首页> 外文期刊>European Journal of Pharmacology: An International Journal >Involvement of serotonergic and dopaminergic mechanisms in hyperthermia induced by a serotonin-releasing drug, p-chloroamphetamine in mice.
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Involvement of serotonergic and dopaminergic mechanisms in hyperthermia induced by a serotonin-releasing drug, p-chloroamphetamine in mice.

机译:血清素和多巴胺能机制与5-羟色胺释放药物对氯苯丙胺诱导的高热有关。

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摘要

Serotonergic and dopaminergic involvement in hyperthermia induced by a serotonin (5-hydroxytryptamine, 5-HT)-releasing drug, p-chloroamphetamine, was investigated in mice. Neither the 5-HT transporter inhibitor fluoxetine nor the 5-HT depleter p-chlorophenylalanine affected p-chloroamphetamine-induced hyperthermia. The dopamine depleter alpha-methyl-p-tyrosine significantly reduced p-chloroamphetamine-induced hyperthermia. The dopamine D(1) receptor antagonist 7-chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine (SCH 23390) antagonized p-chloroamphetamine-induced hyperthermia, although the dopamine D(2) receptor antagonist sulpiride was without effect. These results indicate that p-chloroamphetamine-induced hyperthermia in mice is mediated by dopamine release followed by activation of the dopamine D(1) receptor.
机译:在小鼠中研究了血清素(5-羟色胺,5-HT)释放药物对氯苯丙胺引起的血清素能和多巴胺能参与的热疗。 5-HT转运蛋白抑制剂氟西汀和5-HT耗尽型对氯苯丙氨酸均不影响对氯苯丙胺诱导的体温过高。消耗多巴胺的α-甲基-对-酪氨酸可显着降低对氯苯丙胺诱导的体温过高。多巴胺D(1)受体拮抗剂7-氯-8-羟基-3-甲基-1-苯基-2,3,4,5-四氢-1H-3-苯并ze庚因(SCH 23390)拮抗对氯苯丙胺诱导的体温过高,尽管多巴胺D(2)受体拮抗剂舒必利没有作用。这些结果表明,对氯苯丙胺诱导的小鼠高热是由多巴胺释放介导的,然后激活多巴胺D(1)受体。

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