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一氧化碳与腺苷在大鼠孤束核中的相互作用。

Interaction of carbon monoxide and adenosine in the nucleus tractus solitarii of rats.

作者信息

Lin Chia-Hui, Lo Wan-Chen, Hsiao Michael, Tseng Ching-Jiunn

机构信息

Department of Medical Education and Research, Kaohsiung Veterans General Hospital, 386-Ta-Chung 1st Rd, Kaohsiung, Taiwan, ROC.

出版信息

Hypertension. 2003 Sep;42(3):380-5. doi: 10.1161/01.HYP.0000088561.17252.42. Epub 2003 Aug 11.

Abstract

Carbon monoxide has been identified as an endogenous biological messenger in the brain. Heme oxygenase catalyzes the metabolism of heme to carbon monoxide and biliverdin. Previously, we have shown the involvement of carbon monoxide in central cardiovascular regulation, baroreflex modulation, and glutamatergic neurotransmission in the nucleus tractus solitarii of rats. We also showed that adenosine increased the release of glutamate in the nucleus tractus solitarii. In this study, we investigated the possible interactions of carbon monoxide and adenosine in the nucleus tractus solitarii. Male Sprague-Dawley rats were anesthetized with urethane, and blood pressure were monitored intra-arterially. Unilateral microinjection of increasing doses of hemin (0.01 to 3.3 nmol), a heme molecule cleaved by heme oxygenase to yield carbon monoxide, produced a significant decrease in blood pressure and heart rate in a dose-dependent manner. In addition, similar cardiovascular effects were observed after injection of adenosine (2.3 nmol). These cardiovascular effects of hemin were attenuated by prior administration of the adenosine receptor antagonist 1,3-dipropyl-8-sulfophenylxanthine. Similarly, pretreatment of the heme oxygenase inhibitor zinc protoporphyrin IX or zinc deuteroporphyrin 2,4-bis glycol also attenuated the depressor and bradycardic effects of adenosine. These results indicate that the interaction between carbon monoxide and adenosine may contribute to the activation of heme oxygenase in central cardiovascular regulation.

摘要

一氧化碳已被确认为大脑中的一种内源性生物信使。血红素加氧酶催化血红素代谢生成一氧化碳和胆绿素。此前,我们已证明一氧化碳参与大鼠孤束核的中枢心血管调节、压力反射调节和谷氨酸能神经传递。我们还表明,腺苷可增加孤束核中谷氨酸的释放。在本研究中,我们研究了孤束核中一氧化碳与腺苷之间可能的相互作用。雄性Sprague-Dawley大鼠用乌拉坦麻醉,动脉内监测血压。单侧微量注射递增剂量的血红素(0.01至3.3 nmol),血红素分子经血红素加氧酶裂解产生一氧化碳,可使血压和心率呈剂量依赖性显著降低。此外,注射腺苷(2.3 nmol)后也观察到类似的心血管效应。腺苷受体拮抗剂1,3-二丙基-8-磺基苯基黄嘌呤预先给药可减弱血红素的这些心血管效应。同样,血红素加氧酶抑制剂原卟啉锌IX或氘代原卟啉锌2,4-双二醇预处理也可减弱腺苷的降压和减慢心率作用。这些结果表明,一氧化碳与腺苷之间的相互作用可能有助于在中枢心血管调节中激活血红素加氧酶。

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