Polettini A, Groppi A, Montagna M
Department of Legal Medicine and Public Health, University of Pavia, Italy.
J Anal Toxicol. 1999 Nov-Dec;23(7):570-6. doi: 10.1093/jat/23.7.570.
In order to evaluate pharmacokinetic interactions between heroin and alcohol and their role in the etiology of heroin-related deaths (HRD), the alcohol concentration in blood (BAC), the free (FM) and total morphine (TM) concentrations in blood (determined by DPC Coat-A-Count radioimmunoassay before and after enzymatic hydrolysis), and the TM concentration in urine and bile (DPC Coat-A-Count after enzymatic hydrolysis) in a population of 39 lethal cases included in the records of the Department of Legal Medicine and Public Health at the University of Pavia from the period January 1997-April 1998 were examined. The cause of death in each case was attributed to either heroin or associated heroin-ethanol intoxication. Cases were arbitrarily divided into two groups according to BAC (low-ethanol group, LE, BAC < or = 1000 mg/L and high-ethanol group, HE, BAC > 1000 mg/L). The differences in the FM and TM concentrations in blood, bile, and urine and in the FM/TM ratios between the two . groups were statistically evaluated (Mann-Whitney U test). A similar statistical evaluation was carried out on data from a previously published study concerning the disposition of heroin and its metabolites (6-acetylmorphine and morphine) in blood and urine in 23 lethal cases attributed to either heroin or heroin and alcohol intoxication. The values of the following variables in the LE and HE groups were compared: FM, TM, and 6-acetylmorphine concentrations in blood (6-AM); the FM/ (FM + 6-AM) ratio; the FM/TM ratio; and the urinary concentrations of heroin, 6-acetylmorphine, and free morphine. Statistical analyses of data indicated that high BACs are associated with reduced hydrolysis of 6-AM to morphine (FM/[FM + 6-AM], p = 0.0022) and that a good inverse correlation exists between BAC and hydrolysis of 6-AM to morphine (r2 = 0.67). High BACs were also found to be associated with an increased FM/TM ratio and with reduced excretion of free and total morphine. These results suggest the hypothesis that pharmacokinetic interactions between heroin and alcohol do occur in individuals exposed to high doses of these substances.
为了评估海洛因与酒精之间的药代动力学相互作用及其在海洛因相关死亡(HRD)病因中的作用,对1997年1月至1998年4月期间帕维亚大学法医学与公共卫生系记录中的39例致死病例进行了研究,检测了其血液中的酒精浓度(BAC)、血液中游离吗啡(FM)和总吗啡(TM)浓度(酶水解前后通过DPC Coat - A - Count放射免疫分析测定)以及尿液和胆汁中的TM浓度(酶水解后用DPC Coat - A - Count测定)。每例病例的死亡原因归因于海洛因或相关的海洛因 - 乙醇中毒。根据BAC将病例任意分为两组(低乙醇组,LE,BAC≤1000mg/L;高乙醇组,HE,BAC>1000mg/L)。对两组血液、胆汁和尿液中FM和TM浓度以及FM/TM比值的差异进行了统计学评估(曼 - 惠特尼U检验)。对先前发表的一项关于23例归因于海洛因或海洛因与酒精中毒致死病例血液和尿液中海洛因及其代谢物(6 - 乙酰吗啡和吗啡)处置情况的研究数据进行了类似的统计学评估。比较了LE组和HE组中以下变量的值:血液中FM、TM和6 - 乙酰吗啡(6 - AM)浓度;FM/(FM + 6 - AM)比值;FM/TM比值;以及尿液中海洛因、6 - 乙酰吗啡和游离吗啡的浓度。数据统计分析表明,高BAC与6 - AM向吗啡的水解减少有关(FM/[FM + 6 - AM],p = 0.0022),并且BAC与6 - AM向吗啡的水解之间存在良好的负相关(r2 = 0.67)。还发现高BAC与FM/TM比值增加以及游离和总吗啡排泄减少有关。这些结果提示了一个假设,即在接触高剂量这些物质的个体中,海洛因与酒精之间确实发生了药代动力学相互作用。