Department of Psychology, University of Michigan-Flint, 415 East Kearsley St, Flint, MI 48502, United States.
Neurosci Lett. 2013 Oct 11;553:196-200. doi: 10.1016/j.neulet.2013.08.008. Epub 2013 Aug 28.
Behavioral sensitization is thought to play a significant role in drug addiction. L-type calcium channels have been implicated in sensitization to stimulant and opiate drugs but it is unclear if these channels also contribute to sensitization to ethanol. The effects of three L-type calcium channel blockers, nifedipine (1-7.5 mg/kg), diltiazem (12.5-50 mg/kg), and verapamil (12.5 and 25 mg/kg), on sensitization to ethanol (2 g/kg) were examined in DBA/2J mice. All three blockers reduced but did not prevent expression of sensitization. Only nifedipine blocked acquisition of sensitization. Nifedipine and verapamil decreased blood ethanol levels. The current findings suggest L-type calcium channels do not play a substantial role in sensitization to ethanol and that the neural mechanisms underlying sensitization to ethanol are distinct from those mediating sensitization to stimulants and opiates.
行为敏化被认为在药物成瘾中起重要作用。L 型钙通道与兴奋剂和阿片类药物的敏化有关,但尚不清楚这些通道是否也有助于对乙醇的敏化。在 DBA/2J 小鼠中,研究了三种 L 型钙通道阻滞剂硝苯地平(1-7.5mg/kg)、地尔硫卓(12.5-50mg/kg)和维拉帕米(12.5 和 25mg/kg)对乙醇(2g/kg)敏化的影响。所有三种阻滞剂均减轻但不能预防敏化的表达。只有硝苯地平可阻断敏化的获得。硝苯地平和维拉帕米可降低血乙醇水平。目前的研究结果表明,L 型钙通道在乙醇敏化中不起重要作用,并且介导乙醇敏化的神经机制与介导兴奋剂和阿片类药物敏化的机制不同。