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血管紧张素II调节足细胞的细胞功能。

Angiotensin II modulates cellular functions of podocytes.

作者信息

Gloy J, Henger A, Fischer K G, Nitschke R, Bleich M, Mundel P, Schollmeyer P, Greger R, Pavenstädt H

机构信息

Department of Medicine, University of Freiburg, Germany.

出版信息

Kidney Int Suppl. 1998 Sep;67:S168-70. doi: 10.1046/j.1523-1755.1998.06736.x.

Abstract

Angiotensin II modulates cellular functions of podocytes. The aim of this study was to examine the effects of angiotensin II (Ang II) on membrane voltage (Vm) and cytosolic calcium activity ([Ca2+]i) of rat podocytes. To approach better the in vivo situation, we have developed an experimental approach that allows podocytes to be studied in the intact microdissected glomerulus. Ang II depolarized podocytes in the glomerulus (EC50 15 nM, N = 49). Like podocytes in the glomerulus, podocytes in short-term culture also depolarized in response to Ang II (10 nM, N = 5). Ang II increased [Ca2+]i in podocytes in culture (EC50 3 nM, N = 229). In a solution with reduced extracellular [Ca2+] (10 microM), Ang II-mediated [Ca2+]i increase was significantly reduced by 60% +/- 20% (N = 12). Flufenamate, an inhibitor of nonselective ion channels, inhibited Ang II-mediated increase of [Ca2+]i (IC50 20 microM, N = 29). The Ang subtype 1 (AT1) receptor antagonist losartan inhibited both Ang II-mediated depolarization and [Ca2+]i increase in podocytes (N = 5 to 35). Our results support the concept that Ang II might influence podocyte function directly via an AT1 receptor.

摘要

血管紧张素II调节足细胞的细胞功能。本研究旨在探讨血管紧张素II(Ang II)对大鼠足细胞膜电压(Vm)和胞质钙活性([Ca2+]i)的影响。为了更接近体内情况,我们开发了一种实验方法,可在完整的显微解剖肾小球中研究足细胞。Ang II使肾小球中的足细胞去极化(半数有效浓度为15 nM,N = 49)。与肾小球中的足细胞一样,短期培养的足细胞对Ang II(10 nM,N = 5)也会去极化。Ang II使培养的足细胞中的[Ca2+]i增加(半数有效浓度为3 nM,N = 229)。在细胞外[Ca2+]降低的溶液(10 microM)中,Ang II介导的[Ca2+]i增加显著降低了60%±20%(N = 12)。非选择性离子通道抑制剂氟灭酸抑制了Ang II介导的[Ca2+]i增加(半数抑制浓度为20 microM,N = 29)。血管紧张素1型(AT1)受体拮抗剂氯沙坦抑制了Ang II介导的足细胞去极化和[Ca2+]i增加(N = 5至35)。我们的结果支持Ang II可能通过AT1受体直接影响足细胞功能这一概念。

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