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控制磷脂酸磷酸水解酶和磷脂酸胞苷酰转移酶活性的因素。氯丙嗪、去甲基丙咪嗪、辛可卡因、诺氟拉明、美吡拉敏和镁离子的作用。

Factors controlling the activities of phosphatidate phosphohydrolase and phosphatidate cytidylyltransferase. The effects of chlorpromazine, demethylimipramine, cinchocaine, norfenfluramine, mepyramine and magnesium ions.

作者信息

Sturton R G, Brindley D N

出版信息

Biochem J. 1977 Jan 15;162(1):25-32. doi: 10.1042/bj1620025.

DOI:10.1042/bj1620025
PMID:192211
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1164565/
Abstract
  1. Microsomal membranes from rat liver were incubated with ATP, CoA, Mg2+, [14C]palmitate, F- and sn-glycerol 3-phosphate in order to label them with [14C]phosphatidate. These membranes were isolated and used in a second incubation in which [3H]CTP was present, and the simultaneous synthesis of [14C]diacylglycerol and [3H]CDP-diacylglycerol was measured. 2. The addition of phosphatidate phosphohydrolase, which had been partially purified from the particle-free supernatant, supplemented the activity of the endogenous phosphohydrolase, but it did not alter the rate of CDP-diacylglycerol formation. 3. Adding EDTA inhibited phosphatidate cytidylyl-transferase activity and stimulated the activity of the phosphohydrolases by removing excess of Mg2+. 4. Increasing the concentration of Mg2+, norfenfluramine or chlorpromazine in the assay system stimulated cytidylyltransferase activity, but decreased the activities of both phosphohydrolases. 5. The mechanism for the stimulation of cytidylyl=transferase activity by the cationic drugs and Mg2+ was investigated with emulsions of phosphatidate and the microsomal fraction of rat liver. 6. There was a threshold concentration of about 5mM-MgCl2 below which no cytidylyltransferase activity was detected in the presence or absence of norfenfluramine. Just above this threshold concentration norfenfluramine stimulated cytidylyltransferase activity, but this stimulation disappeared as the Mg2+ concentration was raised to its optimum of 20mM. Norfenfluramine therefore partially replaced the bivalent-cation requirement. 7. At 30 mM-MgCl2 amphiphilic cationic drugs inhibited cytidylyltransferase activity at relatively high concentrations in a non-competitive manner with respect to phosphatidate. 8. The implications of these results are discussed with respect to the regulation of the synthesis of the acidic phospholipids compared with the synthesis of phosphatidylcholine, phosphatidylethanolamine and triacylglycerol.
摘要
  1. 将大鼠肝脏的微粒体膜与ATP、辅酶A、Mg2+、[14C]棕榈酸、F-和sn-甘油3-磷酸一起孵育,以便用[14C]磷脂酸对其进行标记。分离这些膜并用于第二次孵育,其中存在[3H]CTP,并测定[14C]二酰基甘油和[3H]CDP-二酰基甘油的同时合成。2. 加入从无颗粒上清液中部分纯化的磷脂酸磷酸水解酶,补充了内源性磷酸水解酶的活性,但未改变CDP-二酰基甘油的形成速率。3. 添加EDTA通过去除过量的Mg2+抑制磷脂酸胞苷酰转移酶活性并刺激磷酸水解酶的活性。4. 在测定系统中增加Mg2+、去甲氟西汀或氯丙嗪的浓度刺激胞苷酰转移酶活性,但降低了两种磷酸水解酶的活性。5. 用磷脂酸乳液和大鼠肝脏微粒体部分研究了阳离子药物和Mg2+刺激胞苷酰转移酶活性的机制。6. 存在约5mM-MgCl2的阈值浓度,低于该浓度时,无论是否存在去甲氟西汀,均未检测到胞苷酰转移酶活性。略高于该阈值浓度时,去甲氟西汀刺激胞苷酰转移酶活性,但随着Mg2+浓度升高至其最佳值20mM,这种刺激消失。因此,去甲氟西汀部分替代了二价阳离子的需求。7. 在30mM-MgCl2时,两亲性阳离子药物在相对高浓度下以相对于磷脂酸非竞争性的方式抑制胞苷酰转移酶活性。8. 相对于磷脂酰胆碱、磷脂酰乙醇胺和三酰甘油的合成,讨论了这些结果对于酸性磷脂合成调节的意义。

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Factors controlling the activities of phosphatidate phosphohydrolase and phosphatidate cytidylyltransferase. The effects of chlorpromazine, demethylimipramine, cinchocaine, norfenfluramine, mepyramine and magnesium ions.控制磷脂酸磷酸水解酶和磷脂酸胞苷酰转移酶活性的因素。氯丙嗪、去甲基丙咪嗪、辛可卡因、诺氟拉明、美吡拉敏和镁离子的作用。
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