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曲马多及其代谢物在一例过量致死病例中的组织分布

Tissue distribution of tramadol and metabolites in an overdose fatality.

作者信息

Moore K A, Cina S J, Jones R, Selby D M, Levine B, Smith M L

机构信息

Armed Forces Institute of Pathology, Division of Forensic Toxicology, Rockville, Maryland 20850-3125, USA.

出版信息

Am J Forensic Med Pathol. 1999 Mar;20(1):98-100. doi: 10.1097/00000433-199903000-00023.

Abstract

Tramadol (Ultram) is a centrally acting, synthetic analgesic agent. Although it has some affinity for the opiate receptors, tramadol is believed to exert its analgesic effect by inhibiting the re-uptake of norepinephrine and serotonin. There are several published cases of tramadol's involvement in drug-related deaths and impairment. Reports of deaths involving tramadol alone with associated tissue concentrations are rare. This report documents a case in which tramadol overdose was identified as the cause of death. The following tramadol concentrations were found in various tissues: blood, 20 mg/L; urine, 110.2 mg/L; liver, 68.9 mg/kg; and kidney, 37.5 mg/kg. Tissue distributions of the two primary metabolites, N-desmethyl and O-desmethyl tramadol, are also reported. In each tissue or fluid except urine, the tramadol concentration was greater than either metabolite, consistent with other reports of drug-impaired drivers and postmortem cases. The O-desmethyl metabolite concentration was greater than the N-desmethyl metabolite concentration in all tissues; this is in contrast to other postmortem reports, in which the majority of cases report concentrations of O-desmethyl as less than those of N-desmethyl. This may be useful as an indicator of time lapse between ingestion and death.

摘要

曲马多(奇曼丁)是一种中枢性作用的合成镇痛药。尽管它对阿片受体有一定亲和力,但据信曲马多是通过抑制去甲肾上腺素和5-羟色胺的再摄取来发挥镇痛作用的。已有数例曲马多与药物相关死亡及损害事件的报道。单独涉及曲马多且有相关组织浓度的死亡报告较为罕见。本报告记录了一例经鉴定曲马多过量为死亡原因的病例。在各种组织中发现了以下曲马多浓度:血液,20毫克/升;尿液,110.2毫克/升;肝脏,68.9毫克/千克;肾脏,37.5毫克/千克。还报告了两种主要代谢物N-去甲基曲马多和O-去甲基曲马多的组织分布情况。在除尿液外的每个组织或液体中,曲马多浓度均高于任何一种代谢物,这与其他关于药物致驾驶能力受损者及尸检病例的报告一致。在所有组织中,O-去甲基代谢物浓度均高于N-去甲基代谢物浓度;这与其他尸检报告相反,在其他报告中,大多数病例报告O-去甲基浓度低于N-去甲基浓度。这可能作为摄入与死亡之间时间间隔的一个指标。

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