Effects of statins on liver cell function and inflammation in septic rats

Abstract Background Several studies suggest that the presence of statins may be beneficial during sepsis, but this idea is controversial. The aim of this study was to investigate the effects of long-term statin treatment in the livers of septic animals, focusing on its antioxidant, antiinflammatory,...

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Veröffentlicht in:The Journal of surgical research 2012-12, Vol.178 (2), p.888-897
Hauptverfasser: Stolf, Aline Maria, MSc, Lívero, Francislaine dos Reis, MSc, Dreifuss, Arturo Alejandro, MSc, Bastos-Pereira, Amanda Leite, MSc, Fabosi, Isabella Aviles, Alves de Souza, Carlos Eduardo, Gomes, Liana de Oliveira, Chicorski, Raphaella, Brandt, Anna Paula, MSc, Cadena, Silvia Maria Suter, PhD, Telles, José Ederaldo Queiroz, PhD, Hauser, Aline Borsato, PhD, Elferink, Ronald Oude, PhD, Zampronio, Aleksander Roberto, PhD, Acco, Alexandra, PhD
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container_issue 2
container_start_page 888
container_title The Journal of surgical research
container_volume 178
creator Stolf, Aline Maria, MSc
Lívero, Francislaine dos Reis, MSc
Dreifuss, Arturo Alejandro, MSc
Bastos-Pereira, Amanda Leite, MSc
Fabosi, Isabella Aviles
Alves de Souza, Carlos Eduardo
Gomes, Liana de Oliveira
Chicorski, Raphaella
Brandt, Anna Paula, MSc
Cadena, Silvia Maria Suter, PhD
Telles, José Ederaldo Queiroz, PhD
Hauser, Aline Borsato, PhD
Elferink, Ronald Oude, PhD
Zampronio, Aleksander Roberto, PhD
Acco, Alexandra, PhD
description Abstract Background Several studies suggest that the presence of statins may be beneficial during sepsis, but this idea is controversial. The aim of this study was to investigate the effects of long-term statin treatment in the livers of septic animals, focusing on its antioxidant, antiinflammatory, and metabolic properties. Materials and methods Male Wistar rats were treated orally with simvastatin, atorvastatin, or vehicle once a d. After 30 d, sepsis was induced by cecal ligation and puncture (CLP) in Control, Simvastatin-treated, and Atorvastatin-treated groups, while the Sham group underwent only laparotomy. The Basal Simvastatin and Basal Atorvastatin groups received only their respective drugs without surgery. Twenty-four h after CLP or laparotomy, samples were collected from anesthetized rats for evaluation of hepatic oxidative stress, liver histology, hepatic mitochondria enzyme activity, leukocyte counts in blood and peritoneal cavity, gene expression of hepatic superoxide dismutase and TNF-2 , and plasma biochemistry. Results Most parameters that we tested exhibited expected changes upon sepsis induction. However, statin treatment only improved liver mitochondrial enzymatic activity. In other parameters, simvastatin and atorvastatin failed to protect the liver against injuries incurred upon the CLP-induced polymicrobial sepsis model. Conclusions Pretreatment with simvastatin or atorvastatin alone before sepsis induction improved mitochondrial activity in the liver; however, this result was not reproduced in other biomarkers of liver function and leukocyte migration during sepsis. Future studies should be performed to evaluate whether statins can be combined with other drugs to increase the efficacy of sepsis therapy.
doi_str_mv 10.1016/j.jss.2012.08.019
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The aim of this study was to investigate the effects of long-term statin treatment in the livers of septic animals, focusing on its antioxidant, antiinflammatory, and metabolic properties. Materials and methods Male Wistar rats were treated orally with simvastatin, atorvastatin, or vehicle once a d. After 30 d, sepsis was induced by cecal ligation and puncture (CLP) in Control, Simvastatin-treated, and Atorvastatin-treated groups, while the Sham group underwent only laparotomy. The Basal Simvastatin and Basal Atorvastatin groups received only their respective drugs without surgery. Twenty-four h after CLP or laparotomy, samples were collected from anesthetized rats for evaluation of hepatic oxidative stress, liver histology, hepatic mitochondria enzyme activity, leukocyte counts in blood and peritoneal cavity, gene expression of hepatic superoxide dismutase and TNF-2 , and plasma biochemistry. Results Most parameters that we tested exhibited expected changes upon sepsis induction. However, statin treatment only improved liver mitochondrial enzymatic activity. In other parameters, simvastatin and atorvastatin failed to protect the liver against injuries incurred upon the CLP-induced polymicrobial sepsis model. Conclusions Pretreatment with simvastatin or atorvastatin alone before sepsis induction improved mitochondrial activity in the liver; however, this result was not reproduced in other biomarkers of liver function and leukocyte migration during sepsis. Future studies should be performed to evaluate whether statins can be combined with other drugs to increase the efficacy of sepsis therapy.</description><identifier>ISSN: 0022-4804</identifier><identifier>EISSN: 1095-8673</identifier><identifier>DOI: 10.1016/j.jss.2012.08.019</identifier><identifier>PMID: 22954522</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Atorvastatin ; Hepatocytes - drug effects ; Hepatocytes - pathology ; Hepatocytes - physiology ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use ; Inflammation - drug therapy ; Leukocytes ; Liver ; Male ; Mitochondria ; Oxidative stress ; Oxidative Stress - drug effects ; Rats ; Rats, Wistar ; Sepsis ; Sepsis - drug therapy ; Sepsis - metabolism ; Sepsis - pathology ; Simvastatin ; Superoxide Dismutase - genetics ; Superoxide Dismutase-1 ; Surgery ; Tumor Necrosis Factor-alpha - genetics</subject><ispartof>The Journal of surgical research, 2012-12, Vol.178 (2), p.888-897</ispartof><rights>Elsevier Inc.</rights><rights>2012 Elsevier Inc.</rights><rights>Copyright © 2012 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-ec120ddd9c282a943d52ba5cc564f863b2ab7a1aa60e306f98808910166562eb3</citedby><cites>FETCH-LOGICAL-c441t-ec120ddd9c282a943d52ba5cc564f863b2ab7a1aa60e306f98808910166562eb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jss.2012.08.019$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22954522$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Stolf, Aline Maria, MSc</creatorcontrib><creatorcontrib>Lívero, Francislaine dos Reis, MSc</creatorcontrib><creatorcontrib>Dreifuss, Arturo Alejandro, MSc</creatorcontrib><creatorcontrib>Bastos-Pereira, Amanda Leite, MSc</creatorcontrib><creatorcontrib>Fabosi, Isabella Aviles</creatorcontrib><creatorcontrib>Alves de Souza, Carlos Eduardo</creatorcontrib><creatorcontrib>Gomes, Liana de Oliveira</creatorcontrib><creatorcontrib>Chicorski, Raphaella</creatorcontrib><creatorcontrib>Brandt, Anna Paula, MSc</creatorcontrib><creatorcontrib>Cadena, Silvia Maria Suter, PhD</creatorcontrib><creatorcontrib>Telles, José Ederaldo Queiroz, PhD</creatorcontrib><creatorcontrib>Hauser, Aline Borsato, PhD</creatorcontrib><creatorcontrib>Elferink, Ronald Oude, PhD</creatorcontrib><creatorcontrib>Zampronio, Aleksander Roberto, PhD</creatorcontrib><creatorcontrib>Acco, Alexandra, PhD</creatorcontrib><title>Effects of statins on liver cell function and inflammation in septic rats</title><title>The Journal of surgical research</title><addtitle>J Surg Res</addtitle><description>Abstract Background Several studies suggest that the presence of statins may be beneficial during sepsis, but this idea is controversial. The aim of this study was to investigate the effects of long-term statin treatment in the livers of septic animals, focusing on its antioxidant, antiinflammatory, and metabolic properties. Materials and methods Male Wistar rats were treated orally with simvastatin, atorvastatin, or vehicle once a d. After 30 d, sepsis was induced by cecal ligation and puncture (CLP) in Control, Simvastatin-treated, and Atorvastatin-treated groups, while the Sham group underwent only laparotomy. The Basal Simvastatin and Basal Atorvastatin groups received only their respective drugs without surgery. Twenty-four h after CLP or laparotomy, samples were collected from anesthetized rats for evaluation of hepatic oxidative stress, liver histology, hepatic mitochondria enzyme activity, leukocyte counts in blood and peritoneal cavity, gene expression of hepatic superoxide dismutase and TNF-2 , and plasma biochemistry. Results Most parameters that we tested exhibited expected changes upon sepsis induction. However, statin treatment only improved liver mitochondrial enzymatic activity. In other parameters, simvastatin and atorvastatin failed to protect the liver against injuries incurred upon the CLP-induced polymicrobial sepsis model. Conclusions Pretreatment with simvastatin or atorvastatin alone before sepsis induction improved mitochondrial activity in the liver; however, this result was not reproduced in other biomarkers of liver function and leukocyte migration during sepsis. 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The aim of this study was to investigate the effects of long-term statin treatment in the livers of septic animals, focusing on its antioxidant, antiinflammatory, and metabolic properties. Materials and methods Male Wistar rats were treated orally with simvastatin, atorvastatin, or vehicle once a d. After 30 d, sepsis was induced by cecal ligation and puncture (CLP) in Control, Simvastatin-treated, and Atorvastatin-treated groups, while the Sham group underwent only laparotomy. The Basal Simvastatin and Basal Atorvastatin groups received only their respective drugs without surgery. Twenty-four h after CLP or laparotomy, samples were collected from anesthetized rats for evaluation of hepatic oxidative stress, liver histology, hepatic mitochondria enzyme activity, leukocyte counts in blood and peritoneal cavity, gene expression of hepatic superoxide dismutase and TNF-2 , and plasma biochemistry. Results Most parameters that we tested exhibited expected changes upon sepsis induction. However, statin treatment only improved liver mitochondrial enzymatic activity. In other parameters, simvastatin and atorvastatin failed to protect the liver against injuries incurred upon the CLP-induced polymicrobial sepsis model. Conclusions Pretreatment with simvastatin or atorvastatin alone before sepsis induction improved mitochondrial activity in the liver; however, this result was not reproduced in other biomarkers of liver function and leukocyte migration during sepsis. Future studies should be performed to evaluate whether statins can be combined with other drugs to increase the efficacy of sepsis therapy.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22954522</pmid><doi>10.1016/j.jss.2012.08.019</doi><tpages>10</tpages></addata></record>
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subjects Animals
Atorvastatin
Hepatocytes - drug effects
Hepatocytes - pathology
Hepatocytes - physiology
Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology
Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use
Inflammation - drug therapy
Leukocytes
Liver
Male
Mitochondria
Oxidative stress
Oxidative Stress - drug effects
Rats
Rats, Wistar
Sepsis
Sepsis - drug therapy
Sepsis - metabolism
Sepsis - pathology
Simvastatin
Superoxide Dismutase - genetics
Superoxide Dismutase-1
Surgery
Tumor Necrosis Factor-alpha - genetics
title Effects of statins on liver cell function and inflammation in septic rats
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