In Vitro Study of the Metabolic Characteristics of Eight Isoquinoline Alkaloids from Natural Plants in Rat Gut Microbiota

• Published in: Molecules (Basel, Switzerland) Vol. 22; no. 6; p. 932
• Main Authors: He, Chi-Yu, Fu, Jie, Shou, Jia-Wen, Zhao, Zhen-Xiong, Ren, Long, Wang, Yan, Jiang, Jian-Dong
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 04.06.2017; MDPI
• Subjects: 14α-demethylase; Alkaloids; Alkaloids - chemistry; Alkaloids - metabolism; Animals; Benzylisoquinolines - chemistry; Binding; Computer applications; Demethylation; Digestive system; Docking; Gastrointestinal Microbiome - physiology; gut microbiota; Hydrophobicity; Intestinal microflora; Intestine; isoquinoline alkaloids; Isoquinolines - chemistry; Isoquinolines - metabolism; LC/MSn-IT-TOF; Male; Metabolism; Metabolites; Metabolomics; Microbiota; Microorganisms; Molecular Docking Simulation; Rats; Rats, Sprague-Dawley; Steric hindrance; Tandem Mass Spectrometry; Tetrandrine; isoquinoline alkaloids; docking; 14α-demethylase; metabolites; LC/MSn-IT-TOF; gut microbiota
• DOI: 10.3390/molecules22060932
• ISSN: 1420-3049

Gut microbiota is populated with an immense number of microorganisms, which can be regulated by dietary components and drugs to markedly affect the nutritional and health status of the host. Eight medicinal isoquinoline alkaloids from natural plants were cultured anaerobically with rat gut microbiota and an LC/MS -IT-TOF technique was used to identify the resulting metabolites. Palmatine, tetrahydropalmatine, dauricine, and tetrandrine containing nitro-hexatomic isoquinoline rings could be easily transformed by the intestinal flora in vitro and a total of nine demethylated metabolites were detected. However, sinomenine, homoharringtonine, harringtonine, and galanthamine, which all contained benzazepine, could not undergo demethylation. Computer-assisted docking was used to analyze the binding between these compounds and sterol 14α-demethylase. The computational results demonstrated that hydrophobic interactions were the main driving force for binding, but the steric hindrance produced by the benzazepine structure resulted in a weak interaction between the hit compounds and the enzyme. This work illustrated that gut microbiota were important in the metabolism of isoquinoline alkaloids.