Citrus sinensis, Persea americana, and Allium sativum Extracts’ Antihyperglycemic Mechanisms: Impact on Glucose Adsorption and Absorption on Yeast Cells and Psoas Muscles, and Inhibition of Digestive Enzymes
Keywords:
Mechanism, Absorption, Yeast cell, Psoas, Enzymes inhibition, Antihyperglycemic PlantsAbstract
Background
Mechanisms by which some plants with antihyperglycemic effects reduce postprandial hyperglycemiaare not fully elucidated. This study was designed to investigate some action mechanisms of extracts from stem bark of Citrus sinensis, seeds of Persea americana and bulbs of Allium sativum including in vitro inhibition of α-amylase and invertase; glucophagic capacity, absorption capacity on yeast cells and psoas tissues.
Methods
Ethanolic (EE) and aqueous (AE) extracts were tested on α-amylase and invertase activities. Glucose remaining in the medium was measured after direct interactions of: Glucose-extracts; Glucose-yeast-extracts and Glucose-psoas-extracts at different doses 0, 5, 7.5, 10 mg/ml.
Results
All extracts inhibited invertase with IC50 varying from 1.92 to 4.81 mg/ml for Allium sativum extracts. α-amylase was inhibited by EE
C. sinensis (IC50=0.063 vs 2.73 mg/ml for arcabose) and not by EE of A. sativum and EE of P. americana. Glucophagic capacity of extracts varied signicanty from 47.55 % of AE P. americana (5 mg/ml) to 100% with C. sinensis (5 mg/ml). All extracts stimulated glucose uptake (p<0.05) from 2.62 % AE C. sinensis (2.5 mg/ml) to 54.74% for EE of Persea americana (10 mg/ml). All extracts enhanced glucose uptake by psoas tissues increasing absorption capacity to up to 38.56 % with A. sativum (10.45% insulin, p<0.05).
Conclusion
Cumulative actions of each plant extract on inhibition of carbohydrates’ digestive enzymes, adsorption of glucose in intestine and blood, stimulation of glucose uptake and insulin action on yeast cells and psoas tissues, contribute to lower hyperglycemia and diabetes related complications. Therefore, extracts from the plants could be good candidates for diabetes therapy.