Effects of β-carotene on cell viability and antioxidant status of hepatocytes from chronically ethanol-fed rats

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Abstract

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.

Original languageEnglish
Pages (from-to)209-215
Number of pages7
JournalBritish Journal of Nutrition
Volume92
Issue number2
DOIs
Publication statusPublished - Aug 2004

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Carotenoids
Hepatocytes
Cell Survival
Ethanol
Antioxidants
Catalase
L-Lactate Dehydrogenase
Glutathione
Diet
Control Groups
Glutathione Reductase
Lipid Peroxides
Glutathione Peroxidase
Superoxide Dismutase

Keywords

  • β-carotene
  • Antioxidant status
  • Chronic ethanol feeding
  • Hepatocytes

ASJC Scopus subject areas

  • Medicine (miscellaneous)

Cite this

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title = "Effects of β-carotene on cell viability and antioxidant status of hepatocytes from chronically ethanol-fed rats",
abstract = "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.",
keywords = "β-carotene, Antioxidant status, Chronic ethanol feeding, Hepatocytes",
author = "Suh-Ching Yang and Huang, {Chi Chang} and Jan-Show Chu and Jiun-Rong Chen",
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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

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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.

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