TY - JOUR
T1 - Effects of β-carotene on cell viability and antioxidant status of hepatocytes from chronically ethanol-fed rats
AU - Yang, Suh-Ching
AU - Huang, Chi Chang
AU - Chu, Jan-Show
AU - Chen, Jiun-Rong
PY - 2004/8
Y1 - 2004/8
N2 - The purpose of the present study was to evaluate the effects of β-carotene on the cell viability and antioxidant status of hepatocytes from chronically ethanol-fed rats. Rats in the ethanol group were given an ethanol-containing liquid diet that provided 36 % of total energy as ethanol, while rats in the control group were fed an isoenergetic diet without ethanol. After 4 weeks, hepatocytes were taken out and cultured for 24 h. Hepatocytes from the rats in the control and ethanol groups were cultured in medium without (HC, HE) or with β -carotene (HC + B, HE + B). The results showed that lactate dehydrogenase leakage was significantly increased in the HE compared with that in the HC group. However, lactate dehydrogenase leakage of the HE + B group was similar to that of the HC group. When compared with the HC group, activities of glutathione peroxidase and catalase in the HE group were significantly decreased by 54 and 31 %, respectively. Catalase activity in the HE + B group was significantly increased by 61 % compared with that in the HE group. However, activities of glutathione reductase and superoxide dismutase sbowed no difference among the groups. The level of glutathione in the HC + B and HE + B groups was significantly increased to 155 and 143 % compared with those in the HC and HE groups, respectively. The concentration of lipid peroxides showed no difference among the groups. The present results demonstrate that β-carotene improved the cell viability of hepatocytes, and increased catalase activities and glutathione levels in hepatocytes from chronically ethanol-fed rats.
AB - The purpose of the present study was to evaluate the effects of β-carotene on the cell viability and antioxidant status of hepatocytes from chronically ethanol-fed rats. Rats in the ethanol group were given an ethanol-containing liquid diet that provided 36 % of total energy as ethanol, while rats in the control group were fed an isoenergetic diet without ethanol. After 4 weeks, hepatocytes were taken out and cultured for 24 h. Hepatocytes from the rats in the control and ethanol groups were cultured in medium without (HC, HE) or with β -carotene (HC + B, HE + B). The results showed that lactate dehydrogenase leakage was significantly increased in the HE compared with that in the HC group. However, lactate dehydrogenase leakage of the HE + B group was similar to that of the HC group. When compared with the HC group, activities of glutathione peroxidase and catalase in the HE group were significantly decreased by 54 and 31 %, respectively. Catalase activity in the HE + B group was significantly increased by 61 % compared with that in the HE group. However, activities of glutathione reductase and superoxide dismutase sbowed no difference among the groups. The level of glutathione in the HC + B and HE + B groups was significantly increased to 155 and 143 % compared with those in the HC and HE groups, respectively. The concentration of lipid peroxides showed no difference among the groups. The present results demonstrate that β-carotene improved the cell viability of hepatocytes, and increased catalase activities and glutathione levels in hepatocytes from chronically ethanol-fed rats.
KW - Antioxidant status
KW - Chronic ethanol feeding
KW - Hepatocytes
KW - β-carotene
UR - http://www.scopus.com/inward/record.url?scp=4544242212&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=4544242212&partnerID=8YFLogxK
U2 - 10.1079/BJN20041190
DO - 10.1079/BJN20041190
M3 - Article
C2 - 15333151
AN - SCOPUS:4544242212
SN - 0007-1145
VL - 92
SP - 209
EP - 215
JO - British Journal of Nutrition
JF - British Journal of Nutrition
IS - 2
ER -