Hepatotoxicity of the opioids morphine, heroin, meperidine, and methadone to cultured human hepatocytes.

Molecular toxicology Pub Date : 1987-09-01
M J Gómez-Lechón, X Ponsoda, R Jover, R Fabra, R Trullenque, J V Castell
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Abstract

Adult human hepatocytes in chemically defined culture conditions were incubated with morphine, heroin, meperidine, and methadone to investigate their potential hepatotoxicity to human liver. Cytotoxic effects were observed at about 100 times the plasma concentrations required to produce analgesia in human nonaddicts. Concentrations of 1 mM morphine, heroin, and meperidine reduced the glycogen content by 50%, while even 0.2 mM methadone produced a depletion of 70% after 24 h of treatment. Concentrations of 0.8 mM morphine and heroin, 0.4 mM meperidine, and 0.005 mM methadone inhibited the albumin synthesis by about 50% after 24 h of pretreatment. Intracellular glutathione was reduced to 50% of that of controls after 2-3 h of incubation with 2 mM morphine and 1 mM heroin, while 1 mM meperidine and 0.2 mM methadone produced a reduction of about 30% after 6 h incubation. The results show that therapeutic doses of the opioids is unlikely to produce irreversible damage to human hepatocytes, but opiate doses during tolerance or abuse may be a cause of liver dysfunction.

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阿片类药物吗啡、海洛因、哌替啶和美沙酮对培养人肝细胞的肝毒性。
在化学规定的培养条件下,将成人肝细胞与吗啡、海洛因、哌替啶和美沙酮一起培养,研究其对人肝脏的潜在毒性。细胞毒性作用观察到约100倍的血浆浓度需要产生镇痛的人类非成瘾。浓度为1 mM的吗啡、海洛因和哌嗪使糖原含量降低50%,而0.2 mM的美沙酮在治疗24小时后也使糖原含量减少70%。预处理24 h后,0.8 mM吗啡和海洛因、0.4 mM哌嗪、0.005 mM美沙酮对白蛋白合成的抑制作用约为50%。2 mM吗啡和1 mM海洛因孵育2-3 h后,细胞内谷胱甘肽含量降低至对照组的50%,而1 mM哌啶和0.2 mM美沙酮孵育6 h后,细胞内谷胱甘肽含量降低约30%。结果表明,治疗剂量的阿片类药物不太可能对人肝细胞产生不可逆的损伤,但耐受或滥用期间的阿片类药物剂量可能导致肝功能障碍。
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Xenobiotic regulation of glutathione S-transferase Ya gene expression. Review: gene amplification--a cellular response to genotoxic stress. Limitations of the fluorescent probe viability assay. Induction of a novel damage-specific DNA binding protein correlates with enhanced DNA repair in primate cells. Induction of a novel damage-specific DNA binding protein correlates with enhanced DNA repair in primate cells.
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