Berger Karen H, Heberlein Ulrike, Moore Monica S
Ernest Gallo Clinic and Research Center, Emeryville, California 94608, USA.
Alcohol Clin Exp Res. 2004 Oct;28(10):1469-80. doi: 10.1097/01.alc.0000141817.15993.98.
Ethanol tolerance, defined as a reduction in the intensity of the effects of ethanol upon continuous or repeated exposure, is a hallmark of alcoholism. Tolerance may develop at the cellular or neural systems levels. The molecular changes underlying ethanol tolerance are not well understood. We therefore explored the utility of Drosophila, with its accessibility to genetic, molecular, and behavioral analyses, as a model organism to study tolerance development in response to different ethanol-exposure regimens.
We describe a new assay that quantifies recovery from ethanol intoxication in Drosophila. Using this recovery assay, we define ethanol pre-exposure paradigms that lead to the development of tolerance. We also use the inebriometer, an assay that measures the onset of intoxication, to study the effects of pharmacological and genetic manipulations on tolerance development.
We show that flies develop different forms of ethanol tolerance: rapid tolerance, induced by a single short exposure to a high concentration of ethanol, and chronic tolerance, elicited by prolonged exposure to a low concentration of the drug. Neither rapid nor chronic tolerance involves changes in ethanol pharmacokinetics, implying that they represent functional rather than dispositional tolerance. Chronic and rapid tolerance can be distinguished mechanistically: chronic tolerance is disrupted by treatment with the protein synthesis inhibitor cycloheximide, whereas rapid tolerance is resistant to this treatment. Furthermore, rapid and chronic tolerance rely on distinct genetic pathways: a mutant defective for octopamine biosynthesis shows reduced rapid tolerance but normal chronic tolerance.
Flies, like mammals, develop tolerance in response to different ethanol-exposure regimens, and this tolerance affects both the onset of and the recovery from acute intoxication. Two forms of tolerance, rapid and chronic, are mechanistically distinct, because they can be dissociated genetically and pharmacologically.
乙醇耐受性被定义为在持续或反复接触乙醇后,其效应强度降低,是酒精中毒的一个标志。耐受性可能在细胞或神经系统水平上产生。乙醇耐受性背后的分子变化尚未完全了解。因此,我们探索了果蝇作为一种模式生物的实用性,它便于进行遗传、分子和行为分析,以研究对不同乙醇暴露方案的耐受性发展。
我们描述了一种新的测定方法,用于量化果蝇从乙醇中毒中恢复的情况。使用这种恢复测定方法,我们定义了导致耐受性发展的乙醇预暴露范式。我们还使用醉度计,一种测量中毒发作的测定方法,来研究药理学和基因操作对耐受性发展的影响。
我们表明果蝇会产生不同形式的乙醇耐受性:快速耐受性,由单次短时间暴露于高浓度乙醇诱导产生;慢性耐受性,由长时间暴露于低浓度药物引起。快速耐受性和慢性耐受性均不涉及乙醇药代动力学的变化,这意味着它们代表功能性而非处置性耐受性。慢性耐受性和快速耐受性在机制上可以区分:用蛋白质合成抑制剂环己酰亚胺处理会破坏慢性耐受性,而快速耐受性对此处理具有抗性。此外,快速耐受性和慢性耐受性依赖于不同的遗传途径:一种章鱼胺生物合成缺陷的突变体显示快速耐受性降低,但慢性耐受性正常。
果蝇与哺乳动物一样,会对不同的乙醇暴露方案产生耐受性,并且这种耐受性会影响急性中毒的发作和恢复。快速耐受性和慢性耐受性这两种形式在机制上是不同的,因为它们在遗传和药理学上可以分离。