2012•Linchuang huicuiRequires access

Effect of H2S on apoptosis of lung tissue attacked by lipopolysaccharide and lung protection mechanism

Xiaowei Zhang

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Abstract

Objective To observe the effect of hydrogen sulfide(H2S) on apoptosis of lung tissue in lipopolysaccharide(LPS)-induced acute lung injury(ALI) in rats.Methods 140 Sprague-Dawley rats were randomly divided into four groups:sham-operated group,model group(LPS was instilled intratracheally to induce ALI),LPS+NaHS(H2S donor) group,and LPS+PPG(propargylglycin,CSE inhibitor) group.Seven rats of each group,right heart catheter method was used to monitor and record MPAP before agent administration and 2,4,6 and 8 hours after agent administration.Twenty-eight rats were sacrificed at 4 h(14 rats) or 8 h(14 rats) after agent administration.Protein expression of Bcl-2 and Fas were detected by immunohistochemical method.Lung histomorphological changes were observed under microscope and index of quantitative assessment(IQA) was calculated to measure the lung injury severity.Results Compared with sham-operated group,severe injuries of lung tissues and raised IQA,MPAP in each time,higher expression of Fas protein,lower expression of Bcl-2 protein were observed in rats treated with LPS(all P0.01).Pre-administration of NaSH not only alleviated the injuries induced by LPS,but increased expression of Bcl-2 protein,decreased IQA,MPAP in each time and expression of Fas protein.Pre-administration of PPG exacerbated the injuries induced by LPS(all P0.01).Also,decreased expression of Bcl-2 protein,increased IQA,MPAP in each time and expression of Fas protein were observed(all P0.01).Conclusion H2S can protect lung tissue of ALI rats by alleviating apoptosis of lung tissue attacked by LPS.

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Objective To observe the effect of hydrogen sulfide(H2S) on apoptosis of lung tissue in lipopolysaccharide(LPS)-induced acute lung injury(ALI) in rats.Methods 140 Sprague-Dawley rats were randomly divided into four groups:sham-operated group,model group(LPS was instilled intratracheally to induce ALI),LPS+NaHS(H2S donor) group,and LPS+PPG(propargylglycin,CSE inhibitor) group.Seven rats of each group,right heart catheter method was used to monitor and record MPAP before agent administration and 2,4,6 and 8 hours after agent administration.Twenty-eight rats were sacrificed at 4 h(14 rats) or 8 h(14 rats) after agent administration.Protein expression of Bcl-2 and Fas were detected by immunohistochemical method.Lung histomorphological changes were observed under microscope and index of quantitative assessment(IQA) was calculated to measure the lung injury severity.Results Compared with sham-operated group,severe injuries of lung tissues and raised IQA,MPAP in each time,higher expression of Fas protein,lower expression of Bcl-2 protein were observed in rats treated with LPS(all P0.01).Pre-administration of NaSH not only alleviated the injuries induced by LPS,but increased expression of Bcl-2 protein,decreased IQA,MPAP in each time and expression of Fas protein.Pre-administration of PPG exacerbated the injuries induced by LPS(all P0.01).Also,decreased expression of Bcl-2 protein,increased IQA,MPAP in each time and expression of Fas protein were observed(all P0.01).Conclusion H2S can protect lung tissue of ALI rats by alleviating apoptosis of lung tissue attacked by LPS.

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Available abstract

Objective To observe the effect of hydrogen sulfide(H2S) on apoptosis of lung tissue in lipopolysaccharide(LPS)-induced acute lung injury(ALI) in rats.Methods 140 Sprague-Dawley rats were randomly divided into four groups:sham-operated group,model group(LPS was instilled intratracheally to induce ALI),LPS+NaHS(H2S donor) group,and LPS+PPG(propargylglycin,CSE inhibitor) group.Seven rats of each group,right heart catheter method was used to monitor and record MPAP before agent administration and 2,4,6 and 8 hours after agent administration.Twenty-eight rats were sacrificed at 4 h(14 rats) or 8 h(14 rats) after agent administration.Protein expression of Bcl-2 and Fas were detected by immunohistochemical method.Lung histomorphological changes were observed under microscope and index of quantitative assessment(IQA) was calculated to measure the lung injury severity.Results Compared with sham-operated group,severe injuries of lung tissues and raised IQA,MPAP in each time,higher expression of Fas protein,lower expression of Bcl-2 protein were observed in rats treated with LPS(all P0.01).Pre-administration of NaSH not only alleviated the injuries induced by LPS,but increased expression of Bcl-2 protein,decreased IQA,MPAP in each time and expression of Fas protein.Pre-administration of PPG exacerbated the injuries induced by LPS(all P0.01).Also,decreased expression of Bcl-2 protein,increased IQA,MPAP in each time and expression of Fas protein were observed(all P0.01).Conclusion H2S can protect lung tissue of ALI rats by alleviating apoptosis of lung tissue attacked by LPS.

Key concepts: Medicine, Lipopolysaccharide, Lung, Apoptosis, Immunohistochemistry, Pathology, Internal medicine, Endocrinology

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