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Propofol attenuated liver transplantation-induced acute lung injury via connexin43 gap junction inhibition
- Source :
- Journal of Translational Medicine
- Publisher :
- Springer Nature
-
Abstract
- Background Postoperative acute lung injury (ALI) is a severe complication after liver transplantation, which influences patient survival rate obviously. However, its mechanisms are unclear and effective therapies are still lacking. The current study focused on effects of propofol on liver transplantation-induced ALI and whether its underlying mechanism was relative with connexin43 (Cx43) alternation. The authors postulated that endotoxin induced enhancement of Cx43 gap junction (GJ) plays a critical role in mediating post liver transplantation ALI and that pretreatment with the anesthetic propofol, known to inhibit gap junction, can confer effective protection. Methods Male Sprague–Dawley rats underwent autologous orthotopic liver transplantation (AOLT) in the absence or presence of treatments with the selective Cx43 inhibitor, enanthol (0.1 mg/kg) and propofol (50 mg/kg), a commonly used anesthetic in clinical anesthesia. In vitro study, BEAS-2B cells, a kind of lung epithelial cell line expressing Cx43, exposed to lipopolysaccharide (LPS), which mainly contributed to ALI. Function of Cx43 GJ was regulated by Cx43 specific inhibitors, gap26 (300 μM) or enhancer, retinoic acid (10 μM) and two specific siRNAs. Results Compared with the sham group, AOLT results in ALI obviously with plasma endotoxin increase. Cx43 inhibition decreased ALI through inflammatory reaction reduction. In vitro studies, LPS-induced BEAS-2B cells damage was attenuated by Cx43 function inhibition, but amplified by enhancement. Another important finding was propofol reduced Cx43 function and protected against LPS-mediated BEAS-2B cells damage or AOLT-induced ALI, mechanisms of which were also associated with inflammatory reaction decrease. Conclusion Cx43 plays a vital role in liver transplantation-induced ALI. Propofol decreased Cx43 function and protected against ALI in vivo and in vitro. This finding provide a new basis for targeted intervention of organ protection in liver transplantation, even in other kinds of operations.
- Subjects :
- Lipopolysaccharides
Male
0301 basic medicine
Lipopolysaccharide
medicine.medical_treatment
Acute Lung Injury
Liver transplantation
Pharmacology
Lung injury
Transplantation, Autologous
Connexins
General Biochemistry, Genetics and Molecular Biology
Cell Line
Rats, Sprague-Dawley
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
In vivo
medicine
Connexin43
Animals
Humans
RNA, Small Interfering
Propofol
Medicine(all)
Lung
business.industry
Biochemistry, Genetics and Molecular Biology(all)
Research
Gap Junctions
General Medicine
In vitro
respiratory tract diseases
030104 developmental biology
medicine.anatomical_structure
chemistry
Connexin 43
Gene Knockdown Techniques
030220 oncology & carcinogenesis
Anesthesia
Anesthetic
cardiovascular system
business
medicine.drug
Subjects
Details
- Language :
- English
- ISSN :
- 14795876
- Volume :
- 14
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Journal of Translational Medicine
- Accession number :
- edsair.doi.dedup.....8f2901ea45407bbbfebc3a8f73898684
- Full Text :
- https://doi.org/10.1186/s12967-016-0954-1