Furman University Greenville, SC, USA.
Front Mol Neurosci. 2012 Aug 29;5:87. doi: 10.3389/fnmol.2012.00087. eCollection 2012.
Alcohol use disorders, like all drug addictions, involve a constellation of adaptive changes throughout the brain. Neural activity underlying changes in the rewarding properties of alcohol reflect changes in dopamine transmission in mesolimbic and nigrostriatal pathways and these effects are modulated by endogenous opioids such as β-Endorphin. In order to study the role of β-Endorphin in the development of locomotor sensitization to repeated EtOH exposure, we tested transgenic mice that vary in their capacity to synthesize this peptide as a result of constitutive modification of the Pomc gene. Our results indicate that mice deficient in β-Endorphin show attenuated locomotor activation following an acute injection of EtOH (2.0 g/kg) and, in contrast to wildtype mice, fail to demonstrate locomotor sensitization after 12 days of repeated EtOH injections. These data support the idea that β-Endorphin modulates the locomotor effects of EtOH and contributes to the neuroadaptive changes associated with chronic use.
酒精使用障碍与所有药物成瘾一样,涉及大脑中一系列适应性变化。酒精奖赏特性变化背后的神经活动反映了中脑边缘和黑质纹状体通路中多巴胺传递的变化,这些效应受内源性阿片样物质如β-内啡肽的调节。为了研究β-内啡肽在反复乙醇暴露引起的运动敏化发展中的作用,我们测试了由于 Pomc 基因组成型修饰而在合成这种肽的能力上有所不同的转基因小鼠。我们的结果表明,β-内啡肽缺乏的小鼠在急性注射乙醇(2.0 g/kg)后表现出运动激活减弱,与野生型小鼠不同,在 12 天的重复乙醇注射后未能表现出运动敏化。这些数据支持β-内啡肽调节乙醇的运动效应并有助于与慢性使用相关的神经适应性变化的观点。