2011Chinese Journal of AsthmaRequires access

Relationship between apoptosis in lung and changes of serum cytokines

Yi-nan Yue

Open publisher page 0 citations

Abstract

Objective To investigate changes of apoptosis in lung and serum cytokines, and to explore the role of them in lung injury after renal ischemia reperfusion. Methods The animal model of renal ischemia reperfusion injury was made by clamping bilateral renal pedicle for 45 minutes. At 2 h, 6 h,12 h,24 h,72 h after ischemia reperfusion,the serum interleukin-1β(IL-1β) and nitric oxide (NO) were detected,the changes of histopathology and apoptosis in lung were observed. Results After ischemia reperfusion,lung apoptosis,serum IL-1β and NO gradually increased. They reached to a peak value at 12 h after ischemia reperfusion. They gradually decreased at 24 h after ischemia reperfusion. The changes of lung injury were consistent to the changes of detected parameters at each time point after ischemia reperfusion. Conclusions IL-1β and NO released after renal ischemia reperfusion may be one of the reasons of apoptosis and injury in lung. Key words: Acute lung injury; Ischemia reperfusion; Apoptosis; Interleukin-1β;  Nitric oxide

About this research paper

What this paper is about

Objective To investigate changes of apoptosis in lung and serum cytokines, and to explore the role of them in lung injury after renal ischemia reperfusion. Methods The animal model of renal ischemia reperfusion injury was made by clamping bilateral renal pedicle for 45 minutes. At 2 h, 6 h,12 h,24 h,72 h after ischemia reperfusion,the serum interleukin-1β(IL-1β) and nitric oxide (NO) were detected,the changes of histopathology and apoptosis in lung were observed. Results After ischemia reperfusion,lung apoptosis,serum IL-1β and NO gradually increased. They reached to a peak value at 12 h after ischemia reperfusion. They gradually decreased at 24 h after ischemia reperfusion. The changes of lung injury were consistent to the changes of detected parameters at each time point after ischemia reperfusion. Conclusions IL-1β and NO released after renal ischemia reperfusion may be one of the reasons of apoptosis and injury in lung. Key words: Acute lung injury; Ischemia reperfusion; Apoptosis; Interleukin-1β;  Nitric oxide

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 investigate changes of apoptosis in lung and serum cytokines, and to explore the role of them in lung injury after renal ischemia reperfusion. Methods The animal model of renal ischemia reperfusion injury was made by clamping bilateral renal pedicle for 45 minutes. At 2 h, 6 h,12 h,24 h,72 h after ischemia reperfusion,the serum interleukin-1β(IL-1β) and nitric oxide (NO) were detected,the changes of histopathology and apoptosis in lung were observed. Results After ischemia reperfusion,lung apoptosis,serum IL-1β and NO gradually increased. They reached to a peak value at 12 h after ischemia reperfusion. They gradually decreased at 24 h after ischemia reperfusion. The changes of lung injury were consistent to the changes of detected parameters at each time point after ischemia reperfusion. Conclusions IL-1β and NO released after renal ischemia reperfusion may be one of the reasons of apoptosis and injury in lung. Key words: Acute lung injury; Ischemia reperfusion; Apoptosis; Interleukin-1β;  Nitric oxide

Key concepts: Medicine, Ischemia, Lung, Nitric oxide, Apoptosis, Renal ischemia, Reperfusion injury, Kidney

Related papers

Back to paper searchBrowse research topicsOriginal source
Relationship between apoptosis in lung and changes of serum cytokines — Research Paper | ScholarLens