Role of serine threonine protein kinase-1 and Smad3 in lung tissues in development of hepatopulmonary syndrome in rats
10.3760/cma.j.issn.0254-1416.2013.08.019
- VernacularTitle:肺组织Akt1和Smad3在大鼠肝肺综合征形成中的作用
- Author:
Baoli ZU
;
Yang CHEN
;
Bing CHEN
;
Yong YANG
;
Bin YI
;
Kaizhi LU
- Publication Type:Journal Article
- Keywords:
Hepatopulmonary syndrome;
Lung;
Protein-serine-threonine kinases;
Smad3 protein
- From:
Chinese Journal of Anesthesiology
2013;33(8):980-982
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the role of serine threonine protein kinase-1 (Akt1) and Smad3 in lung tissues in development of hepatopulmonary syndrome in rats.Methods Seventy-two healthy male SpragueDawley rats,aged 3-4 months,weighing 200-250 g,were randomly divided into 3 groups (n=24 each):control group (C group),sham operation group (S group) and common bile duct ligation (CBDL) group.The rats were anesthetized with 3％ pentobarbital sodium 45 mg/kg.In group CBDL,laparotomy was performed,the common bile duct was ligated and then the abdomen was closed,while the common bile duct was only exposed,but not ligated and then the abdomen was closed in group S.At 1st,3rd and 5th weeks (T1-3),8 rats were chosen randomly in each group and blood samples were obtained from the abdominal aorta for blood gas analysis.The rats were then sacrificed and lungs were isolated to detect the expression of Aktl and Smad3 mRNA and protein in lung tissues (by RT-PCR and Western blot).The lung tissues were sliced and stained with hematoxylin eosin for examination of the pathological changes of pulmonary capillaries.Results Compared with C and S groups,the expression of Akt1 and Smad3 mRNA and protein in lung tissues was significantly up-regulated at T2,3,and alveolar-arterial oxygen tension difference was increased at T3 in CBDL group (P ＜ 0.05).The pulmonary capillary was obviously dilated at T3 in CBDL group.Conclusion The expression of Akt1 and Smad3 in lung tissues is up-regulated,which may be one of the mechanisms of development of hepatopulmonary syndrome in rats.
