Xie Guozhen, Zhou Rongrong, Huang Lili, Zhang Shuihan, Tan Zhoujin
School of Pharmacy, Hunan University of Chinese Medicine, Changsha, China.
The Affiliated Hospital of Hunan Academy of Chinese Medicine, Changsha, China.
Front Chem. 2022 Jun 20;10:907886. doi: 10.3389/fchem.2022.907886. eCollection 2022.
The gut microbiota (GM) is involved in the metabolism of glycosides and is beneficial for enhancing their bioactivity. However, the metabolism of multi-glycosides by the GM under normal and pathological conditions is unclear. In this study, the total glycosides (TG) of the traditional Chinese medicine (TCM) formula Qiwei Baizhu Powder (QWBZP) were extracted to represent a multi-glycoside system. Ultra-high-performance liquid chromatography quadrupole time-of-flight tandem mass spectrometry (UHPLC-Q-TOF-MS/MS) was used to rapidly identify the components and metabolites of QWBZP-TG. The metabolic profiles of QWBZP-TG in the GM of normal and diarrheal mice were also compared. A total of 68 compounds and seven metabolites were identified in the QWBZP-TG and metabolic samples, respectively. Deglycosylation was the main metabolic pathway of multi-glycoside metabolism. Liquiritin apioside, isoliquiritin apioside, liquiritin, protopanaxadiol (PPD)-type, and oleanane (OLE)-type ginsenosides were relatively easy to metabolize by the GM. At first, the deglycosylation capability of the GM of normal mice was superior to that of diarrheal mice, but the deglycosylation capability of diarrheal mice gradually recovered and produced abundant deglycosylation metabolites. In conclusion, deglycosylation metabolites may be the bioactive components of QWBZP. Glycoside-bacteria interaction may be a key mechanism for QWBZP to therapy diarrhea.
肠道微生物群(GM)参与糖苷代谢,有助于增强其生物活性。然而,GM在正常和病理条件下对多糖苷的代谢尚不清楚。在本研究中,提取了中药七味白术散(QWBZP)的总糖苷(TG)以代表一个多糖苷系统。采用超高效液相色谱四极杆飞行时间串联质谱(UHPLC-Q-TOF-MS/MS)快速鉴定QWBZP-TG的成分和代谢产物。还比较了QWBZP-TG在正常小鼠和腹泻小鼠GM中的代谢谱。在QWBZP-TG和代谢样品中分别鉴定出68种化合物和7种代谢产物。去糖基化是多糖苷代谢的主要途径。甘草苷芹菜糖苷、异甘草苷芹菜糖苷、甘草苷、原人参二醇(PPD)型和齐墩果烷(OLE)型人参皂苷相对容易被GM代谢。起初,正常小鼠GM的去糖基化能力优于腹泻小鼠,但腹泻小鼠的去糖基化能力逐渐恢复并产生大量去糖基化代谢产物。总之,去糖基化代谢产物可能是QWBZP的生物活性成分。糖苷-细菌相互作用可能是QWBZP治疗腹泻的关键机制。