Zabøocka B, Domańska-Janik K
Department of Neurochemistry, Polish Academy of Sciences, Warsaw.
Neuroreport. 1994 Dec 30;6(1):85-8. doi: 10.1097/00001756-199412300-00023.
The effect of the platelet activating factor (PAF) antagonist BN52021 on [3H]D-aspartate (D-Asp) release was investigated in rat hippocampal slices during and after incubation (20 min) in ischaemia-like conditions. Ischaemia did not influence spontaneous D-Asp outflow whereas K(+)-evoked, calcium-dependent release was markedly enhanced in reoxygenated, post-ischaemic slices. These slices also showed a substantial translocation/activation of protein kinase C (PKC). BN52021 blocked both ischaemia-induced effects. Moreover, the PKC inhibitor H7 attenuated post-ischaemic K(+)-evoked D-Asp release when beta-PDBu, a PKC activator, was used to enhance the response of normoxic slices. Assuming that PKC is activated by ischaemia in a PAF-dependent manner and that this activation proceeds to enhanced glutamate exocytosis, we speculate on the involvement of PAF receptor stimulation in the pathology of cerebral ischaemia.
在大鼠海马切片中,于类似缺血条件下孵育(20分钟)期间及之后,研究了血小板活化因子(PAF)拮抗剂BN52021对[3H]D-天冬氨酸(D-Asp)释放的影响。缺血不影响D-Asp的自发流出,而在复氧的缺血后切片中,钾离子诱发的、钙依赖性释放显著增强。这些切片还显示蛋白激酶C(PKC)有大量的易位/激活。BN52021可阻断缺血诱导的两种效应。此外,当使用PKC激活剂β-佛波醇酯(β-PDBu)增强常氧切片的反应时,PKC抑制剂H7可减弱缺血后钾离子诱发的D-Asp释放。假设PKC通过PAF依赖性方式被缺血激活,且这种激活会导致谷氨酸胞吐作用增强,我们推测PAF受体刺激参与了脑缺血的病理过程。