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体外暴露于锂的离体人淋巴细胞中钠钾泵数量增加。肌醇、蛋白激酶C抑制剂和钠氢反向转运体抑制剂可使其逆转。

Increases in Na/K pump numbers in isolated human lymphocytes exposed to lithium in vitro. Reversal by myo-inositol and by inhibitors of protein kinase C and the Na/H antiport.

作者信息

Jenkins R J, Aronson J K, Brearley C J

机构信息

MRC Unit, Radcliffe Infirmary, Oxford, U.K.

出版信息

Biochim Biophys Acta. 1991 Apr 17;1092(2):138-44. doi: 10.1016/0167-4889(91)90147-p.

Abstract

Lithium (1-8 mM) caused a dose-dependent increase in the number of [3H]ouabain binding sites and in sodium/potassium (Na/K) pump activity in normal lymphocytes after incubation for 72 h. The increase in Na/K pump activity was due to an increase in the Vmax of the pump, with no change in the apparent affinity (Km) for potassium (rubidium). There was no change in the turnover number of the pump and the intracellular sodium concentration fell. The increase in [3H]ouabain binding sites was prevented by the addition of myo-inositol (10 mM), by inhibition of the protein kinase C with staurosporine (100 nM) and by inhibition of the Na/H antiport with dimethylamiloride (50 microM). These results suggest that the increase in Na/K pump activity caused by lithium is due to an increase in pump numbers and not due to increased activity of individual pumps or to an alteration in the affinity of the pumps for potassium. The increase in Na/K pump numbers and activity in lymphocytes exposed to lithium for 72 h may be related to altered Na/H antiport activity secondary to inhibition of phosphoinositol breakdown by lithium.

摘要

锂(1 - 8 mM)在正常淋巴细胞孵育72小时后,使[3H]哇巴因结合位点数量和钠/钾(Na/K)泵活性呈剂量依赖性增加。Na/K泵活性的增加是由于泵的Vmax增加,而对钾(铷)的表观亲和力(Km)没有变化。泵的周转数没有变化,细胞内钠浓度下降。添加肌醇(10 mM)、用星形孢菌素(100 nM)抑制蛋白激酶C以及用二甲基氨氯吡脒(50 microM)抑制Na/H反向转运体可阻止[3H]哇巴因结合位点的增加。这些结果表明,锂引起的Na/K泵活性增加是由于泵数量增加,而不是由于单个泵活性增加或泵对钾的亲和力改变。暴露于锂72小时的淋巴细胞中Na/K泵数量和活性的增加可能与锂抑制磷酸肌醇分解继发的Na/H反向转运体活性改变有关。

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