beta-Carotene inhibits inflammatory gene expression in lipopolysaccharide-stimulated macro phages by suppressing redox-based NF-kappaB activation.
- Author:
Se Kyung BAI
1
;
Seon Jin LEE
;
Hee Jun NA
;
Kwon Soo HA
;
Jeong A HAN
;
Hansoo LEE
;
Young Guen KWON
;
Cha Kwon CHUNG
;
Young Myeong KIM
Author Information
1. Vascular System Research Center, Department of Molecular and Cellular Biochemistry, School of Medicine, Kangwon National University, Chunchon, Kangwon-do 200-701, Korea. ymkim@kangwon.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
beta-carotene;
cytokines;
macrophages;
nitric oxide;
NF-kappaB;
reactive oxygen species.
- MeSH:
Animals;
Anti-Inflammatory Agents/*pharmacology;
Antioxidants/*pharmacology;
Dinoprostone/metabolism;
Female;
Gene Expression/drug effects;
Inflammation Mediators/*metabolism;
Lipopolysaccharides/pharmacology;
Macrophages/*drug effects;
Mice;
Mice, Inbred BALB C;
NF-kappa B/*antagonists & inhibitors/genetics/metabolism;
Nitric Oxide/metabolism;
Oxidation-Reduction;
Research Support, Non-U.S. Gov't;
beta Carotene/*pharmacology
- From:Experimental & Molecular Medicine
2005;37(4):323-334
- CountryRepublic of Korea
- Language:English
-
Abstract:
beta-Carotene has shown antioxidant and antiinflammatory activities; however, its molecular mechanism has not been clearly defined. We examined in vitro and in vivo regulatory function of beta-carotene on the production of nitric oxide (NO) and PGE2 as well as expression of inducible NO synthase (iNOS), cyclooxygenase-2, TNF-alpha, and IL-1beta. beta-Carotene inhibited the expression and production of these inflammatory mediators in both LPSstimulated RAW264.7 cells and primary macrophages in a dose-dependent fashion as well as in LPS-administrated mice. Furthermore, this compound suppressed NF-kappaB activation and iNOS promoter activity in RAW264.7 cells stimulated with LPS. beta-Carotene blocked nuclear translocation of NF-kappaB p65 subunit, which correlated with its inhibitory effect on IkappaBalpha phosphorylation and degradation. This compound directly blocked the intracellular accumulation of reactive oxygen species in RAW264.7 cells stimulated with LPS as both the NADPH oxidase inhibitor diphenylene iodonium and antioxidant pyrrolidine dithiocarbamate did. The inhibition of NADPH oxidase also inhibited NO production, iNOS expression, and iNOS promoter activity. These results suggest that beta-carotene possesses anti-inflammatory activity by functioning as a potential inhibitor for redox-based NF-kappaB activation, probably due to its antioxidant activity.
