Calcium-stimulated adenylyl cyclase activity is critical for hippocampus-dependent long-term memory and late phase LTP

被引:400
作者
Wong, ST
Athos, J
Figueroa, XA
Pineda, VV
Schaefer, ML
Chavkin, CC
Muglia, LJ
Storm, DR [1 ]
机构
[1] Univ Washington, Sch Med, Dept Pharmacol, Seattle, WA 98195 USA
[2] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63130 USA
[3] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63130 USA
关键词
D O I
10.1016/S0896-6273(01)80036-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
It is hypothesized that Ca2+ stimulation of calmodulin (CaM)-activated adenylyl cyclases (AC1 or AC8) generates cAMP signals critical for late phase LTP (L-LTP) and long-term memory (LTM). However, mice lacking either AC1 or AC8 exhibit normal L-LTP and LTM. Here, we report that mice lacking both enzymes (DKO) do not exhibit L-LTP or LTM. To determine if these defects are due to a loss of cAMP increases in the hippocampus, DKO mice were unilaterally cannulated to deliver forskolin. Administration of forskolin to area CA1 before training restored normal LTM. We conclude that Ca2+-stimulated adenylyl cyclase activity is essential for L-LTP and LTM and that AC1 or AC8 can produce the necessary cAMP signal.
引用
收藏
页码:787 / 798
页数:12
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