Suppr超能文献

通过高分辨率质谱分析,比较人肝微粒体与雅致小克银汉霉对具有溴萘基部分的合成大麻素JWH-424进行生物转化的情况。

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.

作者信息

Watanabe Shimpei, Iwai Takahiro, Matsushita Ritsuko, Nakanishi Toshio, Kuzhiumparambil Unnikrishnan, Fu Shanlin, Seto Yasuo

机构信息

Forensic Science Group, Photon Science Research Division, RIKEN SPring-8 Center, Physical Science Research Building, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo, 679-5148, Japan.

Climate Change Cluster, University of Technology Sydney, PO Box 123, Broadway, NSW, 2007, Australia.

出版信息

Forensic Toxicol. 2022 Jul;40(2):278-288. doi: 10.1007/s11419-022-00612-2. Epub 2022 Feb 14.

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.

摘要

目的

JWH - 424,即(8 - 溴 - 1 - 萘基)(1 - 戊基 - 1H - 吲哚 - 3 - 基)甲酮,是一种合成大麻素,它是最著名的合成大麻素之一JWH - 018的溴化类似物。尽管与JWH - 018结构相似,但关于JWH - 424的信息知之甚少,包括其代谢情况。本研究的目的是比较人肝微粒体(HLM)和雅致小克银汉霉作为JWH - 424的代谢催化剂,以更好地了解该真菌在合成大麻素代谢中的特征作用。

方法

将JWH - 424与人肝微粒体孵育1小时,与雅致小克银汉霉孵育长达72小时。人肝微粒体孵育混合物用甲醇稀释,真菌孵育混合物用二氯甲烷萃取并在甲醇中复溶,然后通过液相色谱 - 高分辨率质谱(LC - HRMS)进行分析。

结果

人肝微粒体孵育通过二氢二醇形成、羟基化和/或溴被羟基的原位取代产生了10种代谢产物。真菌孵育通过羧基化、二氢二醇形成、羟基化、酮形成、葡萄糖苷化和/或硫酸化产生了23种代谢产物。

结论

一般来说,人肝微粒体模型能很好地预测人体代谢产物,结构类似物以相似方式代谢。然而,人肝微粒体产生的主要羟基代谢产物是那些在萘环上羟基化而非戊基部分羟基化的产物,戊基部分是JWH - 018羟基化的主要位点。另一方面,真菌代谢产物主要在戊基部分发生了羟基化。这种代谢差异表明有必要在真实尿液样本中验证人体代谢产物,同时推荐H9和H10(羟基萘)、H8(原位取代产物)、F22(羟基戊基)和F17(二羟基戊基)用于尿液分析中JWH - 424的监测。

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