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血管活性药物对培养的牛主动脉和肺动脉内皮细胞中环磷酸腺苷生成的刺激作用。

Stimulation of cyclic AMP production by vasoactive agents in cultured bovine aortic and pulmonary artery endothelial cells.

作者信息

Makarski J S

出版信息

In Vitro. 1981 May;17(5):450-8. doi: 10.1007/BF02626746.

Abstract

The ability of selected vasoactive agents to influence cyclic AMP levels of confluent, early-passaged bovine calf aortic and pulmonary artery endothelial cells was investigated. Among the agents tested, only the catecholamines (isoproterenol, epinephrine, norepinephrine) and prostaglandins (PGE1, PGE2, PGF2 alpha) resulted consistently in increased cyclic AMP production in both cell populations. The degree of cyclic AMP stimulation obtained with other vasoactive compounds (angiotensins I and II, bradykinin, and serotonin) tended to be either very small or difficult to reproduce. Isoproterenol stimulation was blocked completely by propanolol, a beta-blocking agent, but not by phentolamine, and alpha-blocking agent. These results reveal that bovine calf aortic and pulmonary artery endothelial cells are responsive to catecholamines and prostaglandins, and therefore presumably possess both sensitive adenylate cyclases and plasma membrane receptors for these compounds.

摘要

研究了所选血管活性药物对汇合的、传代早期的小牛主动脉和肺动脉内皮细胞中环磷酸腺苷(cAMP)水平的影响。在测试的药物中,只有儿茶酚胺(异丙肾上腺素、肾上腺素、去甲肾上腺素)和前列腺素(PGE1、PGE2、PGF2α)能持续使两种细胞群体中的cAMP生成增加。用其他血管活性化合物(血管紧张素I和II、缓激肽和5-羟色胺)获得的cAMP刺激程度往往非常小或难以重复。异丙肾上腺素刺激被β受体阻滞剂普萘洛尔完全阻断,但未被α受体阻滞剂酚妥拉明阻断。这些结果表明,小牛主动脉和肺动脉内皮细胞对儿茶酚胺和前列腺素敏感,因此推测这些细胞具有对这些化合物敏感的腺苷酸环化酶和质膜受体。

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