Desalinated underground seawater of Jeju Island (Korea) improves lipid metabolism in mice fed diets containing high fat and increases antioxidant potential in t-BHP treated HepG2 cells.
- Author:
Jung Ran NOH
1
;
Gil Tae GANG
;
Yong Hoon KIM
;
Keum Jin YANG
;
Chul Ho LEE
;
O Su NA
;
Gi Ju KIM
;
Won Keun OH
;
Young Don LEE
Author Information
- Publication Type:In Vitro ; Original Article
- Keywords: Underground seawater; lipid metabolism; hepatic lipid; antioxidant effect
- MeSH: Animals; Antioxidants; Body Weight Changes; Carnitine O-Palmitoyltransferase; Catalase; Diet; Diet, High-Fat; Fats; Fatty Acid Synthetase Complex; Fluorescence; Glutathione Reductase; Hep G2 Cells; Korea; Lipid Metabolism; Lipogenesis; Liver; Mice; Microscopy; Oxidative Stress; Plasma; Reactive Oxygen Species; Real-Time Polymerase Chain Reaction; RNA, Messenger; Seawater; tert-Butylhydroperoxide; Water
- From:Nutrition Research and Practice 2010;4(1):3-10
- CountryRepublic of Korea
- Language:English
- Abstract: This study was performed to investigate the effect of desalinated underground seawater (named as 'magma seawater', MSW) of Jeju Island in Korea on lipid metabolism and antioxidant activity. MSW was collected from underground of Han-Dong in Jeju Island, and freely given to high fat diet (HFD)-fed C57BL/6 mice for 10 weeks. Although there were no significant differences in the body weight changes and plasma lipid levels, hepatic triglyceride levels were significantly lower in the MSW group than in the normal tap water (TW)-drunken control group. Furthermore, the activity of fatty acid synthase (FAS) was significantly decreased and carnitine palmitoyltransferase (CPT) activity was increased in MSW group compared to TW group. Similarly, real-time PCR analysis revealed that mRNA expressions of lipogenic genes were lowered in MSW groups compared to the control group. In a morphometric observation on the liver tissue, accumulation of fats was remarkably reduced in MSW group. Meanwhile, in vitro assay, free radical scavenging activity measured by using diphenylpicrylhydrazyl (DPPH) was increased in MSW group. The 2'-7'-dichlorofluorescein diacetate (DCF-DA) staining followed with fluorescent microscopy showed a low intensity of fluorescence in MSW-treated HepG2 cells, compared to TW-treated HepG2 cells, which indicated that the production of reactive oxygen species by tert-butyl hydroperoxide (t-BHP) in HepG2 cells was decreased by MSW treatment. The antioxidant effect of MSW on t-BHP-induced oxidative stress in HepG2 cells was supported by the increased activities of intracellular antioxidant enzymes such as catalase and glutathione reductase. From these results, we speculate that MSW has an inhibitory effect on lipogenesis in liver and might play a protective role against cell damage by t-BHP-induced oxidative stress.
