2010•Zhongguo yaofangRequires access

Effects of Lycopene on the Expression of Cytochrome P_(450)2E1 and Tumor Necrosis Factor-α in Liver Tissues of Rats with Nonalcoholic Fatty Liver

Zhao Chun-jing

Open publisher page 0 citations

Abstract

OBJECTIVE: To explore the effects of lycopene on the expression of cytochrome P450 2E1 and tumor necrosis factor-α in liver tissues of rats with nonalcoholic fatty liver. METHODS: Rats were divided into normal control (N) group and modeling group. Modeling group was given high-fat diet for 8 weeks to establish fatty liver model. Then model rats were divided into model control (M) group (high-fat diet), lycopene low-dose (L) group (normal diet, lycopene 10 mg·kg-1), lycopene high-dose (H) group (normal diet, lycopene 20 mg·kg-1) and natural recovery (NR) group (normal diet) with 10 rats of each group. Those groups were given diet for 4 weeks then sacrificed. The change of histopathology was observed. The levels of CYP2E1, TNF-α, SOD, MDA and FFA in liver tissue were detected. RESULTS: Compared with M group, the changes of histopathology in NR group, L group and H group were improved, especially in L group and H group. Compared with NR group, the levels of CYP2E1, TNF-α, MDA and FFA in liver tissue of L group and H group were decreased significantly (P0.05); the level of SOD was increased significantly (P0.05 or P0.01). CONCLUSION: Lycopene can significantly inhibit the expression of CYP2El and TNF-α in fatty liver rats and reduce lipid peroxidation so as to improve fatty liver.

About this research paper

What this paper is about

OBJECTIVE: To explore the effects of lycopene on the expression of cytochrome P450 2E1 and tumor necrosis factor-α in liver tissues of rats with nonalcoholic fatty liver. METHODS: Rats were divided into normal control (N) group and modeling group. Modeling group was given high-fat diet for 8 weeks to establish fatty liver model. Then model rats were divided into model control (M) group (high-fat diet), lycopene low-dose (L) group (normal diet, lycopene 10 mg·kg-1), lycopene high-dose (H) group (normal diet, lycopene 20 mg·kg-1) and natural recovery (NR) group (normal diet) with 10 rats of each group. Those groups were given diet for 4 weeks then sacrificed. The change of histopathology was observed. The levels of CYP2E1, TNF-α, SOD, MDA and FFA in liver tissue were detected. RESULTS: Compared with M group, the changes of histopathology in NR group, L group and H group were improved, especially in L group and H group. Compared with NR group, the levels of CYP2E1, TNF-α, MDA and FFA in liver tissue of L group and H group were decreased significantly (P0.05); the level of SOD was increased significantly (P0.05 or P0.01). CONCLUSION: Lycopene can significantly inhibit the expression of CYP2El and TNF-α in fatty liver rats and reduce lipid peroxidation so as to improve fatty liver.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

OBJECTIVE: To explore the effects of lycopene on the expression of cytochrome P450 2E1 and tumor necrosis factor-α in liver tissues of rats with nonalcoholic fatty liver. METHODS: Rats were divided into normal control (N) group and modeling group. Modeling group was given high-fat diet for 8 weeks to establish fatty liver model. Then model rats were divided into model control (M) group (high-fat diet), lycopene low-dose (L) group (normal diet, lycopene 10 mg·kg-1), lycopene high-dose (H) group (normal diet, lycopene 20 mg·kg-1) and natural recovery (NR) group (normal diet) with 10 rats of each group. Those groups were given diet for 4 weeks then sacrificed. The change of histopathology was observed. The levels of CYP2E1, TNF-α, SOD, MDA and FFA in liver tissue were detected. RESULTS: Compared with M group, the changes of histopathology in NR group, L group and H group were improved, especially in L group and H group. Compared with NR group, the levels of CYP2E1, TNF-α, MDA and FFA in liver tissue of L group and H group were decreased significantly (P0.05); the level of SOD was increased significantly (P0.05 or P0.01). CONCLUSION: Lycopene can significantly inhibit the expression of CYP2El and TNF-α in fatty liver rats and reduce lipid peroxidation so as to improve fatty liver.

Key concepts: Lycopene, CYP2E1, Internal medicine, Endocrinology, Fatty liver, Histopathology, Tumor necrosis factor alpha, Nonalcoholic fatty liver disease

Related papers

Back to paper searchBrowse research topicsOriginal source
Effects of Lycopene on the Expression of Cytochrome P_(450)2E1 and Tumor Necrosis Factor-α in Liver Tissues of Rats with Nonalcoholic Fatty Liver — Research Paper | ScholarLens