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The role of lipoprotein-associated phospholipase A2 in acute kidney injury of septic mice

BACKGROUND: This experiment aimed to investigate the role and mechanism of lipoprotein-associated phospholipase A2 (Lp-PLA2) in kidney injury in septic mice induced by cecal ligation and perforation (CLP). METHODS: Male BALB/c mice were randomly divided into two groups: sham-operation group (Sham gr...

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Autores principales: Liang, Guiwen, Wu, Ruo, Jiang, Lan, Liu, Yanfang, Mao, Guomin, Huang, Zhongwei, Qi, Lei, Jiang, Haiyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658152/
https://www.ncbi.nlm.nih.gov/pubmed/33209683
http://dx.doi.org/10.21037/tau-20-1173
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author Liang, Guiwen
Wu, Ruo
Jiang, Lan
Liu, Yanfang
Mao, Guomin
Huang, Zhongwei
Qi, Lei
Jiang, Haiyan
author_facet Liang, Guiwen
Wu, Ruo
Jiang, Lan
Liu, Yanfang
Mao, Guomin
Huang, Zhongwei
Qi, Lei
Jiang, Haiyan
author_sort Liang, Guiwen
collection PubMed
description BACKGROUND: This experiment aimed to investigate the role and mechanism of lipoprotein-associated phospholipase A2 (Lp-PLA2) in kidney injury in septic mice induced by cecal ligation and perforation (CLP). METHODS: Male BALB/c mice were randomly divided into two groups: sham-operation group (Sham group) and septic group (CLP group). The septic model was simulated by cecal ligation and puncture method, but only cecal ligation was used for the sham operation group. The whole serum and renal tissue samples of the mice were collected 24 hours after modeling in both groups. Hematoxylin-eosin (HE) staining was used to observe the pathological changes of renal tissue, the renal injury score was recorded, and the creatinine (Cr) and blood urea nitrogen (BUN) levels were detected by automatic biochemical analyzer, while the serum Lp-PLA2 level was detected by enzyme-linked immunosorbent assay (ELISA). The 7-day survival rate and the survival curve of the two groups were statistically analyzed. RESULTS: Compared with the Sham group, the pathological score of renal injury in the CLP Group was higher, the level of Lp-PLA2 in serum was significantly increased (all P<0.01), and the expression of Lp-PLA2 in renal tissue was significantly elevated (all P<0.01). Furthermore, the 7-day survival rate of the Sham group was 90%, while that of CLP group was 25%. CONCLUSIONS: The expression level of Lp-PLA2 in blood and kidney tissue of septic mice was increased and correlated with prognosis. However, the predictive value of Lp-PLA2 for prognosis in septic mice needs further study.
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spelling pubmed-76581522020-11-17 The role of lipoprotein-associated phospholipase A2 in acute kidney injury of septic mice Liang, Guiwen Wu, Ruo Jiang, Lan Liu, Yanfang Mao, Guomin Huang, Zhongwei Qi, Lei Jiang, Haiyan Transl Androl Urol Original Article BACKGROUND: This experiment aimed to investigate the role and mechanism of lipoprotein-associated phospholipase A2 (Lp-PLA2) in kidney injury in septic mice induced by cecal ligation and perforation (CLP). METHODS: Male BALB/c mice were randomly divided into two groups: sham-operation group (Sham group) and septic group (CLP group). The septic model was simulated by cecal ligation and puncture method, but only cecal ligation was used for the sham operation group. The whole serum and renal tissue samples of the mice were collected 24 hours after modeling in both groups. Hematoxylin-eosin (HE) staining was used to observe the pathological changes of renal tissue, the renal injury score was recorded, and the creatinine (Cr) and blood urea nitrogen (BUN) levels were detected by automatic biochemical analyzer, while the serum Lp-PLA2 level was detected by enzyme-linked immunosorbent assay (ELISA). The 7-day survival rate and the survival curve of the two groups were statistically analyzed. RESULTS: Compared with the Sham group, the pathological score of renal injury in the CLP Group was higher, the level of Lp-PLA2 in serum was significantly increased (all P<0.01), and the expression of Lp-PLA2 in renal tissue was significantly elevated (all P<0.01). Furthermore, the 7-day survival rate of the Sham group was 90%, while that of CLP group was 25%. CONCLUSIONS: The expression level of Lp-PLA2 in blood and kidney tissue of septic mice was increased and correlated with prognosis. However, the predictive value of Lp-PLA2 for prognosis in septic mice needs further study. AME Publishing Company 2020-10 /pmc/articles/PMC7658152/ /pubmed/33209683 http://dx.doi.org/10.21037/tau-20-1173 Text en 2020 Translational Andrology and Urology. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Liang, Guiwen
Wu, Ruo
Jiang, Lan
Liu, Yanfang
Mao, Guomin
Huang, Zhongwei
Qi, Lei
Jiang, Haiyan
The role of lipoprotein-associated phospholipase A2 in acute kidney injury of septic mice
title The role of lipoprotein-associated phospholipase A2 in acute kidney injury of septic mice
title_full The role of lipoprotein-associated phospholipase A2 in acute kidney injury of septic mice
title_fullStr The role of lipoprotein-associated phospholipase A2 in acute kidney injury of septic mice
title_full_unstemmed The role of lipoprotein-associated phospholipase A2 in acute kidney injury of septic mice
title_short The role of lipoprotein-associated phospholipase A2 in acute kidney injury of septic mice
title_sort role of lipoprotein-associated phospholipase a2 in acute kidney injury of septic mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658152/
https://www.ncbi.nlm.nih.gov/pubmed/33209683
http://dx.doi.org/10.21037/tau-20-1173
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