Abstract
Cytokine-induced beta cell destruction may be mediated by the generation of nitric oxide and or reactive oxygen species. The relative importance of NO and ROS in cytokine-induced beta cell pathophysiology remains unclear. This investigation evaluates and contrasts the cytoprotective potential of antioxidant gene transfer, versus NF-kappa B inhibition, using a degradation-resistant mutant of I kappa B alpha. NF-kappa B inhibition conferred significant protection against cytokine-induced damage whereas antioxidant overexpression failed to provide protection. Conferred cytoprotection was associated with a suppression of iNOS activation and nitrite accumulation. Our data implicates NOS, as opposed to ROS, as the pivotal player in cytokine-induced beta cell damage. From a therapeutic standpoint, strategies aimed at targeting the activation of iNOS may harbor therapeutic potential in preserving beta cell survival in the face of proinflammatory cytokine exposure. (c) 2006 Elsevier Inc. All rights reserved.
| Original language | English (Ireland) |
|---|---|
| Pages (from-to) | 1240-1248 |
| Number of pages | 9 |
| Journal | Biochemical And Biophysical Research Communications |
| Volume | 342 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 1 Apr 2006 |
Keywords
- Adenovirus
- Antioxidants
- Cytokines
- Cytoprotection
- Gene transfer
- Inducible nitric oxide synthase
- IκBα
- Reactive oxygen species
- β cells
Authors (Note for portal: view the doc link for the full list of authors)
- Authors
- McCabe, C,Samali, A,O'Brien, T