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PMID: 10927169 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Reactive oxygen species, cell signaling, and cell injury.

Free radical biology & medicine ·Vol. 28 ·No. 10 ·2000-05-15 ·Pages 1456-62

Hensley K, Robinson KA, Gabbita SP, Salsman S, Floyd RA

Abstract

Oxidative stress has traditionally been viewed as a stochastic process of cell damage resulting from aerobic metabolism, and antioxidants have been viewed simply as free radical scavengers. Only recently has it been recognized that reactive oxygen species (ROS) are widely used as second messengers to propagate proinflammatory or growth-stimulatory signals. With this knowledge has come the corollary realization that oxidative stress and chronic inflammation are related, perhaps inseparable phenomena. New pharmacological strategies aimed at supplementing antioxidant defense systems while antagonizing redox-sensitive signal transduction may allow improved clinical management of chronic inflammatory or degenerative conditions, including Alzheimer's disease. Introduction of antioxidant therapies into mainstream medicine is possible and promising, but will require significant advances in basic cell biology, pharmacology, and clinical bioanalysis.

MeSH Terms
Antioxidants/pharmacology Free Radical Scavengers/pharmacology Humans Inflammation/etiology,metabolism,therapy Oxidation-Reduction Oxidative Stress Reactive Oxygen Species/metabolism Second Messenger Systems Signal Transduction/physiology
Chemicals
Antioxidants Free Radical Scavengers Reactive Oxygen Species
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hensley K
Free Radical Biology and Aging Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104, USA. [email protected]
Robinson K A
Gabbita S P
Salsman S
Floyd R A
Article Info
Journal
Free radical biology & medicine
Abbr.
Free Radic Biol Med
ISSN
0891-5849
Published
2000-05-15
Pages
1456-62
Language
English
Region
United States
NLM ID
8709159
Subset
IM
Grants
NINDS NIH HHS · NS35747 · United States
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