Mutant mice lacking ryanodine receptor type 3 exhibit deficits of contextual fear conditioning and activation of calcium/calmodulin-dependent protein kinase II in the hippocampus

Yasuko Kouzu, Takahiro Moriya, Hiroshi Takeshima, Tohru Yoshioka, Shigenobu Shibata

研究成果: Article

53 被引用数 (Scopus)

抄録

As it is known that ryanodine receptor type 3 is expressed in the hippocampus, we examined the contribution of this receptor to contextual fear conditioning behavior and to the activation of Ca2+/calmodulin-dependent protein kinase II using mice lacking the receptor. Ryanodine receptor type 3-deficient mice exhibited impairments of performance in the contextual fear conditioning test, passive avoidance test, and Y-maze learning test. Both the activities of Ca2+/calmodulin-dependent protein kinase IIβ and Ca2+/calmodulin-dependent protein kinase IIα were significantly increased in the experimental group compared to the control group in the hippocampus, but not in the cingulate cortex on the testing day 24 h after contextual fear training. However, the activities of Ca2+/calmodulin-dependent protein kinase IIβ and α were almost the same in the experimental and control groups in the hippocampus on the training day. Ryanodine receptor type 3-deficient mice did not show the increment of Ca2+/calmodulin-dependent protein kinase IIβ and α activities in the hippocampus on the testing day. In addition, these mutant mice showed the reduction of fear response in the elevated plus-maze test. The present results suggest that calcium-induced calcium release through the activation of ryanodine receptor type 3 in the hippocampus is important to the expression of the performance of contextual learning through the elevation of Ca2+/calmodulin-dependent protein kinase IIβ and α activities. Copyright (C) 2000 Elsevier Science B.V.

本文言語English
ページ(範囲)142-150
ページ数9
ジャーナルMolecular Brain Research
76
1
DOI
出版ステータスPublished - 2000 3 10

ASJC Scopus subject areas

  • Molecular Biology
  • Cellular and Molecular Neuroscience

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