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α-Glucosidase inhibition by green, white and oolong teas: in vitro activity and computational studies
被引:0
|作者:
Esposito, Fabio
[1
]
Pala, Nicolino
[1
]
Carcelli, Mauro
[2
]
Boateng, Samuel T.
[3
]
D'Aquila, Paolo S.
[4
]
Mariani, Alberto
[5
]
Satta, Sandro
[6
]
Chamcheu, Jean Christopher
[3
]
Sechi, Mario
[1
,9
]
Sanna, Vanna
[7
,8
]
机构:
[1] Univ Sassari, Dept Med Surg & Pharm, Lab Drug Design & Nanomed, Sassari, Italy
[2] Univ Parma, Dept Chem Life Sci & Environm Sustainabil, Parma, Italy
[3] Univ Louisiana, Coll Pharm, Sch Basic Pharmaceut & Toxicol Sci, Monroe, LA USA
[4] Univ Sassari, Dept Biomed Sci, Sassari, Italy
[5] Univ Sassari, Dept Chem Phys Math & Nat Sci, Sassari, Italy
[6] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA USA
[7] Nanomater Srl, Alghero, Italy
[8] Porto Conte Ric, Nanomater Srl, SP 55 Porto Conte Capo Caccia,Km 8-400 Loc Tramari, I-07041 Alghero, Italy
[9] Univ Sassari, Dept Med Surg & Pharm, Via Vienna 2,Adm Viale S Pietro 43, I-07100 Sassari, Italy
关键词:
& alpha;
-glucosidase inhibition;
tea;
polyphenols;
catechins;
molecular docking;
ALPHA-GLUCOSIDASE;
ANTIOXIDANT ACTIVITIES;
NATURAL-PRODUCTS;
PHENOLIC CONTENT;
EXTRACTS;
CATECHINS;
AMYLASE;
HYPERGLYCEMIA;
ENZYMES;
WINE;
D O I:
10.1080/14756366.2023.2236802
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Natural a-glucosidase inhibitors from plant-based foods such as catechins offer an attractive strategy for their potential anti-diabetic effects. In this study, infusions of three different tea types (green, white, and oolong) were investigated for their total phenolic (TPC) and catechins (EGCG, ECG, EGC, and EC) content, and for their a-glucosidase inhibitory activities. We observed that the level of TPC in white tea was significantly higher compared to oolong and green tea, which suggests higher content of EGCG and ECG catechins in fresh young leaves. Our findings showed that the higher content of such catechins in the infusion of white tea well correlated with a strong inhibition of a-glucosidase, and such inhibition was demonstrated to be more effective than the FDA-approved drug acarbose. Then, we computationally explored the molecular requirements for enzyme inhibition, especially for the most active catechins EGCG and ECG, as well as their disposition/stability within the active site.
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页数:10
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