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丘脑N-甲基-D-天冬氨酸受体与伤害性感觉突触传递。

Thalamic NMDA receptors and nociceptive sensory synaptic transmission.

作者信息

Eaton S A, Salt T E

机构信息

Department of Visual Science, Institute of Ophthalmology, London, U.K.

出版信息

Neurosci Lett. 1990 Mar 14;110(3):297-302. doi: 10.1016/0304-3940(90)90863-5.

Abstract

The responses of single thalamic neurones to noxious thermal stimulation were recorded in anaesthetized rats. The selective N-methyl-D-aspartate (NMDA) receptor antagonist, 3-((+-)-2-carboxypiperazin-4-yl)propyl-l-phosphonate (CPP), antagonised nociceptive responses when ejected iontophoretically with currents which produced selective antagonism at NMDA receptors. In contrast, the non-NMDA excitatory amino acid receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (CNOX) had little or no effect on nociceptive responses, although it was able to reduce responses to non-nociceptive mechanoreceptor input. These results show that there is substantial NMDA receptor involvement in thalamic nociceptive responses, and that the contribution of CNQX-sensitive non-NMDA receptors to these responses is not extensive. Furthermore, it appears that nociceptive and non-nociceptive input to the thalamus have distinct synaptic pharmacologies.

摘要

在麻醉大鼠中记录了单个丘脑神经元对伤害性热刺激的反应。选择性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂3-((±)-2-羧基哌嗪-4-基)丙基-1-膦酸酯(CPP),当以在NMDA受体上产生选择性拮抗作用的电流进行离子电泳注射时,可拮抗伤害性反应。相比之下,非NMDA兴奋性氨基酸受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNOX)对伤害性反应几乎没有影响,尽管它能够减少对非伤害性机械感受器输入的反应。这些结果表明,NMDA受体大量参与丘脑伤害性反应,且CNQX敏感的非NMDA受体对这些反应的贡献并不广泛。此外,似乎丘脑的伤害性和非伤害性输入具有不同的突触药理学特性。

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