Zhao Zhi-Qi, Lacey Gary, Hendry Ian A, Morton Cecil R
Division of Neuroscience, The John Curtin School of Medical Research, Australian National University, Canberra, ACT 0200, Australia.
Neurosci Lett. 2004 May 6;361(1-3):216-9. doi: 10.1016/j.neulet.2003.12.070.
In anaesthetized cats, antibody microprobes were used to measure the release of immunoreactive substance P (irSP) in the lumbar dorsal horn during electrical stimulation of primary afferent fibres at intensities suprathreshold for unmyelinated fibres. Release of irSP was detected in the region of the superficial dorsal horn. This evoked release was not reduced by clonidine hydrochloride, administered intravenously or by superfusion of the dorsal cord surface. Microprobes inserted during cord superfusion with lignocaine hydrochloride detected less irSP along their entire length, including in the region of evoked release. The results suggest that the analgesic action of clonidine does not involve reduced release of SP from the central terminals of nociceptors in the spinal cord.
在麻醉猫中,使用抗体微探针测量在以高于无髓鞘纤维阈值的强度电刺激初级传入纤维时,腰段背角中免疫反应性P物质(irSP)的释放。在浅表背角区域检测到irSP的释放。静脉注射盐酸可乐定或在脊髓表面进行灌流,均不能减少这种诱发释放。在脊髓用盐酸利多卡因灌流期间插入的微探针,在其整个长度上,包括在诱发释放区域,检测到的irSP较少。结果表明,可乐定的镇痛作用并不涉及脊髓中伤害感受器的中枢终末释放SP减少。