Department of Physiology, School of Medicine, Keio University, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.
Neurochem Res. 2011 Jul;36(7):1314-22. doi: 10.1007/s11064-010-0392-z. Epub 2011 Jan 9.
Mice with spontaneous and induced mutations causing cerebellar phenotypes have provided key insights into how motor-related memories are stored in cerebellar circuits. Delayed eyeblink conditioning is a form of associative motor learning that depends on the cerebellum. However, neurochemical investigation of the underlying mechanisms has been hampered by the long training period (usually several days) required to establish conditioning. Here, we report a new rapid-training protocol that reliably induced delayed eyeblink conditioning within a single day. The associative memory formation depended on the expression of the δ2 glutamate receptor (GluD2) in cerebellar Purkinje cells. It lasted for several weeks, but could be erased by extinction sessions in a single day. In addition, using the rapid protocol, we found that eyeblink conditioning could be induced in juvenile mice at postnatal day 21, and that the Sindbis-virus-mediated expression of GluD2 could rescue the impaired eyeblink conditioning in GluD2-null mice in vivo.
自发性和诱导性突变导致小脑表型的小鼠为小脑回路中运动相关记忆的存储方式提供了重要的见解。延迟性眨眼条件反射是一种依赖小脑的联想性运动学习形式。然而,由于建立条件反射需要很长的训练期(通常需要几天),因此对潜在机制的神经化学研究受到了阻碍。在这里,我们报告了一种新的快速训练方案,可以在一天内可靠地诱导延迟性眨眼条件反射。联想记忆的形成取决于小脑浦肯野细胞中 δ2 谷氨酸受体(GluD2)的表达。它可以持续数周,但可以通过一天内的消退训练来消除。此外,使用快速方案,我们发现眨眼条件反射可以在出生后第 21 天的幼鼠中诱导,并且 Sindbis 病毒介导的 GluD2 表达可以挽救体内 GluD2 缺失小鼠受损的眨眼条件反射。