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
Hauptverfasser: 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
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container_end_page 234
container_issue 1
container_start_page 223
container_title Toxicological sciences
container_volume 128
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. 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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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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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