Treatment with cannabidiol reverses oxidative stress parameters, cognitive impairment and mortality in rats submitted to sepsis by cecal ligation and puncture
Abstract Oxidative stress plays an important role in the development of cognitive impairment in sepsis. Here we assess the effects of acute and extended administration of cannabidiol (CBD) on oxidative stress parameters in peripheral organs and in the brain, cognitive impairment, and mortality in ra...
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Veröffentlicht in: | Brain research 2010-08, Vol.1348, p.128-138 |
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creator | Cassol-Jr, Omar J Comim, Clarissa M Silva, Bruno R Hermani, Fernanda V Constantino, Larissa S Felisberto, Francine Petronilho, Fabricia Hallak, Jaime Eduardo C De Martinis, Bruno S Zuardi, Antonio W Crippa, José A.S Quevedo, João Dal-Pizzol, Felipe |
description | Abstract Oxidative stress plays an important role in the development of cognitive impairment in sepsis. Here we assess the effects of acute and extended administration of cannabidiol (CBD) on oxidative stress parameters in peripheral organs and in the brain, cognitive impairment, and mortality in rats submitted to sepsis by cecal ligation and perforation (CLP). To this aim, male Wistar rats underwent either sham operation or CLP. Rats subjected to CLP were treated by intraperitoneal injection with “basic support” and CBD (at 2.5, 5, or 10 mg/kg once or daily for 9 days after CLP) or vehicle. Six hours after CLP (early times), the rats were killed and samples from lung, liver, kidney, heart, spleen, and brain (hippocampus, striatum, and cortex) were obtained and assayed for thiobarbituric acid reactive species (TBARS) formation and protein carbonyls. On the 10th day (late times), the rats were submitted to the inhibitory avoidance task. After the test, the animals were killed and samples from lung, liver, kidney, heart, spleen, and brain (hippocampus) were obtained and assayed for TBARS formation and protein carbonyls. The acute and extended administration of CBD at different doses reduced TBARS and carbonyl levels in some organs and had no effects in others, ameliorated cognitive impairment, and significantly reduced mortality in rats submitted to CLP. Our data provide the first experimental demonstration that CBD reduces the consequences of sepsis induced by CLP in rats, by decreasing oxidative stress in peripheral organs and in the brain, improving impaired cognitive function, and decreasing mortality. |
doi_str_mv | 10.1016/j.brainres.2010.06.023 |
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Here we assess the effects of acute and extended administration of cannabidiol (CBD) on oxidative stress parameters in peripheral organs and in the brain, cognitive impairment, and mortality in rats submitted to sepsis by cecal ligation and perforation (CLP). To this aim, male Wistar rats underwent either sham operation or CLP. Rats subjected to CLP were treated by intraperitoneal injection with “basic support” and CBD (at 2.5, 5, or 10 mg/kg once or daily for 9 days after CLP) or vehicle. Six hours after CLP (early times), the rats were killed and samples from lung, liver, kidney, heart, spleen, and brain (hippocampus, striatum, and cortex) were obtained and assayed for thiobarbituric acid reactive species (TBARS) formation and protein carbonyls. On the 10th day (late times), the rats were submitted to the inhibitory avoidance task. After the test, the animals were killed and samples from lung, liver, kidney, heart, spleen, and brain (hippocampus) were obtained and assayed for TBARS formation and protein carbonyls. The acute and extended administration of CBD at different doses reduced TBARS and carbonyl levels in some organs and had no effects in others, ameliorated cognitive impairment, and significantly reduced mortality in rats submitted to CLP. Our data provide the first experimental demonstration that CBD reduces the consequences of sepsis induced by CLP in rats, by decreasing oxidative stress in peripheral organs and in the brain, improving impaired cognitive function, and decreasing mortality.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/j.brainres.2010.06.023</identifier><identifier>PMID: 20561509</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Analysis of Variance ; Animals ; Avoidance Learning - drug effects ; Brain - drug effects ; Brain - metabolism ; Cannabidiol ; Cannabidiol - therapeutic use ; Cecum - injuries ; Disease Models, Animal ; Dose-Response Relationship, Drug ; Male ; Memory ; Memory Disorders - drug therapy ; Memory Disorders - etiology ; Mortality ; Neurology ; Oxidative stress ; Protein Carbonylation - drug effects ; Punctures - adverse effects ; Rats ; Rats, Wistar ; Sepsis ; Sepsis - complications ; Sepsis - etiology ; Stress, Psychological - drug therapy ; Stress, Psychological - etiology ; Thiobarbituric Acid Reactive Substances - metabolism ; Time Factors</subject><ispartof>Brain research, 2010-08, Vol.1348, p.128-138</ispartof><rights>Elsevier B.V.</rights><rights>2010 Elsevier B.V.</rights><rights>Copyright 2010 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c454t-bebaaffa7f62a515edb46d4e953de4cda12f2155818c8da6950d6c337b72956b3</citedby><cites>FETCH-LOGICAL-c454t-bebaaffa7f62a515edb46d4e953de4cda12f2155818c8da6950d6c337b72956b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006899310013582$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20561509$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cassol-Jr, Omar J</creatorcontrib><creatorcontrib>Comim, Clarissa M</creatorcontrib><creatorcontrib>Silva, Bruno R</creatorcontrib><creatorcontrib>Hermani, Fernanda V</creatorcontrib><creatorcontrib>Constantino, Larissa S</creatorcontrib><creatorcontrib>Felisberto, Francine</creatorcontrib><creatorcontrib>Petronilho, Fabricia</creatorcontrib><creatorcontrib>Hallak, Jaime Eduardo C</creatorcontrib><creatorcontrib>De Martinis, Bruno S</creatorcontrib><creatorcontrib>Zuardi, Antonio W</creatorcontrib><creatorcontrib>Crippa, José A.S</creatorcontrib><creatorcontrib>Quevedo, João</creatorcontrib><creatorcontrib>Dal-Pizzol, Felipe</creatorcontrib><title>Treatment with cannabidiol reverses oxidative stress parameters, cognitive impairment and mortality in rats submitted to sepsis by cecal ligation and puncture</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>Abstract Oxidative stress plays an important role in the development of cognitive impairment in sepsis. Here we assess the effects of acute and extended administration of cannabidiol (CBD) on oxidative stress parameters in peripheral organs and in the brain, cognitive impairment, and mortality in rats submitted to sepsis by cecal ligation and perforation (CLP). To this aim, male Wistar rats underwent either sham operation or CLP. Rats subjected to CLP were treated by intraperitoneal injection with “basic support” and CBD (at 2.5, 5, or 10 mg/kg once or daily for 9 days after CLP) or vehicle. Six hours after CLP (early times), the rats were killed and samples from lung, liver, kidney, heart, spleen, and brain (hippocampus, striatum, and cortex) were obtained and assayed for thiobarbituric acid reactive species (TBARS) formation and protein carbonyls. On the 10th day (late times), the rats were submitted to the inhibitory avoidance task. After the test, the animals were killed and samples from lung, liver, kidney, heart, spleen, and brain (hippocampus) were obtained and assayed for TBARS formation and protein carbonyls. The acute and extended administration of CBD at different doses reduced TBARS and carbonyl levels in some organs and had no effects in others, ameliorated cognitive impairment, and significantly reduced mortality in rats submitted to CLP. Our data provide the first experimental demonstration that CBD reduces the consequences of sepsis induced by CLP in rats, by decreasing oxidative stress in peripheral organs and in the brain, improving impaired cognitive function, and decreasing mortality.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Avoidance Learning - drug effects</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Cannabidiol</subject><subject>Cannabidiol - therapeutic use</subject><subject>Cecum - injuries</subject><subject>Disease Models, Animal</subject><subject>Dose-Response Relationship, Drug</subject><subject>Male</subject><subject>Memory</subject><subject>Memory Disorders - drug therapy</subject><subject>Memory Disorders - etiology</subject><subject>Mortality</subject><subject>Neurology</subject><subject>Oxidative stress</subject><subject>Protein Carbonylation - drug effects</subject><subject>Punctures - adverse effects</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Sepsis</subject><subject>Sepsis - complications</subject><subject>Sepsis - etiology</subject><subject>Stress, Psychological - drug therapy</subject><subject>Stress, Psychological - etiology</subject><subject>Thiobarbituric Acid Reactive Substances - metabolism</subject><subject>Time Factors</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUstu1DAUjRCIDoVfqLxjwwx-xE6yQaAKClIlFpS15dg35Q6JHWxnYH6Gb61npmXBpivr-p6HdM6tqgtGN4wy9Xa76aNBHyFtOC2fVG0oF0-qFWsbvla8pk-rFaVUrduuE2fVi5S2ZRSio8-rM06lYpJ2q-rvTQSTJ_CZ_Mb8g1jjvenRYRhJhB3EBImEP-hMxh2QlItjIrOJZoJctm-IDbcej0ucZoPxqGW8I1OI2YyY9wQ9iSYnkpZ-wpzBkRxIgjlhIv2eWLBmJCPeFo_gj9x58TYvEV5WzwYzJnh1_55X3z99vLn8vL7-evXl8sP12tayzuseemOGwTSD4kYyCa6vlauhk8JBbZ1hfOBMypa1tnVGdZI6ZYVo-oZ3UvXivHp90p1j-LVAynrCZGEcjYewJN3ShismGvEosqk7ypVoWUGqE9LGkFKEQc8RJxP3mlF9KFFv9UOJ-lCipkqXEgvx4t6i5AXuH-2htQJ4fwJAiWSHEHWyCN6Cwwg2axfwcY93_0nYET2WIn7CHtI2LNGXwDXTiWuqvx1O6XBJjFImZMvFHRq4yx0</recordid><startdate>20100812</startdate><enddate>20100812</enddate><creator>Cassol-Jr, Omar J</creator><creator>Comim, Clarissa M</creator><creator>Silva, Bruno R</creator><creator>Hermani, Fernanda V</creator><creator>Constantino, Larissa S</creator><creator>Felisberto, Francine</creator><creator>Petronilho, Fabricia</creator><creator>Hallak, Jaime Eduardo C</creator><creator>De Martinis, Bruno S</creator><creator>Zuardi, Antonio W</creator><creator>Crippa, José A.S</creator><creator>Quevedo, João</creator><creator>Dal-Pizzol, Felipe</creator><general>Elsevier B.V</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><scope>7QL</scope><scope>7TK</scope><scope>C1K</scope></search><sort><creationdate>20100812</creationdate><title>Treatment with cannabidiol reverses oxidative stress parameters, cognitive impairment and mortality in rats submitted to sepsis by cecal ligation and puncture</title><author>Cassol-Jr, Omar J ; Comim, Clarissa M ; Silva, Bruno R ; Hermani, Fernanda V ; Constantino, Larissa S ; Felisberto, Francine ; Petronilho, Fabricia ; Hallak, Jaime Eduardo C ; De Martinis, Bruno S ; Zuardi, Antonio W ; Crippa, José A.S ; Quevedo, João ; Dal-Pizzol, Felipe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c454t-bebaaffa7f62a515edb46d4e953de4cda12f2155818c8da6950d6c337b72956b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Avoidance Learning - drug effects</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Cannabidiol</topic><topic>Cannabidiol - therapeutic use</topic><topic>Cecum - injuries</topic><topic>Disease Models, Animal</topic><topic>Dose-Response Relationship, Drug</topic><topic>Male</topic><topic>Memory</topic><topic>Memory Disorders - drug therapy</topic><topic>Memory Disorders - etiology</topic><topic>Mortality</topic><topic>Neurology</topic><topic>Oxidative stress</topic><topic>Protein Carbonylation - drug effects</topic><topic>Punctures - adverse effects</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Sepsis</topic><topic>Sepsis - complications</topic><topic>Sepsis - etiology</topic><topic>Stress, Psychological - drug therapy</topic><topic>Stress, Psychological - etiology</topic><topic>Thiobarbituric Acid Reactive Substances - metabolism</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cassol-Jr, Omar J</creatorcontrib><creatorcontrib>Comim, Clarissa M</creatorcontrib><creatorcontrib>Silva, Bruno R</creatorcontrib><creatorcontrib>Hermani, Fernanda V</creatorcontrib><creatorcontrib>Constantino, Larissa S</creatorcontrib><creatorcontrib>Felisberto, Francine</creatorcontrib><creatorcontrib>Petronilho, Fabricia</creatorcontrib><creatorcontrib>Hallak, Jaime Eduardo C</creatorcontrib><creatorcontrib>De Martinis, Bruno S</creatorcontrib><creatorcontrib>Zuardi, Antonio W</creatorcontrib><creatorcontrib>Crippa, José A.S</creatorcontrib><creatorcontrib>Quevedo, João</creatorcontrib><creatorcontrib>Dal-Pizzol, Felipe</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><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Neurosciences Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cassol-Jr, Omar J</au><au>Comim, Clarissa M</au><au>Silva, Bruno R</au><au>Hermani, Fernanda V</au><au>Constantino, Larissa S</au><au>Felisberto, Francine</au><au>Petronilho, Fabricia</au><au>Hallak, Jaime Eduardo C</au><au>De Martinis, Bruno S</au><au>Zuardi, Antonio W</au><au>Crippa, José A.S</au><au>Quevedo, João</au><au>Dal-Pizzol, Felipe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Treatment with cannabidiol reverses oxidative stress parameters, cognitive impairment and mortality in rats submitted to sepsis by cecal ligation and puncture</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2010-08-12</date><risdate>2010</risdate><volume>1348</volume><spage>128</spage><epage>138</epage><pages>128-138</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><abstract>Abstract Oxidative stress plays an important role in the development of cognitive impairment in sepsis. Here we assess the effects of acute and extended administration of cannabidiol (CBD) on oxidative stress parameters in peripheral organs and in the brain, cognitive impairment, and mortality in rats submitted to sepsis by cecal ligation and perforation (CLP). To this aim, male Wistar rats underwent either sham operation or CLP. Rats subjected to CLP were treated by intraperitoneal injection with “basic support” and CBD (at 2.5, 5, or 10 mg/kg once or daily for 9 days after CLP) or vehicle. Six hours after CLP (early times), the rats were killed and samples from lung, liver, kidney, heart, spleen, and brain (hippocampus, striatum, and cortex) were obtained and assayed for thiobarbituric acid reactive species (TBARS) formation and protein carbonyls. On the 10th day (late times), the rats were submitted to the inhibitory avoidance task. After the test, the animals were killed and samples from lung, liver, kidney, heart, spleen, and brain (hippocampus) were obtained and assayed for TBARS formation and protein carbonyls. The acute and extended administration of CBD at different doses reduced TBARS and carbonyl levels in some organs and had no effects in others, ameliorated cognitive impairment, and significantly reduced mortality in rats submitted to CLP. Our data provide the first experimental demonstration that CBD reduces the consequences of sepsis induced by CLP in rats, by decreasing oxidative stress in peripheral organs and in the brain, improving impaired cognitive function, and decreasing mortality.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>20561509</pmid><doi>10.1016/j.brainres.2010.06.023</doi><tpages>11</tpages></addata></record> |
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subjects | Analysis of Variance Animals Avoidance Learning - drug effects Brain - drug effects Brain - metabolism Cannabidiol Cannabidiol - therapeutic use Cecum - injuries Disease Models, Animal Dose-Response Relationship, Drug Male Memory Memory Disorders - drug therapy Memory Disorders - etiology Mortality Neurology Oxidative stress Protein Carbonylation - drug effects Punctures - adverse effects Rats Rats, Wistar Sepsis Sepsis - complications Sepsis - etiology Stress, Psychological - drug therapy Stress, Psychological - etiology Thiobarbituric Acid Reactive Substances - metabolism Time Factors |
title | Treatment with cannabidiol reverses oxidative stress parameters, cognitive impairment and mortality in rats submitted to sepsis by cecal ligation and puncture |
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