Neurotoxicity of anhydroecgonine methyl ester, a crack cocaine pyrolysis product
Smoking crack cocaine involves the inhalation of cocaine and its pyrolysis product, anhydroecgonine methyl ester (AEME). Although there is evidence that cocaine is neurotoxic, the neurotoxicity of AEME has never been evaluated. AEME seems to have cholinergic agonist properties in the cardiovascular...
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Veröffentlicht in: | Toxicological sciences 2012-07, Vol.128 (1), p.223-234 |
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creator | Garcia, Raphael Caio Tamborelli Dati, Livia Mendonça Munhoz Fukuda, Suelen Torres, Larissa Helena Lobo Moura, Sidnei de Carvalho, Nathalia Delazeri Carrettiero, Daniel Carneiro Camarini, Rosana Levada-Pires, Adriana Cristina Yonamine, Mauricio Negrini-Neto, Osvaldo Abdalla, Fernando Maurício Francis Sandoval, Maria Regina Lopes Afeche, Solange Castro Marcourakis, Tania |
description | Smoking crack cocaine involves the inhalation of cocaine and its pyrolysis product, anhydroecgonine methyl ester (AEME). Although there is evidence that cocaine is neurotoxic, the neurotoxicity of AEME has never been evaluated. AEME seems to have cholinergic agonist properties in the cardiovascular system; however, there are no reports on its effects in the central nervous system. The aim of this study was to investigate the neurotoxicity of AEME and its possible cholinergic effects in rat primary hippocampal cell cultures that were exposed to different concentrations of AEME, cocaine, and a cocaine-AEME combination. We also evaluated the involvement of muscarinic cholinergic receptors in the neuronal death induced by these treatments using concomitant incubation of the cells with atropine. Neuronal injury was assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and lactate dehydrogenase (LDH) assays. The results of the viability assays showed that AEME is a neurotoxic agent that has greater neurotoxic potential than cocaine after 24 and 48 h of exposure. We also showed that incubation for 48 h with a combination of both compounds in equipotent concentrations had an additive neurotoxic effect. Although both substances decreased cell viability in the MTT assay, only cocaine increased LDH release. Caspase-3 activity was increased after 3 and 6 h of incubation with 1mM cocaine and after 6 h of 0.1 and 1.0mM AEME exposure. Atropine prevented the AEME-induced neurotoxicity, which suggests that muscarinic cholinergic receptors are involved in AEME's effects. In addition, binding experiments confirmed that AEME has an affinity for muscarinic cholinergic receptors. Nevertheless, atropine was not able to prevent the neurotoxicity produced by cocaine and the cocaine-AEME combination, suggesting that these treatments activated other neuronal death pathways. Our results suggest a higher risk for neurotoxicity after smoking crack cocaine than after cocaine use alone. |
doi_str_mv | 10.1093/toxsci/kfs140 |
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Although there is evidence that cocaine is neurotoxic, the neurotoxicity of AEME has never been evaluated. AEME seems to have cholinergic agonist properties in the cardiovascular system; however, there are no reports on its effects in the central nervous system. The aim of this study was to investigate the neurotoxicity of AEME and its possible cholinergic effects in rat primary hippocampal cell cultures that were exposed to different concentrations of AEME, cocaine, and a cocaine-AEME combination. We also evaluated the involvement of muscarinic cholinergic receptors in the neuronal death induced by these treatments using concomitant incubation of the cells with atropine. Neuronal injury was assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and lactate dehydrogenase (LDH) assays. The results of the viability assays showed that AEME is a neurotoxic agent that has greater neurotoxic potential than cocaine after 24 and 48 h of exposure. We also showed that incubation for 48 h with a combination of both compounds in equipotent concentrations had an additive neurotoxic effect. Although both substances decreased cell viability in the MTT assay, only cocaine increased LDH release. Caspase-3 activity was increased after 3 and 6 h of incubation with 1mM cocaine and after 6 h of 0.1 and 1.0mM AEME exposure. Atropine prevented the AEME-induced neurotoxicity, which suggests that muscarinic cholinergic receptors are involved in AEME's effects. In addition, binding experiments confirmed that AEME has an affinity for muscarinic cholinergic receptors. Nevertheless, atropine was not able to prevent the neurotoxicity produced by cocaine and the cocaine-AEME combination, suggesting that these treatments activated other neuronal death pathways. Our results suggest a higher risk for neurotoxicity after smoking crack cocaine than after cocaine use alone.</description><identifier>ISSN: 1096-6080</identifier><identifier>EISSN: 1096-0929</identifier><identifier>DOI: 10.1093/toxsci/kfs140</identifier><identifier>PMID: 22523227</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Cells, Cultured ; Cocaine - analogs & derivatives ; Cocaine - toxicity ; Female ; Hippocampus - cytology ; Hippocampus - drug effects ; Immunohistochemistry ; Pregnancy ; Quinuclidinyl Benzilate - metabolism ; Radioligand Assay ; Rats ; Rats, Wistar ; Tritium</subject><ispartof>Toxicological sciences, 2012-07, Vol.128 (1), p.223-234</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c332t-b9fce761a7aa68f79366cf5845a41c4b3919aff8b1e39406563c4012ec6e82903</citedby><cites>FETCH-LOGICAL-c332t-b9fce761a7aa68f79366cf5845a41c4b3919aff8b1e39406563c4012ec6e82903</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22523227$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Garcia, Raphael Caio Tamborelli</creatorcontrib><creatorcontrib>Dati, Livia Mendonça Munhoz</creatorcontrib><creatorcontrib>Fukuda, Suelen</creatorcontrib><creatorcontrib>Torres, Larissa Helena Lobo</creatorcontrib><creatorcontrib>Moura, Sidnei</creatorcontrib><creatorcontrib>de Carvalho, Nathalia Delazeri</creatorcontrib><creatorcontrib>Carrettiero, Daniel Carneiro</creatorcontrib><creatorcontrib>Camarini, Rosana</creatorcontrib><creatorcontrib>Levada-Pires, Adriana Cristina</creatorcontrib><creatorcontrib>Yonamine, Mauricio</creatorcontrib><creatorcontrib>Negrini-Neto, Osvaldo</creatorcontrib><creatorcontrib>Abdalla, Fernando Maurício Francis</creatorcontrib><creatorcontrib>Sandoval, Maria Regina Lopes</creatorcontrib><creatorcontrib>Afeche, Solange Castro</creatorcontrib><creatorcontrib>Marcourakis, Tania</creatorcontrib><title>Neurotoxicity of anhydroecgonine methyl ester, a crack cocaine pyrolysis product</title><title>Toxicological sciences</title><addtitle>Toxicol Sci</addtitle><description>Smoking crack cocaine involves the inhalation of cocaine and its pyrolysis product, anhydroecgonine methyl ester (AEME). Although there is evidence that cocaine is neurotoxic, the neurotoxicity of AEME has never been evaluated. AEME seems to have cholinergic agonist properties in the cardiovascular system; however, there are no reports on its effects in the central nervous system. The aim of this study was to investigate the neurotoxicity of AEME and its possible cholinergic effects in rat primary hippocampal cell cultures that were exposed to different concentrations of AEME, cocaine, and a cocaine-AEME combination. We also evaluated the involvement of muscarinic cholinergic receptors in the neuronal death induced by these treatments using concomitant incubation of the cells with atropine. Neuronal injury was assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and lactate dehydrogenase (LDH) assays. The results of the viability assays showed that AEME is a neurotoxic agent that has greater neurotoxic potential than cocaine after 24 and 48 h of exposure. We also showed that incubation for 48 h with a combination of both compounds in equipotent concentrations had an additive neurotoxic effect. Although both substances decreased cell viability in the MTT assay, only cocaine increased LDH release. Caspase-3 activity was increased after 3 and 6 h of incubation with 1mM cocaine and after 6 h of 0.1 and 1.0mM AEME exposure. Atropine prevented the AEME-induced neurotoxicity, which suggests that muscarinic cholinergic receptors are involved in AEME's effects. In addition, binding experiments confirmed that AEME has an affinity for muscarinic cholinergic receptors. Nevertheless, atropine was not able to prevent the neurotoxicity produced by cocaine and the cocaine-AEME combination, suggesting that these treatments activated other neuronal death pathways. Our results suggest a higher risk for neurotoxicity after smoking crack cocaine than after cocaine use alone.</description><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Cocaine - analogs & derivatives</subject><subject>Cocaine - toxicity</subject><subject>Female</subject><subject>Hippocampus - cytology</subject><subject>Hippocampus - drug effects</subject><subject>Immunohistochemistry</subject><subject>Pregnancy</subject><subject>Quinuclidinyl Benzilate - metabolism</subject><subject>Radioligand Assay</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Tritium</subject><issn>1096-6080</issn><issn>1096-0929</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1PwzAMhiMEYmNw5Ipy5EBZPtq0OaKJL2kCDnCuUs9hZW0zklai_55OLZxs2Y9eWw8hl5zdcqblsnU_AcrlzgYesyMyH4YqYlro46lXLGMzchbCF2OcK6ZPyUyIREgh0jl5e8HOuyGkhLLtqbPUNNt-4x3Cp2vKBmmN7bavKIYW_Q01FLyBHQUH5rDd995VfSgD3Xu36aA9JyfWVAEvprogHw_376unaP36-Ly6W0cgpWijQlvAVHGTGqMym2qpFNgkixMTc4gLqbk21mYFR6ljphIlIWZcICjMhGZyQa7H3OHudzd8l9dlAKwq06DrQs6ZiGXCBU8HNBpR8C4Ejzbf-7I2vh-g_CAxHyXmo8SBv5qiu6LGzT_9Z03-AvXCcEs</recordid><startdate>201207</startdate><enddate>201207</enddate><creator>Garcia, Raphael Caio Tamborelli</creator><creator>Dati, Livia Mendonça Munhoz</creator><creator>Fukuda, Suelen</creator><creator>Torres, Larissa Helena Lobo</creator><creator>Moura, Sidnei</creator><creator>de Carvalho, Nathalia Delazeri</creator><creator>Carrettiero, Daniel Carneiro</creator><creator>Camarini, Rosana</creator><creator>Levada-Pires, Adriana Cristina</creator><creator>Yonamine, Mauricio</creator><creator>Negrini-Neto, Osvaldo</creator><creator>Abdalla, Fernando Maurício Francis</creator><creator>Sandoval, Maria Regina Lopes</creator><creator>Afeche, Solange Castro</creator><creator>Marcourakis, Tania</creator><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></search><sort><creationdate>201207</creationdate><title>Neurotoxicity of anhydroecgonine methyl ester, a crack cocaine pyrolysis product</title><author>Garcia, Raphael Caio Tamborelli ; 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Although there is evidence that cocaine is neurotoxic, the neurotoxicity of AEME has never been evaluated. AEME seems to have cholinergic agonist properties in the cardiovascular system; however, there are no reports on its effects in the central nervous system. The aim of this study was to investigate the neurotoxicity of AEME and its possible cholinergic effects in rat primary hippocampal cell cultures that were exposed to different concentrations of AEME, cocaine, and a cocaine-AEME combination. We also evaluated the involvement of muscarinic cholinergic receptors in the neuronal death induced by these treatments using concomitant incubation of the cells with atropine. Neuronal injury was assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and lactate dehydrogenase (LDH) assays. The results of the viability assays showed that AEME is a neurotoxic agent that has greater neurotoxic potential than cocaine after 24 and 48 h of exposure. We also showed that incubation for 48 h with a combination of both compounds in equipotent concentrations had an additive neurotoxic effect. Although both substances decreased cell viability in the MTT assay, only cocaine increased LDH release. Caspase-3 activity was increased after 3 and 6 h of incubation with 1mM cocaine and after 6 h of 0.1 and 1.0mM AEME exposure. Atropine prevented the AEME-induced neurotoxicity, which suggests that muscarinic cholinergic receptors are involved in AEME's effects. In addition, binding experiments confirmed that AEME has an affinity for muscarinic cholinergic receptors. Nevertheless, atropine was not able to prevent the neurotoxicity produced by cocaine and the cocaine-AEME combination, suggesting that these treatments activated other neuronal death pathways. Our results suggest a higher risk for neurotoxicity after smoking crack cocaine than after cocaine use alone.</abstract><cop>United States</cop><pmid>22523227</pmid><doi>10.1093/toxsci/kfs140</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry |
subjects | Animals Cells, Cultured Cocaine - analogs & derivatives Cocaine - toxicity Female Hippocampus - cytology Hippocampus - drug effects Immunohistochemistry Pregnancy Quinuclidinyl Benzilate - metabolism Radioligand Assay Rats Rats, Wistar Tritium |
title | Neurotoxicity of anhydroecgonine methyl ester, a crack cocaine pyrolysis product |
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