Lutein decreases oxidative stress and inflammation in liver and eyes of guinea pigs fed a hypercholesterolemic diet.
- Author:
Jung Eun KIM
1
;
Richard M CLARK
;
Youngki PARK
;
Jiyoung LEE
;
Maria Luz FERNANDEZ
Author Information
- Publication Type:Original Article
- Keywords: Lutein; lipid peroxidation; inflammation; guinea pigs
- MeSH: Animals; Cholesterol; Cytokines; Diet; DNA; Eye; Guinea; Guinea Pigs; Inflammation; Lipid Peroxidation; Liver; Lutein; Malondialdehyde; NF-kappa B; Oxidative Stress; Plasma; Tumor Necrosis Factor-alpha
- From:Nutrition Research and Practice 2012;6(2):113-119
- CountryRepublic of Korea
- Language:English
- Abstract: Guinea pigs were fed a hypercholesterolemic diet (0.25 g/100 g cholesterol) and randomly allocated either to a Control group (n = 9) or to a Lutein (0.1 g/100 g) group (n = 10) for 12 weeks to evaluate oxidative stress and inflammation in both liver and eyes. Malondialdehyde (MDA) concentrations and inflammatory cytokines were measured as well as hepatic nuclear factor-kappaB (NF-kappaB) binding. Lutein concentrations were greater in eyes (P < 0.01) and liver (P < 0.001) in the Lutein group. All guinea pigs had high concentrations of hepatic cholesterol as well as high plasma ALT and AST levels indicative of liver injury. However, the Lutein group had 43% lower hepatic free cholesterol than the Controls (P < 0.05). Hepatic MDA and MDA in the eye were lower in the Lutein compared to the Control group (P < 0.05). Hepatic tumor necrosis factor-alpha was 32% lower in the Lutein group (P < 0.05). Lastly, the Lutein group presented lower NF-kappaB DNA binding activity than the Control group (P < 0.001). These results suggest that in the presence of high cholesterol, lutein exerts both antioxidant and anti-inflammatory effects, which can be explained by attenuated NF-kappaB DNA binding activity. Furthermore, results also suggest that lutein accumulates in the eyes of guinea pigs to protect against oxidative stress.
