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丙泊酚刺激培养的猪主动脉内皮细胞释放一氧化氮。

Propofol stimulates nitric oxide release from cultured porcine aortic endothelial cells.

作者信息

Petros A J, Bogle R G, Pearson J D

机构信息

Intensive Therapy Unit, St. George's Hospital, London.

出版信息

Br J Pharmacol. 1993 May;109(1):6-7. doi: 10.1111/j.1476-5381.1993.tb13523.x.

Abstract

Propofol, an intravenous anaesthetic agent, causes marked vasodilatation in vivo. In the present study the effects of propofol on the release of nitric oxide (NO) from vascular endothelial cells was determined in vitro. Application of propofol to co-cultures of porcine aortic endothelial and smooth muscle cells resulted in a rapid increase in cyclic GMP formation. This increase was significantly inhibited following pretreatment of the cells with either NG-nitro-L-arginine (L-NOARG) or in the presence of haemoglobin. When applied to smooth muscle cells alone, propofol did not result in an increase in cyclic GMP levels. These results demonstrate that propofol stimulates the production and release of NO from cultured endothelial cells and suggest that the vasodilatation and hypotension observed when propofol is given in vivo may be due to NO release.

摘要

丙泊酚是一种静脉麻醉剂,在体内可引起显著的血管扩张。在本研究中,在体外测定了丙泊酚对血管内皮细胞释放一氧化氮(NO)的影响。将丙泊酚应用于猪主动脉内皮细胞和平滑肌细胞的共培养物中,导致环磷酸鸟苷(cGMP)生成迅速增加。在用NG-硝基-L-精氨酸(L-NOARG)预处理细胞后或在血红蛋白存在的情况下,这种增加被显著抑制。当单独应用于平滑肌细胞时,丙泊酚不会导致cGMP水平升高。这些结果表明,丙泊酚刺激培养的内皮细胞产生和释放NO,并提示在体内给予丙泊酚时观察到的血管扩张和低血压可能归因于NO的释放。

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