首页> 外文期刊>Journal of Poultry Science >Intracerebroventricular Injection of L-Pipecolic Acid Exerts Hypnotic Effects Without Activating NMDA Receptors in Neonatal Chicks under Social Isolation-induced Stress
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Intracerebroventricular Injection of L-Pipecolic Acid Exerts Hypnotic Effects Without Activating NMDA Receptors in Neonatal Chicks under Social Isolation-induced Stress

机译:脑内注射L-哌啶酸在社会隔离诱导的应力下在新生儿雏虫中施用催眠作用而不激活NMDA受体

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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 γ -aminobutyric acid-A and γ -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.
机译:L-哌啶酸是L-赖氨酸分解代谢的中间体。其中央注射对脑部的催眠作用施加了催眠作用,其通过γ-氨基丁酸-A和γ-氨基丁酸-B受体的活化部分介导。还显示L-脯氨酸对N-甲基-D-天冬氨酸受体产生类似的效果。此外,L-哌啶醇称为L-同催化剂,L-哌啶醇和L-脯氨酸属于亚氨基酸基团;因此,它们具有卓越的共享某些共性,包括类似功能。然而,尚未检查N-甲基-D-天冬氨酸受体关于L-哌啶醇的影响的作用。在本研究中,在新生儿雏鸡中研究了N-甲基-D-天冬氨酸受体与L-哌啶醇的中心功能的关系。在脑内注射L-哌啶醇后,随着眼睛的活跃清醒和坐姿的行为姿势显着影响;虽然,头部下垂(睡眠姿势)坐在一无所转动的情况下显着提升。然而,N-甲基-D-天冬氨酸受体拮抗剂MK-801不影响这些变化。总之,L-哌啶酸的中央施用通过在新生儿雏鸡中的N-甲基-D-天冬氨酸受体的激活而没有发挥催眠作用。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。

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