4-Methylthioamphetamine Increases Dopamine in the Rat Striatum and has Rewarding Effects In Vivo
Author
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Sotomayor Zárate, Ramón
Author
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Quiroz, Gabriel
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Araya, Katherine A.
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Abarca, Jorge
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Ibáñez, María R.
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Montecinos, Alejandro
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Guajardo, Carlos
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Núñez, Gabriel
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Fierro, Angélica
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Moya, Pablo R.
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Iturriaga-Vásquez, Patricio
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Gómez-Molina, Cristóbal
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Gysling, Katia
Author
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Reyes Parada, Miguel
Admission date
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2019-03-15T16:03:26Z
Available date
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2019-03-15T16:03:26Z
Publication date
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2012
Cita de ítem
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Basic and Clinical Pharmacology and Toxicology, Volumen 111, Issue 6, 2018, Pages 371-379
Identifier
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17427835
Identifier
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17427843
Identifier
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10.1111/j.1742-7843.2012.00926.x
Identifier
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https://repositorio.uchile.cl/handle/2250/165836
Abstract
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4-Methylthioamphetamine (MTA) is a phenylisopropylamine derivative whose use has been associated with severe intoxications. MTA is usually regarded as a selective serotonin-releasing agent. Nevertheless, previous data have suggested that its mechanism of action probably involves a catecholaminergic component. As little is known about dopaminergic effects of this drug, in this work the actions of MTA upon the dopamine (DA) transporter (DAT) were studied in vitro, in vivo and in silico. Also, the possible abuse liability of MTA was behaviourally assessed. MTA exhibited an in vitro affinity for the rat DAT in the low micromolar range (6.01 μM) and induced a significant, dose-dependent increase in striatal DA. MTA significantly increased c-Fos-positive cells in striatum and nucleus accumbens, induced conditioned place preference and increased locomotor activity. Docking experiments were performed in a homology model of the DAT. In conclusion, our results show that MTA is able to increase e