4.7 Article

Central injection of L- and D-aspartate attenuates isolation-induced stress behavior in chicks possibly through different mechanisms

期刊

EUROPEAN JOURNAL OF PHARMACOLOGY
卷 736, 期 -, 页码 138-142

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2014.04.042

关键词

Intracerebroventricular; L-Aspartate; D-Aspartate; NMDA receptor; Chick

资金

  1. Japan Society for the Promotion of Science [23248046]
  2. Directorate General of Higher Education (DGHE) of Indonesia
  3. Grants-in-Aid for Scientific Research [23248046] Funding Source: KAKEN

向作者/读者索取更多资源

Intracerebroventricular (i.c.v.) injection of L- and D-aspartate (L- and D-Asp) has been shown to have a sedative effect with and without a hypnotic effect, respectively, in neonatal chicks experiencing isolation stress. However, the mechanisms of the different stress-attenuating functions of L- and D-Asp have not yet been fully clarified. In the present study, we investigated the involvement of the N-methyl-D-aspartate (NMDA) receptor in order to reveal the receptor-mediated function of L- and D-Asp. To reveal whether L-and D-Asp act through the NMDA receptor, (+)-MK-801, which is an antagonist of NMDA receptors, was used in the current study. In experiment 1, the chicks were injected i.c.v. with either saline, (+)-MK-801, L-Asp or L-Asp plus (+)-MK-801. The sedative and hypnotic effects induced by L-Asp were blocked by co-administration with (+)-MK-801. In experiment 2, the chicks were injected i.c.v. with either saline, (+)-MK-801, D-Asp or D-Asp plus (+)-MK-801. Importantly, the sedative effects induced by D-Asp were shifted to hypnotic effects by co-administration with (+)-MK-801. Taken together, L-Asp could induce sedative and hypnotic effects for stress behaviors through the NMDA receptor, but the attenuation of stress behaviors by D-Asp might be via simultaneous involvement of other receptors besides the NMDA receptor in this process. These differences may explain the different functional mechanisms of L- and D-Asp in the central nervous system. (C) 2014 Elsevier B.V. All rights reserved.

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