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甲氨蝶呤在细胞内的蓄积和叶酸耗竭可能是该药物产生慢性毒性的一种机制。

Methotrexate accumulation and folate depletion in cells as a possible mechanism of chronic toxicity to the drug.

作者信息

Kamen B A, Nylen P A, Camitta B M, Bertino J R

出版信息

Br J Haematol. 1981 Nov;49(3):355-60. doi: 10.1111/j.1365-2141.1981.tb07237.x.

Abstract

Methotrexate has been associated with chronic toxicities such as cirrhosis and neurological impairments ranging from mild learning disorders to a fatal leucoencephalopathy. The mechanism(s) for this toxicity is not completely understood. Certain tissues can convert methotrexate to polyglutamates. This results in a more persistent intracellular form of the drug. In this study the intracellular levels of folate and methotrexate were measured in the erythrocytes and liver of patients treated chronically with methotrexate. These tissues showed an accumulation of methotrexate as polyglutamates and a concomitant loss of folate. Folate concentrations were below normal in nine of 12 red cell and three of five liver samples. It is proposed that persistent methotrexate concentrations and/or the associated folate deficiency may be related to the toxicity of methotrexate, especially in time of cellular stress.

摘要

甲氨蝶呤与慢性毒性有关,如肝硬化和神经功能障碍,范围从轻度学习障碍到致命的白质脑病。这种毒性的机制尚未完全了解。某些组织可将甲氨蝶呤转化为多聚谷氨酸盐。这导致药物在细胞内的形式更持久。在本研究中,对长期接受甲氨蝶呤治疗的患者的红细胞和肝脏中的叶酸和甲氨蝶呤的细胞内水平进行了测量。这些组织显示甲氨蝶呤以多聚谷氨酸盐的形式积累,同时叶酸流失。12个红细胞样本中的9个和5个肝脏样本中的3个叶酸浓度低于正常水平。有人提出,持续的甲氨蝶呤浓度和/或相关的叶酸缺乏可能与甲氨蝶呤的毒性有关,尤其是在细胞应激时。

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