Effects of combined arsenic and lead exposure on the brain monoaminergic system and behavioral functions in rats: Reversal effect of MiADMSA
In this study, we evaluated the therapeutic efficacy of monoisoamyldimercaptosuccinic acid (MiADMSA) against individual and combined effects of arsenic (As) and lead (Pb) on the monoaminergic system and behavioral functions in rats. Pregnant rats were exposed to sodium metaarsenite (50 ppm) and lead...
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Veröffentlicht in: | Toxicology and industrial health 2019-02, Vol.35 (2), p.89-108 |
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description | In this study, we evaluated the therapeutic efficacy of monoisoamyldimercaptosuccinic acid (MiADMSA) against individual and combined effects of arsenic (As) and lead (Pb) on the monoaminergic system and behavioral functions in rats. Pregnant rats were exposed to sodium metaarsenite (50 ppm) and lead acetate (0.2%) individually and in combination (As = 25 ppm + Pb = 0.1%) via drinking water from gestation day (GD) 6 to postnatal day (PND) 21. MiADMSA (50 mg/kg body weight) was given orally through gavage for 3 consecutive days to pups from PND 18 to PND 20. The results showed increases in synaptosomal epinephrine, dopamine, and norepinephrine levels with individual metal exposures and decreases with combined exposure to As and Pb in the cortex, cerebellum, and hippocampus in PND 21, PND 28, and 3 months age-group rats. We found decreased activity of mitochondrial monoamine oxidase in the selected brain regions following individual and combined exposures to Pb and As. In addition, rats treated with Pb and As alone or in combination showed significant deficits in open-field behavior, grip strength, locomotor activity, and exploratory behavior at PND 28 and 3 months of age. However, MiADMSA administration showed reversal effects against the As- and/or Pb-induced impairments in the monoaminergic system as well as in behavioral functions of rats. Our data demonstrated that the mixture of Pb and As induced synergistic toxicity to developing brain leading to impairments in neurobehavioral functions and also suggest therapeutic efficacy of MiADMSA against Pb- and/or As-induced developmental neurotoxicity. |
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Pregnant rats were exposed to sodium metaarsenite (50 ppm) and lead acetate (0.2%) individually and in combination (As = 25 ppm + Pb = 0.1%) via drinking water from gestation day (GD) 6 to postnatal day (PND) 21. MiADMSA (50 mg/kg body weight) was given orally through gavage for 3 consecutive days to pups from PND 18 to PND 20. The results showed increases in synaptosomal epinephrine, dopamine, and norepinephrine levels with individual metal exposures and decreases with combined exposure to As and Pb in the cortex, cerebellum, and hippocampus in PND 21, PND 28, and 3 months age-group rats. We found decreased activity of mitochondrial monoamine oxidase in the selected brain regions following individual and combined exposures to Pb and As. In addition, rats treated with Pb and As alone or in combination showed significant deficits in open-field behavior, grip strength, locomotor activity, and exploratory behavior at PND 28 and 3 months of age. However, MiADMSA administration showed reversal effects against the As- and/or Pb-induced impairments in the monoaminergic system as well as in behavioral functions of rats. Our data demonstrated that the mixture of Pb and As induced synergistic toxicity to developing brain leading to impairments in neurobehavioral functions and also suggest therapeutic efficacy of MiADMSA against Pb- and/or As-induced developmental neurotoxicity.</description><identifier>ISSN: 0748-2337</identifier><identifier>EISSN: 1477-0393</identifier><identifier>DOI: 10.1177/0748233718814990</identifier><identifier>PMID: 30526433</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Age ; Amine oxidase (flavin-containing) ; Arsenic ; Behavior ; Body weight ; Brain ; Cerebellum ; Dopamine ; Drinking water ; Epinephrine ; Exploratory behavior ; Exposure ; Gestation ; Grip strength ; Lead ; Lead acetates ; Locomotor activity ; Mitochondria ; Neurotoxicity ; Norepinephrine ; Open-field behavior ; Rodents ; Sodium ; Toxicity</subject><ispartof>Toxicology and industrial health, 2019-02, Vol.35 (2), p.89-108</ispartof><rights>The Author(s) 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-53a3a0acb573562bd17157acf345fef015e39fd3cf445f9786c3d19789353c3b3</citedby><cites>FETCH-LOGICAL-c365t-53a3a0acb573562bd17157acf345fef015e39fd3cf445f9786c3d19789353c3b3</cites><orcidid>0000-0002-6492-6529</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0748233718814990$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0748233718814990$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21798,27901,27902,43597,43598</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30526433$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saritha, S</creatorcontrib><creatorcontrib>Davuljigari, Chand Basha</creatorcontrib><creatorcontrib>Kumar, K Praveen</creatorcontrib><creatorcontrib>Reddy, G Rajrami</creatorcontrib><title>Effects of combined arsenic and lead exposure on the brain monoaminergic system and behavioral functions in rats: Reversal effect of MiADMSA</title><title>Toxicology and industrial health</title><addtitle>Toxicol Ind Health</addtitle><description>In this study, we evaluated the therapeutic efficacy of monoisoamyldimercaptosuccinic acid (MiADMSA) against individual and combined effects of arsenic (As) and lead (Pb) on the monoaminergic system and behavioral functions in rats. Pregnant rats were exposed to sodium metaarsenite (50 ppm) and lead acetate (0.2%) individually and in combination (As = 25 ppm + Pb = 0.1%) via drinking water from gestation day (GD) 6 to postnatal day (PND) 21. MiADMSA (50 mg/kg body weight) was given orally through gavage for 3 consecutive days to pups from PND 18 to PND 20. The results showed increases in synaptosomal epinephrine, dopamine, and norepinephrine levels with individual metal exposures and decreases with combined exposure to As and Pb in the cortex, cerebellum, and hippocampus in PND 21, PND 28, and 3 months age-group rats. We found decreased activity of mitochondrial monoamine oxidase in the selected brain regions following individual and combined exposures to Pb and As. In addition, rats treated with Pb and As alone or in combination showed significant deficits in open-field behavior, grip strength, locomotor activity, and exploratory behavior at PND 28 and 3 months of age. However, MiADMSA administration showed reversal effects against the As- and/or Pb-induced impairments in the monoaminergic system as well as in behavioral functions of rats. Our data demonstrated that the mixture of Pb and As induced synergistic toxicity to developing brain leading to impairments in neurobehavioral functions and also suggest therapeutic efficacy of MiADMSA against Pb- and/or As-induced developmental neurotoxicity.</description><subject>Age</subject><subject>Amine oxidase (flavin-containing)</subject><subject>Arsenic</subject><subject>Behavior</subject><subject>Body weight</subject><subject>Brain</subject><subject>Cerebellum</subject><subject>Dopamine</subject><subject>Drinking water</subject><subject>Epinephrine</subject><subject>Exploratory behavior</subject><subject>Exposure</subject><subject>Gestation</subject><subject>Grip strength</subject><subject>Lead</subject><subject>Lead acetates</subject><subject>Locomotor activity</subject><subject>Mitochondria</subject><subject>Neurotoxicity</subject><subject>Norepinephrine</subject><subject>Open-field behavior</subject><subject>Rodents</subject><subject>Sodium</subject><subject>Toxicity</subject><issn>0748-2337</issn><issn>1477-0393</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kEtLxDAUhYMoOj72riTgupr0Nk3rbvANI4KPdUnTG61MkzFpB_0P_mgzMz5AcHXhnu-cA4eQfc6OOJfymMmsSAEkLwqelSVbIyOeSZkwKGGdjBZystC3yHYIL4yxPBfpJtkCJtI8AxiRj3NjUPeBOkO16-rWYkOVD2hbTZVt6BRVQ_Ft5sLgkTpL-2ektVetpZ2zTnXR4Z8iHN5Dj93SU-OzmrfOqyk1g9V962yg0eBVH07oHc7Rh6jhsnrRfNOOz27ux7tkw6hpwL2vu0MeL84fTq-Sye3l9el4kmjIRZ8IUKCY0rWQIPK0brjkQiptIBMGDeMCoTQNaJPFRymLXEPD4y1BgIYadsjhKnfm3euAoa9e3OBtrKxSXjCRCV6WkWIrSnsXgkdTzXzbKf9ecVYt5q_-zh8tB1_BQ91h82P43jsCyQoI6gl_W_8N_AQYDI1u</recordid><startdate>201902</startdate><enddate>201902</enddate><creator>Saritha, S</creator><creator>Davuljigari, Chand Basha</creator><creator>Kumar, K Praveen</creator><creator>Reddy, G Rajrami</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T2</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>7U7</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9.</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><orcidid>https://orcid.org/0000-0002-6492-6529</orcidid></search><sort><creationdate>201902</creationdate><title>Effects of combined arsenic and lead exposure on the brain monoaminergic system and behavioral functions in rats: Reversal effect of MiADMSA</title><author>Saritha, S ; Davuljigari, Chand Basha ; Kumar, K Praveen ; Reddy, G Rajrami</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-53a3a0acb573562bd17157acf345fef015e39fd3cf445f9786c3d19789353c3b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Age</topic><topic>Amine oxidase (flavin-containing)</topic><topic>Arsenic</topic><topic>Behavior</topic><topic>Body weight</topic><topic>Brain</topic><topic>Cerebellum</topic><topic>Dopamine</topic><topic>Drinking water</topic><topic>Epinephrine</topic><topic>Exploratory behavior</topic><topic>Exposure</topic><topic>Gestation</topic><topic>Grip strength</topic><topic>Lead</topic><topic>Lead acetates</topic><topic>Locomotor activity</topic><topic>Mitochondria</topic><topic>Neurotoxicity</topic><topic>Norepinephrine</topic><topic>Open-field behavior</topic><topic>Rodents</topic><topic>Sodium</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saritha, S</creatorcontrib><creatorcontrib>Davuljigari, Chand Basha</creatorcontrib><creatorcontrib>Kumar, K Praveen</creatorcontrib><creatorcontrib>Reddy, G Rajrami</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><jtitle>Toxicology and industrial health</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saritha, S</au><au>Davuljigari, Chand Basha</au><au>Kumar, K Praveen</au><au>Reddy, G Rajrami</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of combined arsenic and lead exposure on the brain monoaminergic system and behavioral functions in rats: Reversal effect of MiADMSA</atitle><jtitle>Toxicology and industrial health</jtitle><addtitle>Toxicol Ind Health</addtitle><date>2019-02</date><risdate>2019</risdate><volume>35</volume><issue>2</issue><spage>89</spage><epage>108</epage><pages>89-108</pages><issn>0748-2337</issn><eissn>1477-0393</eissn><abstract>In this study, we evaluated the therapeutic efficacy of monoisoamyldimercaptosuccinic acid (MiADMSA) against individual and combined effects of arsenic (As) and lead (Pb) on the monoaminergic system and behavioral functions in rats. Pregnant rats were exposed to sodium metaarsenite (50 ppm) and lead acetate (0.2%) individually and in combination (As = 25 ppm + Pb = 0.1%) via drinking water from gestation day (GD) 6 to postnatal day (PND) 21. MiADMSA (50 mg/kg body weight) was given orally through gavage for 3 consecutive days to pups from PND 18 to PND 20. The results showed increases in synaptosomal epinephrine, dopamine, and norepinephrine levels with individual metal exposures and decreases with combined exposure to As and Pb in the cortex, cerebellum, and hippocampus in PND 21, PND 28, and 3 months age-group rats. We found decreased activity of mitochondrial monoamine oxidase in the selected brain regions following individual and combined exposures to Pb and As. In addition, rats treated with Pb and As alone or in combination showed significant deficits in open-field behavior, grip strength, locomotor activity, and exploratory behavior at PND 28 and 3 months of age. However, MiADMSA administration showed reversal effects against the As- and/or Pb-induced impairments in the monoaminergic system as well as in behavioral functions of rats. Our data demonstrated that the mixture of Pb and As induced synergistic toxicity to developing brain leading to impairments in neurobehavioral functions and also suggest therapeutic efficacy of MiADMSA against Pb- and/or As-induced developmental neurotoxicity.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>30526433</pmid><doi>10.1177/0748233718814990</doi><tpages>20</tpages><orcidid>https://orcid.org/0000-0002-6492-6529</orcidid></addata></record> |
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subjects | Age Amine oxidase (flavin-containing) Arsenic Behavior Body weight Brain Cerebellum Dopamine Drinking water Epinephrine Exploratory behavior Exposure Gestation Grip strength Lead Lead acetates Locomotor activity Mitochondria Neurotoxicity Norepinephrine Open-field behavior Rodents Sodium Toxicity |
title | Effects of combined arsenic and lead exposure on the brain monoaminergic system and behavioral functions in rats: Reversal effect of MiADMSA |
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