Mullany P, Connolly S, Lynch M A
Department of Physiology, Trinity College, Dublin, Ireland.
Eur J Pharmacol. 1996 Aug 15;309(3):311-5. doi: 10.1016/0014-2999(96)00464-5.
We have used synaptosomes prepared from rat hippocampus to investigate the role of protein tyrosine kinase and Ca2+/calmodulin-dependent protein kinase II in modulating glutamate release in young animals and to investigate possible parallel age-related changes in release and kinase activity. We report that depolarization of synaptosomes with 40 mM KCl, which stimulated glutamate release, also significantly increased activity of both kinases, while the protein tyrosine kinase inhibitor, genistein and the Ca2+/calmodulin-dependent protein kinase II inhibitor, KN62 (1-(N,O-bis[5-isoquinolinesulfonyl]-N-methyl-tyrosyl)-4-phenylpiperax ine) decreased K(+)-stimulated, Ca2(+)-dependent release of glutamate. K(+)-stimulated release of glutamate was significantly decreased in hippocampal synaptosomes prepared from aged, compared to young, animals. In parallel with these changes in release, we report an age-related decrease in activities of both protein tyrosine kinase and Ca2+/calmodulin-dependent protein kinase II. We conclude that these kinases play a role in modulating release of glutamate in hippocampus and that the age-related decrease in glutamate release may be partly due to an age-related decrease in kinase activities.
我们利用从大鼠海马体制备的突触体来研究蛋白酪氨酸激酶和钙调蛋白依赖性蛋白激酶II在调节幼龄动物谷氨酸释放中的作用,并研究释放和激酶活性中可能存在的与年龄相关的平行变化。我们报告称,用40 mM KCl使突触体去极化,刺激谷氨酸释放的同时,也显著增加了这两种激酶的活性,而蛋白酪氨酸激酶抑制剂染料木黄酮和钙调蛋白依赖性蛋白激酶II抑制剂KN62(1-(N,O-双[5-异喹啉磺酰基]-N-甲基-酪氨酰)-4-苯基哌嗪)减少了K(+)刺激的、Ca(2+)依赖性的谷氨酸释放。与幼龄动物相比,从老龄动物制备的海马体突触体中,K(+)刺激的谷氨酸释放显著减少。与这些释放变化平行,我们报告了蛋白酪氨酸激酶和钙调蛋白依赖性蛋白激酶II的活性与年龄相关的降低。我们得出结论,这些激酶在调节海马体中谷氨酸的释放中起作用,并且谷氨酸释放与年龄相关的减少可能部分归因于激酶活性与年龄相关的降低。