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吗啡和施他宁对大鼠肝脏脂质含量的影响。

Effect of morphine and stadol on lipid content in liver of rat.

作者信息

el Daly E S

机构信息

Zoology Department, Faculty of Science, Assiut University, Egypt.

出版信息

Life Sci. 1994;55(18):1419-26. doi: 10.1016/0024-3205(94)00756-x.

Abstract

The effects of repeated accumulative increasing doses (5, 10, 20 and 40 mg/kg body weight) of morphine and stadol on lipid content have been studied in liver of rat. The results obtained indicate that significant increases were recorded in hepatic triglycerides (TG) content after 1 and 12 hrs of morphine treatment while non-significant increases were recorded after stadol administration. After 36 hrs of treatment with either of the two drugs, the liver TG content was decreased which may indicate that drug tolerance might have developed. The phospholipids content showed increases especially after 12 hrs of morphine or stadol administration. The results obtained suggest enhanced phospholipid synthesis under the action of both drugs. Highly significant increases occurred in cholesterol content after 1, 12 and 24 hrs of treatment of both drugs. This might reflect the occurrence of decreased catabolism and turnover of cholesterol during the experiment. Total lipids content of liver showed marked and highly significant increases after 12 hrs of morphine and after 12 and 24 hrs of stadol administration respectively. The data obtained suggest that morphine and stadol may be hepatotoxic to rats.

摘要

已在大鼠肝脏中研究了重复累积递增剂量(5、10、20和40毫克/千克体重)的吗啡和镇痛新对脂质含量的影响。所得结果表明,吗啡治疗1小时和12小时后,肝脏甘油三酯(TG)含量显著增加,而使用镇痛新后记录到的增加不显著。用这两种药物中的任何一种治疗36小时后,肝脏TG含量降低,这可能表明已经产生了药物耐受性。磷脂含量尤其是在给予吗啡或镇痛新12小时后有所增加。所得结果表明,在两种药物的作用下磷脂合成增强。两种药物治疗1小时、12小时和24小时后,胆固醇含量均出现高度显著增加。这可能反映了实验期间胆固醇分解代谢和周转减少的情况。肝脏总脂质含量在给予吗啡12小时后以及分别给予镇痛新12小时和24小时后均出现显著且高度显著的增加。所得数据表明,吗啡和镇痛新可能对大鼠具有肝毒性。

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