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选择性α2-肾上腺素能拮抗剂对去大脑家兔运动及心血管系统的影响。

Motor and cardiovascular effects of selective alpha 2-adrenoceptor antagonists in the decerebrated rabbit.

作者信息

Harris J, Clarke R W

机构信息

Department of Physiology and Environmental Science, University of Nottingham, Loughborough, Leicestershire, UK.

出版信息

Eur J Pharmacol. 1993 Jun 24;237(2-3):323-8. doi: 10.1016/0014-2999(93)90285-p.

Abstract

In the decerebrated rabbit, intrathecal administration of the alpha 2-adrenoceptor antagonists idazoxan and yohimbine increases reflex responses of gastrocnemius motoneurones to electrical stimulation of the sural nerve. The maximum effect of idazoxan is about twice that of yohimbine, suggesting that part of the effect of idazoxan may be due to an action at non-adrenergic idazoxan or imidazoline binding sites. RX811059 and RX821002 are selective alpha 2-adrenoceptor antagonists with minimal affinity for imidazoline binding sites. In the present study it was found that intrathecal administration of these compounds in doses of 5-200 micrograms increased the sural-gastrocnemius reflex to the same level as idazoxan, confirming that this reflex is subject to powerful adrenergic inhibition mediated through spinal alpha 2-adrenoceptors. RX811059 and RX821002 also increased arterial blood pressure and heart rate. A retrospective analysis of data from earlier studies showed that whereas intrathecal yohimbine had increased blood pressure, idazoxan had not. It is possible that idazoxan acts at non-adrenergic idazoxan binding sites to cancel out the hypertensive effects which are associated with alpha 2-adrenoceptor blockade.

摘要

在去大脑的兔子中,鞘内注射α₂肾上腺素能受体拮抗剂咪唑克生和育亨宾可增强腓肠肌运动神经元对腓肠神经电刺激的反射反应。咪唑克生的最大效应约为育亨宾的两倍,这表明咪唑克生的部分效应可能归因于其作用于非肾上腺素能的咪唑克生或咪唑啉结合位点。RX811059和RX821002是对咪唑啉结合位点亲和力极小的选择性α₂肾上腺素能受体拮抗剂。在本研究中发现,鞘内注射剂量为5 - 200微克的这些化合物可使腓肠肌-腓肠神经反射增强至与咪唑克生相同的水平,证实该反射受到通过脊髓α₂肾上腺素能受体介导的强大肾上腺素能抑制作用的影响。RX811059和RX821002还可升高动脉血压和心率。对早期研究数据的回顾性分析表明,鞘内注射育亨宾可升高血压,而咪唑克生则不然。咪唑克生可能作用于非肾上腺素能的咪唑克生结合位点,以抵消与α₂肾上腺素能受体阻断相关的高血压效应。

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