Abstract
Aldose reductase, although identified initially as a glucose-reducing enzyme via polyol pathway, is believed to be an important component of antioxidant defense system as well as a key mediator of oxidative stress-induced molecular signaling. The dual role played by AR has made it a very important enzyme for the regulation of not only the cellular redox state by detoxifying the reactive lipid-aldehydes generated by lipid peroxidation which is crucial in the cellular homeostasis, but also in the regulation of molecular signaling cascade that may regulate oxidative stress-induced cytotoxic events. Search for the new molecular targets to restrain the oxidative stress-induced inflammation has resulted in the identification of AR as an unanticipated mediator of oxidative stress-induced signaling. Although, in last one decade or so AR has been implicated in various inflammation-related disease conditions ranging from diabetes, sepsis, cancer, cardiovascular and airway inflammation, however, a critical evaluation of the clinical efficacy of AR inhibitors awaits a better understanding of the role of AR in regulating inflammation, especially in ocular inflammation.
Original language | English (US) |
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Pages (from-to) | 540-549 |
Number of pages | 10 |
Journal | Current molecular medicine |
Volume | 10 |
Issue number | 6 |
DOIs | |
State | Published - 2010 |
Externally published | Yes |
Keywords
- Aldose reductase
- Autoimmunity
- GS-DHN
- Infection
- Inflammation
- NF-κB
- Uveitis
ASJC Scopus subject areas
- Biochemistry
- Molecular Medicine
- Molecular Biology