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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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. Future studies should be performed to evaluate whether statins can be combined with other drugs to increase the efficacy of sepsis therapy.</description><subject>Animals</subject><subject>Atorvastatin</subject><subject>Hepatocytes - drug effects</subject><subject>Hepatocytes - pathology</subject><subject>Hepatocytes - physiology</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</subject><subject>Inflammation - drug therapy</subject><subject>Leukocytes</subject><subject>Liver</subject><subject>Male</subject><subject>Mitochondria</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Sepsis</subject><subject>Sepsis - drug therapy</subject><subject>Sepsis - metabolism</subject><subject>Sepsis - pathology</subject><subject>Simvastatin</subject><subject>Superoxide Dismutase - genetics</subject><subject>Superoxide Dismutase-1</subject><subject>Surgery</subject><subject>Tumor Necrosis Factor-alpha - genetics</subject><issn>0022-4804</issn><issn>1095-8673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcFu1TAQRS1ERR-FD2CDsmSTMHbsxBESEqpaqFSJRWFtOc5Yckichyep1L-vw2tZsGDl8ejeq5kzjL3jUHHgzcexGokqAVxUoCvg3Qt24NCpUjdt_ZIdAIQopQZ5zl4TjZD_XVu_YudCdEoqIQ7s5sp7dCsViy9otWuIuYzFFO4xFQ6nqfBbdGvIPRuHIkQ_2Xm2fxohFoTHNbgi2ZXesDNvJ8K3T-8F-3l99ePyW3n7_evN5Zfb0knJ1xIdFzAMQ-eEFraT9aBEb5VzqpFeN3UvbN9abm0DWEPjO61Bd_u6jWoE9vUF-3DKPabl94a0mjnQPqmNuGxkOFe8zXJeZyk_SV1aiBJ6c0xhtunBcDB7pBlNJmh2gga0yQSz5_1T_NbPOPx1PCPLgk8nAeYl7wMmQy5gdDiElEmaYQn_jf_8j9tNIQZnp1_4gDQuW4qZnuGGssfc7SfcL5ihQSulqh8Bzy-VNw</recordid><startdate>20121201</startdate><enddate>20121201</enddate><creator>Stolf, Aline Maria, MSc</creator><creator>Lívero, Francislaine dos Reis, MSc</creator><creator>Dreifuss, Arturo Alejandro, MSc</creator><creator>Bastos-Pereira, Amanda Leite, MSc</creator><creator>Fabosi, Isabella Aviles</creator><creator>Alves de Souza, Carlos Eduardo</creator><creator>Gomes, Liana de Oliveira</creator><creator>Chicorski, Raphaella</creator><creator>Brandt, Anna Paula, MSc</creator><creator>Cadena, Silvia Maria Suter, PhD</creator><creator>Telles, José Ederaldo Queiroz, PhD</creator><creator>Hauser, Aline Borsato, PhD</creator><creator>Elferink, Ronald Oude, PhD</creator><creator>Zampronio, Aleksander Roberto, PhD</creator><creator>Acco, Alexandra, PhD</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20121201</creationdate><title>Effects of statins on liver cell function and inflammation in septic rats</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-ec120ddd9c282a943d52ba5cc564f863b2ab7a1aa60e306f98808910166562eb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Atorvastatin</topic><topic>Hepatocytes - drug effects</topic><topic>Hepatocytes - pathology</topic><topic>Hepatocytes - physiology</topic><topic>Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology</topic><topic>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</topic><topic>Inflammation - drug therapy</topic><topic>Leukocytes</topic><topic>Liver</topic><topic>Male</topic><topic>Mitochondria</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Sepsis</topic><topic>Sepsis - drug therapy</topic><topic>Sepsis - metabolism</topic><topic>Sepsis - pathology</topic><topic>Simvastatin</topic><topic>Superoxide Dismutase - genetics</topic><topic>Superoxide Dismutase-1</topic><topic>Surgery</topic><topic>Tumor Necrosis Factor-alpha - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of surgical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stolf, Aline Maria, MSc</au><au>Lívero, Francislaine dos Reis, MSc</au><au>Dreifuss, Arturo Alejandro, MSc</au><au>Bastos-Pereira, Amanda Leite, MSc</au><au>Fabosi, Isabella Aviles</au><au>Alves de Souza, Carlos Eduardo</au><au>Gomes, Liana de Oliveira</au><au>Chicorski, Raphaella</au><au>Brandt, Anna Paula, MSc</au><au>Cadena, Silvia Maria Suter, PhD</au><au>Telles, José Ederaldo Queiroz, PhD</au><au>Hauser, Aline Borsato, PhD</au><au>Elferink, Ronald Oude, PhD</au><au>Zampronio, Aleksander Roberto, PhD</au><au>Acco, Alexandra, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of statins on liver cell function and inflammation in septic rats</atitle><jtitle>The Journal of surgical research</jtitle><addtitle>J Surg Res</addtitle><date>2012-12-01</date><risdate>2012</risdate><volume>178</volume><issue>2</issue><spage>888</spage><epage>897</epage><pages>888-897</pages><issn>0022-4804</issn><eissn>1095-8673</eissn><abstract>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.</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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