| Literature DB >> 33536920 |
Yifan Zhao1,2, Peng Sun1,2, Yue Ma1,2, Xiaoqiang Chang1,2, Xingyu Chen1,2, Xin Ji1,2, Yue Bai1,2, Dong Zhang1,2, Lan Yang1,2.
Abstract
Dihydroartemisinin (DHA) and its' derivatives have been employed as the most powerful first-line drugs for malarial treatment for several decades. The metabolism of DHA has not been studied clearly. Previous reports were focused on the pharmacokinetics procedure of DHA in healthy rats. The metabolites of DHA in red blood cells (RBC), especially in the RBC from Plasmodium-infected models, have rarely been studied. The Plasmodium species parasitize inside RBC, and these cells should be the final place where DHA performs its activity. In this study, the profile of DHA metabolites in biosample (blood, plasma, and RBC) of the infected and healthy mice was investigated with UPLC-Q-TOF-MS and UNIFI platform to gain insight into DHA metabolism. Results show that a total of 25 metabolites were successfully identified in infected (30 in healthy) blood, 27 in infected (27 in healthy) plasma, and 15 in infected (22 in healthy) RBC. Results show that hydroxylation, OH-dehydration, and glucuronidation reactions were important in the metabolic pathway in vivo. Significantly, DHA metabolites inside RBC were identified for the first time. 8-Hydroxy (8-OH) DHA, 4α-OH deoxy ART, and 6β-OH deoxy ART were identified in vivo for the first time.Entities:
Keywords: Plasmodium berghei ANKA; UNIFI platform; UPLC-ESI-Q-TOF-MSE; blood; dihydroartemisinin (DHA); metabolite profiling; plasma; red blood cell
Year: 2021 PMID: 33536920 PMCID: PMC7848114 DOI: 10.3389/fphar.2020.614159
Source DB: PubMed Journal: Front Pharmacol ISSN: 1663-9812 Impact factor: 5.810