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培养的内皮细胞中氧合血红蛋白对内皮素生成的刺激作用。

Oxyhemoglobin stimulation of endothelin production in cultured endothelial cells.

作者信息

Ohlstein E H, Storer B L

机构信息

Department of Pharmacology, SmithKline Beecham Research Laboratories, King of Prussia, Pennsylvania.

出版信息

J Neurosurg. 1992 Aug;77(2):274-8. doi: 10.3171/jns.1992.77.2.0274.

Abstract

Oxyhemoglobin and endothelin have both been linked to the development of the severe and sustained cerebral vasospasm associated with subarachnoid hemorrhage. The effects of oxyhemoglobin on endothelin biosynthesis in cultured endothelial cells were evaluated. Oxyhemoglobin (0.01 to 100 microM) produced concentration-dependent increases in immunoreactive endothelin levels in bovine pulmonary artery endothelial cell-conditioned medium. The median effective concentration for oxyhemoglobin-induced increases in immunoreactive endothelin levels was approximately 0.5 microM, and the maximum stimulation of immunoreactive endothelin levels was approximately 5.5-fold over basal conditions. In addition to directly stimulating basal production of immunoreactive endothelin, oxyhemoglobin significantly augmented immunoreactive endothelin production following platelet-mediated stimulation of endothelin production. An l-arginine analog inhibitor of nitric oxide synthase, L-NG-monomethyl arginine (L-NMMA, 200 microM), did not significantly affect basal immunoreactive endothelin levels. However, L-NMMA significantly augmented platelet-induced immunoreactive endothelin production. Methylene blue (10 microM), an inhibitor of soluble guanylate cyclase, did not significantly affect basal immunoreactive endothelin levels, nor did it significantly affect the platelet-mediated stimulation of immunoreactive endothelin production in cultured endothelial cells. The present results reveal that oxyhemoglobin can directly stimulate endothelin biosynthesis in cultured endothelial cells. This newly identified property of oxyhemoglobin suggests a potential mechanism for the sustained and severe cerebral vasospasm associated with subarachnoid hemorrhage.

摘要

氧合血红蛋白和内皮素均与蛛网膜下腔出血相关的严重且持续性脑血管痉挛的发生有关。我们评估了氧合血红蛋白对培养的内皮细胞中内皮素生物合成的影响。氧合血红蛋白(0.01至100微摩尔)使牛肺动脉内皮细胞条件培养基中免疫反应性内皮素水平呈浓度依赖性升高。氧合血红蛋白诱导免疫反应性内皮素水平升高的半数有效浓度约为0.5微摩尔,免疫反应性内皮素水平的最大刺激约为基础条件下的5.5倍。除了直接刺激免疫反应性内皮素的基础产生外,氧合血红蛋白在血小板介导的内皮素产生刺激后还显著增强了免疫反应性内皮素的产生。一氧化氮合酶的L - 精氨酸类似物抑制剂L - NG - 单甲基精氨酸(L - NMMA,200微摩尔)对基础免疫反应性内皮素水平无显著影响。然而,L - NMMA显著增强了血小板诱导的免疫反应性内皮素产生。可溶性鸟苷酸环化酶抑制剂亚甲蓝(10微摩尔)对基础免疫反应性内皮素水平无显著影响,对培养的内皮细胞中血小板介导的免疫反应性内皮素产生刺激也无显著影响。目前的结果表明,氧合血红蛋白可直接刺激培养的内皮细胞中内皮素的生物合成。氧合血红蛋白这一新发现的特性提示了与蛛网膜下腔出血相关的持续性严重脑血管痉挛的潜在机制。

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