| Literature DB >> 28629538 |
Chang-Li Sun1, Chang-An Geng2, Xiao-Yan Huang2, Yun-Bao Ma2, Xiao-Hong Zheng1, Tong-Hua Yang1, Xing-Long Chen1, Xiu-Juan Yin1, Xue-Mei Zhang2, Ji-Jun Chen3.
Abstract
5-Hydroxytryptamine 2C (5-HT2C) receptor is one of the major targets of anti-obesity agents, due to its role in regulation of appetite. In the present study, the 70% EtOH extract of the roots of Bupleurum chinense was revealed to have agonistic activity on 5-HT2C receptor, and the subsequent bioassay-guided isolation led to identification of several saikosaponins as the active constituents with 5-HT2C receptor agonistic activity in vitro and anti-obesity activity in vivo. The new compound, 22-oxosaikosaponin d (1), was determined by extensive spectroscopic analyses (HR-ESI-MS, IR, and 1D and 2D NMR). The primary structure-activity relationship study suggested that the intramolecular ether bond between C-13 and C-28 and the number of sugars at C-3 position were closely related to the 5-HT2C receptor agonistic activity. Saikosaponin a (3), the main saponin in B. chinense, showed obviously agonistic activity on 5-HT2C receptor with an EC50 value of 21.08 ± 0.33 μmol·L-1in vitro and could reduce food intake by 39.1% and 69.2%, and weight gain by 13.6% and 16.4%, respectively, at 3.0 and 6.0 mg·kg-1in vivo. This investigation provided valuable information for the potential use of B. chinense as anti-obesity agent.Entities:
Keywords: 5-hydroxytryptamine 2C (5-HT(2C)) receptor; Anti-obesity; Bupleurum chinense; Saikosaponins
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Year: 2017 PMID: 28629538 DOI: 10.1016/S1875-5364(17)30070-5
Source DB: PubMed Journal: Chin J Nat Med ISSN: 1875-5364