The chemical constituents and hypoglycemic activity of alcoholic extract of sea buckthorn leaves
- VernacularTitle:沙棘叶醇提物的化学成分与降糖活性研究
- Author:
Chang-yu YAN
1
;
Zhao-jun DING
2
;
Xiao-min LI
3
;
Xin-liang MAO
3
;
Zong-sheng YU
3
;
Zhi-fang WANG
3
;
Jian-wen YE
3
;
Kurihara HIROSHI
4
;
Yi-fang LI
5
;
Lei LIANG
5
;
Rong-rong HE
5
Author Information
- Publication Type:Research Article
- Keywords: sea buckthorn leave; chemical composition; hypoglycemic; italic>α-glucosidase; glucose tolerance; streptozocin
- From: Acta Pharmaceutica Sinica 2023;58(2):396-404
- CountryChina
- Language:Chinese
-
Abstract:
The purpose of this research is to identify the chemical constituents of sea buckthorn leaves extract (SBLE) and explore its hypoglycemic biological activity. SBLE was prepared by hot reflux extraction with 65% ethanol, and its chemical composition was analyzed by ultra-high-performance liquid chromatography-photodiode array-mass spectrometry/mass spectrometry (UHPLC-PDA-MS/MS) system. The animal experiments were compliant with ethical principles for animal use and had been approved by the Animal Experiment Ethics Committee of Jinan University. Mice were injected with streptozocin (STZ) to establish a hyperglycemic animal model, and SBLE (1.5 g·kg-1) was administered by gavage for 5 weeks. The fasting blood glucose (FBG) and oral glucose tolerance were detected. Normal mice were given SBLE (1.5 g·kg-1) by intragastric administration for 10 days, and blood was collected from the tail vein to detect the changes in blood glucose within 120 min after sucrose or starch loading. The mucous membrane of the small intestine of mice was taken to detect the activity of
α -glucosidase (AG), and the activity of yeast-derived AG incubated with SBLE was evaluated. The glucose uptake by Caco-2 cells treated with SBLE was detected by fluorescence microscopy and cytometry, and the gene expression of sodium-dependent glucose transporter 1 (SGLT1 ) and glucose transporter 2 (GLUT2 ) in Caco-2 cells were detected by real-time quantitative PCR (qPCR). A total of 18 compounds were identified, mainly including tannins and flavonoids. SBLE reduced FBG and increased oral glucose tolerance in STZ hyperglycemic mice. SBLE effectively inhibited the increase of blood glucose caused by starch intake in normal mice. SBLE exerted good inhibitory activity on yeast-derived AG (IC50 = 16.94 μg·mL-1) and small intestinal mucosa AG with an inhibition rate of 15.48%. SBLE (25-100 μg·mL-1) dose-dependently inhibited glucose uptake by Caco-2 cells, and SBLE significantly reduced the mRNA level ofSGLT1 without changing the expression ofGLUT2 . In conclusion, the UHPLC characteristic fingerprint of SBLE is established with 18 chemical components identified by mass spectrometry, and SBLE exerts hypoglycemic effect by inhibiting the activity of AG and the absorption of glucose by intestinal epithelial cells.
