| Literature DB >> 27503750 |
Yinghua Ma1, Weiwei Xie1, Tingting Tian1, Yiran Jin2, Huijun Xu1, Kerong Zhang3, Yingfeng Du4.
Abstract
Oridonin (ORI) is an active natural ent-kaurene diterpenoid ingredient with notable anti-cancer and anti-inflammation activities. Currently, a strategy was developed to identify metabolites and to assess the metabolic profiles of ORI in vitro using ultra-high-performance liquid chromatography-Triple/time-of-flight mass spectrometry (UPLC-Triple-TOF-MS/MS). Meanwhile, the metabolism differences of ORI in the liver microsomes of four different species were investigated using a principal component analysis (PCA) based on the metabolite absolute peak area values as the variables. Based on the proposed methods, 27 metabolites were structurally characterized. The results indicate that ORI is universally metabolized in vitro, and the metabolic pathway mainly includes dehydration, hydroxylation, di-hydroxylation, hydrogenation, decarboxylation, and ketone formation. Overall, there are obvious inter-species differences in types and amounts of ORI metabolites in the four species. These results will provide basic data for future pharmacological and toxicological studies of ORI and for other ent-kauranes diterpenoids. Meanwhile, studying the ORI metabolic differences helps to select the proper animal model for further pharmacology and toxicological assessment.Entities:
Keywords: In vitro; Liver microsomes; Metabolites; Oridonin; UPLC-Triple-TOF-MS/MS
Mesh:
Substances:
Year: 2016 PMID: 27503750 DOI: 10.1016/j.ab.2016.08.004
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365