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DOI 10.1002/cbdv.202401765

Медицинская библиотека · Chemistry & biodiversity · 2024

Bioactivity-Based Analysis and Chemical Characterization of Hypoglycemic Components from Helicteres angustifolia L.

Tian Xiaoli, Zhao Yu, Zhang Ayu, Zhang Dongmei, Ren Jiayi, Bai Yidan, Yang Xi, Jantrawut Pensak, Cheng Delin, Zhang Jie

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Аннотация

Helicteres angustifolia L. (H. angustifolia), a well-known traditional Chinese medicine, has been demonstrated to have hypoglycemic activity. We found that the EtOAc extract of H. angustifolia (HAEF) showed stronger α-glucosidase inhibitory activity than that of positive control. Furthermore, the hypoglycemic activity of HAEF was evaluated in streptozotocin (STZ)-induced type 2 diabetes mellitus (T2DM) rats. The results demonstrated that HAEF reduced the drinking quantity, feeding quantity, and controlled weight loss in diabetic rats. Besides, the fasting blood glucose (FBG), viscera index, and the area under time-blood glucose curve (AUC) were significantly decreased, and the oral glucose tolerance was also improved after 5 weeks. Then, the high-performance liquid chromatography with quadrupole time of flight tandem mass spectrometry (HPLC-Q-TOF-MS/MS) method was performed for qualitative analysis of the chemical constituents in HAEF. Twenty-one compounds were identified from in HAEF. Four compounds were further isolated from HAEF and subjected to α-glucosidase inhibition experiments. At the end, molecular docking was empolyed simulate the interaction of three compounds with α-glucosidase. This is the first report on major hypoglycaemic components has been identified in the roots of H. angustifolia. These findings provide a material basis for the use of H. angustifolia in the treatment of diabetes.

Для цитирования: Tian Xiaoli, Zhao Yu, Zhang Ayu, Zhang Dongmei, Ren Jiayi, Bai Yidan, Yang Xi, Jantrawut Pensak, Cheng Delin, Zhang Jie. Bioactivity-Based Analysis and Chemical Characterization of Hypoglycemic Components from Helicteres angustifolia L.. Chemistry & biodiversity. 2024. DOI: 10.1002/cbdv.202401765.

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