State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, 132# Lanhei Road, Kunming 650201, Yunnan, PR China; Yunnan Key Laboratory of Natural Medicinal Chemistry, Kunming 650201, PR China.
State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, 132# Lanhei Road, Kunming 650201, Yunnan, PR China; Yunnan Key Laboratory of Natural Medicinal Chemistry, Kunming 650201, PR China; University of Chinese Academy of Sciences, Beijing 100049, PR China.
J Ethnopharmacol. 2019 Mar 25;232:39-46. doi: 10.1016/j.jep.2018.12.013. Epub 2018 Dec 10.
Traditional Chinese medicines (TCMs) are fascinating sources for natural drug candidates. Uncaria rhynchophylla (Gouteng) is a famous TCM used for alleviating central nervous system (CNS) disorders, while its antidepressant constituents are still disputed.
The present study was designed to assess the antidepressant property of U. rhynchophylla and characterize the active constituents targeting melatonin receptors which are closely related to CNS diseases.
The total extract and each fraction of U. rhynchophylla were extensively assessed for their agonistic activity on melatonin receptors in vitro. The following bioassay-guided fractionation yielded the active constituents, whose activity was confirmed by dose-dependent bioassay and antagonistic experiment on HEK293 cells. Their antidepressant effects were evaluated on forced swimming test (FST), tail suspension test (TST) and open-field test (OFT) mice models in vivo. Their metabolic profiles in mice plasma were analyzed by LCMS-IT-TOF.
The stems and hooks of U. rhynchophylla were revealed with agonistic activity on melatonin receptors (MT and MT). Under the guidance of bioassay, two flavanols, catechin and epicatechin were obtained and showed obviously activity agitating MT (EC = 25.8 and 156.1 μM) and MT (EC = 47.3 and 208.8 μM) receptors. The agonistic activity of catechin on melatonin receptors can be antagonized by luzindole at the concentrations of 1.57-100 μM. Catechin could significantly reduce the immobility time in both FST and TST mice models at doses of 80 and 40 mg/kg, without obvious effect on locomotor activity in OFT mice model. Five phase II (M1-M5) and one phase I (M6) metabolites of catechin were detected in mice plasma after intragastric (i.g.) administration.
Catechin is a potent antidepressant candidate from U. rhynchophylla by targeting melatonin receptors. The main metabolic pathways of catechin in mice plasma are glucuronidation (M3) and methylated glucuronidation (M4 and M5). This study provides valuable information for understanding the antidepressant potency of Gouteng and its active constituents.
传统中药(TCM)是天然药物候选物的迷人来源。钩藤(Gouteng)是一种著名的中药,用于缓解中枢神经系统(CNS)疾病,但其抗抑郁成分仍存在争议。
本研究旨在评估钩藤的抗抑郁特性,并表征针对与 CNS 疾病密切相关的褪黑素受体的活性成分。
广泛评估钩藤的总提取物和各馏分在体外对褪黑素受体的激动活性。以下基于生物测定的分步分离得到了活性成分,其活性通过剂量依赖性生物测定和对 HEK293 细胞的拮抗实验得到证实。在体内通过强迫游泳试验(FST)、悬尾试验(TST)和旷场试验(OFT)小鼠模型评估它们的抗抑郁作用。通过 LCMS-IT-TOF 分析小鼠血浆中的代谢谱。
钩藤的茎和钩被发现具有对褪黑素受体(MT 和 MT)的激动活性。在生物测定的指导下,获得了两种黄烷醇,儿茶素和表儿茶素,它们对 MT(EC=25.8 和 156.1μM)和 MT(EC=47.3 和 208.8μM)受体表现出明显的活性。儿茶素对褪黑素受体的激动活性可被 1.57-100μM 的 luzindole 拮抗。儿茶素在 80 和 40mg/kg 剂量下可显著减少 FST 和 TST 小鼠模型中的不动时间,而在 OFT 小鼠模型中对运动活性无明显影响。在灌胃(i.g.)给予后,在小鼠血浆中检测到儿茶素的五个 II 期(M1-M5)和一个 I 期(M6)代谢物。
儿茶素是一种通过靶向褪黑素受体的钩藤潜在抗抑郁候选物。儿茶素在小鼠血浆中的主要代谢途径是葡萄糖醛酸化(M3)和甲基化葡萄糖醛酸化(M4 和 M5)。本研究为了解钩藤及其活性成分的抗抑郁作用提供了有价值的信息。