Stereoselective in vitro metabolism of rhynchophylline and isorhynchophylline epimers of Uncaria rhynchophylla in rat liver microsomes

Abstract

1. The objective was to investigate the underlying mechanism of the stereoselectivity in the metabolism of rhynchophylline (RIN) and isorhynchophylline (IRN) epimers in rat liver microsomes (RLM).

2. After incubation, eight metabolites of RIN (M1-5) and IRN (M6-8) reacted at A- and C-ring were identified using LC-Q-TOF/MS. Metabolic pathways included oxidation, hydroxylation, N-oxidation and dehydrogenation. In addition, hydroxylation at A-ring was the major metabolic pathway for RIN whereas the oxidation at C-ring was the major one for IRN.

3. Enzyme kinetics showed that the intrinsic clearance (CL_int) for IRN elimination was 1.9-fold higher than RIN and the degradation half-life (T_1/2) of RIN was 4.7-fold higher than that of IRN, indicating IRN was more favorable to be metabolized than RIN in RLM.

4. Data from chemical inhibition study demonstrated CYP3A was the predominant isoform involved in the metabolic elimination of both epimers, as well as the formation of M1-8.

5. In conclusion, data revealed that due to the spatial configurations at C-7 position, RIN and IRN epimers possessed different hepatic metabolic pathways and elimination rates which were mainly mediated by CYP3A.

Keywords:

• Isorhynchophylline
• rat liver microsomes
• rhynchophylline
• stereoselective metabolism
• uncaria rhynchophylla

Acknowledgements

This project was supported by the National Natural Science Foundation of China (Grant No. 81573557 and 81373956).

Declaration of interest

No potential conflict of interest was reported by the authors.

Supplementary material available online