作者: M. Hudspith , G.R. John , P.T. Nhamburo , J.M. Littleton
DOI: 10.1016/0741-8329(85)90030-8
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摘要: Abstract Phospholipase C (PLC) activity was measured by the incorporation of [3H]-inositol into lipids and breakdown [3H]-inositol-labelled phosphatidylinositols (PI) polyphosphatidylinositols (PPI) to phosphates; phospholipase A2 (PLA2) [3H]oleic acid-labelled phosphatidylcholine ([3H]PC) acid enzymes phospholipid base exchange (PLBE) [14C]serine membrane lipids. The activities these in rat brain preparations were all increased procedures which increase intracellular Ca2+, inhibited a varying extent presence ethanol, 50 mM, vitro. In contrast, PLA2 PLBE markedly from animals had received ethanol chronically vivo. Similarly, although basal PLC only slightly such preparations, depolarization induced significantly greater fraction radiolabelled PI than that obtained control preparations. results suggest compensatory alterations Ca2+-activated metabolism tissue during continued