Sun Chang-Li, Geng Chang-An, Huang Xiao-Yan, Ma Yun-Bao, Zheng Xiao-Hong, Yang Tong-Hua, Chen Xing-Long, Yin Xiu-Juan, Zhang Xue-Mei, Chen Ji-Jun
State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China; University of Chinese Academy of Sciences, Beijing 100049, China.
State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China.
Chin J Nat Med. 2017 Jun;15(6):467-473. doi: 10.1016/S1875-5364(17)30070-5.
5-Hydroxytryptamine 2C (5-HT) 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-HT receptor, and the subsequent bioassay-guided isolation led to identification of several saikosaponins as the active constituents with 5-HT 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-HT receptor agonistic activity. Saikosaponin a (3), the main saponin in B. chinense, showed obviously agonistic activity on 5-HT receptor with an EC value of 21.08 ± 0.33 μmol·Lin 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·kgin vivo. This investigation provided valuable information for the potential use of B. chinense as anti-obesity agent.
5-羟色胺2C(5-HT)受体是抗肥胖药物的主要靶点之一,因为它在食欲调节中起作用。在本研究中,柴胡根的70%乙醇提取物被发现对5-HT受体具有激动活性,随后通过生物测定引导的分离鉴定出几种柴胡皂苷为具有体外5-HT受体激动活性和体内抗肥胖活性的活性成分。新化合物22-氧代柴胡皂苷d(1)通过广泛的光谱分析(高分辨电喷雾电离质谱、红外光谱以及一维和二维核磁共振谱)得以确定。初步的构效关系研究表明,C-13和C-28之间的分子内醚键以及C-3位糖的数量与5-HT受体激动活性密切相关。柴胡中的主要皂苷柴胡皂苷a(3)在体外对5-HT受体表现出明显的激动活性,其半数有效浓度(EC)值为21.08±0.33μmol·L,在体内3.0和6.0mg·kg剂量下分别可使食物摄入量减少39.1%和69.2%,体重增加减少13.6%和16.4%。本研究为柴胡作为抗肥胖药物的潜在应用提供了有价值的信息。