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内皮源性舒张因子和心房肽II可提高猪主动脉内皮细胞中的环磷酸鸟苷水平。

Endothelium-derived relaxing factor and atriopeptin II elevate cyclic GMP levels in pig aortic endothelial cells.

作者信息

Martin W, White D G, Henderson A H

机构信息

Department of Cardiology, University of Wales College of Medicine, Heath Park, Cardiff.

出版信息

Br J Pharmacol. 1988 Jan;93(1):229-39. doi: 10.1111/j.1476-5381.1988.tb11426.x.

Abstract
  1. Two directly-acting stimulants of soluble guanylate cyclase, glyceryl trinitrate (0.1 microM) and sodium azide (10 microM), and a receptor-mediated stimulant of particulate guanylate cyclase, atriopeptin II (10 nM), each elevated the cyclic GMP content of primary cultures of pig aortic endothelial cells without affecting the cyclic AMP content. 2. Two receptor-mediated stimulants of adenylate cyclase, glucagon (1 microM) and isoprenaline (10 microM), had no effect on the cyclic AMP or cyclic GMP content of these cells, but the directly acting stimulant, forskolin (30 microM), induced a small increase in cyclic AMP content. 3. Three agents that release endothelium-derived relaxing factor (EDRF); bradykinin (0.1 microM), ATP (10 microM) and ionophore A23187 (0.1 microM), each markedly elevated the cyclic GMP content of pig aortic endothelial cells, but acetylcholine (1 microM) had no effect. None of these agents had any effect on cyclic AMP content. 4. Two agents that potentiate the actions of EDRF; M & B 22948 (100 microM) and superoxide dismutase (30 units ml-1), each elevated the cyclic GMP content of pig aortic endothelial cells without affecting the cyclic AMP content. Pretreating cells with catalase (100 units ml-1) did not affect the rise in cyclic GMP content induced by superoxide dismutase (30 units ml-1). 5. Pretreatment of pig aortic endothelial cells with haemoglobin (10 microM) reduced the resting content of cyclic GMP and blocked the increase in cyclic GMP content induced by glyceryl trinitrate (0.1 microM), sodium azide (10 microM), bradykinin (0.1 microM), ATP (10 microM), ionophore A23187 (0.1 microM), M & B 22948 (100 microM) and superoxide dismutase (30 units ml-1), but not that induced by atriopeptin II (10 nM). 6. Pretreatment of pig aortic endothelial cells with an inhibitor of soluble guanylate cyclase, methylene blue (20 microM), had no effect on the resting content of cyclic GMP. Methylene blue (20 microM) blocked the increase in cyclic GMP content induced by glyceryl trinitrate (0.1 microM), M & B22948 (100 microM) and bradykinin (0.1 microM), but not that induced by atriopeptin II (10 nM). 7. The data show that soluble guanylate cyclase, particulate guanylate cyclase and adenylate cyclase are present in pig aortic endothelial cells. They further suggest that EDRF, produced spontaneously or in response to vasoactive agents, elevates endothelial cyclic GMP content by stimulating soluble guanylate cyclase. It is possible that this may serve as a feedback loop by which the endothelial cell modulates EDRF production.
摘要
  1. 两种可溶性鸟苷酸环化酶的直接作用刺激剂,硝酸甘油(0.1微摩尔)和叠氮化钠(10微摩尔),以及一种颗粒性鸟苷酸环化酶的受体介导刺激剂,心房肽II(10纳摩尔),均能提高猪主动脉内皮细胞原代培养物中的环鸟苷酸含量,而不影响环腺苷酸含量。2. 两种腺苷酸环化酶的受体介导刺激剂,胰高血糖素(1微摩尔)和异丙肾上腺素(10微摩尔),对这些细胞的环腺苷酸或环鸟苷酸含量没有影响,但直接作用刺激剂福斯高林(30微摩尔)可使环腺苷酸含量略有增加。3. 三种释放内皮源性舒张因子(EDRF)的物质;缓激肽(0.1微摩尔)、三磷酸腺苷(10微摩尔)和离子载体A23187(0.1微摩尔),均能显著提高猪主动脉内皮细胞的环鸟苷酸含量,但乙酰胆碱(1微摩尔)没有作用。这些物质均对环腺苷酸含量没有影响。4. 两种增强EDRF作用的物质;M&B 22948(100微摩尔)和超氧化物歧化酶(30单位/毫升),均能提高猪主动脉内皮细胞的环鸟苷酸含量,而不影响环腺苷酸含量。用过氧化氢酶(100单位/毫升)预处理细胞并不影响超氧化物歧化酶(30单位/毫升)诱导的环鸟苷酸含量升高。5. 用血红蛋白(10微摩尔)预处理猪主动脉内皮细胞可降低环鸟苷酸的基础含量,并阻断硝酸甘油(0.1微摩尔)、叠氮化钠(10微摩尔)、缓激肽(0.1微摩尔)、三磷酸腺苷(10微摩尔)、离子载体A23187(0.1微摩尔)、M&B 22948(100微摩尔)和超氧化物歧化酶(30单位/毫升)诱导的环鸟苷酸含量升高,但不阻断心房肽II(10纳摩尔)诱导的升高。6. 用可溶性鸟苷酸环化酶抑制剂亚甲蓝(20微摩尔)预处理猪主动脉内皮细胞对环鸟苷酸的基础含量没有影响。亚甲蓝(20微摩尔)阻断了硝酸甘油(0.1微摩尔)、M&B22948(100微摩尔)和缓激肽(0.1微摩尔)诱导的环鸟苷酸含量升高,但不阻断心房肽II(10纳摩尔)诱导的升高。7. 数据表明猪主动脉内皮细胞中存在可溶性鸟苷酸环化酶、颗粒性鸟苷酸环化酶和腺苷酸环化酶。它们进一步表明,自发产生或对血管活性物质作出反应而产生的EDRF,通过刺激可溶性鸟苷酸环化酶提高内皮细胞环鸟苷酸含量。这有可能作为一种反馈环,内皮细胞借此调节EDRF的产生。

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