SI, sucrase-isomaltase, 6476

N. diseases: 117; N. variants: 15
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE In this study, the inhibitory effects of loquat leaf extract (LLE) on pancreatic α-amylase and α-glucosidase, and the preventative effects of LLE on hyperlipidemia and hyperglycemia in rats induced by a high fat and fructose diet have been evaluated. 28124052 2017
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE Inhibition of α-amylase and α-glucosidase enzymes using natural products (especially polyphenols) is a novel oral policy to regulate carbohydrate metabolism and hyperglycemia. 28470323 2017
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE This study also shows that n-hexane, chloroform, ethyl acetate and aqueous extracts of A. bracteosa root possess α-glucosidase inhibitory activities and therefore it may be used as hypoglycemic agents in the management of postprandial hyperglycemia. 28294059 2017
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 AlteredExpression disease BEFREE Our studies demonstrate that the dietary polyphenols resveratrol and piceatannol lower postprandial hyperglycemia and indicate that inhibition of intestinal α-glucosidase activity may be a potential mechanism contributing to their antidiabetic property. 28570943 2017
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 AlteredExpression disease BEFREE Taken together, these results suggest that 2 has dual inhibitory activity against α-glucosidase and α-amylase and alleviates diabetic hyperglycemia and hyperlipidemia, making it a potential functional food ingredient and drug candidate for management of type 2 diabetes. 28132506 2017
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE Inhibition of α-amylase and α-glucosidase enzymes retards the rate of carbohydrate digestion, thereby provides an alternative and a less evasive strategy of reducing postprandial hyperglycaemia in diabetic patients.The AgNps derived from <i>O. sanctum</i> and <i>O. basilicum</i>, respectively displayed an inhibitory effect at 89.31 ± 5.32%, and 79.74 ± 9.51%, respectively, against <i>Bacillus stearothermophilus</i> α-glucosidase enzyme model, indicating an enhanced biocatalytic potential compared to their respective crude extracts and the control. 28855825 2017
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 GeneticVariation disease BEFREE This study investigated the inhibitory effects of 2,7″-phloroglucinol-6,6'-bieckol on activities of α-glucosidase and α-amylase as well as its alleviating effect on postprandial hyperglycaemia in streptozotocin-induced diabetic mice. 28219252 2017
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE These results suggest that both products assayed could be effective in the management of postprandial hyperglycemia through inhibition of α-glucosidase in the small intestine. 28161878 2017
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE α-Glucosidase inhibitors (AGIs) have been reported for their clinical potential against postprandial hyperglycemia, which is responsible for the risks associated with diabetes mellitus 2 and cardiovascular diseases (CVDs). 28745232 2017
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 AlteredExpression disease BEFREE Our results suggest that PB2 is useful for protection against hyperglycemia through inhibiting the activity of α-glucosidase. 30188554 2018
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE Efficacy of Alpha Glucosidase Inhibitor from Marine Actinobacterium in the Control of Postprandial Hyperglycaemia in Streptozotocin (STZ) Induced Diabetic Male Albino Wister Rats. 29755552 2018
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE The α-amylase and α-glucosidase inhibitory activities of UIOPS-1 were significantly increased after digestion indicating a good control of postprandial hyperglycemia (P<0.001). 29389616 2018
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE The present study provides new insight into the potential application of Lu'an GuaPian green tea as a functional food ingredient to regulate postprandial hyperglycemia through inhibition of α-glucosidase/α-amylase by FGs, particularly the mono- and di- glycosides of kaempferol. 29989631 2018
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 AlteredExpression disease BEFREE UIOPC also showed significant inhibitory capacity on α-amylase and α-glucosidase than UIOPS (P < 0.05), suggesting a good regulation of the postprandial hyperglycemia. 29689356 2018
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE The inhibition of α-glucosidase and α-amylase is a clinical strategy for the treatment of type II diabetes, and herbal medicines have been reported to credibly alleviate hyperglycemia. 30189596 2018
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE This study has identified two novel and active α-glucosidase inhibitory peptides that could resist GIT digestion and therefore, have the potential to retard postprandial hyperglycemia in diabetic patients. 30096627 2018
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 AlteredExpression disease BEFREE The inhibition of α-glucosidase, a key carbohydrate hydrolyzing enzyme, could serve as one of the effective methodology in both preventing and treating diabetes through controlling the postprandial glucose levels and suppressing postprandial hyperglycemia. 29421697 2018
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE Scopoletin inhibits α-glucosidase in vitro and alleviates postprandial hyperglycemia in mice with diabetes. 30031794 2018
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE Inhibition of α-glucosidase is an effective strategy for controlling the post-prandial hyperglycemia in diabetic patients. 30118991 2018
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE Inhibition of α-glucosidase is an effective strategy for controlling post-prandial hyperglycemia in diabetic patients. 29223804 2018
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE α-glucosidase is involved in the hydrolyses of disaccharide into monosaccharides and results in hyperglycemia. 29885400 2018
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 Biomarker disease BEFREE The study provides informative data on the potential α-glucosidase inhibitors identified in <i>C. nutans</i> leaves, indicating the plant's therapeutic effect to manage hyperglycemia. 30235889 2018
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 AlteredExpression disease BEFREE The inhibition of α-glucosidase activity is a prospective approach to prevent postprandial hyperglycemia. 31765755 2019
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 AlteredExpression disease BEFREE α-glucosidase inhibitors compete with the α-glucosidase enzyme activity, which helps to reduce the conversion of carbohydrates into glucose and thereby control the postprandial hyperglycemia incidence. 31808390 2019
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
0.100 AlteredExpression disease BEFREE Functional foods that inhibit α-amylase and α-glucosidase activity are effective for regulating the blood glucose level and preventing hyperglycemia. 31613007 2019