6 周,并通过渗透微型泵双侧 PVN 输注 PD-98059(0.025μg/h),一种 p44/42 MAPK 抑制剂,或载体。HS 导致平均动脉压 (MAP) 和 Fra-like (Fra-LI) 活性升高,以及血浆和 PVN 去甲肾上腺素 (NE)、酪氨酸羟化酶 (TH)、NOX2 和 NOX4 水平升高,PVN 水平下降 γ-氨基丁酸 (GABA)、铜/锌超氧化物歧化酶 (Cu/Zn-SOD) 和谷氨酸脱羧酶 67 kDa 同工型 (GAD67),与 NS 组相比。PD-98059 输注减少了 PVN 中的 NE、TH、NOX2 和 NOX4,并诱导了 PVN 中的 Cu/Zn-SOD 和 GAD67。这表明 PVN 中 p44/42 MAPK 的阻断通过调节神经递质和减轻氧化应激来减轻高血压。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/10c846366286/srep43038-f10.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/08c95fb5bb14/srep43038-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/a4e456733164/srep43038-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/dc4c7f5315dd/srep43038-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/3547ce52768d/srep43038-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/10c846366286/srep43038-f10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/388383facc17/srep43038-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/f1591304b89f/srep43038-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/12006d6c3437/srep43038-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/c301b93a60c2/srep43038-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/676ed5400e00/srep43038-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/08c95fb5bb14/srep43038-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/a4e456733164/srep43038-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/dc4c7f5315dd/srep43038-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/3547ce52768d/srep43038-f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48bc/5320530/10c846366286/srep43038-f10.jpg

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