Effects of propofol pretreatment on the AQP-1 expression after HK-2 cells injured by anoxia-reoxygenation.
Yani Feng, Dazhi Sun, Hong Ma
Abstract
Yani Feng, Dazhi Sun, Hong Ma
Abstract
Objective To determine what effects propofol exerts on aqp-1 mRNA expression after HK-2 cells injured by anoxiareoxygenation.Methods HK-2 cells were randomly assigned to one of 4 groups:Control group(group A),CoCl2 group(group B).300 μmol/L CoCl2 were added to the cultured HK-2 cells,and then maintained with no serum media for 24 h.In intralipid group(group C),HK-2 cells were pretreated with 10% intralipid 90 μl 1h and treated as group B.In propofol group(group D)HK-2 cells were pretreated with 25 μmol/L propofol for 1 hour and treated as group B.MTT method was employed to detect the proliferation of HK-2 cells and RT-PCR to show AQP-1 mRNA and bcl-2 mRNA expression.Results After pretreated with 25 μmol/L propofol,the proliferation of HK-2 cells was increased(P 0.01).The expression of AQP-1 gene was significantly down-regulated and bcl-2 gene significantly up-regulated(P 0.01).Conclusion Pretreatment with 25 μmol/L propofol can protect HK-2 cells against anoxia-reoxygenation injury by regulating the expression of AQP-1 mRNA and bcl-2 mRNA.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To determine what effects propofol exerts on aqp-1 mRNA expression after HK-2 cells injured by anoxiareoxygenation.Methods HK-2 cells were randomly assigned to one of 4 groups:Control group(group A),CoCl2 group(group B).300 μmol/L CoCl2 were added to the cultured HK-2 cells,and then maintained with no serum media for 24 h.In intralipid group(group C),HK-2 cells were pretreated with 10% intralipid 90 μl 1h and treated as group B.In propofol group(group D)HK-2 cells were pretreated with 25 μmol/L propofol for 1 hour and treated as group B.MTT method was employed to detect the proliferation of HK-2 cells and RT-PCR to show AQP-1 mRNA and bcl-2 mRNA expression.Results After pretreated with 25 μmol/L propofol,the proliferation of HK-2 cells was increased(P 0.01).The expression of AQP-1 gene was significantly down-regulated and bcl-2 gene significantly up-regulated(P 0.01).Conclusion Pretreatment with 25 μmol/L propofol can protect HK-2 cells against anoxia-reoxygenation injury by regulating the expression of AQP-1 mRNA and bcl-2 mRNA.
Key concepts: Propofol, Messenger RNA, Molecular biology, Chemistry, Apoptosis, Gene expression, Andrology, MTT assay