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Effects of melatonin on aluminium-induced neurobehavioral and neurochemical changes in aging rats
•Reactive oxygen species (ROS) play a strong role in the aging process.•Aluminium supplementation enhanced behavioral declines in aging circumstances.•Assessment was performed by ‘open fields’, ‘elevated plus maze’ and ‘Radial 8-arms maze’ tasks.•Melatonin plays a neuroprotective role against alumin...
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Published in: | Food and chemical toxicology 2014-08, Vol.70, p.84-93 |
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description | •Reactive oxygen species (ROS) play a strong role in the aging process.•Aluminium supplementation enhanced behavioral declines in aging circumstances.•Assessment was performed by ‘open fields’, ‘elevated plus maze’ and ‘Radial 8-arms maze’ tasks.•Melatonin plays a neuroprotective role against aluminium-induced neurobehavioral changes.•Melatonin offers neuroprotection against cholinergic and oxidative damages in aging rats.
This study aimed to investigate the potential protective effects of melatonin (Mel) against aluminium-induced neurodegenerative changes in aging Wistar rats (24–28months old). Herein, aluminium chloride (AlCl3) (50mg/kg BW/day) was administered by gavage, and melatonin (Mel) was co-administered to a group of Al-treated rats by an intra-peritoneal injection at a daily dose of 10mg/kg BW for four months. The findings revealed that aluminium administration induced a significant decrease in body weight associated with marked mortality for the old group of rats, which was more pronounced in old Al-treated rats. Behavioural alterations were assessed by ‘open fields’, ‘elevated plus maze’ and ‘Radial 8-arms maze’ tests. The results demonstrated that Mel co-administration alleviated neurobehavioral changes in both old and old Al-treated rats. Melatonin was noted to play a good neuroprotective role, reducing lipid peroxidation (TBARs), and enhancing enzymatic (SOD, CAT and GPx) activities in the brain organs of old control and old Al-treated rats. Mel treatment also reversed the decrease of AChE activity in the brain tissues, which was confirmed by histological sections. Overall, the results showed that Mel administration can induce beneficial effects for the treatment of Al-induced neurobehavioral and neurochemical changes in the central nervous system (CNS). |
doi_str_mv | 10.1016/j.fct.2014.03.043 |
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This study aimed to investigate the potential protective effects of melatonin (Mel) against aluminium-induced neurodegenerative changes in aging Wistar rats (24–28months old). Herein, aluminium chloride (AlCl3) (50mg/kg BW/day) was administered by gavage, and melatonin (Mel) was co-administered to a group of Al-treated rats by an intra-peritoneal injection at a daily dose of 10mg/kg BW for four months. The findings revealed that aluminium administration induced a significant decrease in body weight associated with marked mortality for the old group of rats, which was more pronounced in old Al-treated rats. Behavioural alterations were assessed by ‘open fields’, ‘elevated plus maze’ and ‘Radial 8-arms maze’ tests. The results demonstrated that Mel co-administration alleviated neurobehavioral changes in both old and old Al-treated rats. Melatonin was noted to play a good neuroprotective role, reducing lipid peroxidation (TBARs), and enhancing enzymatic (SOD, CAT and GPx) activities in the brain organs of old control and old Al-treated rats. Mel treatment also reversed the decrease of AChE activity in the brain tissues, which was confirmed by histological sections. Overall, the results showed that Mel administration can induce beneficial effects for the treatment of Al-induced neurobehavioral and neurochemical changes in the central nervous system (CNS).</description><identifier>ISSN: 0278-6915</identifier><identifier>EISSN: 1873-6351</identifier><identifier>DOI: 10.1016/j.fct.2014.03.043</identifier><identifier>PMID: 24727051</identifier><identifier>CODEN: FCTOD7</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Acetylcholinesterase - metabolism ; AChE activity ; Aging ; Aging - drug effects ; Aluminium toxicity ; Aluminum ; Aluminum - administration & dosage ; Aluminum - toxicity ; Animals ; Behavior, Animal - drug effects ; Biological and medical sciences ; Body Weight - drug effects ; Brain ; Brain - drug effects ; Brain - metabolism ; Catalase - metabolism ; Central nervous system ; Chemical and industrial products toxicology. Toxic occupational diseases ; Food toxicology ; Glutathione Peroxidase - metabolism ; Lipid Peroxidation - drug effects ; Lipids ; Male ; Medical sciences ; Melatonin ; Melatonin - administration & dosage ; Melatonin - toxicity ; Metals and various inorganic compounds ; Mortality ; Neurodegenerative Diseases - chemically induced ; Neurodegenerative Diseases - pathology ; Oxidative stress ; Oxidative Stress - drug effects ; Protective ; Rats ; Rats, Wistar ; Superoxide Dismutase - metabolism ; Thiobarbituric Acid Reactive Substances - metabolism ; Toxicology</subject><ispartof>Food and chemical toxicology, 2014-08, Vol.70, p.84-93</ispartof><rights>2014 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c449t-4d8e21bfe0ff5fc1ec03dc6a3052d983e395c6ae38aa72b187fe664aacc405733</citedby><cites>FETCH-LOGICAL-c449t-4d8e21bfe0ff5fc1ec03dc6a3052d983e395c6ae38aa72b187fe664aacc405733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28600442$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24727051$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Allagui, M.S.</creatorcontrib><creatorcontrib>Feriani, A.</creatorcontrib><creatorcontrib>Saoudi, M.</creatorcontrib><creatorcontrib>Badraoui, R.</creatorcontrib><creatorcontrib>Bouoni, Z.</creatorcontrib><creatorcontrib>Nciri, R.</creatorcontrib><creatorcontrib>Murat, J.C.</creatorcontrib><creatorcontrib>Elfeki, A.</creatorcontrib><title>Effects of melatonin on aluminium-induced neurobehavioral and neurochemical changes in aging rats</title><title>Food and chemical toxicology</title><addtitle>Food Chem Toxicol</addtitle><description>•Reactive oxygen species (ROS) play a strong role in the aging process.•Aluminium supplementation enhanced behavioral declines in aging circumstances.•Assessment was performed by ‘open fields’, ‘elevated plus maze’ and ‘Radial 8-arms maze’ tasks.•Melatonin plays a neuroprotective role against aluminium-induced neurobehavioral changes.•Melatonin offers neuroprotection against cholinergic and oxidative damages in aging rats.
This study aimed to investigate the potential protective effects of melatonin (Mel) against aluminium-induced neurodegenerative changes in aging Wistar rats (24–28months old). Herein, aluminium chloride (AlCl3) (50mg/kg BW/day) was administered by gavage, and melatonin (Mel) was co-administered to a group of Al-treated rats by an intra-peritoneal injection at a daily dose of 10mg/kg BW for four months. The findings revealed that aluminium administration induced a significant decrease in body weight associated with marked mortality for the old group of rats, which was more pronounced in old Al-treated rats. Behavioural alterations were assessed by ‘open fields’, ‘elevated plus maze’ and ‘Radial 8-arms maze’ tests. The results demonstrated that Mel co-administration alleviated neurobehavioral changes in both old and old Al-treated rats. Melatonin was noted to play a good neuroprotective role, reducing lipid peroxidation (TBARs), and enhancing enzymatic (SOD, CAT and GPx) activities in the brain organs of old control and old Al-treated rats. Mel treatment also reversed the decrease of AChE activity in the brain tissues, which was confirmed by histological sections. Overall, the results showed that Mel administration can induce beneficial effects for the treatment of Al-induced neurobehavioral and neurochemical changes in the central nervous system (CNS).</description><subject>Acetylcholinesterase - metabolism</subject><subject>AChE activity</subject><subject>Aging</subject><subject>Aging - drug effects</subject><subject>Aluminium toxicity</subject><subject>Aluminum</subject><subject>Aluminum - administration & dosage</subject><subject>Aluminum - toxicity</subject><subject>Animals</subject><subject>Behavior, Animal - drug effects</subject><subject>Biological and medical sciences</subject><subject>Body Weight - drug effects</subject><subject>Brain</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Catalase - metabolism</subject><subject>Central nervous system</subject><subject>Chemical and industrial products toxicology. Toxic occupational diseases</subject><subject>Food toxicology</subject><subject>Glutathione Peroxidase - metabolism</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Lipids</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Melatonin</subject><subject>Melatonin - administration & dosage</subject><subject>Melatonin - toxicity</subject><subject>Metals and various inorganic compounds</subject><subject>Mortality</subject><subject>Neurodegenerative Diseases - chemically induced</subject><subject>Neurodegenerative Diseases - pathology</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Protective</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Thiobarbituric Acid Reactive Substances - metabolism</subject><subject>Toxicology</subject><issn>0278-6915</issn><issn>1873-6351</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkU1r3DAQhkVpaLZpf0AvxZdCL3b0LZueSkg_INBLchaz8mhXiy2lkh3ov4-W3ba30pPQ8Mxo9D6EvGO0Y5Tp60Pn3dJxymRHRUeleEE2rDei1UKxl2RDuelbPTB1SV6XcqCUGmb0K3LJpeGGKrYhcOs9uqU0yTczTrCkGGKTYgPTOocY1rkNcVwdjk3ENact7uEppAxTA_Fcc3ucg6sVt4e4w9LUCbALcddkWMobcuFhKvj2fF6Rhy-39zff2rsfX7_ffL5rnZTD0sqxR862Hqn3yjuGjorRaRBU8XHoBYpB1SuKHsDwbf2mR60lgHOSKiPEFfl4mvuY088Vy2LnUBxOE0RMa7FMa0ql5kr-B8rNYLQSvKLshLqcSsno7WMOM-RfllF7lGAPtkqwRwmWClsl1J735_HrdsbxT8fv1Cvw4QxAqbn5DNGF8pfrj5vK4-OfThzW3J4CZltcwFhlhFyl2TGFf6zxDBC5pVU</recordid><startdate>20140801</startdate><enddate>20140801</enddate><creator>Allagui, M.S.</creator><creator>Feriani, A.</creator><creator>Saoudi, M.</creator><creator>Badraoui, R.</creator><creator>Bouoni, Z.</creator><creator>Nciri, R.</creator><creator>Murat, J.C.</creator><creator>Elfeki, A.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><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>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>7QF</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope></search><sort><creationdate>20140801</creationdate><title>Effects of melatonin on aluminium-induced neurobehavioral and neurochemical changes in aging rats</title><author>Allagui, M.S. ; Feriani, A. ; Saoudi, M. ; Badraoui, R. ; Bouoni, Z. ; Nciri, R. ; Murat, J.C. ; Elfeki, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c449t-4d8e21bfe0ff5fc1ec03dc6a3052d983e395c6ae38aa72b187fe664aacc405733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Acetylcholinesterase - metabolism</topic><topic>AChE activity</topic><topic>Aging</topic><topic>Aging - drug effects</topic><topic>Aluminium toxicity</topic><topic>Aluminum</topic><topic>Aluminum - administration & dosage</topic><topic>Aluminum - toxicity</topic><topic>Animals</topic><topic>Behavior, Animal - drug effects</topic><topic>Biological and medical sciences</topic><topic>Body Weight - drug effects</topic><topic>Brain</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Catalase - metabolism</topic><topic>Central nervous system</topic><topic>Chemical and industrial products toxicology. Toxic occupational diseases</topic><topic>Food toxicology</topic><topic>Glutathione Peroxidase - metabolism</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Lipids</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Melatonin</topic><topic>Melatonin - administration & dosage</topic><topic>Melatonin - toxicity</topic><topic>Metals and various inorganic compounds</topic><topic>Mortality</topic><topic>Neurodegenerative Diseases - chemically induced</topic><topic>Neurodegenerative Diseases - pathology</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Protective</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Superoxide Dismutase - metabolism</topic><topic>Thiobarbituric Acid Reactive Substances - metabolism</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Allagui, M.S.</creatorcontrib><creatorcontrib>Feriani, A.</creatorcontrib><creatorcontrib>Saoudi, M.</creatorcontrib><creatorcontrib>Badraoui, R.</creatorcontrib><creatorcontrib>Bouoni, Z.</creatorcontrib><creatorcontrib>Nciri, R.</creatorcontrib><creatorcontrib>Murat, J.C.</creatorcontrib><creatorcontrib>Elfeki, A.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Aluminium Industry Abstracts</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><jtitle>Food and chemical toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Allagui, M.S.</au><au>Feriani, A.</au><au>Saoudi, M.</au><au>Badraoui, R.</au><au>Bouoni, Z.</au><au>Nciri, R.</au><au>Murat, J.C.</au><au>Elfeki, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of melatonin on aluminium-induced neurobehavioral and neurochemical changes in aging rats</atitle><jtitle>Food and chemical toxicology</jtitle><addtitle>Food Chem Toxicol</addtitle><date>2014-08-01</date><risdate>2014</risdate><volume>70</volume><spage>84</spage><epage>93</epage><pages>84-93</pages><issn>0278-6915</issn><eissn>1873-6351</eissn><coden>FCTOD7</coden><abstract>•Reactive oxygen species (ROS) play a strong role in the aging process.•Aluminium supplementation enhanced behavioral declines in aging circumstances.•Assessment was performed by ‘open fields’, ‘elevated plus maze’ and ‘Radial 8-arms maze’ tasks.•Melatonin plays a neuroprotective role against aluminium-induced neurobehavioral changes.•Melatonin offers neuroprotection against cholinergic and oxidative damages in aging rats.
This study aimed to investigate the potential protective effects of melatonin (Mel) against aluminium-induced neurodegenerative changes in aging Wistar rats (24–28months old). Herein, aluminium chloride (AlCl3) (50mg/kg BW/day) was administered by gavage, and melatonin (Mel) was co-administered to a group of Al-treated rats by an intra-peritoneal injection at a daily dose of 10mg/kg BW for four months. The findings revealed that aluminium administration induced a significant decrease in body weight associated with marked mortality for the old group of rats, which was more pronounced in old Al-treated rats. Behavioural alterations were assessed by ‘open fields’, ‘elevated plus maze’ and ‘Radial 8-arms maze’ tests. The results demonstrated that Mel co-administration alleviated neurobehavioral changes in both old and old Al-treated rats. Melatonin was noted to play a good neuroprotective role, reducing lipid peroxidation (TBARs), and enhancing enzymatic (SOD, CAT and GPx) activities in the brain organs of old control and old Al-treated rats. Mel treatment also reversed the decrease of AChE activity in the brain tissues, which was confirmed by histological sections. Overall, the results showed that Mel administration can induce beneficial effects for the treatment of Al-induced neurobehavioral and neurochemical changes in the central nervous system (CNS).</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>24727051</pmid><doi>10.1016/j.fct.2014.03.043</doi><tpages>10</tpages></addata></record> |
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subjects | Acetylcholinesterase - metabolism AChE activity Aging Aging - drug effects Aluminium toxicity Aluminum Aluminum - administration & dosage Aluminum - toxicity Animals Behavior, Animal - drug effects Biological and medical sciences Body Weight - drug effects Brain Brain - drug effects Brain - metabolism Catalase - metabolism Central nervous system Chemical and industrial products toxicology. Toxic occupational diseases Food toxicology Glutathione Peroxidase - metabolism Lipid Peroxidation - drug effects Lipids Male Medical sciences Melatonin Melatonin - administration & dosage Melatonin - toxicity Metals and various inorganic compounds Mortality Neurodegenerative Diseases - chemically induced Neurodegenerative Diseases - pathology Oxidative stress Oxidative Stress - drug effects Protective Rats Rats, Wistar Superoxide Dismutase - metabolism Thiobarbituric Acid Reactive Substances - metabolism Toxicology |
title | Effects of melatonin on aluminium-induced neurobehavioral and neurochemical changes in aging rats |
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