2006•Di-Si Junyi Daxue xuebaoRequires access

Effects of DDFA on cell apoptosis and expressions of Bax and Bcl-2 in lung tissue of rats with severe acute pancreatitis

Shi Xue

Open publisher page 1 citations

Abstract

AIM: To explore the effects of DDFA on cell apoptosis and expressions of Bax and Bcl-2 in lung tissue of rats with severe acute pancreatitis(SAP). METHODS: 45 rats weighting 200-250 g were randomized into 3 groups: control group (n=15), SAP group (n=15) and DDFA group (n=15). The models of SAP were established by the injection of 200 g/L arginine solution ip(once a hour for 2 h) into the rats. At the 24, 48 and 72 h after establishment of models, serum amylase, TNF-a and calcium were determined. The left lungs were taken for light and electron microscopic observation. Cell apoptosis in lung tissue was determined by TUNEL method. Expressions of Bax and Bcl-2 were detected by immunohistochemical staining of SABC. RESULTS: In the SAP group, serum amylase, TNF-a, apoptotic index, expressions of Bax and Bcl-2 markedly increased. Lung tissue injuries were significant under a light microscope. As compared with SAP group at the same phase, serum amylase, TNF-a, apoptotic index and expressions of Bax in DDFA group decreased significantly. While the expression of Bcl-2 increased significantly. The injury of lung tissue was relieved by DDFA. CONCLUSION: The apoptosis and the expressions of Bax and Bcl-2 in lung tissue might be involved in pathogenesis of SAP. DDFA administration in the early stage is helpful for diminishing lung injury induced by SAP.

About this research paper

What this paper is about

AIM: To explore the effects of DDFA on cell apoptosis and expressions of Bax and Bcl-2 in lung tissue of rats with severe acute pancreatitis(SAP). METHODS: 45 rats weighting 200-250 g were randomized into 3 groups: control group (n=15), SAP group (n=15) and DDFA group (n=15). The models of SAP were established by the injection of 200 g/L arginine solution ip(once a hour for 2 h) into the rats. At the 24, 48 and 72 h after establishment of models, serum amylase, TNF-a and calcium were determined. The left lungs were taken for light and electron microscopic observation. Cell apoptosis in lung tissue was determined by TUNEL method. Expressions of Bax and Bcl-2 were detected by immunohistochemical staining of SABC. RESULTS: In the SAP group, serum amylase, TNF-a, apoptotic index, expressions of Bax and Bcl-2 markedly increased. Lung tissue injuries were significant under a light microscope. As compared with SAP group at the same phase, serum amylase, TNF-a, apoptotic index and expressions of Bax in DDFA group decreased significantly. While the expression of Bcl-2 increased significantly. The injury of lung tissue was relieved by DDFA. CONCLUSION: The apoptosis and the expressions of Bax and Bcl-2 in lung tissue might be involved in pathogenesis of SAP. DDFA administration in the early stage is helpful for diminishing lung injury induced by SAP.

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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

AIM: To explore the effects of DDFA on cell apoptosis and expressions of Bax and Bcl-2 in lung tissue of rats with severe acute pancreatitis(SAP). METHODS: 45 rats weighting 200-250 g were randomized into 3 groups: control group (n=15), SAP group (n=15) and DDFA group (n=15). The models of SAP were established by the injection of 200 g/L arginine solution ip(once a hour for 2 h) into the rats. At the 24, 48 and 72 h after establishment of models, serum amylase, TNF-a and calcium were determined. The left lungs were taken for light and electron microscopic observation. Cell apoptosis in lung tissue was determined by TUNEL method. Expressions of Bax and Bcl-2 were detected by immunohistochemical staining of SABC. RESULTS: In the SAP group, serum amylase, TNF-a, apoptotic index, expressions of Bax and Bcl-2 markedly increased. Lung tissue injuries were significant under a light microscope. As compared with SAP group at the same phase, serum amylase, TNF-a, apoptotic index and expressions of Bax in DDFA group decreased significantly. While the expression of Bcl-2 increased significantly. The injury of lung tissue was relieved by DDFA. CONCLUSION: The apoptosis and the expressions of Bax and Bcl-2 in lung tissue might be involved in pathogenesis of SAP. DDFA administration in the early stage is helpful for diminishing lung injury induced by SAP.

Key concepts: TUNEL assay, Apoptosis, Lung, Immunohistochemistry, Pathology, Pathogenesis, Necrosis, Pancreatitis

Related papers

Back to paper searchBrowse research topicsOriginal source
Effects of DDFA on cell apoptosis and expressions of Bax and Bcl-2 in lung tissue of rats with severe acute pancreatitis — Research Paper | ScholarLens