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关于兴奋性氨基酸在中缝正中核中发挥功能性作用的行为学和生物化学证据。

Behavioral and biochemical evidence for a functional role of excitatory amino acids in the median raphe nucleus.

作者信息

Wirtshafter D, Trifunovic R, Krebs J C

机构信息

Department of Psychology, University of Illinois, Chicago, IL 60680.

出版信息

Brain Res. 1989 Mar 20;482(2):225-34. doi: 10.1016/0006-8993(89)91185-2.

Abstract

Recent experiments have suggested the existence of excitatory amino acid (EAA)-containing afferents to the median raphe nucleus. In the present study we investigated the functional significance of EAAs in the median raphe (MR) by examining the behavioral and biochemical effects of intra-raphe injections of EAA antagonists. Injections of kynurenic acid, gamma-glutamylglycine, 2-amino-5-phosphonovaleric acid (2-APV) and 2-amino-7-phosphonoheptanoic acid (2-APH) into the median raphe resulted in marked hyperactivity. In contrast to the effect of 2-APV and 2-APH, intra-raphe injections of the homologues of these compounds with 4, 6 or 8 carbon atoms, which have a lower affinity for excitatory amino acid receptors, were without significant effects on activity. Additionally, the effects of 2-APV were shown to be stereospecific to the active D-isomer further suggesting receptor mediation of the effect. Injections of EAA antagonists into the dorsal raphe nucleus or the ventral tegmental area were much less effective in increasing activity than were injections into the MR, suggesting anatomical specificity of the effect. Injections of 2-APV into the median raphe were also shown to result in a reduction of serotonin metabolism within the hippocampus and an increase in dopamine metabolism within the nucleus accumbens and the magnitude of both of these effects was positively correlated with the behavioral responses to the injections. These findings suggest that cells within the median raphe may be subject to a tonic excitation exerted through EAA receptors.

摘要

近期实验表明,存在含兴奋性氨基酸(EAA)的传入神经至中缝正中核。在本研究中,我们通过检查向中缝内注射EAA拮抗剂的行为和生化效应,来研究EAA在中缝正中核(MR)中的功能意义。向中缝正中核注射犬尿氨酸、γ-谷氨酰甘氨酸、2-氨基-5-磷酸戊酸(2-APV)和2-氨基-7-磷酸庚酸(2-APH)会导致明显的活动亢进。与2-APV和2-APH的作用相反,向中缝内注射这些化合物具有4、6或8个碳原子的同系物,它们对兴奋性氨基酸受体的亲和力较低,对活动没有显著影响。此外,2-APV的作用显示对活性D-异构体具有立体特异性,这进一步表明该效应是由受体介导的。向背侧中缝核或腹侧被盖区注射EAA拮抗剂在增加活动方面比向中缝正中核注射的效果要小得多,这表明该效应具有解剖学特异性。向中缝正中核注射2-APV还显示会导致海马体内血清素代谢减少以及伏隔核内多巴胺代谢增加,并且这两种效应的程度与对注射的行为反应呈正相关。这些发现表明,中缝正中核内的细胞可能受到通过EAA受体施加的紧张性兴奋作用。

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