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阿片样物质在脊髓水平介导去甲肾上腺素诱导而非5-羟色胺诱导的抗伤害感受:通过大鼠福尔马林试验的电生理模型进行重新评估

Opiate-like substances mediate norepinephrine-induced but not serotonin-induced antinociception at spinal level: reevaluation by an electrophysiological model of formalin test in rats.

作者信息

Ma J, Qiao J T, Dafny N

机构信息

Department of Neurobiology, Shanxi Medical University, Taiyuan, P.R. China.

出版信息

Life Sci. 2001 Jul 13;69(8):969-76. doi: 10.1016/s0024-3205(01)01191-2.

Abstract

After subcutaneous injection of formalin (5%, 50 microl) into a hindpaw of rats, biphasic excitatory nociceptive discharges were recorded extracellularly in thalamic parafascicular neurons. Intrathecal (i.t.) administration of either norepinephrine (NE. 6 nmol, 10 microl) or serotonin (5-HT, 120 nmol, 10 microl) prior to the second phase significantly inhibited the second phase of the formalin-induced parafascicular nociceptive discharges. Intrathecal naloxone (Nal, 50 nmol, 10 microl) did not show any effect on the parafascicular nociceptive discharges. However, when i.t. Nal was given 5 min before NE, Nal prevented the NE antinociceptive effect. Pre-administration of Nal before 5-HT did not affect the antinociceptive effects of 5-HT on the second phase of nociceptive discharges. These results indicate that opiate-like substances are involved in the mediation of NE-induced antinociception. It is suggested that endogenous NE and 5-HT released from brainstem descending terminals at the spinal level carry out their antinociceptive actions differently.

摘要

给大鼠后爪皮下注射福尔马林(5%,50微升)后,在丘脑束旁核神经元中细胞外记录到双相兴奋性伤害性放电。在第二阶段之前鞘内注射去甲肾上腺素(NE,6纳摩尔,10微升)或5-羟色胺(5-HT,120纳摩尔,10微升)可显著抑制福尔马林诱导的束旁核伤害性放电的第二阶段。鞘内注射纳洛酮(Nal,50纳摩尔,10微升)对束旁核伤害性放电没有任何影响。然而,当在NE注射前5分钟鞘内给予Nal时,Nal可阻止NE的抗伤害作用。在5-HT之前预先给予Nal并不影响5-HT对伤害性放电第二阶段的抗伤害作用。这些结果表明阿片样物质参与了NE诱导的抗伤害作用的介导。提示从脑干下行终末在脊髓水平释放的内源性NE和5-HT以不同方式发挥其抗伤害作用。

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