Comparison between human liver microsomes and the fungus Cunninghamella elegans for biotransformation of the synthetic cannabinoid JWH-424 having a bromo-naphthyl moiety analysed by high-resolution mass spectrometry.

IF 2.8 4区 医学 Q2 TOXICOLOGY
Shimpei Watanabe, Takahiro Iwai, Ritsuko Matsushita, Toshio Nakanishi, Unnikrishnan Kuzhiumparambil, Shanlin Fu, Yasuo Seto
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引用次数: 1

Abstract

Purpose: JWH-424, (8-bromo-1-naphthyl)(1-pentyl-1H-indol-3-yl)methanone, is a synthetic cannabinoid, which is a brominated analogue of JWH-018, one of the best-known synthetic cannabinoids. Despite the structural similarity to JWH-018, little is known about JWH-424 including its metabolism. The aim of the study was to compare human liver microsomes (HLM) and the fungus Cunninghamella elegans as the metabolism catalysts for JWH-424 to better understand the characteristic actions of the fungus in the synthetic cannabinoid metabolism.

Methods: JWH-424 was incubated with HLM for 1 h and Cunninghamella elegans for up to 72 h. The HLM incubation mixtures were diluted with methanol and fungal incubation mixtures were extracted with dichloromethane and reconstituted in methanol before analyses by liquid chromatography-high-resolution mass spectrometry (LC-HRMS).

Results: HLM incubation resulted in production of ten metabolites through dihydrodiol formation, hydroxylation, and/or ipso substitution of the bromine with a hydroxy group. Fungal incubation led to production of 23 metabolites through carboxylation, dihydrodiol formation, hydroxylation, ketone formation, glucosidation and/or sulfation.

Conclusions: Generally, HLM models give good predictions of human metabolites and structural analogues are metabolised in a similar fashion. However, major hydroxy metabolites produced by HLM were those hydroxylated at naphthalene instead of pentyl moiety, the major site of hydroxylation for JWH-018. Fungal metabolites, on the other hand, had undergone hydroxylation mainly at pentyl moiety. The metabolic disagreement suggests the necessity to verify the human metabolites in authentic urine samples, while H9 and H10 (hydroxynaphthalene), H8 (ipso substitution), F22 (hydroxypentyl), and F17 (dihydroxypentyl) are recommended for monitoring of JWH-424 in urinalysis.

用高分辨率质谱分析了人肝微粒体与秀丽隐杆线虫真菌对合成大麻素JWH-424生物转化的比较。
目的:JWH-424(8-溴-1-萘基)(1-戊基- 1h -吲哚-3-基)甲烷酮是一种合成大麻素,它是JWH-018的溴化类似物,JWH-018是最著名的合成大麻素之一。尽管结构与JWH-018相似,但对JWH-424及其代谢知之甚少。本研究的目的是比较人肝微粒体(HLM)和真菌秀丽隐杆线虫(Cunninghamella elegans)作为JWH-424代谢催化剂,以更好地了解真菌在合成大麻素代谢中的特征作用。方法:JWH-424与HLM孵育1 h,与秀丽隐杆线虫孵育72 h。HLM孵育混合物用甲醇稀释,真菌孵育混合物用二氯甲烷提取,在甲醇中重组,然后采用液相色谱-高分辨率质谱(LC-HRMS)分析。结果:HLM通过形成二氢二醇、羟基化和/或用羟基取代溴产生十种代谢物。真菌培养通过羧基化、二氢二醇形成、羟基化、酮形成、葡萄糖苷化和/或磺化产生23种代谢物。结论:一般来说,HLM模型能很好地预测人体代谢物和结构类似物以类似的方式代谢。然而,HLM产生的主要羟基代谢物是萘羟基化的产物,而不是JWH-018的主要羟基化位点戊基部分。另一方面,真菌代谢物主要在戊基部分发生羟基化。代谢差异提示有必要对真实尿样中的人体代谢物进行验证,建议在尿液分析中监测JWH-424的H9和H10(羟基萘)、H8(羟基取代)、F22(羟基戊基)和F17(二羟基戊基)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Forensic Toxicology
Forensic Toxicology TOXICOLOGY-
CiteScore
5.80
自引率
9.10%
发文量
40
审稿时长
3 months
期刊介绍: The journal Forensic Toxicology provides an international forum for publication of studies on toxic substances, drugs of abuse, doping agents, chemical warfare agents, and their metabolisms and analyses, which are related to laws and ethics. It includes original articles, reviews, mini-reviews, short communications, and case reports. Although a major focus of the journal is on the development or improvement of analytical methods for the above-mentioned chemicals in human matrices, appropriate studies with animal experiments are also published. Forensic Toxicology is the official publication of the Japanese Association of Forensic Toxicology (JAFT) and is the continuation of the Japanese Journal of Forensic Toxicology (ISSN 0915-9606).
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