2006Shiyong yixue zazhiRequires access

The relationgship between uncoupling protein gene mRNA expression and insulin resistance induced by feeding high-fat.

Quanmin Li

Open publisher page 0 citations

Abstract

Objective To explore the relationship between insulin sensitivity and uncoupling protein gene(UCP) mRNA expression in high-fat rat model of insulin resistance. Methods Twenty Wistar rats were randomly divided into to general feed group(n=10) and high-fat feed group(n=10). The model of insulin resistance was made by feeding high-fat. In the experimental study, the change of insulin sensitivity was valued by euglycomic-hyperinsulin clamp and the change of UCP mRNA in liver and muscle was measured by using RT-PCR. Results In the high-fat feed group, the body weight of animal was increased significantly; glucose disposal rate was reduced significantly(GIR, 28.03±8.02 vs 9.89±3.28, P 0.01); and the expression of UCP-2 mRNA in liver and UCP-3 mRNA in muscle decreased remarkably(0.63±0.18 vs 0.43±0.15, P 0.05;1.22±0.24 vs 0.78±0.17, P 0.01). Conclusions The high-fat diet can result in the reduced insulin sensitivity. Its causes may be related with the decreased UCPs gene mRNA expression.

About this research paper

What this paper is about

Objective To explore the relationship between insulin sensitivity and uncoupling protein gene(UCP) mRNA expression in high-fat rat model of insulin resistance. Methods Twenty Wistar rats were randomly divided into to general feed group(n=10) and high-fat feed group(n=10). The model of insulin resistance was made by feeding high-fat. In the experimental study, the change of insulin sensitivity was valued by euglycomic-hyperinsulin clamp and the change of UCP mRNA in liver and muscle was measured by using RT-PCR. Results In the high-fat feed group, the body weight of animal was increased significantly; glucose disposal rate was reduced significantly(GIR, 28.03±8.02 vs 9.89±3.28, P 0.01); and the expression of UCP-2 mRNA in liver and UCP-3 mRNA in muscle decreased remarkably(0.63±0.18 vs 0.43±0.15, P 0.05;1.22±0.24 vs 0.78±0.17, P 0.01). Conclusions The high-fat diet can result in the reduced insulin sensitivity. Its causes may be related with the decreased UCPs gene mRNA expression.

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 relationship between insulin sensitivity and uncoupling protein gene(UCP) mRNA expression in high-fat rat model of insulin resistance. Methods Twenty Wistar rats were randomly divided into to general feed group(n=10) and high-fat feed group(n=10). The model of insulin resistance was made by feeding high-fat. In the experimental study, the change of insulin sensitivity was valued by euglycomic-hyperinsulin clamp and the change of UCP mRNA in liver and muscle was measured by using RT-PCR. Results In the high-fat feed group, the body weight of animal was increased significantly; glucose disposal rate was reduced significantly(GIR, 28.03±8.02 vs 9.89±3.28, P 0.01); and the expression of UCP-2 mRNA in liver and UCP-3 mRNA in muscle decreased remarkably(0.63±0.18 vs 0.43±0.15, P 0.05;1.22±0.24 vs 0.78±0.17, P 0.01). Conclusions The high-fat diet can result in the reduced insulin sensitivity. Its causes may be related with the decreased UCPs gene mRNA expression.

Key concepts: Insulin resistance, Endocrinology, Internal medicine, Uncoupling protein, Messenger RNA, Insulin, Gene expression, Biology

Related papers

Back to paper searchBrowse research topicsOriginal source
The relationgship between uncoupling protein gene mRNA expression and insulin resistance induced by feeding high-fat. — Research Paper | ScholarLens