Acute effect of aspartame-induced oxidative stress in Wistar albino rat brain
The present study was carried out to investigate the acute effect of aspartame on oxidative stress in the Wistar albino rat brain. We sought to investigate whether acute administration of aspartame (75 mg/kg) could release methanol and induce oxidative stress in the rat brain 24 hours after administ...
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Veröffentlicht in: | Journal of biomedical research 2015-01, Vol.29 (5), p.390-396 |
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description | The present study was carried out to investigate the acute effect of aspartame on oxidative stress in the Wistar albino rat brain. We sought to investigate whether acute administration of aspartame (75 mg/kg) could release methanol and induce oxidative stress in the rat brain 24 hours after administration. To mimic human methanol metabolism, methotrexate treated rats were used to study aspartame effects. Wistar strain male albino rats were administered with aspartame orally as a single dose and studied along with controls and methotrexate treated controls. Blood methanol and formate level were estimated after 24 hours and rats were sacrificed and free radical changes were observed in discrete regions by assessing the scavenging enzymes, reduce dglutathione (GSH), lipid peroxidation and protein thiol levels. There was a significant increase in lipid peroxidation levels, superoxide dismutase activity (SOD), glutathione peroxidase levels (GPx), and catalase activity (CAT) with a significant decrease in GSH and protein thiol. Aspartame exposure resulted in detectable methanol even after 24 hours. Methanol and its metabolites may be responsible for the generation of oxidative stress in brain regions. The observed alteration in aspartame fed animals may be due to its metabolite methanol and elevated formate. The elevated free radicals due to methanol induced oxidative stress. |
doi_str_mv | 10.7555/JBR.28.20120118 |
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We sought to investigate whether acute administration of aspartame (75 mg/kg) could release methanol and induce oxidative stress in the rat brain 24 hours after administration. To mimic human methanol metabolism, methotrexate treated rats were used to study aspartame effects. Wistar strain male albino rats were administered with aspartame orally as a single dose and studied along with controls and methotrexate treated controls. Blood methanol and formate level were estimated after 24 hours and rats were sacrificed and free radical changes were observed in discrete regions by assessing the scavenging enzymes, reduce dglutathione (GSH), lipid peroxidation and protein thiol levels. There was a significant increase in lipid peroxidation levels, superoxide dismutase activity (SOD), glutathione peroxidase levels (GPx), and catalase activity (CAT) with a significant decrease in GSH and protein thiol. Aspartame exposure resulted in detectable methanol even after 24 hours. Methanol and its metabolites may be responsible for the generation of oxidative stress in brain regions. The observed alteration in aspartame fed animals may be due to its metabolite methanol and elevated formate. The elevated free radicals due to methanol induced oxidative stress.</description><identifier>ISSN: 1674-8301</identifier><identifier>DOI: 10.7555/JBR.28.20120118</identifier><identifier>PMID: 26445572</identifier><language>eng</language><publisher>China: Editorial Department of Journal of Biomedical Research</publisher><subject>Original ; Wistar大鼠 ; 急性 ; 氧化应激 ; 脑组织 ; 诱导 ; 谷胱甘肽过氧化物酶 ; 超氧化物歧化酶 ; 阿斯巴甜</subject><ispartof>Journal of biomedical research, 2015-01, Vol.29 (5), p.390-396</ispartof><rights>2015 by the Journal of Biomedical Research. All rights reserved. 2015</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-8f18b6dd44ece07a537d079652869a0ae60859cc5a8ba3f1653380a643d2ad833</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/85389A/85389A.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585433/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585433/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26445572$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ashok, Iyaswamy</creatorcontrib><creatorcontrib>Sheeladevi, Rathinasamy</creatorcontrib><creatorcontrib>Wankhar, Dapkupar</creatorcontrib><title>Acute effect of aspartame-induced oxidative stress in Wistar albino rat brain</title><title>Journal of biomedical research</title><addtitle>Journal of Biomedical Research</addtitle><description>The present study was carried out to investigate the acute effect of aspartame on oxidative stress in the Wistar albino rat brain. We sought to investigate whether acute administration of aspartame (75 mg/kg) could release methanol and induce oxidative stress in the rat brain 24 hours after administration. To mimic human methanol metabolism, methotrexate treated rats were used to study aspartame effects. Wistar strain male albino rats were administered with aspartame orally as a single dose and studied along with controls and methotrexate treated controls. Blood methanol and formate level were estimated after 24 hours and rats were sacrificed and free radical changes were observed in discrete regions by assessing the scavenging enzymes, reduce dglutathione (GSH), lipid peroxidation and protein thiol levels. There was a significant increase in lipid peroxidation levels, superoxide dismutase activity (SOD), glutathione peroxidase levels (GPx), and catalase activity (CAT) with a significant decrease in GSH and protein thiol. Aspartame exposure resulted in detectable methanol even after 24 hours. Methanol and its metabolites may be responsible for the generation of oxidative stress in brain regions. The observed alteration in aspartame fed animals may be due to its metabolite methanol and elevated formate. The elevated free radicals due to methanol induced oxidative stress.</description><subject>Original</subject><subject>Wistar大鼠</subject><subject>急性</subject><subject>氧化应激</subject><subject>脑组织</subject><subject>诱导</subject><subject>谷胱甘肽过氧化物酶</subject><subject>超氧化物歧化酶</subject><subject>阿斯巴甜</subject><issn>1674-8301</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNpVkM9rFTEQx3NQbKk9e5Pgycu-5vdmL0It_qQiiOIxzCazr5F9yWuSLfrfu6WvDw0DOcxnvjN8CHnB2abXWl98fvttI-xGML4Wt0_IKTe96qxk_ISc1_qLrU8ORij7jJwIo5TWvTglXy790pDiNKFvNE8U6h5Kgx12MYXFY6D5dwzQ4h3S2grWSmOiP2NtUCjMY0yZFmh0LBDTc_J0grni-eE_Iz_ev_t-9bG7_vrh09XldeeVYK2zE7ejCUEp9Mh60LIPrB-MFtYMwAANs3rwXoMdQU7caCktA6NkEBCslGfkzUPufhl3GDymVmB2-xJ3UP64DNH930nxxm3znVPaaiXvA14fAkq-XbA2t4vV4zxDwrxUx3vBpRo0Myt68YD6kmstOB3XcObu3bvVvRPWPbpfJ17-e92Rf7S-Aq8OkTc5bW9j2h4ZY4y0Vggr_wKL8o0n</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Ashok, Iyaswamy</creator><creator>Sheeladevi, Rathinasamy</creator><creator>Wankhar, Dapkupar</creator><general>Editorial Department of Journal of Biomedical Research</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150101</creationdate><title>Acute effect of aspartame-induced oxidative stress in Wistar albino rat brain</title><author>Ashok, Iyaswamy ; Sheeladevi, Rathinasamy ; Wankhar, Dapkupar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-8f18b6dd44ece07a537d079652869a0ae60859cc5a8ba3f1653380a643d2ad833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Original</topic><topic>Wistar大鼠</topic><topic>急性</topic><topic>氧化应激</topic><topic>脑组织</topic><topic>诱导</topic><topic>谷胱甘肽过氧化物酶</topic><topic>超氧化物歧化酶</topic><topic>阿斯巴甜</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ashok, Iyaswamy</creatorcontrib><creatorcontrib>Sheeladevi, Rathinasamy</creatorcontrib><creatorcontrib>Wankhar, Dapkupar</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of biomedical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ashok, Iyaswamy</au><au>Sheeladevi, Rathinasamy</au><au>Wankhar, Dapkupar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute effect of aspartame-induced oxidative stress in Wistar albino rat brain</atitle><jtitle>Journal of biomedical research</jtitle><addtitle>Journal of Biomedical Research</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>29</volume><issue>5</issue><spage>390</spage><epage>396</epage><pages>390-396</pages><issn>1674-8301</issn><abstract>The present study was carried out to investigate the acute effect of aspartame on oxidative stress in the Wistar albino rat brain. We sought to investigate whether acute administration of aspartame (75 mg/kg) could release methanol and induce oxidative stress in the rat brain 24 hours after administration. To mimic human methanol metabolism, methotrexate treated rats were used to study aspartame effects. Wistar strain male albino rats were administered with aspartame orally as a single dose and studied along with controls and methotrexate treated controls. Blood methanol and formate level were estimated after 24 hours and rats were sacrificed and free radical changes were observed in discrete regions by assessing the scavenging enzymes, reduce dglutathione (GSH), lipid peroxidation and protein thiol levels. There was a significant increase in lipid peroxidation levels, superoxide dismutase activity (SOD), glutathione peroxidase levels (GPx), and catalase activity (CAT) with a significant decrease in GSH and protein thiol. Aspartame exposure resulted in detectable methanol even after 24 hours. Methanol and its metabolites may be responsible for the generation of oxidative stress in brain regions. The observed alteration in aspartame fed animals may be due to its metabolite methanol and elevated formate. The elevated free radicals due to methanol induced oxidative stress.</abstract><cop>China</cop><pub>Editorial Department of Journal of Biomedical Research</pub><pmid>26445572</pmid><doi>10.7555/JBR.28.20120118</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Original Wistar大鼠 急性 氧化应激 脑组织 诱导 谷胱甘肽过氧化物酶 超氧化物歧化酶 阿斯巴甜 |
title | Acute effect of aspartame-induced oxidative stress in Wistar albino rat brain |
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