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采用 UPLC-Q-TOF-MS 技术鉴定 和 的降血糖活性成分。

Identification of the Hypoglycemic Active Components of Thunb. and Miq. by UPLC-Q-TOF-MS.

机构信息

Hunan Provincial Key Laboratory of the Traditional Chinese Medicine Agricultural Biogenomics, The "Double-First Class" Application Characteristic Discipline of Hunan Province (Pharmaceutical Science), Changsha Medical University, Changsha 410219, China.

Hunan Pharmaceutical Development and investment Group Co., Ltd., Changsha 410219, China.

出版信息

Molecules. 2024 Oct 13;29(20):4848. doi: 10.3390/molecules29204848.

Abstract

Thunb. and are famous Chinese medicines used for hyperglycemia; however, the specific compounds that contributed to the hypoglycemic activity and mechanism are still unknown. In this study, the antidiabetic activity of buds and buds, roots, stems, and leaves extracts was primarily evaluated, and the buds and buds, roots, and stems extracts displayed significant hypoglycemic activity, especially for the buds of . A total of 72 high-level compounds, including 9 iridoid glycosides, 12 flavonoids, 34 organic acids, and 17 saponins, were identified by ultra-performance liquid chromatography/quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS) combined with the fragmentation pathways of standards from different parts of and extracts. Among them, 19 metabolites, including 13 saponins, were reported for the first time from both medicines. Seven high-content compounds identified from buds extract were further evaluated for hypoglycemic activity. The result indicated that neochlorogenic acid, chlorogenic acid, isochlorogenic acid A, isochlorogenic acid B, and isochlorogenic acid C displayed significant antidiabetic activity, especially for isochlorogenic acid A and isochlorogenic acid C, which demonstrated that the five chlorogenic-acid-type compounds were the active ingredients of hypoglycemic activity for and . The potential mechanism of hypoglycemic activity for isochlorogenic acid A and isochlorogenic acid C was inhibiting the intestinal α-glucosidase activity to block the supply of glucose. This study was the first to clarify the hypoglycemic active ingredients and potential mechanism of and , providing new insights for the comprehensive utilization of both resources and the development of hypoglycemic drugs.

摘要

山茱萸和女贞子是用于治疗高血糖的著名中药,但导致其降血糖活性和机制的特定化合物仍不清楚。在本研究中,主要评估了山茱萸芽和女贞子芽、根、茎和叶提取物的抗糖尿病活性,结果表明,山茱萸芽和女贞子芽、根和茎提取物具有显著的降血糖活性,尤其是山茱萸芽。通过超高效液相色谱/四极杆飞行时间质谱(UPLC-Q-TOF-MS)结合不同部位提取物的标准碎片途径,共鉴定出 72 种高水平化合物,包括 9 种环烯醚萜苷、12 种黄酮类、34 种有机酸和 17 种皂苷。其中,有 19 种代谢物,包括 13 种皂苷,首次从这两种药物中报道。进一步评价了从山茱萸芽提取物中鉴定出的 7 种高含量化合物的降血糖活性。结果表明,新绿原酸、绿原酸、异绿原酸 A、异绿原酸 B 和异绿原酸 C 具有显著的抗糖尿病活性,特别是异绿原酸 A 和异绿原酸 C,表明这 5 种绿原酸类化合物是山茱萸和女贞子降血糖活性的有效成分。异绿原酸 A 和异绿原酸 C 的降血糖活性的潜在机制是抑制肠道α-葡萄糖苷酶活性,阻止葡萄糖的供应。本研究首次阐明了山茱萸和女贞子的降血糖活性成分和潜在机制,为两种资源的综合利用和降血糖药物的开发提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d1c/11510595/0c51ede4ce99/molecules-29-04848-g001.jpg

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