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ATORVASTATIN CAN PREVENT HEPATIC REMOTE REPERFUSION INJURY

BACKGROUND: Some studies have shown that statins have a promising effect on protection against reperfusion injury. AIM: To evaluate the ability of ischemic postconditioning, statins and both associated to prevent or minimize reperfusion injury in the liver of rats subjected to ischemia and reperfusi...

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Autores principales: dos SANTOS, Carlos Henrique Marques, DOURADO, Doroty Mesquita, da SILVA, Baldomero Antonio Kato, PONTES, Henrique Budib Dorsa, de AZEVEDO-NETO, Euler, VENDAS, Giovanna Serra da Cruz, CHAVES, Ian de Oliveira, MIRANDA, João Victor Cunha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Colégio Brasileiro de Cirurgia Digestiva 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630213/
https://www.ncbi.nlm.nih.gov/pubmed/29019561
http://dx.doi.org/10.1590/0102-6720201700030008
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author dos SANTOS, Carlos Henrique Marques
DOURADO, Doroty Mesquita
da SILVA, Baldomero Antonio Kato
PONTES, Henrique Budib Dorsa
de AZEVEDO-NETO, Euler
VENDAS, Giovanna Serra da Cruz
CHAVES, Ian de Oliveira
MIRANDA, João Victor Cunha
author_facet dos SANTOS, Carlos Henrique Marques
DOURADO, Doroty Mesquita
da SILVA, Baldomero Antonio Kato
PONTES, Henrique Budib Dorsa
de AZEVEDO-NETO, Euler
VENDAS, Giovanna Serra da Cruz
CHAVES, Ian de Oliveira
MIRANDA, João Victor Cunha
author_sort dos SANTOS, Carlos Henrique Marques
collection PubMed
description BACKGROUND: Some studies have shown that statins have a promising effect on protection against reperfusion injury. AIM: To evaluate the ability of ischemic postconditioning, statins and both associated to prevent or minimize reperfusion injury in the liver of rats subjected to ischemia and reperfusion by abdominal aorta clamping. METHOD: Were used 41 Wistar rats, which were distributed into five groups: ischemia and reperfusion (I/R), ischemic postcondictioning (IPC), postconditioning + statin (IPC+S), statin (S) and Sham. It was performed a medium laparotomy, dissection and isolation of the infra-renal abdominal aorta; excepting Sham group, all the others were submitted to the aorta clamping for 70 min (ischemia) and posterior clamping removing (reperfusion, 70 min). In the IPC and IPC+S groups, postconditioning was performed between the ischemia and reperfusion phases by four cycles of reperfusion and ischemia lasting 30 s each. In IPC+S and S groups, preceding the surgical procedure, administration of 3.4 mg/day of atorvastatin was performed for seven days by gavage. The left hepatic lobe was removed for histological study and euthanasia was performed. RESULTS: The mean hepatic injury was 3 in the I/R group, 1.5 in the IPC group, 1.2 in the IPC+S group, 1.2 in the S group, and 0 in the SHAM group. The I/R group had a higher degree of tissue injury compared to the others in the statistical analysis and there was no difference between the others (p<0.01). CONCLUSION: Ischemic postconditioning and atorvastatin were able to minimize hepatic reperfusion injury, either alone or in combination.
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spelling pubmed-56302132017-10-13 ATORVASTATIN CAN PREVENT HEPATIC REMOTE REPERFUSION INJURY dos SANTOS, Carlos Henrique Marques DOURADO, Doroty Mesquita da SILVA, Baldomero Antonio Kato PONTES, Henrique Budib Dorsa de AZEVEDO-NETO, Euler VENDAS, Giovanna Serra da Cruz CHAVES, Ian de Oliveira MIRANDA, João Victor Cunha Arq Bras Cir Dig Original Article BACKGROUND: Some studies have shown that statins have a promising effect on protection against reperfusion injury. AIM: To evaluate the ability of ischemic postconditioning, statins and both associated to prevent or minimize reperfusion injury in the liver of rats subjected to ischemia and reperfusion by abdominal aorta clamping. METHOD: Were used 41 Wistar rats, which were distributed into five groups: ischemia and reperfusion (I/R), ischemic postcondictioning (IPC), postconditioning + statin (IPC+S), statin (S) and Sham. It was performed a medium laparotomy, dissection and isolation of the infra-renal abdominal aorta; excepting Sham group, all the others were submitted to the aorta clamping for 70 min (ischemia) and posterior clamping removing (reperfusion, 70 min). In the IPC and IPC+S groups, postconditioning was performed between the ischemia and reperfusion phases by four cycles of reperfusion and ischemia lasting 30 s each. In IPC+S and S groups, preceding the surgical procedure, administration of 3.4 mg/day of atorvastatin was performed for seven days by gavage. The left hepatic lobe was removed for histological study and euthanasia was performed. RESULTS: The mean hepatic injury was 3 in the I/R group, 1.5 in the IPC group, 1.2 in the IPC+S group, 1.2 in the S group, and 0 in the SHAM group. The I/R group had a higher degree of tissue injury compared to the others in the statistical analysis and there was no difference between the others (p<0.01). CONCLUSION: Ischemic postconditioning and atorvastatin were able to minimize hepatic reperfusion injury, either alone or in combination. Colégio Brasileiro de Cirurgia Digestiva 2017 /pmc/articles/PMC5630213/ /pubmed/29019561 http://dx.doi.org/10.1590/0102-6720201700030008 Text en http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License
spellingShingle Original Article
dos SANTOS, Carlos Henrique Marques
DOURADO, Doroty Mesquita
da SILVA, Baldomero Antonio Kato
PONTES, Henrique Budib Dorsa
de AZEVEDO-NETO, Euler
VENDAS, Giovanna Serra da Cruz
CHAVES, Ian de Oliveira
MIRANDA, João Victor Cunha
ATORVASTATIN CAN PREVENT HEPATIC REMOTE REPERFUSION INJURY
title ATORVASTATIN CAN PREVENT HEPATIC REMOTE REPERFUSION INJURY
title_full ATORVASTATIN CAN PREVENT HEPATIC REMOTE REPERFUSION INJURY
title_fullStr ATORVASTATIN CAN PREVENT HEPATIC REMOTE REPERFUSION INJURY
title_full_unstemmed ATORVASTATIN CAN PREVENT HEPATIC REMOTE REPERFUSION INJURY
title_short ATORVASTATIN CAN PREVENT HEPATIC REMOTE REPERFUSION INJURY
title_sort atorvastatin can prevent hepatic remote reperfusion injury
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630213/
https://www.ncbi.nlm.nih.gov/pubmed/29019561
http://dx.doi.org/10.1590/0102-6720201700030008
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