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在社会隔离诱导的应激状态下,向新生雏鸡脑室内注射L-哌啶酸可产生催眠作用而不激活NMDA受体。

Intracerebroventricular Injection of L-Pipecolic Acid Exerts Hypnotic Effects Without Activating NMDA Receptors in Neonatal Chicks under Social Isolation-induced Stress.

作者信息

Shigemura Asako, Chowdhury Vishwajit S, Furuse Mitsuhiro

机构信息

Laboratory of Regulation in Metabolism and Behavior, Faculty of Agriculture, Kyushu University, Fukuoka 819-0395, Japan.

Laboratory of Stress Physiology and Metabolism, Faculty of Arts and Science, Kyushu University, Fukuoka 819-0395, Japan.

出版信息

J Poult Sci. 2020 Jan 25;57(1):84-87. doi: 10.2141/jpsa.0190067.

Abstract

L-Pipecolic acid is an intermediate of L-lysine catabolism. Its central injection exerted a hypnotic effect on the brain, which was partially mediated by the activation of -aminobutyric acid-A and -aminobutyric acid-B receptors. L-Proline has also been shown to exert a similar effect on N-methyl-D-aspartate receptors. Furthermore, L-pipecolic acid is known as L-homoproline, and both L-pipecolic acid and L-proline belong to the imino acid group; therefore, it is plausible that they share certain commonalities, including similar functions. However, the role of N-methyl-D-aspartate receptors with respect to the effects of L-pipecolic acid has not been examined yet. In the present study, the relationship between N-methyl-D-aspartate receptors and the central function of L-pipecolic acid was investigated in neonatal chicks. The behavioral postures for active wakefulness and standing/sitting motionless with eyes opened were significantly affected after intracerebroventricular injection of L-pipecolic acid; whereas, sitting motionless with head drooped (sleeping posture) was significantly enhanced. However, the N-methyl-D-aspartate receptor antagonist, MK-801, did not affect these changes. In conclusion, the central administration of L-pipecolic acid did not exert hypnotic effects through the activation of N-methyl-D-aspartate receptors in neonatal chicks. These results suggest that the imino group is not a determinant for activating N-methyl-D-aspartate receptors.

摘要

L-哌啶酸是L-赖氨酸分解代谢的中间体。向脑内注射L-哌啶酸可对大脑产生催眠作用,这部分是由γ-氨基丁酸-A和γ-氨基丁酸-B受体的激活介导的。L-脯氨酸也已被证明对N-甲基-D-天冬氨酸受体有类似作用。此外,L-哌啶酸被称为L-高脯氨酸,L-哌啶酸和L-脯氨酸都属于亚氨基酸组;因此,它们具有某些共同特性,包括相似功能,这是合理的。然而,关于L-哌啶酸作用方面N-甲基-D-天冬氨酸受体的作用尚未得到研究。在本研究中,在新生雏鸡中研究了N-甲基-D-天冬氨酸受体与L-哌啶酸中枢功能之间的关系。脑室内注射L-哌啶酸后,主动觉醒以及睁眼静止站立/坐立的行为姿势受到显著影响;而低头静止坐立(睡眠姿势)则显著增强。然而,N-甲基-D-天冬氨酸受体拮抗剂MK-801并未影响这些变化。总之,在新生雏鸡中,脑内给予L-哌啶酸不会通过激活N-甲基-D-天冬氨酸受体发挥催眠作用。这些结果表明,亚氨基不是激活N-甲基-D-天冬氨酸受体的决定因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/817a/7063071/59b3dc4668db/57_84_1.jpg

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