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微量注射去甲肾上腺素或美托咪定对猫脊髓中P物质刺激诱发释放无影响:一项使用抗体微探针的研究

Lack of effect of microinjection of noradrenaline or medetomidine on stimulus-evoked release of substance P in the spinal cord of the cat: a study with antibody microprobes.

作者信息

Lang C W, Hope P J, Grubb B D, Duggan A W

机构信息

Department of Preclinical Veterinary Sciences, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Summerhall.

出版信息

Br J Pharmacol. 1994 Jul;112(3):951-7. doi: 10.1111/j.1476-5381.1994.tb13173.x.

Abstract
  1. Experiments were performed on barbiturate anaesthetized, spinalized cats to investigate the effect of microinjected noradrenaline or medetomidine on the release of immunoreactive substance P in the dorsal spinal cord following peripheral nerve stimulation. The presence of immunoreactive substance P was assessed with microprobes bearing C-terminus-directed antibodies to substance P. 2. Noradrenaline or medetomidine were microinjected into the grey matter of the spinal cord, near microprobe insertion sites, at depths of 2.5, 2.0, 1.5 and 1.0 mm below the spinal cord surface with volumes of approximately 0.125 microliters and a concentration of 10(-3) M. 3. In the untreated spinal cord, electrical stimulation of the ipsilateral tibial nerve (suprathreshold for C-fibres) elicited release of immunoreactive substance P which was centred in and around lamina II. Neither noradrenaline nor medetomidine administration in the manner described produced significant alterations in this pattern of nerve stimulus-evoked release. 4. In agreement with recent ultrastructural studies these results do not support a control of substance P release by catecholamines released from sites near to the central terminals of small diameter primary afferent fibres.
摘要
  1. 实验在巴比妥酸盐麻醉、脊髓横断的猫身上进行,以研究微量注射去甲肾上腺素或美托咪定对周围神经刺激后脊髓背角中免疫反应性P物质释放的影响。使用带有针对P物质C末端抗体的微探针评估免疫反应性P物质的存在。2. 将去甲肾上腺素或美托咪定微量注射到脊髓灰质中,靠近微探针插入部位,在脊髓表面以下2.5、2.0、1.5和1.0毫米深处,体积约为0.125微升,浓度为10(-3)M。3. 在未处理的脊髓中,电刺激同侧胫神经(C纤维阈上刺激)引起免疫反应性P物质的释放,其集中在Ⅱ层及其周围。以所述方式给予去甲肾上腺素或美托咪定均未使这种神经刺激诱发的释放模式产生显著改变。4. 与最近的超微结构研究一致,这些结果不支持由小直径初级传入纤维中枢终末附近部位释放的儿茶酚胺对P物质释放的控制。

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