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鲎(美洲鲎)心肌上胺类和肽类作用的第二信使系统。

Second-messenger systems underlying amine and peptide actions on cardiac muscle in the horseshoe crab Limulus polyphemus.

作者信息

Groome J R, Watson W H

机构信息

Zoology Department, University of New Hampshire, Durham 03824.

出版信息

J Exp Biol. 1989 Sep;145:419-37. doi: 10.1242/jeb.145.1.419.

Abstract

The biochemical mechanisms by which octopamine, catecholamines and the peptide proctolin exert their actions on Limulus cardiac muscle were investigated. Amines produced long-lasting increases in the amplitude of contractions evoked by electrical stimulation. At 10(-5) mol l-1, the apparent order of potency for amine-induced increases in evoked contraction amplitude was dopamine approximately equal to octopamine greater than norepinephrine approximately equal to epinephrine. At this dose, amines produced long-lasting increases in the levels of cyclic AMP (octopamine greater than dopamine approximately equal to norepinephrine approximately equal to epinephrine), but not of cyclic GMP, in Limulus cardiac muscle. Like the amines, the adenylate cyclase activator forskolin enhanced cardiac muscle contractility and increased levels of cyclic AMP, but not of cyclic GMP. The phosphodiesterase inhibitor IBMX produced a transient increase in cardiac muscle contractility, but typically produced long-lasting negative inotropy. This agent increased levels of both cyclic AMP and cyclic GMP in Limulus cardiac muscle. Proctolin and the protein kinase C activator phorbol dB increased the contraction amplitude of the intact heart and the electrically stimulated myocardium. These compounds, as well as dopamine, elicited sustained contractures and rhythmic contractions when applied to deganglionated Limulus cardiac muscle rings. Unlike the amines, proctolin and phorbol dB did not increase cardiac muscle cyclic AMP levels. These results suggest that several second-messenger systems may be utilized by amines and peptides to produce excitatory actions on cardiac muscle fibers of the Limulus heart. Cyclic AMP appears to be an important second messenger underlying the effects of amines to enhance cardiac muscle contractility. Pharmacological data suggest that proctolin may alter cardiac muscle contractility and excitability by a mechanism which involves the phosphatidylinositol pathway. Dopamine, unlike the other amines, produces a number of proctolin-like effects and may activate both the cyclic AMP and the phosphatidylinositol systems in Limulus cardiac muscle.

摘要

研究了章鱼胺、儿茶酚胺和肽类促肠肌肽对鲎心肌发挥作用的生化机制。胺类物质使电刺激诱发的收缩幅度产生持久增加。在10⁻⁵mol/L时,胺类物质诱发收缩幅度增加的效力表观顺序为:多巴胺≈章鱼胺>去甲肾上腺素≈肾上腺素。在此剂量下,胺类物质使鲎心肌中环磷酸腺苷(cAMP)水平产生持久增加(章鱼胺>多巴胺≈去甲肾上腺素≈肾上腺素),但环磷酸鸟苷(cGMP)水平未增加。与胺类物质一样,腺苷酸环化酶激活剂福斯高林增强心肌收缩力并增加cAMP水平,但不增加cGMP水平。磷酸二酯酶抑制剂异丁基甲基黄嘌呤(IBMX)使心肌收缩力产生短暂增加,但通常产生持久的负性肌力作用。该药物使鲎心肌中的cAMP和cGMP水平均增加。促肠肌肽和蛋白激酶C激活剂佛波醇酯增加完整心脏和电刺激心肌的收缩幅度。当将这些化合物以及多巴胺应用于去神经节的鲎心肌环时,会引发持续挛缩和节律性收缩。与胺类物质不同,促肠肌肽和佛波醇酯不会增加心肌cAMP水平。这些结果表明,胺类物质和肽类可能利用多种第二信使系统对鲎心脏的心肌纤维产生兴奋作用。cAMP似乎是胺类物质增强心肌收缩力作用背后的重要第二信使。药理学数据表明,促肠肌肽可能通过涉及磷脂酰肌醇途径的机制改变心肌收缩力和兴奋性。与其他胺类物质不同,多巴胺产生许多类似促肠肌肽的作用,并可能激活鲎心肌中的cAMP和磷脂酰肌醇系统。

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