共 97 条
Polyphenolic inhibition of enterocytic starch digestion enzymes and glucose transporters for managing type 2 diabetes may be reduced in food systems
被引:49
作者:
Ayua, Emmanuel O.
[1
]
Nkhata, Smith G.
[2
,3
]
Namaumbo, Sydney J.
[2
,3
]
Kamau, Elijah Heka
[1
]
Ngoma, Theresa N.
[2
,3
]
Aduol, Kevin Omondi
[1
]
机构:
[1] Univ Eldoret, Dept Food Sci & Nutr, POB 1125-30100, Eldoret, Kenya
[2] Lilongwe Univ Agr & Nat Resources, Nat Resources Coll, Fac Life Sci & Nat Resources, Agrofood Proc Technol, POB 143, Lilongwe, Malawi
[3] Lilongwe Univ Agr & Nat Resources, Nat Resources Coll, Fac Life Sci & Nat Resources, Food Technol, POB 143, Lilongwe, Malawi
来源:
关键词:
Polyphenols;
Type II diabetes;
Enzyme inhibition;
Starch digestion;
Glucose transporter;
DIFFERENT BOTANICAL SOURCES;
PANCREATIC ALPHA-AMYLASE;
IN-VITRO;
PHENOLIC-COMPOUNDS;
TEA POLYPHENOLS;
ANTIOXIDANT CAPACITY;
DIETARY POLYPHENOLS;
QUALITY ATTRIBUTES;
GLYCEMIC RESPONSE;
GREEN COFFEE;
D O I:
10.1016/j.heliyon.2021.e06245
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
With the current global surge in diabetes cases, there is a growing interest in slowing and managing diabetes and its effects. While there are medications that can be used, they have adverse side effects such as hypoglycemia and weight gain. To overcome these problems, bioactive compounds commonly found in fruits, vegetables and cereal grains are used to slow starch digestion and transport of simple sugars across the intestinal epithelia thereby reducing plasma blood glucose spike. These effects are achieved through inhibition of amylases, glucosidases and glucose transporters present in the gastrointestinal tract and brush boarder membrane. The extent of inhibition by polyphenols is dependent on molecular structure, doses and food matrix. Glycemic lowering effect of polyphenols have been demonstrated both in in vivo and in vitro studies. However, when these compounds are incorporated in food systems, they can interact with other polymers in the food matrix leading to lesser inhibition of digestion and/or glucose transporters compared to isolated or pure compounds as often witnessed in most in vitro studies.
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