Antiamyloidogenic Effects of Ellagic Acid on Human Serum Albumin Fibril Formation Induced by Potassium Sorbate and Glucose.
Creators
- 1. Tarbiat Modares University
- 2. University of Tehran
- 3. Iran University of Medical Sciences
- 4. University of Saskatchewan
- 5. Tehran University of Medical Sciences
- 6. Institut national de la recherche agronomique
- 7. INRAE
Description
Oxidative stress has the main role in protein conformational changes and consequent direct involvement in different kind of diseases. Potassium sorbate as a widespread industrial preservative and glucose are two important oxidants that can be involved in oxidative stress. In this study the effect of ellagic acid as a phenolic antioxidant on amyloid fibril formation of human serum albumin upon incubation of potassium sorbate and glucose was studied using thioflavin T assay, surface tension, atomic force microscopy, Amadori product, and carbonyl content assays. The thioflavin T assay and atomic force microscopy micrographs demonstrated the antiamyloidogenic effect of ellagic acid on the human serum albumin fibril formation. This antioxidant also had the repair effect on surface tension of the modified human serum albumin (amyloid intermediates), which was destructed, caused by potassium sorbate and glucose. This mechanism takes place because of potent carbonyl stress suppression effect of ellagic acid, which was strengthening by potassium sorbate in the presence and absence of glucose.
Publication Details
Journal article
Journal:
Journal of molecular recognition : JMR
Publisher:
John Wiley and Sons Ltd
ISSN:
10991352
Volume:
29
Pages:
611-618
Funding
Financial Support
UNESCO Chair on Interdisciplinary Research in Diabetes at University of Tehran
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Iran National Elites Foundation
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Iran National Science Foundation
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Center of Excellence in Biothermodynamics
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International Scientific Studies and Collaboration (CISSC)-Ministry of Science, Research, and Technology
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University of Tehran
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References
Scholarly Citations
MeSH Terms
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Chemical Substances
4 chemical substances identified from Medical Subject Headings (MeSH).