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利用HeLa细胞进行药物毒性体外测量有效性的初步研究。III. 43种药物的人类致死作用与致死药物浓度的HeLa细胞毒性的关系

Preliminary studies on the validity of in vitro measurement of drug toxicity using HeLa cells. III. Lethal action to man of 43 drugs related to the HeLa cell toxicity of the lethal drug concentrations.

作者信息

Ekwall B

出版信息

Toxicol Lett. 1980 Apr;5(5):319-31. doi: 10.1016/0378-4274(80)90033-8.

Abstract

The human lethal plasma concentrations of 46 drugs were divided by their IC50 for HeLa cells in vitro to make up a series of cytotoxic quotients (CQLv). CQLv was then compared with the recorded lethal action to man of 43 of the drugs. While the 7 drugs with the lowest CQLv values produce a non-cytotoxic interference with neuro-transmission, most of the remaining 36 drugs have a known local or systemic cytotoxicity to man. A majority of the 36 drugs induces a non-specific central nervous system (CNS)-depression at lethal dosage, intermingled with function loss from organs outside CNS in proportion to decreasing drug accumulation in CNS cells and increasing CQLv. The remaining drugs which do not penetrate CNS cells and at lethal dosage induce a widespread injury and function loss of tissues outside the CNS, have a CQLv near unity. Non-specific CNS-depression may thus be the primary human reaction to lethal systemic drug cytotoxicity, while widespread drug injury to various tissues outside CNS--conventionally considered to be cytotoxic in origin--may be the obligatory human reaction to drugs that do not penetrate cells well. The present findings indicate a relevance to human toxicity of the HeLa toxicity for most drugs.

摘要

将46种药物的人体致死血浆浓度除以它们在体外对HeLa细胞的IC50,以构成一系列细胞毒性商数(CQLv)。然后将CQLv与所记录的43种药物对人体的致死作用进行比较。虽然CQLv值最低的7种药物对神经传递产生非细胞毒性干扰,但其余36种药物中的大多数对人体具有已知的局部或全身细胞毒性。36种药物中的大多数在致死剂量下会引起非特异性中枢神经系统(CNS)抑制,同时随着CNS细胞中药物蓄积的减少和CQLv的增加,CNS外器官的功能丧失也相应增加。其余不穿透CNS细胞且在致死剂量下会引起CNS外组织广泛损伤和功能丧失的药物,其CQLv接近1。因此,非特异性CNS抑制可能是人体对致死性全身药物细胞毒性的主要反应,而CNS外各种组织的广泛药物损伤——传统上认为其起源具有细胞毒性——可能是人体对不能很好穿透细胞的药物的必然反应。目前的研究结果表明,HeLa细胞毒性对大多数药物的人体毒性具有相关性。

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