Sharpe Amanda L, Varela Erika, Beckstead Michael J
Department of Pharmaceutical Sciences, Feik School of Pharmacy, University of the Incarnate Word, San Antonio, Texas, United States of America.
Department of Cellular and Integrative Physiology, UT Health, San Antonio, Texas, United States of America.
PLoS One. 2017 Jul 7;12(7):e0180710. doi: 10.1371/journal.pone.0180710. eCollection 2017.
Methamphetamine (METH) is a psychostimulant that exhibits significant abuse potential. Although METH addiction is a major health and societal concern, no drug is currently approved for its therapeutic management. METH activates the central dopaminergic "reward" circuitry, and with repeated use increases levels of the neuromodulatory peptide neurotensin in the nucleus accumbens and ventral tegmental area. Previous studies in rats suggest that neurotensin agonism decreases METH self-administration, but these studies did not examine the effect of neurotensin agonism on the pattern of self-administration or open field locomotion. In our studies, we established intravenous METH self-administration in male, DBA/2J mice (fixed ratio 3, 2 hr sessions) and examined the effect of pretreatment with the NTS1 receptor agonist PD149163 on METH self-administration behavior. Locomotion following PD149163 was also measured up to 2 hours after injection on a rotarod and in an open field. Pretreatment with PD149163 (0.05 and 0.10 mg/kg, s.c.) significantly decreased METH self-administration. The pattern of responding suggested that PD149163 decreased motivation to self-administer METH initially in the session with more normal intake in the second hour of access. Voluntary movement in the open-field was significantly decreased by both 0.05 and 0.10 mg/kg (s.c.) PD149163 from 10-120 minutes after injection, but rotarod performance suggested that PD149163 did not cause frank sedation. These results suggest that a systemically delivered NTS1 receptor agonist decreases METH self-administration in mice. The pattern of self-administration suggests that PD149163 may acutely decrease motivation to self-administer METH before the drug is experienced, but cannot rule out that depression of voluntary movement plays a role in the decreased self-administration.
甲基苯丙胺(METH)是一种具有显著滥用潜力的精神兴奋剂。尽管METH成瘾是一个主要的健康和社会问题,但目前尚无药物被批准用于其治疗管理。METH激活中枢多巴胺能“奖赏”回路,并且随着反复使用会增加伏隔核和腹侧被盖区中神经调节肽神经降压素的水平。先前对大鼠的研究表明,神经降压素激动作用会减少METH自我给药,但这些研究并未考察神经降压素激动作用对自我给药模式或旷场运动的影响。在我们的研究中,我们在雄性DBA/2J小鼠中建立了静脉注射METH自我给药模型(固定比率3,2小时实验时段),并考察了用NTS1受体激动剂PD149163预处理对METH自我给药行为的影响。在注射后长达2小时的时间里,还在转棒试验和旷场中测量了PD149163注射后的运动情况。用PD149163(0.05和0.10 mg/kg,皮下注射)预处理显著减少了METH自我给药。反应模式表明,PD149163最初在实验时段减少了自我给药METH的动机,在获取药物的第二个小时摄入量更正常。在注射后10 - 120分钟,0.05和0.10 mg/kg(皮下注射)的PD149163均显著减少了旷场中的自主运动,但转棒试验表现表明PD149163并未引起明显的镇静作用。这些结果表明,全身给药的NTS1受体激动剂可减少小鼠的METH自我给药。自我给药模式表明,PD149163可能在体验药物之前急性减少自我给药METH的动机,但不能排除自主运动的抑制在自我给药减少中起作用。