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Behavioral cross-sensitization between cocaine and ethanol is accompanied by parallel changes in the activity of AMPK system

机译:可卡因和乙醇之间的行为交叉敏化伴随着AMPK系统活动的平行变化

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Behavioral sensitization is thought to be relevant to the psychopathology of drug addiction. A previous study from our research group demonstrated cross-sensitization between cocaine and ethanol. Although these findings suggest a common mechanism of action between these two drugs, little is known about the molecular or cellular aspects of this commonality. The AMPK pathway functions as an intracellular energy sensor and plays a critical role in maintaining cellular energy homeostasis. Thus, the present study examined AMPK signaling following reciprocal cross-sensitization between cocaine and ethanol in the rat prefrontal cortex and dorsal striatum. Male Sprague Dawley rats were repeatedly treated with either cocaine (15 mg/kg, 5 times) or ethanol (0.5 g/kg, 15 times) and then challenged reciprocally with the other drug. When sensitized to either cocaine or ethanol, the phosphorylation in response to additional challenges with the same drug was enhanced, indicating the development of sensitization. However, responses to the cocaine challenge were enhanced in the ethanol-sensitized state, whereas the responses to the ethanol challenge were not apparently enhanced in the cocaine-sensitized state. This was likely due to the ceiling effect of cocaine sensitization, which suggested that cocaine had more robust effects than ethanol. Although the same changes were found for two upstream kinases of AMPK (LKB1 and CaMK4), TAK1 responded differently and was not affected by acute challenges from either cocaine or ethanol. In the prefrontal cortex, there was an increase in activity, whereas there was a decrease in activity in the dorsal striatum. This difference might be due to dopamine Di receptor dominance in the prefrontal cortex and D2 receptor dominance in the dorsal striatum. Taken together, these results suggest that both cocaine and ethanol may share overlapping molecular pathways in the process of behavioral sensitization. However, the action of cocaine was stronger than that of ethanol.
机译:认为行为致敏与药物成瘾的精神病理学相关。我们研究组的先前研究表明了可卡因和乙醇之间的交叉敏化。虽然这些研究结果表明这两种药物之间的常见作用机制,但关于这种共性的分子或细胞方面的众所周知。 AMPK途径用作细胞内能量传感器,并在维持细胞能量稳态中起着关键作用。因此,本研究检测了在大鼠前额叶皮层和背纹纹状体中可卡因和乙醇之间的相互交叉敏化之后的AMPK信号传导。用可卡因(15mg / kg,5次)或乙醇(0.5g / kg,15次)重复处理雄性Sprague Dawley大鼠,然后用其他药物往复攻击。当对可卡因或乙醇敏感时,磷酸化响应于具有相同药物的额外挑战,表明致敏的发展。然而,在乙醇致敏状态下提高对可卡因攻击的反应,而对乙醇致敏的挑战的反应在可卡因致敏状态下显然没有显然增强。这可能是由于可卡因敏化的天花板效应,这表明可卡因的效果比乙醇更强大。虽然对AMPK(LKB1和CAMK4)的两个上游激酶发现相同的变化,但TAK1不同地响应不同,并且不受可卡因或乙醇的急性挑战的影响。在前额叶皮质中,活性增加,而背面纹状体的活性会降低。这种差异可能是由于多巴胺DI受体在背体纹状体中的前额叶皮质和D2受体的优势中的优势。总之,这些结果表明可卡因和乙醇可以共享行为敏化过程中的重叠分子途径。然而,可卡因的作用比乙醇更强。

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