Inhibition of α-glucosidase by vitamin D3 and the effect of vitamins B1 and B2. Issue 2 (8th January 2016)
- Record Type:
- Journal Article
- Title:
- Inhibition of α-glucosidase by vitamin D3 and the effect of vitamins B1 and B2. Issue 2 (8th January 2016)
- Main Title:
- Inhibition of α-glucosidase by vitamin D3 and the effect of vitamins B1 and B2
- Authors:
- Peng, Xi
Zhang, Guowen
Zeng, Li - Abstract:
- Abstract : Vitamin D3 occupies the active site of α-glucosidase to avoid the entry of the substrate and causes the inhibition of α-glucosidase. Abstract : α-Glucosidase is a vital enzyme in carbohydrate metabolism. Over-expression of this enzyme is correlated with hyperglycemia. The inhibitory effect of vitamin D3 on α-glucosidase as well as its mechanism of action was investigated in this work. The results showed that vitamin D3 exhibited stronger inhibition on α-glucosidase than acarbose with the IC50 value of 1.28 × 10 −4 mol L −1, and the inhibition was a mixed-type mechanism through a multiphase kinetic process. The inhibition constant was determined to be (5.66 ± 0.03) × 10 −5 mol L −1 . Vitamin D3 interacted with α-glucosidase by hydrophobic interactions, and molecular docking further verified that the inhibitor inserted into the active site pocket of α-glucosidase and interacted with the amino residues, which induced the rearrangement and conformational changes of α-glucosidase, and might move to cover the active pocket, hindering the binding of the substrate leading to the inhibition of the enzyme activity. Moreover, it was found that vitamin D3 combined with vitamin B1 or vitamin B2 exhibited significant synergistic effects on inhibition of α-glucosidase. This study has provided new insights into the role of vitamin D3 in inhibiting α-glucosidase catalysis and offered useful information on the dietary recommendation of vitamin D3 for the treatment of type 2Abstract : Vitamin D3 occupies the active site of α-glucosidase to avoid the entry of the substrate and causes the inhibition of α-glucosidase. Abstract : α-Glucosidase is a vital enzyme in carbohydrate metabolism. Over-expression of this enzyme is correlated with hyperglycemia. The inhibitory effect of vitamin D3 on α-glucosidase as well as its mechanism of action was investigated in this work. The results showed that vitamin D3 exhibited stronger inhibition on α-glucosidase than acarbose with the IC50 value of 1.28 × 10 −4 mol L −1, and the inhibition was a mixed-type mechanism through a multiphase kinetic process. The inhibition constant was determined to be (5.66 ± 0.03) × 10 −5 mol L −1 . Vitamin D3 interacted with α-glucosidase by hydrophobic interactions, and molecular docking further verified that the inhibitor inserted into the active site pocket of α-glucosidase and interacted with the amino residues, which induced the rearrangement and conformational changes of α-glucosidase, and might move to cover the active pocket, hindering the binding of the substrate leading to the inhibition of the enzyme activity. Moreover, it was found that vitamin D3 combined with vitamin B1 or vitamin B2 exhibited significant synergistic effects on inhibition of α-glucosidase. This study has provided new insights into the role of vitamin D3 in inhibiting α-glucosidase catalysis and offered useful information on the dietary recommendation of vitamin D3 for the treatment of type 2 diabetes. … (more)
- Is Part Of:
- Food & function. Volume 7:Issue 2(2016)
- Journal:
- Food & function
- Issue:
- Volume 7:Issue 2(2016)
- Issue Display:
- Volume 7, Issue 2 (2016)
- Year:
- 2016
- Volume:
- 7
- Issue:
- 2
- Issue Sort Value:
- 2016-0007-0002-0000
- Page Start:
- 982
- Page End:
- 991
- Publication Date:
- 2016-01-08
- Subjects:
- Food -- Analysis -- Periodicals
Food -- Composition -- Periodicals
Nutrition -- Periodicals
664.07 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/FO ↗
http://pubs.rsc.org/en/journals/journal/fo ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5fo00992h ↗
- Languages:
- English
- ISSNs:
- 2042-6496
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3977.038457
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 468.xml