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新生大鼠离体脊髓-神经制备中隐神经刺激诱发的C纤维反应的药理学特性。

Pharmacological properties of a C-fibre response evoked by saphenous nerve stimulation in an isolated spinal cord-nerve preparation of the newborn rat.

作者信息

Nussbaumer J C, Yanagisawa M, Otsuka M

机构信息

Department of Pharmacology, Faculty of Medicine, Tokyo Medical and Dental University, Japan.

出版信息

Br J Pharmacol. 1989 Oct;98(2):373-82. doi: 10.1111/j.1476-5381.1989.tb12607.x.

DOI:10.1111/j.1476-5381.1989.tb12607.x
PMID:2479438
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1854704/
Abstract
  1. An isolated spinal cord-peripheral nerve preparation of the newborn rat was developed. In this preparation it is possible to record spinal reflexes from a lumbar ventral root in response to stimulation of the ipsilateral saphenous or obturator nerve. 2. Single shock, weak intensity stimulation of the saphenous nerve induced a fast conducted compound action potential in the L3 dorsal root and a fast depolarizing response in the ipsilateral L3 ventral root. As a stronger stimulus was applied to the saphenous nerve, a slowly conducted compound action potential appeared in the dorsal root and a slow depolarizing ventral root potential (v.r.p.) in the L3 ventral root. 3. Single shock stimulation of the obturator nerve induced a rapidly conducted compound action potential in the L3 dorsal root and monosynaptic and polysynaptic reflexes, with a fast time course, in the ipsilateral L3 ventral root. 4. The slow v.r.p. evoked by saphenous nerve stimulation was depressed by the tachykinin antagonist, [D-Arg1, D-Trp7,9, Leu11] substance P (spantide), 4-16 microM. The response recovered its original shape and size 30-60 min after the removal of this antagonist. 5. The saphenous nerve-evoked slow v.r.p. was depressed by [Met5] enkephalin (0.1-1 microM), dynorphin (1-13)(0.2 microM) and morphine (1-2 microM), and these effects were reversed by naloxone (1 microM). 6. Two endogenous peptides, galanin (1-2 microM) and somatostatin (1-2.5 microM), inhibited the slow v.r.p. evoked by saphenous nerve stimulation, whereas another endogenous peptide, calcitonin gene-related peptide (0.1-0.5 microM), potentiated the slow v.r.p. The slow v.r.p. was also inhibited by gamma-aminobutyric acid (GABA, 20 microM) and muscimol (0.2 microM), and their effects were antagonized by bicuculline (1 microM). 7. The present results suggest that substance P and neurokinin A are involved in the saphenous nerve-evoked C-fibre response in the spinal cord of the newborn rat.
摘要
  1. 建立了新生大鼠的离体脊髓 - 外周神经标本。在此标本中,可以记录腰段腹根对同侧隐神经或闭孔神经刺激的脊髓反射。2. 对隐神经进行单次弱强度刺激,可在L3背根诱发快速传导的复合动作电位,并在同侧L3腹根诱发快速去极化反应。当对隐神经施加更强刺激时,背根会出现缓慢传导的复合动作电位,L3腹根会出现缓慢去极化的腹根电位(v.r.p.)。3. 对闭孔神经进行单次刺激,可在L3背根诱发快速传导的复合动作电位,并在同侧L3腹根诱发具有快速时间进程的单突触和多突触反射。4. 速激肽拮抗剂[D - Arg1,D - Trp7,9,Leu11]P物质(spantide),4 - 16微摩尔,可抑制隐神经刺激诱发的缓慢v.r.p.。去除该拮抗剂30 - 60分钟后,反应恢复其原始形状和大小。5. [Met5]脑啡肽(0.1 - 1微摩尔)、强啡肽(1 - 13)(0.2微摩尔)和吗啡(1 - 2微摩尔)可抑制隐神经诱发的缓慢v.r.p.,这些作用可被纳洛酮(1微摩尔)逆转。6. 两种内源性肽,甘丙肽(1 - 2微摩尔)和生长抑素(1 - 2.5微摩尔),可抑制隐神经刺激诱发的缓慢v.r.p.,而另一种内源性肽,降钙素基因相关肽(0.1 - 0.5微摩尔),可增强缓慢v.r.p.。γ - 氨基丁酸(GABA,20微摩尔)和蝇蕈醇(0.2微摩尔)也可抑制缓慢v.r.p.,其作用可被荷包牡丹碱(1微摩尔)拮抗。7. 目前的结果表明,P物质和神经激肽A参与新生大鼠脊髓中隐神经诱发的C纤维反应。

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