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蓝斑脊髓去甲肾上腺素能通路在大鼠芬太尼诱导的肌肉强直中的作用

Involvement of coerulospinal noradrenergic pathway in fentanyl-induced muscular rigidity in rats.

作者信息

Lui P W, Lee T Y, Chan S H

机构信息

Department of Anesthesiology, Veterans General Hospital, Taipei, Taiwan, Republic of China.

出版信息

Neurosci Lett. 1990 Jan 1;108(1-2):183-8. doi: 10.1016/0304-3940(90)90728-r.

Abstract

Unilateral, site-specific microinjection of fentanyl (2.5 micrograms/50 nl) into the locus coeruleus (LC) in Sprague-Dawley rats anesthetized with ketamine evoked a significant increase in the electromyographic activity recorded from both caudal lateral extensor and gastrocnemius muscles. This correlate of opiate-induced muscular rigidity was appreciably antagonized by a pretreatment with the specific alpha 1-adrenoceptor blocker, prazosin (250 micrograms/kg, i.v.). On the other hand, an equimolar dose (0.65 mumol/kg) of the specific alpha 2-adrenoceptor blocker, yohimbine (0.23 mg/kg, i.v.) failed to prevent the occurrence of fentanyl-induced EMG activation. We suggest that the coerulospinal noradrenergic pathway may be directly involved in the elicitation of muscular rigidity by fentanyl, possibly via alpha 1-adrenoceptors in the spinal cord.

摘要

在氯胺酮麻醉的Sprague-Dawley大鼠中,向蓝斑(LC)进行单侧、位点特异性微量注射芬太尼(2.5微克/50纳升),可使从尾外侧伸肌和腓肠肌记录到的肌电图活动显著增加。阿片类药物诱导的肌肉强直的这种关联可通过用特异性α1肾上腺素能受体阻滞剂哌唑嗪(250微克/千克,静脉注射)预处理而明显拮抗。另一方面,等摩尔剂量(0.65微摩尔/千克)的特异性α2肾上腺素能受体阻滞剂育亨宾(0.23毫克/千克,静脉注射)未能阻止芬太尼诱导的肌电图激活的发生。我们认为,蓝斑脊髓去甲肾上腺素能通路可能直接参与芬太尼诱发的肌肉强直,可能是通过脊髓中的α1肾上腺素能受体。

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