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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Modification of cardiovascular response of adenosine A2 receptor agonist by adenylate cyclase in the spinal cord of rats.
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Modification of cardiovascular response of adenosine A2 receptor agonist by adenylate cyclase in the spinal cord of rats.

机译:腺苷酸环化酶修饰大鼠脊髓中腺苷A2受体激动剂的心血管反应。

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摘要

This study was performed to investigate the influence of spinal adenosine A2 receptors on the central regulation of blood pressure (BP) and heart rate (HR), and to define whether its mechanism is mediated by adenylate cyclase or guanylate cyclase. Intrathecal (i.t.) administration of drugs at the thoracic level were performed in anesthetized, artificially ventilated male Sprague-Dawley rats. Injection (i.t.) of adenosine A2 receptor agonist, 5'-(N-cyclopropyl)-carboxamidoadenosine (CPCA; 1, 2 and 3 nmol) produced a dose dependent decrease of BP and HR. Pretreatment with adenylate cyclase inhibitor, MDL-12,330, attenuated the depressor and bradycardiac effects of CPCA (2 nmol), but not with guanylate cyclase inhibitor, LY-83,583. These results suggest that adenosine A2 receptor in the spinal cord plays an inhibitory role in the central cardiovascular regulation and that the depressor and bradycardiac actions are mediated by adenylate cyclase.
机译:进行这项研究以研究脊髓腺苷A2受体对血压(BP)和心率(HR)的中央调节的影响,并确定其机制是由腺苷酸环化酶还是鸟苷酸环化酶介导的。在麻醉的人工通气雄性Sprague-Dawley大鼠中,进行鞘内(i.t.)胸腔给药。注射(i.t.)腺苷A2受体激动剂5'-(N-环丙基)-羧酰胺基腺苷(CPCA; 1、2和3 nmol)使BP和HR呈剂量依赖性降低。用腺苷酸环化酶抑制剂MDL-12,330预处理可减弱CPCA(2 nmol)的降压和心动过缓作用,但不能用鸟苷酸环化酶抑制剂LY-83,583进行预处理。这些结果表明,脊髓中的腺苷A2受体在中枢心血管调节中起抑制作用,而抑制剂和心动过缓的作用是由腺苷酸环化酶介导的。

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