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血管紧张素II可增加人培养内皮细胞中内皮素-1的释放,但并不调节其循环水平。

Angiotensin II increases the release of endothelin-1 from human cultured endothelial cells but does not regulate its circulating levels.

作者信息

Ferri C, Desideri G, Baldoncini R, Bellini C, Valenti M, Santucci A, De Mattia G

机构信息

University of Rome 'La Sapienza', Andrea Cesalpino Foundation, Rome 00161, Italy.

出版信息

Clin Sci (Lond). 1999 Mar;96(3):261-70.

Abstract

We investigated the effect of angiotensin II on endothelin-1 secretion in vitro and in vivo. In vivo, angiotensin II was given intravenously to 23 essential hypertensive and 8 control subjects according to different protocols: Study A, 1.0 ng x min-1 x kg-1 and 3.0 ng x min-1 x kg-1 angiotensin II for 30 min each; Study B, 1.0 ng x min-1 x kg-1 and 3.0 ng x min-1 x kg-1 angiotensin II for 120 min each; Study C, 3.0 ng x min-1 x kg-1 angiotensin II for 30 min followed by a dose increment of 3.0 ng x min-1 x kg-1 every 30 min until mean blood pressure levels increased by 25 mmHg; Study D, 1.0 ng x min-1 x kg-1 followed by 3.0 ng x min-1 x kg-1 angiotensin II for 60 min each on two different NaCl diets (either 20 mmol NaCl/day or 220 mmol NaCl/day, both for 1 week). In all in vivo studies neither plasma nor urine endothelin-1 levels changed with angiotensin II infusion. In contrast, angiotensin II (10(-9), 10(-8), 10(-7) mol/l) stimulated endothelin-1 secretion from cultured human vascular endothelial cells derived from umbilical cord veins in a time- and dose-dependent manner. The in vitro angiotensin II effects were abolished by candesartan cilexetil, an inhibitor of the membrane-bound AT1 receptor, and also by actinomycin D, an RNA synthesis inhibitor, and cycloheximide, a protein synthesis inhibitor, indicating that endothelin-1 release depended on AT1 receptor subtype and de novo protein synthesis. Our findings indicate that angiotensin II regulates endothelin-1 release by cultured endothelial cells through an AT1 receptor-dependent pathway, but does not influence circulating endothelin-1 levels in vivo.

摘要

我们在体外和体内研究了血管紧张素II对内皮素-1分泌的影响。在体内,根据不同方案对23名原发性高血压患者和8名对照受试者静脉给予血管紧张素II:研究A,分别以1.0 ng·min⁻¹·kg⁻¹和3.0 ng·min⁻¹·kg⁻¹的剂量输注血管紧张素II,各持续30分钟;研究B,分别以1.0 ng·min⁻¹·kg⁻¹和3.0 ng·min⁻¹·kg⁻¹的剂量输注血管紧张素II,各持续120分钟;研究C,先以3.0 ng·min⁻¹·kg⁻¹的剂量输注血管紧张素II 30分钟,随后每30分钟将剂量增加3.0 ng·min⁻¹·kg⁻¹,直至平均血压水平升高25 mmHg;研究D,在两种不同的氯化钠饮食(分别为每天20 mmol氯化钠或每天220 mmol氯化钠,均持续1周)条件下,先以1.0 ng·min⁻¹·kg⁻¹的剂量输注血管紧张素II,随后各以3.0 ng·min⁻¹·kg⁻¹的剂量输注血管紧张素II 60分钟。在所有体内研究中,输注血管紧张素II后血浆和尿液中的内皮素-1水平均未发生变化。相比之下,血管紧张素II(10⁻⁹、10⁻⁸、10⁻⁷ mol/L)能以时间和剂量依赖性方式刺激源自人脐带静脉的培养血管内皮细胞分泌内皮素-1。膜结合型AT1受体抑制剂坎地沙坦酯、RNA合成抑制剂放线菌素D以及蛋白质合成抑制剂环己酰亚胺均可消除血管紧张素II在体外的作用,这表明内皮素-1的释放依赖于AT1受体亚型和从头合成蛋白质。我们的研究结果表明,血管紧张素II通过AT1受体依赖性途径调节培养的内皮细胞释放内皮素-1,但在体内不影响循环内皮素-1水平。

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