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谷氨酸参与大鼠热痛觉过敏的外周调节。

Glutamate participates in the peripheral modulation of thermal hyperalgesia in rats.

作者信息

Jackson D L, Graff C B, Richardson J D, Hargreaves K M

机构信息

Department of Restorative Sciences, School of Dentistry, University of Minnesota, Minneapolis 55455, USA.

出版信息

Eur J Pharmacol. 1995 Sep 25;284(3):321-5. doi: 10.1016/0014-2999(95)00449-u.

Abstract

While the effects of excitatory amino acids have been well characterized in the central nervous system, relatively little is known about their possible modulation of elements responsible for hyperalgesia within peripheral tissue. The presented experiments demonstrate that the intraplantar (i.pl.) injection of L-glutamate (30 nmol) evokes a thermal hyperalgesic response in the paw withdrawal latencies of normal rats which is stereospecific. In addition, the i.pl. injection of either the non-competitive N-methyl-D-aspartate (NMDA) receptor antagonist MK-801 (10 nmol) or the competitive alpha-amino-3-hydroxy-4-methyl-5-isoxazolepropionic acid (AMPA)/kainate receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX)(100 nmol) into hindpaws inflamed with carrageenan significantly reduced the thermal hyperalgesic response in rats. Collectively, these results suggest that excitatory amino acids activate a peripheral target which facilitates a hyperalgesic behavioural response to thermal stimulation via a receptor mediated process.

摘要

虽然兴奋性氨基酸在中枢神经系统中的作用已得到充分表征,但对于它们可能对外周组织中负责痛觉过敏的成分产生的调节作用却知之甚少。所呈现的实验表明,足底内(i.pl.)注射L-谷氨酸(30 nmol)会在正常大鼠的爪退缩潜伏期引发热痛觉过敏反应,且具有立体特异性。此外,将非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂MK-801(10 nmol)或竞争性α-氨基-3-羟基-4-甲基-5-异恶唑丙酸(AMPA)/海人藻酸受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)(100 nmol)注射到用角叉菜胶致炎的后爪中,可显著降低大鼠的热痛觉过敏反应。总体而言,这些结果表明,兴奋性氨基酸激活了一个外周靶点,该靶点通过受体介导的过程促进对热刺激的痛觉过敏行为反应。

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