Herin David V, Liu Shijing, Ullrich Thomas, Rice Kenner C, Cunningham Kathryn A
Department of Pharmacology and Toxicology, Center for Addiction Research, University of Texas Medical Branch, Galveston, TX 77555-1031, USA.
Psychopharmacology (Berl). 2005 Apr;178(4):505-13. doi: 10.1007/s00213-004-2030-4. Epub 2004 Oct 23.
Contradictory evidence exists regarding the role of the 5-HT(2A) receptor (5-HT(2A)R) in hyperactivity and hyperthermia elicited by the substituted amphetamine (+)-3,4-methylenedioxymethamphetamine.
The present studies examined the ability of the selective 5-HT(2A)R antagonist M100907 to block hyperactivity and hyperthermia produced across the (+)-MDMA dose-effect curve.
Male rats were pretreated with M100907 (0, 0.25, 0.5, 1, and 2 mg/kg) followed by treatment with (+)-MDMA (0-12 mg/kg); activity was recorded for 90 min followed by determination of rectal temperature. Additionally, we investigated the ability of M100907 (0 and 0.5 mg/kg) to reverse hyperthermia elicited by (+)-MDMA (12 mg/kg).
The first study demonstrated that M100907 attenuated hyperactivity in the periphery of the monitor and eliminated rearing induced by (+)-MDMA (3 mg/kg) with no effect on basal activity. In two subsequent studies, (+)-MDMA (0-12 mg/kg) dose-dependently increased peripheral activity and rearing and produced hyperthermia. Pretreatment with M100907 decreased peripheral activity evoked by (+)-MDMA, right-shifted the dose-effect curve for rearing, and blocked (+)-MDMA-induced hyperthermia, while having no effect when administered alone. A final study demonstrated the ability of M100907 (0.5 mg/kg) to reverse hyperthermia produced by (+)-MDMA (12 mg/kg).
These results suggest that the 5-HT(2A)R contributes to the generation of peripheral hyperactivity and rearing and, especially, the hyperthermia evoked by (+)-MDMA and that 5-HT(2A)R antagonists should be further investigated as treatments for the psychological and hyperthermic effects of (+/-)-MDMA.
关于5-羟色胺2A受体(5-HT(2A)R)在由取代苯丙胺(+)-3,4-亚甲基二氧甲基苯丙胺引发的多动和体温过高中所起的作用,存在相互矛盾的证据。
本研究考察了选择性5-HT(2A)R拮抗剂M100907阻断(+)-3,4-亚甲基二氧甲基苯丙胺(MDMA)剂量效应曲线上产生的多动和体温过高的能力。
雄性大鼠先用M100907(0、0.25、0.5、1和2毫克/千克)预处理,然后用(+)-MDMA(0 - 12毫克/千克)处理;记录90分钟的活动情况,随后测定直肠温度。此外,我们研究了M100907(0和0.5毫克/千克)逆转(+)-MDMA(12毫克/千克)引发的体温过高的能力。
第一项研究表明,M100907减弱了监测器周边的多动,并消除了(+)-MDMA(3毫克/千克)诱导的竖毛行为,对基础活动没有影响。在随后的两项研究中,(+)-MDMA(0 - 12毫克/千克)剂量依赖性地增加了周边活动和竖毛行为,并导致体温过高。用M100907预处理可减少(+)-MDMA诱发的周边活动,使竖毛行为的剂量效应曲线右移,并阻断(+)-MDMA诱导的体温过高,而单独给药时则没有效果。最后一项研究表明,M100907(0.5毫克/千克)有逆转(+)-MDMA(12毫克/千克)产生的体温过高的能力。
这些结果表明,5-HT(2A)R促成了周边多动和竖毛行为的产生,尤其是(+)-MDMA诱发的体温过高,并且5-HT(2A)R拮抗剂作为(±)-MDMA心理和体温过高效应的治疗方法应进一步研究。