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Folic acid and melatonin ameliorate carbon tetrachloride-induced hepatic injury, oxidative stress and inflammation in rats
This study investigated the protective effects of melatonin and folic acid against carbon tetrachloride (CCl4)-induced hepatic injury in rats. Oxidative stress, liver function, liver histopathology and serum lipid levels were evaluated. The levels of protein kinase B (Akt1), interferon gamma (IFN-γ)...
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Published in: | Nutrition & metabolism 2013-02, Vol.10 (1), p.20-20 |
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description | This study investigated the protective effects of melatonin and folic acid against carbon tetrachloride (CCl4)-induced hepatic injury in rats. Oxidative stress, liver function, liver histopathology and serum lipid levels were evaluated. The levels of protein kinase B (Akt1), interferon gamma (IFN-γ), programmed cell death-receptor (Fas) and Tumor necrosis factor-alpha (TNF-α) mRNA expression were analyzed. CCl4 significantly elevated the levels of lipid peroxidation (MDA), cholesterol, LDL, triglycerides, bilirubin and urea. In addition, CCl4 was found to significantly suppress the activity of both catalase and glutathione (GSH) and decrease the levels of serum total protein and HDL-cholesterol. All of these parameters were restored to their normal levels by treatment with melatonin, folic acid or their combination. An improvement of the general hepatic architecture was observed in rats that were treated with the combination of melatonin and folic acid along with CCl4. Furthermore, the CCl4-induced upregulation of TNF-α and Fas mRNA expression was significantly restored by the three treatments. Melatonin, folic acid or their combination also restored the baseline levels of IFN-γ and Akt1 mRNA expression. The combination of melatonin and folic acid exhibited ability to reduce the markers of liver injury induced by CCl4 and restore the oxidative stability, the level of inflammatory cytokines, the lipid profile and the cell survival Akt1 signals. |
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Oxidative stress, liver function, liver histopathology and serum lipid levels were evaluated. The levels of protein kinase B (Akt1), interferon gamma (IFN-γ), programmed cell death-receptor (Fas) and Tumor necrosis factor-alpha (TNF-α) mRNA expression were analyzed. CCl4 significantly elevated the levels of lipid peroxidation (MDA), cholesterol, LDL, triglycerides, bilirubin and urea. In addition, CCl4 was found to significantly suppress the activity of both catalase and glutathione (GSH) and decrease the levels of serum total protein and HDL-cholesterol. All of these parameters were restored to their normal levels by treatment with melatonin, folic acid or their combination. An improvement of the general hepatic architecture was observed in rats that were treated with the combination of melatonin and folic acid along with CCl4. Furthermore, the CCl4-induced upregulation of TNF-α and Fas mRNA expression was significantly restored by the three treatments. Melatonin, folic acid or their combination also restored the baseline levels of IFN-γ and Akt1 mRNA expression. The combination of melatonin and folic acid exhibited ability to reduce the markers of liver injury induced by CCl4 and restore the oxidative stability, the level of inflammatory cytokines, the lipid profile and the cell survival Akt1 signals.</description><identifier>ISSN: 1743-7075</identifier><identifier>EISSN: 1743-7075</identifier><identifier>DOI: 10.1186/1743-7075-10-20</identifier><identifier>PMID: 23374533</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Akt1 ; Anti-inflammatory effects ; Antioxidants ; blood lipids ; blood proteins ; carbon ; carbon tetrachloride ; catalase ; cholesterol ; Colleges & universities ; Folic acid ; gene expression ; glutathione ; Hepatic injury-markers ; histopathology ; inflammation ; interferon-gamma ; Kinases ; lipid peroxidation ; liver ; liver function ; low density lipoprotein ; Melatonin ; messenger RNA ; oxidative stability ; Oxidative stress ; protective effect ; rats ; Rodents ; triacylglycerols ; tumor necrosis factor-alpha ; urea ; Vitamin B</subject><ispartof>Nutrition & metabolism, 2013-02, Vol.10 (1), p.20-20</ispartof><rights>2013 Ebaid et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright ©2013 Ebaid et al.; licensee BioMed Central Ltd. 2013 Ebaid et al.; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c520t-931ea2ab61ad7516568e59ca2813a861e14595cd2622842e87e3b463708b1ccf3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570377/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1285771689?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23374533$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ebaid, Hossam</creatorcontrib><creatorcontrib>Bashandy, Samir Ae</creatorcontrib><creatorcontrib>Alhazza, Ibrahim M</creatorcontrib><creatorcontrib>Rady, Ahmed</creatorcontrib><creatorcontrib>El-Shehry, Sultan</creatorcontrib><title>Folic acid and melatonin ameliorate carbon tetrachloride-induced hepatic injury, oxidative stress and inflammation in rats</title><title>Nutrition & metabolism</title><addtitle>Nutr Metab (Lond)</addtitle><description>This study investigated the protective effects of melatonin and folic acid against carbon tetrachloride (CCl4)-induced hepatic injury in rats. Oxidative stress, liver function, liver histopathology and serum lipid levels were evaluated. The levels of protein kinase B (Akt1), interferon gamma (IFN-γ), programmed cell death-receptor (Fas) and Tumor necrosis factor-alpha (TNF-α) mRNA expression were analyzed. CCl4 significantly elevated the levels of lipid peroxidation (MDA), cholesterol, LDL, triglycerides, bilirubin and urea. In addition, CCl4 was found to significantly suppress the activity of both catalase and glutathione (GSH) and decrease the levels of serum total protein and HDL-cholesterol. All of these parameters were restored to their normal levels by treatment with melatonin, folic acid or their combination. An improvement of the general hepatic architecture was observed in rats that were treated with the combination of melatonin and folic acid along with CCl4. Furthermore, the CCl4-induced upregulation of TNF-α and Fas mRNA expression was significantly restored by the three treatments. Melatonin, folic acid or their combination also restored the baseline levels of IFN-γ and Akt1 mRNA expression. The combination of melatonin and folic acid exhibited ability to reduce the markers of liver injury induced by CCl4 and restore the oxidative stability, the level of inflammatory cytokines, the lipid profile and the cell survival Akt1 signals.</description><subject>Akt1</subject><subject>Anti-inflammatory effects</subject><subject>Antioxidants</subject><subject>blood lipids</subject><subject>blood proteins</subject><subject>carbon</subject><subject>carbon tetrachloride</subject><subject>catalase</subject><subject>cholesterol</subject><subject>Colleges & universities</subject><subject>Folic acid</subject><subject>gene expression</subject><subject>glutathione</subject><subject>Hepatic injury-markers</subject><subject>histopathology</subject><subject>inflammation</subject><subject>interferon-gamma</subject><subject>Kinases</subject><subject>lipid peroxidation</subject><subject>liver</subject><subject>liver function</subject><subject>low density lipoprotein</subject><subject>Melatonin</subject><subject>messenger RNA</subject><subject>oxidative stability</subject><subject>Oxidative stress</subject><subject>protective effect</subject><subject>rats</subject><subject>Rodents</subject><subject>triacylglycerols</subject><subject>tumor necrosis factor-alpha</subject><subject>urea</subject><subject>Vitamin B</subject><issn>1743-7075</issn><issn>1743-7075</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqFks1v1DAQxSMEoqVw5oYiceFAqL_tXJBQRaFSJS5wtib2bNerxC52UlH-epxuWbVcOHn05vmnmdFrmteUfKDUqFOqBe800bKjpGPkSXN8UJ4-qI-aF6XsCOFc9OR5c8Q410Jyftz8Pk9jcC244FuIvp1whDnFEFuoZUgZZmwd5CHFdsY5g9uOKQePXYh-cejbLV7DXBEh7pZ8-75Nv4Kvwg22Zc5Yyh02xM0I01T1yqnwii0vm2cbGAu-un9Pmh_nn7-ffe0uv325OPt02TnJyNz1nCIwGBQFryVVUhmUvQNmKAejKFIhe-k8U4wZwdBo5INQXBMzUOc2_KS52HN9gp29zmGCfGsTBHsnpHxlIdcNRrREegkDQekIE73DnrOemcFp2g8UjK-sj3vW9TJM6B3GepLxEfRxJ4atvUo3lktNuNYV8O4ekNPPBctsp1AcjiNETEuxVHCqmJBE_t_KjDZGCbJS3_5j3aUlx3rV1SW1psr01XW6d7mcSsm4OcxNiV3jZNfA2DUwq8JI_fHm4boH_9_88D-fQsX2</recordid><startdate>20130203</startdate><enddate>20130203</enddate><creator>Ebaid, Hossam</creator><creator>Bashandy, Samir Ae</creator><creator>Alhazza, Ibrahim M</creator><creator>Rady, Ahmed</creator><creator>El-Shehry, Sultan</creator><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130203</creationdate><title>Folic acid and melatonin ameliorate carbon tetrachloride-induced hepatic injury, oxidative stress and inflammation in rats</title><author>Ebaid, Hossam ; Bashandy, Samir Ae ; Alhazza, Ibrahim M ; Rady, Ahmed ; El-Shehry, Sultan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c520t-931ea2ab61ad7516568e59ca2813a861e14595cd2622842e87e3b463708b1ccf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Akt1</topic><topic>Anti-inflammatory effects</topic><topic>Antioxidants</topic><topic>blood lipids</topic><topic>blood proteins</topic><topic>carbon</topic><topic>carbon tetrachloride</topic><topic>catalase</topic><topic>cholesterol</topic><topic>Colleges & universities</topic><topic>Folic acid</topic><topic>gene expression</topic><topic>glutathione</topic><topic>Hepatic injury-markers</topic><topic>histopathology</topic><topic>inflammation</topic><topic>interferon-gamma</topic><topic>Kinases</topic><topic>lipid peroxidation</topic><topic>liver</topic><topic>liver function</topic><topic>low density lipoprotein</topic><topic>Melatonin</topic><topic>messenger RNA</topic><topic>oxidative stability</topic><topic>Oxidative stress</topic><topic>protective effect</topic><topic>rats</topic><topic>Rodents</topic><topic>triacylglycerols</topic><topic>tumor necrosis factor-alpha</topic><topic>urea</topic><topic>Vitamin B</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ebaid, Hossam</creatorcontrib><creatorcontrib>Bashandy, Samir Ae</creatorcontrib><creatorcontrib>Alhazza, Ibrahim M</creatorcontrib><creatorcontrib>Rady, Ahmed</creatorcontrib><creatorcontrib>El-Shehry, Sultan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Physical Education Index</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Nutrition & metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ebaid, Hossam</au><au>Bashandy, Samir Ae</au><au>Alhazza, Ibrahim M</au><au>Rady, Ahmed</au><au>El-Shehry, Sultan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Folic acid and melatonin ameliorate carbon tetrachloride-induced hepatic injury, oxidative stress and inflammation in rats</atitle><jtitle>Nutrition & metabolism</jtitle><addtitle>Nutr Metab (Lond)</addtitle><date>2013-02-03</date><risdate>2013</risdate><volume>10</volume><issue>1</issue><spage>20</spage><epage>20</epage><pages>20-20</pages><issn>1743-7075</issn><eissn>1743-7075</eissn><abstract>This study investigated the protective effects of melatonin and folic acid against carbon tetrachloride (CCl4)-induced hepatic injury in rats. Oxidative stress, liver function, liver histopathology and serum lipid levels were evaluated. The levels of protein kinase B (Akt1), interferon gamma (IFN-γ), programmed cell death-receptor (Fas) and Tumor necrosis factor-alpha (TNF-α) mRNA expression were analyzed. CCl4 significantly elevated the levels of lipid peroxidation (MDA), cholesterol, LDL, triglycerides, bilirubin and urea. In addition, CCl4 was found to significantly suppress the activity of both catalase and glutathione (GSH) and decrease the levels of serum total protein and HDL-cholesterol. All of these parameters were restored to their normal levels by treatment with melatonin, folic acid or their combination. An improvement of the general hepatic architecture was observed in rats that were treated with the combination of melatonin and folic acid along with CCl4. Furthermore, the CCl4-induced upregulation of TNF-α and Fas mRNA expression was significantly restored by the three treatments. Melatonin, folic acid or their combination also restored the baseline levels of IFN-γ and Akt1 mRNA expression. The combination of melatonin and folic acid exhibited ability to reduce the markers of liver injury induced by CCl4 and restore the oxidative stability, the level of inflammatory cytokines, the lipid profile and the cell survival Akt1 signals.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>23374533</pmid><doi>10.1186/1743-7075-10-20</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Akt1 Anti-inflammatory effects Antioxidants blood lipids blood proteins carbon carbon tetrachloride catalase cholesterol Colleges & universities Folic acid gene expression glutathione Hepatic injury-markers histopathology inflammation interferon-gamma Kinases lipid peroxidation liver liver function low density lipoprotein Melatonin messenger RNA oxidative stability Oxidative stress protective effect rats Rodents triacylglycerols tumor necrosis factor-alpha urea Vitamin B |
title | Folic acid and melatonin ameliorate carbon tetrachloride-induced hepatic injury, oxidative stress and inflammation in rats |
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