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向大鼠延髓腹外侧头端微量注射尾加压素 II 通过 GPR14/ERK 通路增加交感血管运动张力。

Microinjection of urotensin II into the rostral ventrolateral medulla increases sympathetic vasomotor tone via the GPR14/ERK pathway in rats.

机构信息

The Third Hospital of Shijiazhuang, Shijiazhuang, 050017, China.

Department of Physiology, Institute of Basic Medicine, Hebei Medical University, Shijiazhuang, 050017, China.

出版信息

Hypertens Res. 2020 Aug;43(8):765-771. doi: 10.1038/s41440-020-0460-y. Epub 2020 May 8.

Abstract

The present study aimed to reveal the effects of urotensin II (UII) on sympathetic vasomotor tone in the rostral ventrolateral medulla (RVLM). UII (0.3, 3, and 30 nmol/L, 50 nL) was microinjected into the RVLM. Blood pressure (BP), heart rate (HR), and renal sympathetic nerve activity (RSNA) were measured to determine the sympathetic vasomotor tone. BP, HR, and RSNA were simultaneously recorded after drugs had been microinjected into the RVLM. Microinjection of UII (0.3, 3, and 30 nmol/L, 50 nL) into the RVLM significantly increased BP, HR, and RSNA. Pretreatment with BIM23127 (300 nmol/L, 50 nL), a potent antagonist of the UII receptor GPR14, abolished the effect of UII. Previous microinjection of PD98059 (25 μmol/L, 50 nL), an inhibitor of ERK, significantly suppressed the effects of UII. Preinjection of an inhibitor of the N-type Ca channel, ω-conotoxin GVIA (50 nmol/L, 50 nL), inhibited the effects of UII. The present study demonstrated that microinjection of UII into the RVLM significantly increased sympathetic vasomotor tone, which was mediated by the GPR14/ERK/N-type Ca channel pathway. UII may become a novel therapeutic target for autonomic nervous system regulation, especially in hypertension.

摘要

本研究旨在揭示尾加压素 II (UII) 对延髓头端腹外侧区 (RVLM) 交感血管紧张的影响。将 UII(0.3、3 和 30nmol/L,50nL)微注射到 RVLM 中。测量血压 (BP)、心率 (HR) 和肾交感神经活动 (RSNA) 以确定交感血管紧张度。在 RVLM 中微注射药物后,同时记录 BP、HR 和 RSNA。将 UII(0.3、3 和 30nmol/L,50nL)微注射到 RVLM 中可显著增加 BP、HR 和 RSNA。用 BIM23127(300nmol/L,50nL)预处理,一种有效的 UII 受体 GPR14 拮抗剂,可消除 UII 的作用。预先注射 ERK 抑制剂 PD98059(25μmol/L,50nL)可显著抑制 UII 的作用。预先注射 N 型钙通道抑制剂 ω-芋螺毒素 GVIA(50nmol/L,50nL)可抑制 UII 的作用。本研究表明,将 UII 微注射到 RVLM 中可显著增加交感血管紧张度,这是通过 GPR14/ERK/N 型钙通道途径介导的。UII 可能成为自主神经系统调节的一个新的治疗靶点,特别是在高血压中。

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