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兴奋性氨基酸对大鼠离体肠段的影响。

The effects of excitatory amino acids on isolated gut segments of the rat.

作者信息

Janković S M, Milovanović D, Matović M, Irić-Cupić V

机构信息

Center for Clinical and Experimental Pharmacology, Clinical Hospital Center, ul. Zmaj Jovina 30, Kragujevac, Serbia, 34000, Yugoslavia.

出版信息

Pharmacol Res. 1999 Feb;39(2):143-8. doi: 10.1006/phrs.1998.0422.

Abstract

Glutamate and aspartate are excitatory neurotransmitters in both central and peripheral nervous systems, acting on ionotropic and metabotropic receptors. In our study we have examined the effects of glutamate, aspartate, N-methyl-d-aspartate (NMDA), kainic acid and (+/-)-1-aminocyclopentane-cis-1,3-dicarboxylic acid (ACPD) on tone and spontaneous activity of isolated rat gastric fundus, jejunum, ileum, ascending colon and rectum. Both glutamate and aspartate produced concentration-dependent tonic contractions of rat fundus and rectum; the other gut segments used in the study were not responsive. While only NMDA and kainic acid produced concentration-dependent tonic contractions of isolated rat gastric fundus, all three type-selective agonists of glutamate receptors (NMDA, kainic acid and ACPD) produced tonic contractions of isolated rat rectum. The results of our study suggest that glutamate and aspartate in rat gastric fundus activate excitatory intrinsic neurons through only ionotropic receptors (NMDA and non-NMDA receptors), while the same action in rat rectum is mediated through both ionotropic and metabotropic receptors.

摘要

谷氨酸和天冬氨酸在中枢和外周神经系统中都是兴奋性神经递质,作用于离子型受体和代谢型受体。在我们的研究中,我们检测了谷氨酸、天冬氨酸、N-甲基-D-天冬氨酸(NMDA)、 kainic 酸和(±)-1-氨基环戊烷-顺-1,3-二羧酸(ACPD)对离体大鼠胃底、空肠、回肠、升结肠和直肠张力及自发活动的影响。谷氨酸和天冬氨酸均可引起大鼠胃底和直肠的浓度依赖性强直性收缩;研究中使用的其他肠道节段无反应。虽然只有NMDA和kainic酸可引起离体大鼠胃底的浓度依赖性强直性收缩,但谷氨酸受体的所有三种类型选择性激动剂(NMDA、kainic酸和ACPD)均可引起离体大鼠直肠的强直性收缩。我们的研究结果表明,大鼠胃底中的谷氨酸和天冬氨酸仅通过离子型受体(NMDA和非NMDA受体)激活兴奋性内在神经元,而大鼠直肠中的相同作用则通过离子型受体和代谢型受体介导。

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