2008•Neural Injury and Functional ReconstructionRequires access

Cell Apoptosis and the Expression of Apoptosis-inducing Factor in Rats Brain Infectious Injury

Qiao Xiao-hu, Wu Ri Le

Open publisher page 0 citations

Abstract

Objective:To explore the effect of apoptosis-inducing factor(AIF)and the caspase independent pathway in infectious brain injury.Methods:Models of acute infectious brain injury of rats were prepared by injecting LPS via the left internal carotid artery.One hundred and sixty rats were randomly divided into NS and LPS group.At 6 h、12 h、24 h、48 h and 72 h after acute infectious brain injury,ethidium bromide(EB)content was measured by formamide-method,the expression of NSE protein,GFAP protein and AIF were studied by immunohistochemistry,and apoptosis was examined by TUNEL technique.Results:The expression of NSE,GFAP,AIF and the number of apoptosis in LPS group was increased at 6 h and reached the peak at 24 h,and then decreased gradually at 48-72 h,but still significantly higher than in NS group.Conclusion:Apoptosis plays a role in the formation and development of infectious brain injury of rats.Caspase independent pathway was involved in this process through AIF.

About this research paper

What this paper is about

Objective:To explore the effect of apoptosis-inducing factor(AIF)and the caspase independent pathway in infectious brain injury.Methods:Models of acute infectious brain injury of rats were prepared by injecting LPS via the left internal carotid artery.One hundred and sixty rats were randomly divided into NS and LPS group.At 6 h、12 h、24 h、48 h and 72 h after acute infectious brain injury,ethidium bromide(EB)content was measured by formamide-method,the expression of NSE protein,GFAP protein and AIF were studied by immunohistochemistry,and apoptosis was examined by TUNEL technique.Results:The expression of NSE,GFAP,AIF and the number of apoptosis in LPS group was increased at 6 h and reached the peak at 24 h,and then decreased gradually at 48-72 h,but still significantly higher than in NS group.Conclusion:Apoptosis plays a role in the formation and development of infectious brain injury of rats.Caspase independent pathway was involved in this process through AIF.

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 effect of apoptosis-inducing factor(AIF)and the caspase independent pathway in infectious brain injury.Methods:Models of acute infectious brain injury of rats were prepared by injecting LPS via the left internal carotid artery.One hundred and sixty rats were randomly divided into NS and LPS group.At 6 h、12 h、24 h、48 h and 72 h after acute infectious brain injury,ethidium bromide(EB)content was measured by formamide-method,the expression of NSE protein,GFAP protein and AIF were studied by immunohistochemistry,and apoptosis was examined by TUNEL technique.Results:The expression of NSE,GFAP,AIF and the number of apoptosis in LPS group was increased at 6 h and reached the peak at 24 h,and then decreased gradually at 48-72 h,but still significantly higher than in NS group.Conclusion:Apoptosis plays a role in the formation and development of infectious brain injury of rats.Caspase independent pathway was involved in this process through AIF.

Key concepts: Apoptosis, TUNEL assay, Apoptosis-inducing factor, Immunohistochemistry, Medicine, Ethidium bromide, Caspase 3, Andrology

Related papers

Back to paper searchBrowse research topicsOriginal source
Cell Apoptosis and the Expression of Apoptosis-inducing Factor in Rats Brain Infectious Injury — Research Paper | ScholarLens