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Thiamine reverses hyperglycemia-induced dysfunction in cultured endothelial cells
E Ascher1, P V Gade, A Hingorani
1Division of Vascular Surgery, Maimonides Medical Center, Brooklyn, NY 11219, USA.
Surgery
|October 31, 2001
Summary
Thiamine supplementation improved endothelial cell migration and reduced von Willebrand factor secretion under high glucose conditions. This suggests thiamine may help prevent vascular complications associated with diabetes.
Area of Science:
- Biochemistry
- Cell Biology
- Endocrinology
Background:
- High glucose levels impair endothelial cell migration and increase von Willebrand factor (vWF) secretion, indicating endothelial cell damage.
- Thiamine, a crucial coenzyme in glucose metabolism, is investigated for its potential to counteract these hyperglycemic effects.
Purpose of the Study:
- To determine if thiamine improves endothelial cell migration under hyperglycemia.
- To assess if thiamine reduces von Willebrand factor secretion in high glucose conditions.
Main Methods:
- Bovine aortic endothelial cells (BAECs) were cultured in normal (5.5 mmol/L) and high glucose (13.8 and 27.7 mmol/L) with or without thiamine (200 micromol/L).
- Endothelial cell migration was quantified using a scratch-wound assay.
- vWF secretion was measured via enzyme-linked immunosorbent assay (ELISA).
Main Results:
- Hyperglycemia significantly reduced BAEC migration and increased vWF secretion (P <.001).
- Thiamine treatment counteracted the inhibitory effects of high glucose on cell migration.
- Thiamine restored migration distance to 6.94 cm and wound area coverage to 47.7 cm², compared to 4.0 cm and reduced area under hyperglycemia (P <.001).
Conclusions:
- Hyperglycemia activates endothelial cells, increasing vWF secretion and impairing migration.
- Thiamine mitigates hyperglycemia-induced endothelial cell dysfunction.
- Thiamine may prevent vascular complications of diabetes by improving glucose metabolism and reducing endothelial cell damage.