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氯丙嗪对粒细胞超氧化物生成的抑制作用。

Chlorpromazine inhibition of granulocyte superoxide production.

作者信息

Cohen H J, Chovaniec M E, Ellis S E

出版信息

Blood. 1980 Jul;56(1):23-9.

PMID:6248151
Abstract

Superoxide production by granulocytes is a result of the activation of an NAD(P)H-dependent oxidase present in the plasma membrane. Chlorpromazine (5-50 muM) prolongs the time necessary to activation of the superoxide generating system and inhibits the extent of activation. When chlorpromazine is added after activation, there is an inhibition of further superoxide production. These effects are seen with digitonin, phorbol myristate acetate, and opsonized zymosan stimulated guinea pig and human granulocytes. Other phenothiazines (1-20 muM) and tetracaine (0.1-1.0 muM) produce similar effects. Lidocaine (1-10 mM) inhibits superoxide production but has no effect on the rate of activation. The effect of chlorpromazine on the rate of activation is reversible, but its effect on extent of activation is unaffected by extensive washing. Incubation of granulocytes with chlorpromazine results in decreased activation of the plasma membrane superoxide generating NADPH oxidase. Chlorpromazine also competes with NADPH for the membrane oxidase. These data and previously published results provide the basis of a model for the activation of the superoxide generating system.

摘要

粒细胞产生超氧化物是存在于质膜中的NAD(P)H依赖性氧化酶激活的结果。氯丙嗪(5 - 50μM)延长了激活超氧化物生成系统所需的时间,并抑制激活程度。当在激活后加入氯丙嗪时,会抑制进一步的超氧化物产生。在洋地黄皂苷、佛波酯肉豆蔻酸酯乙酸盐以及调理酵母聚糖刺激的豚鼠和人粒细胞中都观察到了这些效应。其他吩噻嗪类药物(1 - 20μM)和丁卡因(0.1 - 1.0μM)也产生类似的效应。利多卡因(1 - 10 mM)抑制超氧化物产生,但对激活速率没有影响。氯丙嗪对激活速率的影响是可逆的,但其对激活程度的影响不受大量洗涤的影响。粒细胞与氯丙嗪一起孵育会导致质膜超氧化物生成NADPH氧化酶的激活减少。氯丙嗪还与NADPH竞争膜氧化酶。这些数据和先前发表的结果为超氧化物生成系统的激活模型提供了基础。

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