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代谢型谷氨酸受体1(mGluR1)突变小鼠的小脑长时程抑制缺陷及运动学习受损。

Deficient cerebellar long-term depression and impaired motor learning in mGluR1 mutant mice.

作者信息

Aiba A, Kano M, Chen C, Stanton M E, Fox G D, Herrup K, Zwingman T A, Tonegawa S

机构信息

Howard Hughes Medical Institute, Center for Learning and Memory, Cambridge, Massachusetts.

出版信息

Cell. 1994 Oct 21;79(2):377-88.

PMID:7954803
Abstract

mGluR1 mutant mice are viable but show characteristic cerebellar symptoms such as ataxic gait and intention tremor. The anatomy of the cerebellum is not overtly disturbed. Excitatory synaptic transmission from parallel fibers (PFs) to Purkinje cells and that from climbing fibers (CFs) to Purkinje cells appear to be functional, and voltage-gated Ca2+ channels of Purkinje cells are normal. Both PF and CF synapses display normal short-term synaptic plasticity to paired stimuli. By marked contrast, long-term depression (LTD) is clearly deficient and conditioned eyeblink response is impaired. We conclude that mGluR1 is required for the induction of LTD and that the ataxic behavior and impaired eyeblink conditioning of the mGluR1 mutant mice are primarily due to deficient LTD.

摘要

代谢型谷氨酸受体1(mGluR1)突变小鼠能够存活,但表现出典型的小脑症状,如共济失调步态和意向性震颤。小脑的解剖结构未受到明显干扰。从平行纤维(PFs)到浦肯野细胞以及从攀缘纤维(CFs)到浦肯野细胞的兴奋性突触传递似乎是正常的,并且浦肯野细胞的电压门控钙通道也是正常的。PF和CF突触对成对刺激均表现出正常的短期突触可塑性。与之形成鲜明对比的是,长时程抑制(LTD)明显缺失,条件性眨眼反应受损。我们得出结论,LTD的诱导需要mGluR1,并且mGluR1突变小鼠的共济失调行为和眨眼条件反射受损主要是由于LTD缺陷所致。

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