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在新生雏鸡的急性应激条件下,脑室内注射L-丝氨酸类似物和衍生物会产生镇静和催眠作用。

Intracerebroventricular injection of L-serine analogs and derivatives induces sedative and hypnotic effects under an acute stressful condition in neonatal chicks.

作者信息

Asechi Mari, Tomonaga Shozo, Tachibana Tetsuya, Han Li, Hayamizu Kohsuke, Denbow D Michael, Furuse Mitsuhiro

机构信息

Laboratory of Advanced Animal and Marine Bioresources, Graduate School of Bioresources and Bioenvironmental Sciences, Kyushu University, Fukuoka 812-8581, Japan.

出版信息

Behav Brain Res. 2006 Jun 3;170(1):71-7. doi: 10.1016/j.bbr.2006.02.005. Epub 2006 Mar 29.

DOI:10.1016/j.bbr.2006.02.005
PMID:16574253
Abstract

Four experiments were conducted to clarify the central functions of L-serine and its analogs on an acute stressful condition. Intracerebroventricular (i.c.v.) injection of L-serine (0.21, 0.42 and 0.84 micromol) attenuated stress responses in a dose-dependent fashion, as well as induced sleep, in Experiment 1. The effects of L- and D-serine in Experiment 2, those of L-serine, phosphoserine, acetylserine and L-cysteine in Experiment 3 and those of L-serine, glycine and lysophosphatidylserine in Experiment 4 were compared at an equimolar basis (0.84 micromol). D-Serine, proposed as an endogenous agonist of N-methyl-D-aspatate (NMDA) receptor, did not have sedative and hypnotic effects as observed with L-serine. In contrast, all the analogs and derivatives of L-serine had a sedative effect, although with a different manner in several behavioral markers of stress such as spontaneous activity and distress vocalizations. No significant changes in plasma corticosterone concentration were observed in any experiment. Taken together, the i.c.v. injection of L-serine analogs and its derivatives have sedative and hypnotic effects under an acute stressful condition, which does not involve the hypothalamic-pituitary-adrenal axis. In conclusion, L-serine may be effective in improving anxiety or sleep disorders induced by psychological stressor.

摘要

进行了四项实验以阐明L-丝氨酸及其类似物在急性应激状态下的中枢功能。在实验1中,脑室内(i.c.v.)注射L-丝氨酸(0.21、0.42和0.84微摩尔)以剂量依赖的方式减轻应激反应,并诱导睡眠。在实验2中,以等摩尔浓度(0.84微摩尔)比较了L-丝氨酸和D-丝氨酸的作用;在实验3中,比较了L-丝氨酸、磷酸丝氨酸、乙酰丝氨酸和L-半胱氨酸的作用;在实验4中,比较了L-丝氨酸、甘氨酸和溶血磷脂酰丝氨酸的作用。作为N-甲基-D-天冬氨酸(NMDA)受体内源性激动剂的D-丝氨酸,没有观察到L-丝氨酸所具有的镇静和催眠作用。相反,L-丝氨酸的所有类似物和衍生物都有镇静作用,尽管在一些应激行为指标(如自发活动和痛苦叫声)上方式不同。在任何实验中均未观察到血浆皮质酮浓度有显著变化。综上所述,脑室内注射L-丝氨酸类似物及其衍生物在急性应激状态下具有镇静和催眠作用,且不涉及下丘脑-垂体-肾上腺轴。总之,L-丝氨酸可能对改善由心理应激源引起的焦虑或睡眠障碍有效。

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