Classical eyeblink conditioning in glutamate receptor subunit δ2 mutant mice is impaired in the delay paradigm but not in the trace paradigm

被引:89
作者
Kishimoto, Y
Kawahara, S
Suzuki, M
Mori, H
Mishina, M
Kirino, Y
机构
[1] Univ Tokyo, Sch Pharmaceut Sci, Lab Neurobiophys, Bunkyo Ku, Tokyo 1130033, Japan
[2] Japan Sci & Technol Corp, CREST, Saitama 3320012, Japan
[3] Univ Tokyo, Sch Med, Dept Mol Neurobiol & Pharmacol, Tokyo 1130033, Japan
关键词
associative learning; cerebellar LTD; motor learning; Purkinje cell;
D O I
10.1046/j.0953-816x.2001.01488.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In mice lacking glutamate receptor subunit delta2 (GluR delta2(-/-) mice), cerebellar long-term depression (LTD) at the parallel fibre-Purkinje cell synapses is disrupted. Unlike the cerebellar LTD-deficient mice previously used for eyeblink conditioning, however, the abnormalities of the GluR delta2(-/-) mice are restricted to the cerebellar cortex. In delay eyeblink conditionings (interstimulus interval of 252 and 852 ms), in which the conditioned stimulus (CS) overlaps temporally with a coterminating unconditioned stimulus (US), GluR delta2(-/-) mice are severely impaired in learning, strongly supporting the hypothesis that cerebellar cortical LTD is essential for delay conditioning. In the trace paradigm, in which a stimulus-free trace interval of 500 ms intervened between the CS and US, GluR delta2(-/-) mice learned as successfully as wild-type mice, indicating that cerebellar LTD is not necessary for trace conditioning. Thus, the present study has revealed a cerebellar LTD-independent learning in eyeblink conditioning.
引用
收藏
页码:1249 / 1253
页数:5
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