Ito I, Hidaka H, Sugiyama H
Fujigotemba Research Labs, Chgai Pharmaceutical Co., Gotemba, Japan.
Neurosci Lett. 1991 Jan 2;121(1-2):119-21. doi: 10.1016/0304-3940(91)90663-e.
Effects of KN-62 (1-[NO-bis-1,5-isoquinolinesulfonyl]-N-methyl-L-tyrosyl- 4-phenylpiperazine), a specific inhibitor of calcium/calmodulin-dependent protein kinase II, were examined using rat hippocampus slices in vitro. The inhibitor, when applied in bathing solutions prior to and present during the tetanic stimulations, blocked the generation of long-term potentiation (LTP) in CA1 regions without affecting basal synaptic transmission itself, suggesting an important role of this kinase in the molecular mechanism of CA1 LTP. In contrast, mossy fiber LTP in CA3 regions was not affected significantly by the inhibitor.
使用大鼠海马体脑片体外研究了钙/钙调蛋白依赖性蛋白激酶II的特异性抑制剂KN-62(1-[N-二(1,5-异喹啉磺酰基)]-N-甲基-L-酪氨酰-4-苯基哌嗪)的作用。该抑制剂在强直刺激之前及刺激期间加入到浴液中时,可阻断CA1区长期增强(LTP)的产生,而不影响基础突触传递本身,提示该激酶在CA1区LTP的分子机制中起重要作用。相反,CA3区苔藓纤维LTP未受该抑制剂的显著影响。