Basavarajappa B S, Saito M, Cooper T B, Hungund B L
Division of Analytical Psychopharmacology, College of Physicians and Surgeons, Columbia University, New York, New York, USA.
Alcohol Clin Exp Res. 1997 Oct;21(7):1199-203.
Human neuroblastoma cells were exposed to ethanol (EtOH; 100 mM) in culture for various time periods. It was found that chronic EtOH exposure increased the arachidonyl-specific phospholipase A2 (PLA2) activity significantly in both cytosol (1.6-fold) and membrane (2.2-fold) fractions when 1-palmitoyl-2-arachidonyl-sn-glycero-3-phosphocholine was used as a substrate. This arachidonyl-specific PLA2 activity progressively increased with increasing duration of EtOH exposure and reached peak level at 72-hr EtOH exposure (chronic). A significant amount of the PLA2 activity was associated with the membrane fraction. No significant difference in PLA2 activity was observed when 1-palmitoyl-2 oleoyl or linoleoyl-sn-glycero-3-phosphocholine was used as a substrate. It was also found that co-treatment of neuroblastoma cells with ganglioside GM1 reduced the EtOH-induced activation of arachidonyl-specific PLA2 activity. The present results indicate that arachidonic acid-specific PLA2 may play a role in adaptation mechanisms to chronic EtOH in cultured neuroblastoma cells. Ganglioside GM1, in part, may exert its neuroprotective effects by modulating arachidonyl-specific PLA2 activity in chronic EtOH-exposed neuroblastoma cells.
将人神经母细胞瘤细胞在培养中暴露于乙醇(EtOH;100 mM)不同时间段。结果发现,当以1-棕榈酰-2-花生四烯酰-sn-甘油-3-磷酸胆碱作为底物时,慢性乙醇暴露显著增加了胞质溶胶(1.6倍)和膜(2.2倍)组分中花生四烯酰特异性磷脂酶A2(PLA2)的活性。这种花生四烯酰特异性PLA2活性随着乙醇暴露时间的延长而逐渐增加,并在乙醇暴露72小时(慢性)时达到峰值水平。大量的PLA2活性与膜组分相关。当以1-棕榈酰-2-油酰或亚油酰-sn-甘油-3-磷酸胆碱作为底物时,未观察到PLA2活性有显著差异。还发现用神经节苷脂GM1共同处理神经母细胞瘤细胞可降低乙醇诱导的花生四烯酰特异性PLA2活性的激活。目前的结果表明,花生四烯酸特异性PLA2可能在培养的神经母细胞瘤细胞对慢性乙醇的适应机制中起作用。神经节苷脂GM1可能部分通过调节慢性乙醇暴露的神经母细胞瘤细胞中花生四烯酰特异性PLA2活性发挥其神经保护作用。