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内皮素对分离的小鼠肾球旁细胞肾素分泌的影响。

Effects of endothelins on renin secretion from isolated mouse renal juxtaglomerular cells.

作者信息

Ritthaler T, Scholz H, Ackermann M, Riegger G, Kurtz A, Krämer B K

机构信息

Physiologisches Institut, Universität Regensburg, Germany.

出版信息

Am J Physiol. 1995 Jan;268(1 Pt 2):F39-45. doi: 10.1152/ajprenal.1995.268.1.F39.

DOI:10.1152/ajprenal.1995.268.1.F39
PMID:7840246
Abstract

This study was performed to examine the effects of endothelin (ET)-1, ET-2, and ET-3 on renin secretion from cultured mouse renal juxtaglomerular (JG) cells. Although different ETs had no consistent effect on basal renin secretion, they equipotently inhibited adenosine 3',5'-cyclic monophosphate (cAMP)-stimulated renin release with a concentration of approximately 3 nM inhibiting 50% of maximal response. ETs did not significantly affect renin release stimulated by the nitric oxide donor sodium nitroprusside (100 microM) or that stimulated by low [2 mM ethylene glycol-bis(beta-aminoethyl ether)-N,N,N',N'-tetraacetic acid] or high (3 mM CaCl2) extracellular calcium. The inhibitory effect of ETs on cAMP-dependent renin secretion was abolished by lowering extracellular calcium concentration to the nanomolar range. However, the action of ETs was not changed by the ETA receptor antagonist BQ-123 (100 nM) and was mimicked by ETB receptor agonists IRL-1620 (1 microM), sarafotoxin S6b (1 microM), and [Ala1,3,11,15]ET-1 (1 microM). All ETs induced calcium oscillations in JG cells that were dependent on extracellular calcium and were associated with prominent calcium-activated chloride currents. These findings suggest that ETs inhibit rather selectively the cAMP-activated pathway of renin secretion through a calcium-sensitive process. The action of ETs on renal JG cells appears to be mediated via ETB receptors and is presumably related to activation of phospholipase C and subsequent events.

摘要

本研究旨在检测内皮素(ET)-1、ET-2和ET-3对培养的小鼠肾球旁(JG)细胞肾素分泌的影响。尽管不同的内皮素对基础肾素分泌没有一致的影响,但它们能同等程度地抑制腺苷3',5'-环磷酸(cAMP)刺激的肾素释放,浓度约为3 nM时可抑制50%的最大反应。内皮素对一氧化氮供体硝普钠(100 μM)刺激的肾素释放或低[2 mM乙二醇双(β-氨基乙醚)-N,N,N',N'-四乙酸]或高(3 mM氯化钙)细胞外钙刺激的肾素释放均无显著影响。将细胞外钙浓度降至纳摩尔范围可消除内皮素对cAMP依赖性肾素分泌的抑制作用。然而,ETA受体拮抗剂BQ-123(100 nM)并未改变内皮素的作用,而ETB受体激动剂IRL-1620(1 μM)、sarafotoxin S6b(1 μM)和[Ala1,3,11,15]ET-1(1 μM)可模拟其作用。所有内皮素均可诱导JG细胞中的钙振荡,该振荡依赖于细胞外钙,并与显著的钙激活氯电流相关。这些发现表明,内皮素通过钙敏感过程选择性地抑制肾素分泌的cAMP激活途径。内皮素对肾JG细胞的作用似乎是通过ETB受体介导的,可能与磷脂酶C的激活及后续事件有关。

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