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向大鼠丘脑正中核微量注射吗啡对福尔马林诱发的脊髓背角神经元伤害性反应的影响。

The effects of microinjection of morphine into thalamic nucleus submedius on formalin-evoked nociceptive responses of neurons in the rat spinal dorsal horn.

作者信息

Zhao Mei, Li Qiang, Tang Jing-Shi

机构信息

Department of Physiology and Pathophysiology, Key Laboratory of Environment and Genes Related to Diseases of Ministry of Education, Xi'an Jiaotong University School of Medicine, Xi'an, Shaanxi 710061, PR China.

出版信息

Neurosci Lett. 2006 Jun 19;401(1-2):103-7. doi: 10.1016/j.neulet.2006.02.075. Epub 2006 Mar 23.

Abstract

Previous studies have indicated that the thalamic nucleus submedius (Sm), as an ascending component, is involved in an endogenous analgesic system consisting of spinal cord-Sm-ventrolateral orbital cortex (VLO)-periaqueductal gray (PAG)-spinal cord loop. To investigate the action of opioid in this antinociception pathway, the effects of microinjection of morphine and naloxone into the Sm on the formalin-induced nociceptive responses of neurons in the spinal dorsal horn were determined in the anesthetized rat. Formalin (5%, 50 microl) subcutaneously injected into unilateral hindpaw produced a biphasic nociceptive response which was similar to that obtained from assessing the nociceptive behavior either in the relative magnitude of response or the time course. A unilateral microinjection of morphine (5 microg, 0.5 microl) into the Sm 15 min after formalin injection significantly depressed the second phasic responses of neurons induced by formalin, and this effect was significantly attenuated by pre-microinjection of opioid receptor antagonist naloxone (1 microg, 0.5 microl) into the same site. The results suggest that the Sm is involved in opioid receptor-mediated antinociceptive effect on the persistent nociception through depression of the nociceptive transmission at the spinal cord level.

摘要

先前的研究表明,丘脑正中核(Sm)作为一个上行成分,参与了由脊髓-Sm-腹外侧眶额皮质(VLO)-导水管周围灰质(PAG)-脊髓环路组成的内源性镇痛系统。为了研究阿片类药物在这条抗伤害感受通路中的作用,在麻醉大鼠中测定了向Sm内微量注射吗啡和纳洛酮对福尔马林诱导的脊髓背角神经元伤害性反应的影响。将5%福尔马林(50微升)皮下注射到单侧后爪会产生双相伤害性反应,这与通过评估伤害性行为在反应的相对幅度或时间进程方面所获得的结果相似。在福尔马林注射15分钟后,向Sm内单侧微量注射吗啡(5微克,0.5微升)可显著抑制福尔马林诱导的神经元的第二相反应,并且预先向同一部位微量注射阿片受体拮抗剂纳洛酮(1微克,0.5微升)可显著减弱这种效应。结果表明,Sm通过抑制脊髓水平的伤害性传递,参与了阿片受体介导的对持续性伤害感受的抗伤害作用。

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