Expression and effects of microRNA-155 in the livers of septic mice

OBJECTIVE: To evaluate the effects of microRNA-155 (miR-155) on liver injury in mice with sepsis

Bibliographische Detailangaben
Veröffentlicht in:Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue. - 1998. - 24(2012), 3 vom: 01. März, Seite 154-7
1. Verfasser: Wang, Zhong-hua (VerfasserIn)
Weitere Verfasser: Liang, Yan-bing, Tang, Hao, Chen, Zhi-bin, Li, Zhen-yu, Wu, Jing-guo, Yang, Qing, Zeng, Li-jin, Hu, Xu-chu, Ma, Zhong-fu
Format: Aufsatz
Sprache:Chinese
Veröffentlicht: 2012
Zugriff auf das übergeordnete Werk:Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue
Schlagworte:English Abstract Journal Article MicroRNAs Mirn155 microRNA, mouse
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100 1 |a Wang, Zhong-hua  |e verfasserin  |4 aut 
245 1 0 |a Expression and effects of microRNA-155 in the livers of septic mice 
264 1 |c 2012 
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500 |a Date Completed 21.02.2013 
500 |a Date Revised 11.06.2012 
500 |a published: Print 
500 |a Citation Status MEDLINE 
520 |a OBJECTIVE: To evaluate the effects of microRNA-155 (miR-155) on liver injury in mice with sepsis 
520 |a METHODS: One hundred and twenty BALB/c mice were randomly divided into two groups of equal number according to random number table. Sepsis was induced by intraperitoneal injection of lipopolysaccharide (LPS,20 mg/kg). The mice were sacrificed at the time-points of 0, 2, 6, 12, 24, 48 hours. Blood and liver tissue were collected, and the levels of tumor necrosis factor- α (TNF- α ), interleukin (IL-6, IL-10) in serum and liver homogenate and alanine transaminase (ALT) in serum were determined by enzyme linked immunosorbent assay(ELISA). The injury of liver tissue was evaluated by histopathology. The expression of miR-155 in liver tissue was assessed by fluorescent quantitation reverse transcription-polymerase chain reaction (RT-PCR) 
520 |a RESULTS: The levels of TNF- α , IL-6 and IL-10 in serum and liver homogenate of septic mice increased with passage of time, and then the levels of TNF-α and IL-6 lowered after reaching the peak value, but remained higher than that of control group.TNF-α (ng/L) reached the peak value at 2 hours post-LPS-injection (serum: 1538.46 ± 102.12 vs. 64.52 ± 18.44,liver homogenate: 255.26 ± 41.23 vs. 60.21 + 13.55, both P<0.05). The level of IL-6 (μg/L) reached the peak value at 6 hours post-LPS-injection (serum: 875.33 ± 102.37 vs. 153.72 ± 20.67, liver homogenate: 9.22 + 0.82 vs. 3.35 ±0.36, both P<0.05), and that of IL-10 (ng/L) reached the peak value at 48 hours post-LPS-injection (serum: 520.13 ± 88.52 vs. 23.43 3.01, liver homogenate: 260.12 + 50.38 vs. 16.37 ± 3.71, both P<0.05). There were significant differences in above indexes between septic and control group (all P<0.05). The serum level of ALT (U/L) rose with passage of time, reaching the peak value at 48 hours post-LPS-injection (603.26 + 70.21 vs. 45.84 + 5.64, P<0.05). The values showed significant differences between septic and control group (P<0.05). A large number of leucocytic infiltration was found in liver. Hepatic tissue showed architectural distortion. Hepatocyte vacuolation and nodular necrosis were obvious at 12 hours post-LPS-injection. Relative expression of miR-155 was found to be increased at 2 hours post-LPS-injection, reaching its peak value at 12 hours post-LPS-injection [(72.96 ± 9.34)-fold of control group, P<0.05] 
520 |a CONCLUSION: The increase in miR-155 expression might play an important role in the mechanism of liver injury during sepsis 
650 4 |a English Abstract 
650 4 |a Journal Article 
650 7 |a MicroRNAs  |2 NLM 
650 7 |a Mirn155 microRNA, mouse  |2 NLM 
700 1 |a Liang, Yan-bing  |e verfasserin  |4 aut 
700 1 |a Tang, Hao  |e verfasserin  |4 aut 
700 1 |a Chen, Zhi-bin  |e verfasserin  |4 aut 
700 1 |a Li, Zhen-yu  |e verfasserin  |4 aut 
700 1 |a Wu, Jing-guo  |e verfasserin  |4 aut 
700 1 |a Yang, Qing  |e verfasserin  |4 aut 
700 1 |a Zeng, Li-jin  |e verfasserin  |4 aut 
700 1 |a Hu, Xu-chu  |e verfasserin  |4 aut 
700 1 |a Ma, Zhong-fu  |e verfasserin  |4 aut 
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