Department of Pharmacology and Toxicology, School of Medicine and Biomedical Sciences, University at Buffalo, 3435 Main Street (Farber Hall 102), Buffalo, NY, 14221, USA.
Psychopharmacology (Berl). 2014 Jan;231(1):257-67. doi: 10.1007/s00213-013-3228-0. Epub 2013 Aug 11.
Melatonin modifies physiological and behavioral responses to psychostimulants, with the MT₁ and MT₂ melatonin receptors specifically implicated in facilitating methamphetamine (METH)-induced sensitization in melatonin-proficient mice.
The objective of the study is to assess differences in locomotor sensitization after a single dose of methamphetamine in low-melatonin-expressing C57BL/6 wild-type and MT₁ receptor knockout (MT₁KO) mice, comparing with melatonin-expressing C3H/HeN mice.
Mice received a vehicle or methamphetamine (1.2 mg/kg, i.p.) pretreatment (day 1) during the light (ZT5-9) or dark (ZT 19-21) periods in novel test arenas. Locomotor sensitization was assessed by methamphetamine challenge after an eight-day abstinence (day 9). TH protein expression was evaluated by immunofluorescence and Western blot analysis.
Methamphetamine pretreatment induced statistically significant locomotor sensitization upon challenge after eight-day abstinence in C3H and C57 wild-type mice during the light period. The magnitude of sensitization in C57 mice was diminished in the dark period and completely abrogated in MT₁KO mice. No differences were observed in tyrosine hydroxylase immunoreactivity in the mesolimbic dopamine system. Additional exposures to the test arenas after methamphetamine pretreatment (nights 2-6) enhanced sensitization.
Deletion of the MT₁ melatonin receptor abolishes sensitization induced by a single METH pretreatment. The magnitude of sensitization is also altered by time of day and contextual cues. We conclude that the MT₁ melatonin receptor is emerging as a novel target of therapeutic intervention for drug abuse disorders.
褪黑素可调节生理和行为对精神兴奋剂的反应,而 MT₁ 和 MT₂ 褪黑素受体特别参与促进褪黑素功能正常的小鼠中甲氧麻黄酮(METH)诱导的敏化作用。
本研究的目的是评估低褪黑素表达的 C57BL/6 野生型和 MT₁ 受体敲除(MT₁KO)小鼠与褪黑素表达的 C3H/HeN 小鼠单次给予 METH 后,在运动敏化方面的差异。
在新的测试场中,小鼠在光照(ZT5-9)或黑暗(ZT 19-21)期间接受载体或 METH(1.2mg/kg,ip)预处理(第 1 天)。在 8 天的禁欲期(第 9 天)后,通过 METH 挑战评估运动敏化。通过免疫荧光和 Western blot 分析评估 TH 蛋白表达。
在光照期,C3H 和 C57 野生型小鼠在 METH 预处理 8 天后,METH 挑战时出现了统计学上显著的运动敏化。在黑暗期,C57 小鼠的敏化程度减弱,而在 MT₁KO 小鼠中则完全消除。在中脑边缘多巴胺系统中,酪氨酸羟化酶免疫反应性无差异。在 METH 预处理后,对测试场的额外暴露(第 2-6 晚)增强了敏化作用。
MT₁ 褪黑素受体的缺失消除了单次 METH 预处理引起的敏化作用。敏化的幅度也受时间和环境线索的影响。我们得出结论,MT₁ 褪黑素受体正成为治疗药物滥用障碍的新靶点。