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锂在人血小板致密体中的优先蓄积。

Preferential accumulation of lithium in the dense bodies of human platelets.

作者信息

Costa J L, Fay D D, Nurnberger J I, Murphy D L

出版信息

Biochem Pharmacol. 1982 Oct 15;31(20):3215-8. doi: 10.1016/0006-2952(82)90552-4.

Abstract

From 50 to 73% of the lithium contained in platelets of patients receiving oral therapy with lithium carbonate was released by brief thrombin treatment. Similarly, about 50% of the lithium in platelets of normal volunteers incubated with lithium chloride was thrombin-releasable. The data indicate that an amount of lithium approximately equal to 10% of the calcium content was sequestered in the dense bodies (amine storage organelles) of human platelets. Electron microprobe analysis of dense bodies suggests that the addition of lithium did not change the phosphorus content but produced a loss of about 10% of the dense-body calcium. Nevertheless, synthetic solid analogues of the dense-body core incubated with lithium chloride did not sequester lithium preferentially over potassium and failed to exchange calcium for lithium. Thus, the mechanism responsible for the observed changes in platelet dense bodies may be related to selective membrane permeability properties rather than to binding of lithium to nucleotides or pyrophosphate in the dense-body core.

摘要

接受碳酸锂口服治疗的患者,其血小板中50%至73%的锂可通过短暂凝血酶处理释放出来。同样,在与氯化锂一起孵育的正常志愿者的血小板中,约50%的锂可被凝血酶释放。数据表明,人体血小板致密体(胺储存细胞器)中螯合的锂量约等于钙含量的10%。致密体的电子微探针分析表明,锂的添加并未改变磷含量,但导致致密体钙含量损失约10%。然而,与氯化锂一起孵育的致密体核心的合成固体类似物并没有比钾更优先地螯合锂,也未能将钙与锂进行交换。因此,导致血小板致密体中观察到的变化的机制可能与选择性膜通透性特性有关,而不是与锂与致密体核心中的核苷酸或焦磷酸的结合有关。

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