Suppr超能文献

大鼠双硫仑-乙醇反应中双硫仑及其代谢产物的比较研究

Comparative aspects of disulfiram and its metabolites in the disulfiram-ethanol reaction in the rat.

作者信息

Yourick J J, Faiman M D

机构信息

Department of Pharmacology and Toxicology, University of Kansas, Lawrence 66045.

出版信息

Biochem Pharmacol. 1989 Feb 1;38(3):413-21. doi: 10.1016/0006-2952(89)90380-8.

Abstract

Diethyldithiocarbamate-methyl ester (DDTC-Me), a metabolite of disulfiram, has been shown recently to produce a disulfiram-ethanol reaction (DER). Studies were carried out to compare the ethanol-sensitizing properties of DDTC-Me with those of disulfiram and diethyldithiocarbamate (DDTC) in the rat. All three drugs inhibited liver mitochondrial low Km aldehyde dehydrogenase (ALDH) in vivo, with maximal ALDH inhibition occurring 8 hr after drug administration. The onset of ALDH inhibition was most rapid after DDTC-Me administration. ALDH was inhibited approximately 50% 0.5 hr after DDTC-Me, whereas ALDH was inhibited only 5 and 10%, respectively, after disulfiram and DDTC. Not until 8 hr after drug treatment was ALDH inhibition the same for disulfiram, DDTC and DDTC-Me. The degree of ALDH inhibition from 8 to 172 hr after dosing was the same for all three drugs. An ethanol (1 g/kg, 20% v/v) challenge administered to rats treated with disulfiram (75 mg/kg), DDTC (114 mg/kg), or DDTC-Me (41.2 mg/kg) for 8 hr produced similar blood acetaldehyde/ethanol concentration-time profiles. In addition, all three agents produced a DER (hypotension, tachycardia). No DER occurred if ethanol was administered more than 24 hr after drug pretreatment. The hypotension associated with the DER correlated with the increased blood acetaldehyde but not blood ethanol. A threshold blood acetaldehyde of 110 microM appeared to be required for hypotension to occur, and this was related to ALDH inhibition of approximately 40%. The tachycardia associated with the DER correlated more with blood ethanol. After DDTC-Me administration, no disulfiram or DDTC could be detected in the plasma. Furthermore, no DDTC-Me was found in the plasma 8 hr after DDTC-Me administration, suggesting that no correlation exists between the DER and plasma concentration of DDTC-Me and most likely disulfiram. These data suggest that the alcohol-sensitizing properties of DDTC-Me are similar to those observed with disulfiram and DDTC. Since DDTC-Me is an active metabolite and more potent than disulfiram and DDTC in producing a DER, disulfiram metabolism is an important consideration in the disulfiram-ethanol reaction.

摘要

二乙基二硫代氨基甲酸盐甲酯(DDTC-Me)是双硫仑的一种代谢产物,最近已证明它会引发双硫仑-乙醇反应(DER)。本研究旨在比较DDTC-Me与双硫仑及二乙基二硫代氨基甲酸盐(DDTC)在大鼠体内的乙醇致敏特性。这三种药物在体内均能抑制肝脏线粒体低Km醛脱氢酶(ALDH),给药后8小时ALDH抑制作用达到最大。DDTC-Me给药后ALDH抑制作用起效最快。DDTC-Me给药后0.5小时,ALDH被抑制约50%,而双硫仑和DDTC给药后,ALDH分别仅被抑制5%和10%。直到药物治疗8小时后,双硫仑、DDTC和DDTC-Me对ALDH的抑制作用才相同。给药后8至172小时,这三种药物对ALDH的抑制程度相同。对用双硫仑(75毫克/千克)、DDTC(114毫克/千克)或DDTC-Me(41.2毫克/千克)治疗8小时的大鼠进行乙醇(1克/千克,20% v/v)激发试验,产生了相似的血液乙醛/乙醇浓度-时间曲线。此外,这三种药物均引发了DER(低血压、心动过速)。如果在药物预处理后24小时以上给予乙醇,则不会发生DER。与DER相关的低血压与血液乙醛升高相关,但与血液乙醇无关。低血压发生似乎需要血液乙醛阈值达到110微摩尔,这与约40%的ALDH抑制有关。与DER相关的心动过速与血液乙醇的相关性更大。给予DDTC-Me后,血浆中未检测到双硫仑或DDTC。此外,DDTC-Me给药8小时后,血浆中未发现DDTC-Me,这表明DER与DDTC-Me以及很可能与双硫仑的血浆浓度之间不存在相关性。这些数据表明,DDTC-Me的乙醇致敏特性与双硫仑和DDTC观察到的相似。由于DDTC-Me是一种活性代谢产物,在引发DER方面比双硫仑和DDTC更有效,双硫仑代谢是双硫仑-乙醇反应中的一个重要考虑因素。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验