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Shen-fu injection alleviates acute renal injury by reducing cytokine levels and modulating apoptosis in a porcine hemorrhagic shock model
PURPOSE: Shen-fu injection (SFI) was used to intervene in the resuscitation of porcine hemorrhagic shock (HS) model to study its protective effects on acute kidney injury. METHODS: After 60 min of HS, 28 animals were randomly assigned into four groups. The groups were as follows: hemorrhagic shock g...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira para o Desenvolvimento da Pesquisa em
Cirurgia
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8184256/ https://www.ncbi.nlm.nih.gov/pubmed/34076082 http://dx.doi.org/10.1590/ACB360405 |
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author | Yuan, Wei Wu, JunYuan Zhang, Qiang Liang, Yong Zhang, MingQqing Qin, HongJie Li, Chun-Sheng |
author_facet | Yuan, Wei Wu, JunYuan Zhang, Qiang Liang, Yong Zhang, MingQqing Qin, HongJie Li, Chun-Sheng |
author_sort | Yuan, Wei |
collection | PubMed |
description | PURPOSE: Shen-fu injection (SFI) was used to intervene in the resuscitation of porcine hemorrhagic shock (HS) model to study its protective effects on acute kidney injury. METHODS: After 60 min of HS, 28 animals were randomly assigned into four groups. The groups were as follows: hemorrhagic shock group (HS); HS resuscitation with shed-blood group (HSR); HS resuscitation with shed-blood and SFI (1 mL·kg(–1)) group (HSR-SFI); and the sham operation group (Sham). The bloods were analyzed for serum creatinine (sCr), cystatin C (CysC) and neutrophil gelatinase-associated lipocalin (NGAL). BAX, Bcl-2, and caspase-3 protein expressions by Western blot analysis and immunohistochemical staining. The renal tissues were removed and pathologic changes were observed. RESULTS: Mean aortic pressure (MAP) in HSR-SFI groups were higher than that in HSR groups after shock. At the 6th hour after shock, the urine volume per hour in the HSR-SFI groups was more than that in the HSR groups. The sCr, NGAL, CysC and cytokine levels of HSR-SFI groups were lower. The Bcl-2 expression was increased in the HSR-SFI groups. The BAX and caspase-3 expressions were reduced. The histopathologic score in the HSR-SFI was lower. CONCLUSIONS: SFI may reduce the risk of acute kidney injury (AKI) following hemorrhagic shock by attenuating systemic inflammatory responses, and regulating the expression of apoptosis-related proteins. |
format | Online Article Text |
id | pubmed-8184256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Sociedade Brasileira para o Desenvolvimento da Pesquisa em
Cirurgia |
record_format | MEDLINE/PubMed |
spelling | pubmed-81842562021-06-21 Shen-fu injection alleviates acute renal injury by reducing cytokine levels and modulating apoptosis in a porcine hemorrhagic shock model Yuan, Wei Wu, JunYuan Zhang, Qiang Liang, Yong Zhang, MingQqing Qin, HongJie Li, Chun-Sheng Acta Cir Bras Original Article PURPOSE: Shen-fu injection (SFI) was used to intervene in the resuscitation of porcine hemorrhagic shock (HS) model to study its protective effects on acute kidney injury. METHODS: After 60 min of HS, 28 animals were randomly assigned into four groups. The groups were as follows: hemorrhagic shock group (HS); HS resuscitation with shed-blood group (HSR); HS resuscitation with shed-blood and SFI (1 mL·kg(–1)) group (HSR-SFI); and the sham operation group (Sham). The bloods were analyzed for serum creatinine (sCr), cystatin C (CysC) and neutrophil gelatinase-associated lipocalin (NGAL). BAX, Bcl-2, and caspase-3 protein expressions by Western blot analysis and immunohistochemical staining. The renal tissues were removed and pathologic changes were observed. RESULTS: Mean aortic pressure (MAP) in HSR-SFI groups were higher than that in HSR groups after shock. At the 6th hour after shock, the urine volume per hour in the HSR-SFI groups was more than that in the HSR groups. The sCr, NGAL, CysC and cytokine levels of HSR-SFI groups were lower. The Bcl-2 expression was increased in the HSR-SFI groups. The BAX and caspase-3 expressions were reduced. The histopathologic score in the HSR-SFI was lower. CONCLUSIONS: SFI may reduce the risk of acute kidney injury (AKI) following hemorrhagic shock by attenuating systemic inflammatory responses, and regulating the expression of apoptosis-related proteins. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia 2021-05-28 /pmc/articles/PMC8184256/ /pubmed/34076082 http://dx.doi.org/10.1590/ACB360405 Text en https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Yuan, Wei Wu, JunYuan Zhang, Qiang Liang, Yong Zhang, MingQqing Qin, HongJie Li, Chun-Sheng Shen-fu injection alleviates acute renal injury by reducing cytokine levels and modulating apoptosis in a porcine hemorrhagic shock model |
title | Shen-fu injection alleviates acute renal injury by reducing cytokine
levels and modulating apoptosis in a porcine hemorrhagic shock
model |
title_full | Shen-fu injection alleviates acute renal injury by reducing cytokine
levels and modulating apoptosis in a porcine hemorrhagic shock
model |
title_fullStr | Shen-fu injection alleviates acute renal injury by reducing cytokine
levels and modulating apoptosis in a porcine hemorrhagic shock
model |
title_full_unstemmed | Shen-fu injection alleviates acute renal injury by reducing cytokine
levels and modulating apoptosis in a porcine hemorrhagic shock
model |
title_short | Shen-fu injection alleviates acute renal injury by reducing cytokine
levels and modulating apoptosis in a porcine hemorrhagic shock
model |
title_sort | shen-fu injection alleviates acute renal injury by reducing cytokine
levels and modulating apoptosis in a porcine hemorrhagic shock
model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8184256/ https://www.ncbi.nlm.nih.gov/pubmed/34076082 http://dx.doi.org/10.1590/ACB360405 |
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