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4-methylthioamphetamine-induced hyperthermia in mice: influence of serotonergic and catecholaminergic pathways

Title
4-methylthioamphetamine-induced hyperthermia in mice: influence of serotonergic and catecholaminergic pathways
Type
Article in International Scientific Journal
Year
2003
Authors
Remiao, F
(Author)
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Carvalho, F
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Fernandes, E
(Author)
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de Boer, D
(Author)
Other
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dos Reys, LA
(Author)
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Bastos, MD
(Author)
FFUP
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Journal
Vol. 190
Pages: 262-271
ISSN: 0041-008X
Publisher: Elsevier
Scientific classification
FOS: Medical and Health sciences > Basic medicine
Other information
Authenticus ID: P-000-FSZ
Abstract (EN): 4-Methylthioamphetamine (4-MTA), also known as p-methylthioamphetamine, is a new amphetamine derivative which in humans has been increasingly associated with severe intoxications and several deaths. As hyperthermia is considered to be one of the most life-threatening acute physiological consequences of amphetamine-related intoxications, it was our aim to determine whether 4-MTA induces changes in body temperature in a mouse model. Accordingly, we measured the subcutaneous temperature after acute administration of 4-MTA in CD1 mice. Because hyperthermia seems to result from the central and peripheral actions of catecholamines and serotonin (5-hydroxytriptamine or 5-HT), we also investigated the possible interactions of some catecholaminergic and serotonergic receptor blockers and the inhibition of monoamine oxidase (MAO) with this effect. 4-MTA induced hyperthermia in CD1 mice. Blockade of the 5-HT receptors with methysergide and MAO inhibition with pargyline resulted in the potentiation of the 4-MTA-induced hyperthermic effect. Blockade of the alpha(1)-adrenergic receptors with prazosin completely reverted the 4-MTA-induced hyperthermia while with the beta-adrenergic receptor blocker dl-propranolol this reversal was not complete. Blockade of the alpha(1)-adrenergic receptors with yohimbine had no effect on the hyperthermia induced by 4-MTA. These results suggest that 4-MTA-induced hyperthermia is highly influenced by the catecholaminergic and serotonergic receptor activation and the MAO activity.
Language: English
Type (Professor's evaluation): Scientific
No. of pages: 10
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