Effects of carbon monoxide on lipopolysaccharide induced damage in rat alveolar macrophages
10.11958/20150377
- VernacularTitle:一氧化碳对脂多糖诱导大鼠肺巨噬细胞损伤的影响
- Author:
Wei LIU
;
Jianbo YU
;
Dan WANG
;
Jia SHI
- Publication Type:Journal Article
- Keywords:
carbon monoxide;
lipopolysaccharides;
macrophages,alveolar;
apoptosis;
adenosine triphosphate;
membrane potential,mitochondrial;
Drp1
- From:
Tianjin Medical Journal
2016;44(6):672-674,675
- CountryChina
- Language:Chinese
-
Abstract:
Objective To evaluate effects of carbon monoxide (CO) on lipopolysaccharide (LPS) induced damage and possible mechanism in rat alveolar macrophages. Methods Rat alveolar macrophages were cultured in DMEM containing 10%fetal bovine serum with 5%CO2 at 37℃in Heraeus sepatech. The cells were divided into four groups using random number table (n=10): control group (group C),CO group, LPS group and LPS+CO group. The CO release molecule-2 (CORM-2) 100 μmol/L was added into CO group,LPS 10 mg/L was added into LPS group, cells were pretreated with CORM-2 100μmol/L for 1 h then LPS 10 mg/L was added into LPS+CO group, the same amount of PBS was added to group C. Proliferation was measured by MTT assay. Apoptosis and mitochondrial membrane potential were detected with flow cytometer. The content of ATP was tested by ATP content kit. Drp1 mRNA was measured by RT-PCR, and Drp1 expression was determined by Western blot assay. Results Compared with group C, the cell vitality, content of ATP and mitochondrial membrane potential were decreased in LPS group and LPS+CO group,and cell apoptosis rate, Drp1 mRNA and protein expression were increased (P<0.05). There were no significant changes were found in CO group. Compared with LPS group, the cell vitality, content of ATP and mitochondrial membrane potential were increased in LPS+CO group,and the cell apoptosis rate, Drp1 mRNA and protein expression were decreased (P<0.05). Conclusion Carbon monoxide can alleviate LPS-induced damage in rat alveolar macrophages, which is related with down-regulation of Drp1 and amelioration of mitochondrial function.
