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缺乏谷氨酸脱羧酶67的小鼠小脑的γ-氨基丁酸与突触抑制

GABA and synaptic inhibition of mouse cerebellum lacking glutamate decarboxylase 67.

作者信息

Obata Kunihiko, Hirono Moritoshi, Kume Nobuko, Kawaguchi Yoshiya, Itohara Shigeyoshi, Yanagawa Yuchio

机构信息

Obata Research Unit, RIKEN Brain Science Institute, 2-1 Hirosawa, Wako, Saitama-ken 351-0198, Japan.

出版信息

Biochem Biophys Res Commun. 2008 Jun 6;370(3):429-33. doi: 10.1016/j.bbrc.2008.03.110. Epub 2008 Mar 31.

Abstract

gamma-Aminobutyric acid (GABA) is a major inhibitory neurotransmitter and also presumed to be a neurotrophic factor. GABA is synthesized by glutamate decarboxylase (GAD). A mouse lacking a 67kDa isoform of GAD (GAD67) has a reduced GABA level in its brain at birth and does not survive postnatally because of cleft palate. In this study, to investigate the functional and developmental roles of GABA in the postnatal cerebellum, selective GAD67 deletion was achieved using a Cre-loxP strategy. In this mouse, GABA level was reduced to 16-44% in the cerebellum but not in the cerebrum. Inhibitory synaptic transmission to Purkinje cells was seriously impaired. However, the morphology of Purkinje cells and the density of synaptic terminals in the cerebellar cortex appeared unaffected, suggesting that GABA does not participate in cerebellar development substantially.

摘要

γ-氨基丁酸(GABA)是一种主要的抑制性神经递质,也被认为是一种神经营养因子。GABA由谷氨酸脱羧酶(GAD)合成。缺乏GAD 67 kDa同工型(GAD67)的小鼠出生时大脑中的GABA水平降低,并且由于腭裂在出生后无法存活。在本研究中,为了研究GABA在出生后小脑的功能和发育作用,使用Cre-loxP策略实现了GAD67的选择性缺失。在这种小鼠中,小脑的GABA水平降低到16%-44%,但大脑中的GABA水平未降低。对浦肯野细胞的抑制性突触传递严重受损。然而,浦肯野细胞的形态和小脑皮质中突触终末的密度似乎未受影响,这表明GABA在小脑发育中基本不发挥作用。

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