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锂对培养体系中粒细胞生成的影响。

Effect of lithium on granulopoiesis in culture.

作者信息

Morley D C, Galbraith P R

出版信息

Can Med Assoc J. 1978 Feb 4;118(3):288-90.

Abstract

Lithium carbonate therapy is associated with polymorphonuclear leukocytosis. In vitro studies have shown that lithium ions stimulate formation of granulocytic colonies. In a study undertaken to determine how lithium acts, colony-forming cells uncontaminated by monocytes (which elaborate colony-stimulating factor [CSF] in vitro) were obtained by means of a two-step cell separation procedure. The effects of lithium on colony formation were then studied in (a) cultures stimulated by humoral CSF, (b) cultures in which monocytes were relied upon to synthesize CSF de novo and (c) unstimulated cultures. Lithium enhanced the action of CSF but did not stimulate colony formation in the absence of CSF. In monocyte-stimulated cultures, colony formation increased with lithium concentrations up to 1 mmol/L but this increase paralleled that in CSF-stimulated cultures and therefore was not due to increased CSF production by monocytes. At higher concentrations of lithium, colony formation decreased in the monocyte-stimulated cultures but increased in the CSF-stimulated cultures. A lithium concentration of 4 mmol/L gave the greatest enhancing effect on colony formation in CSF-stimulated cultures and a concentration greater than 1 mmol/L inhibited de novo synthesis of CSF by monocytes.

摘要

碳酸锂治疗与多形核白细胞增多有关。体外研究表明,锂离子能刺激粒细胞集落的形成。在一项旨在确定锂作用机制的研究中,通过两步细胞分离程序获得了未被单核细胞污染的集落形成细胞(单核细胞在体外可产生集落刺激因子[CSF])。然后在以下几种培养条件下研究锂对集落形成的影响:(a) 由体液性CSF刺激的培养物;(b) 依靠单核细胞重新合成CSF的培养物;(c) 未受刺激的培养物。锂增强了CSF的作用,但在没有CSF的情况下不刺激集落形成。在单核细胞刺激的培养物中,锂浓度高达1 mmol/L时集落形成增加,但这种增加与CSF刺激的培养物中的增加情况相似,因此并非由于单核细胞产生的CSF增加所致。在更高浓度的锂作用下,单核细胞刺激的培养物中集落形成减少,但CSF刺激的培养物中集落形成增加。4 mmol/L的锂浓度对CSF刺激的培养物中的集落形成具有最大的增强作用,而大于1 mmol/L的浓度会抑制单核细胞重新合成CSF。

相似文献

本文引用的文献

1
Leukocytosis during lithium treatment.锂治疗期间的白细胞增多症。
Am J Psychiatry. 1971 May;127(11):1559-61. doi: 10.1176/ajp.127.11.1559.
5
Mechanisms of lithium action.锂的作用机制。
N Engl J Med. 1973 Aug 2;289(5):254-60. doi: 10.1056/NEJM197308022890508.

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