Cancer prevention research 2012; 17(2): 169-175
Published online June 30, 2012
© Korean Society of Cancer Prevention
Hyang Suk Kim1,2, Eun Ok Choi1,2, Cheol Park3, Yung Hyun Choi2,3, Kyung Tae Chung4 and Hye Jin Hwang1
The purpose of this study was to investigate the serum lipid profile and anti-inflammatory effects of Hizikia fusiforme according to the various extracts in Sprague-Dawley rat. Experimental group was divided into 6 groups: a control group (C), H. fusiforme ethanol extract group (EtOH), H. fusiforme dichloromethane fraction group (CH2Cl2), H. fusiforme ethylacetate fraction group (EtOAc), H. fusiforme butanol fraction group (n-BuOH), H. fusiforme water fraction group (H2O), respectively. H. fusiforme extracts (400 mg/kg B.W) were orally administrated into rat every day for 4 weeks. The triglyceride concentrations were significantly decreased in CH2Cl2, n-BuOH and H2O group compared to the control group (p<0.05). The HDL-cholesterol levels of the EtOH and H2O group were significantly higher than the control group (p<0.05). In the muscle tissue, the expression of iNOS was decreased in CH2Cl2 (39%) and EtOAc (28%) group compare to control group. The expression of COX-2 in the liver was inhibited in the CH2Cl2 (60%) and n-BuOH (48%) group compared to control group. In the muscle tissue, the expression of COX-2 were inhibited in the n-BuOH and H2O group (33% and 58%) compared to control group. It was found from the results suggest that H. fusiforme extract could be effective on serum lipid profile and expression of anti-inflammatory mediators. (Cancer Prev Res 17, 17-175, 2012)
Keywords: Hizikia fusiforme, lipid profile, iNOS, COX-2
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