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Chronic Intermittent Hypobaric Hypoxia Reduces Hypothalamic N-Methyl-d-Aspartate Receptor Activity and Sympathetic Outflow in Spontaneously Hypertensive Rats

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机构: [1]Department of Physiology, Hebei Medical University, Shijiazhuang, China. [2]Department of Gynaecology and Obstetrics, Fourth Hospital of Hebei Medical University, Shijiazhuang, China. [3]Hebei Collaborative Innovation Center for Cardio-Cerebrovascular Disease, Shijiazhuang, China. [4]The Key Laboratory of Neural and Vascular Biology, Ministry of Education, Hebei Medical University, Shijiazhuang, China. [5]Key Laboratory of Neurophysiology of Hebei Province, Shijiazhuang, China.
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关键词: chronic intermittent hypobaric hypoxia hypertension hypothalamic paraventricular nucleus NMDA receptor renin-angiotensin system

摘要:
Guo, Xinqi, Hongyu Ma, Ziye Cui, Qiyue Zhao, Ying Zhang, Lu Jia, Liping Zhang, Hui Guo, Xiangjian Zhang, Yi Zhang, Yue Guan, and Huijie Ma. Chronic intermittent hypobaric hypoxia reduces hypothalamic N-Methyl-d-Aspartate Receptor activity and sympathetic outflow in spontaneously hypertensive rats. High Alt Med Biol. 00:000-000, 2024. Objective: This study aims to determine the role of hypothalamic renin-angiotensin system (RAS) in the antihypertensive effect of chronic intermittent hypobaric hypoxia (CIHH). Methods: Wistar-Kyoto (WKY) rats and spontaneously hypertensive rats (SHRs) received 35 days of hypobaric hypoxia simulating an altitude of 4,000 m, 5 h/day. The levels of RAS, blood pressure, and N-methyl-d-aspartate receptor (NMDAR) activities of hypothalamic paraventricular nucleus (PVN) presympathetic neurons from each group of rats were determined. Results: The systolic blood pressure, diastolic blood pressure, and mean arterial blood pressure (MAP) of SHRs significantly decreased from the third week of CIHH treatment. This blood pressure reduction effect could be maintained for at least 2 weeks after stopping the CIHH treatment. CIHH treatment also attenuated the decrease in MAP and renal sympathetic nerve activity induced by hexamethonium administration in SHRs, but not in WKY rats. Furthermore, CIHH reversed the increase in serum angiotensin (Ang)II concentration and the expression of PVN angiotensin-converting enzyme (ACE) and AngII type 1 (AT1) receptors, as well as the decrease in serum Ang1-7 concentration and the expression of PVN ACE2 and Mas receptors in SHRs. In addition, the administration of CIHH resulted in a reduction in the frequency of miniature excitatory postsynaptic currents and amplitude of NMDAR current in PVN presympathetic neurons of SHRs, which means that CIHH decreased the pre- and postsynaptic NMDAR activity of PVN presympathetic neurons in SHRs. However, pretreatment with A779 (a Mas receptor blocker) or AngII abrogated the above effects. Meanwhile, Ang1-7 pretreatment mimicked the CIHH effect on pre- and postsynaptic NMDAR activity of presympathetic neurons in SHRs. Conclusions: Our data indicate that CIHH reduces pre- and postsynaptic NMDAR activity of PVN presympathetic neurons, sympathetic outflow, and blood pressure by decreasing the activity of the ACE/AngII/AT1 axis and increasing the activity of ACE2/Ang1-7/Mas axis in the hypothalamus in hypertension.

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出版当年[2025]版:
大类 | 4 区 医学
小类 | 3 区 生物物理 4 区 公共卫生、环境卫生与职业卫生 4 区 运动科学
最新[2025]版:
大类 | 4 区 医学
小类 | 3 区 生物物理 4 区 公共卫生、环境卫生与职业卫生 4 区 运动科学
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Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Q3 SPORT SCIENCES Q4 BIOPHYSICS

影响因子: 最新[2023版] 最新五年平均 出版当年[2024版] 出版当年五年平均 出版前一年[2023版]

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第一作者机构: [1]Department of Physiology, Hebei Medical University, Shijiazhuang, China.
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通讯机构: [1]Department of Physiology, Hebei Medical University, Shijiazhuang, China. [3]Hebei Collaborative Innovation Center for Cardio-Cerebrovascular Disease, Shijiazhuang, China. [4]The Key Laboratory of Neural and Vascular Biology, Ministry of Education, Hebei Medical University, Shijiazhuang, China. [5]Key Laboratory of Neurophysiology of Hebei Province, Shijiazhuang, China. [*1]Department of Physiology Hebei Medical University 361 Eastern Zhongshan Road Shijiazhuang 050017 China [*2]Department of Physiology Hebei Medical University 361 Eastern Zhongshan Road Shijiazhuang 050017 China
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