Messiha F S, Sproat H F, Striegler R L
Brain Res Bull. 1983 Aug;11(2):249-53. doi: 10.1016/0361-9230(83)90199-5.
Biochemical and histological studies on the effect of separate and combined administration of LiCl and of chlorpromazine (CPZ) on female C57BL/6J mice were performed. Mice were divided into 4 groups. One group was given an intraperitoneal injection daily of CPZ HCl, 5 mg/kg for 4 days followed by 4 more days of a daily dosage of 10 mg/kg. A second group was maintained on 0.4% (w/v) LiCl solution as the sole drinking fluid for 8 consecutive days and a third group received the same LiCl solution but with daily CPZ injection as the initial group for 8 days. The fourth group served as saline-controls. Hepatic liver alcohol dehydrogenase was induced by combined drug treatment from respective controls. The Li-treatment inhibited mitochondrial liver aldehyde dehydrogenase, and coadministration of CPZ with LiCl antagonized this effect. Mice treated with CPZ showed corneal cellularity and mitotic figure appearance without inflammation. The LiCl treated mice displayed variations in base corneal cell size, shape and pigmentation with aggregation of the nuclei, and the presence of mitotic activity inflammation. Mice receiving combined drug treatment showed similar corneal alterations, but mitotic figures were found above base cell layer suggesting an enhanced corneal toxicity. The results suggest a drug-drug interaction phenomenon which may explain some of their adverse reaction when given concurrently.
对雌性C57BL/6J小鼠进行了关于单独及联合给予氯化锂(LiCl)和氯丙嗪(CPZ)的影响的生化和组织学研究。小鼠被分为4组。一组每天腹腔注射盐酸氯丙嗪,剂量为5mg/kg,持续4天,随后4天每天剂量为10mg/kg。第二组连续8天以0.4%(w/v)LiCl溶液作为唯一饮用水,第三组接受相同的LiCl溶液,但与初始组一样每天注射CPZ,持续8天。第四组作为生理盐水对照组。联合药物治疗相对于各自的对照组诱导了肝脏乙醇脱氢酶。锂处理抑制了肝脏线粒体醛脱氢酶,CPZ与LiCl共同给药拮抗了这种作用。用CPZ处理的小鼠出现角膜细胞增多和有丝分裂象,但无炎症。用LiCl处理的小鼠角膜基底细胞大小、形状和色素沉着出现变化,细胞核聚集,且存在有丝分裂活性炎症。接受联合药物治疗的小鼠表现出类似的角膜改变,但在基底细胞层上方发现有丝分裂象,提示角膜毒性增强。结果表明存在药物相互作用现象,这可能解释了它们同时给药时的一些不良反应。