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尾加压素 II 及其特异性受体拮抗剂尿速肽对大鼠血管平滑肌细胞的影响。

Effects of urotensin II and its specific receptor antagonist urantide on rat vascular smooth muscle cells.

机构信息

Department of Pathophysiology, Chengde Medical College, Chengde 067000, China.

出版信息

Bosn J Basic Med Sci. 2013 May;13(2):78-83. doi: 10.17305/bjbms.2013.2369.

Abstract

We investigated the effects of urantide, a receptor antagonist of urotensin II (U-II), on the expression of U-II and its receptor GPR14 in rat vascular smooth muscle cells. Vascular smooth muscle cells from rat thoracic aorta were cultured by explant method. Subjects in this experiment were divided into eight groups: normal control group (group C), U-II group (group M), positive control group (Flu group) and urantide-treated groups (10⁻¹⁰, 10⁻⁹, 10⁻⁸, 10⁻⁷ and 10⁻⁶ mol/L). Cultured vascular smooth muscle cells in vitro were studied by immunocytochemistry, biochemistry, and flow cytometry. U-II (10⁻⁸ mol/L) promoted the proliferation of vascular smooth muscle cells at each time point, influenced cell cycle, increased proliferation index and S-phase cell fraction, and dramatically promoted the expression of U-II and GPR14. In the concentration range from 10⁻¹⁰ to 10⁻⁶ mol/L, urantide dramatically inhibited the proliferation of vascular smooth muscle cells and the protein expression of U-II and GPR14, especially at a concentration of 10⁻⁶ mol/L. U-II, binding with its receptor GPR14, promotes vascular smooth muscle cells proliferation and migration, which can be inhibited by urantide. This study provides an evidence for understanding the effects of U-II and its receptor GPR14 on vascular smooth muscle cells.

摘要

我们研究了尿钠肽,一种对加压素 II(U-II)的受体拮抗剂,对大鼠血管平滑肌细胞中 U-II 及其受体 GPR14 的表达的影响。通过组织块培养法培养大鼠胸主动脉血管平滑肌细胞。本实验将研究对象分为 8 组:正常对照组(C 组)、U-II 组(M 组)、阳性对照组(Flu 组)和尿钠肽处理组(10⁻¹⁰、10⁻⁹、10⁻⁸、10⁻⁷和 10⁻⁶mol/L)。体外培养的血管平滑肌细胞通过免疫细胞化学、生化和流式细胞术进行研究。U-II(10⁻⁸mol/L)在每个时间点都促进血管平滑肌细胞的增殖,影响细胞周期,增加增殖指数和 S 期细胞分数,并显著促进 U-II 和 GPR14 的表达。在 10⁻¹⁰至 10⁻⁶mol/L 的浓度范围内,尿钠肽显著抑制血管平滑肌细胞的增殖和 U-II 和 GPR14 的蛋白表达,特别是在 10⁻⁶mol/L 时。U-II 与 GPR14 结合,促进血管平滑肌细胞增殖和迁移,这可被尿钠肽抑制。本研究为了解 U-II 和其受体 GPR14 对血管平滑肌细胞的影响提供了证据。

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