Neuropsychotoxicity of Abused Drugs: Effects of Serotonin Receptor Ligands on Methamphetamine- and Cocaine-Induced Behavioral Sensitization in Mice

Repeated administration of psychostimulants elicits a progressive enhancement of locomotor activity known as behavioral sensitization. Central dopamine (DA) neurons play key roles as the neural substrates mediating behavioral sensitization, but the role of the serotonin (5-HT) system in the sensitiz...

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Main Authors: Yukio Ago (Author), Shigeo Nakamura (Author), Akemichi Baba (Author), Toshio Matsuda (Author)
Format: Book
Published: Elsevier, 2008-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Yukio Ago  |e author 
700 1 0 |a Shigeo Nakamura  |e author 
700 1 0 |a Akemichi Baba  |e author 
700 1 0 |a Toshio Matsuda  |e author 
245 0 0 |a Neuropsychotoxicity of Abused Drugs: Effects of Serotonin Receptor Ligands on Methamphetamine- and Cocaine-Induced Behavioral Sensitization in Mice 
260 |b Elsevier,   |c 2008-01-01T00:00:00Z. 
500 |a 1347-8613 
500 |a 10.1254/jphs.FM0070121 
520 |a Repeated administration of psychostimulants elicits a progressive enhancement of locomotor activity known as behavioral sensitization. Central dopamine (DA) neurons play key roles as the neural substrates mediating behavioral sensitization, but the role of the serotonin (5-HT) system in the sensitization is not fully elucidated. We have recently demonstrated that osemozotan, a specific 5-HT1A-receptor agonist, and ritanserin, a 5-HT2-receptor antagonist, inhibited the expression and development of both methamphetamine- and cocaine-induced behavioral sensitization in mice and that these drugs attenuated the maintenance of behavioral sensitization of methamphetamine, but not that of cocaine. We also found that azasetron, a 5-HT3-receptor antagonist, inhibited the expression and development of the sensitization induced by methamphetamine and cocaine, respectively. Neurochemical studies using a microdialysis technique showed that repeated methamphetamine enhanced the methamphetamine-induced increase in 5-HT release in the prefrontal cortex. The sensitization of 5-HT release in methamphetamine-treated mice was attenuated by osemozotan and ritanserin. These findings suggest that the 5-HT system plays an important role in methamphetamine- and cocaine-induced behavioral sensitization in mice and imply that 5-HT1A-receptor agonists and 5-HT2-receptor antagonists may have a potential therapeutic value for the treatment of methamphetamine abuse or psychosis. Keywords:: drugs of abuse, behavioral sensitization, methamphetamine, cocaine, serotonin (5-HT)-receptor ligand 
546 |a EN 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Journal of Pharmacological Sciences, Vol 106, Iss 1, Pp 15-21 (2008) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S1347861319315312 
787 0 |n https://doaj.org/toc/1347-8613 
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