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解释物质依赖中药物使用的升级:模型与合适的动物实验室测试。

Explaining the escalation of drug use in substance dependence: models and appropriate animal laboratory tests.

作者信息

Zernig Gerald, Ahmed Serge H, Cardinal Rudolf N, Morgan Drake, Acquas Elio, Foltin Richard W, Vezina Paul, Negus S Stevens, Crespo Jose A, Stöckl Petra, Grubinger Petra, Madlung Ekkehard, Haring Christian, Kurz Martin, Saria Alois

机构信息

Experimental Psychiatry Unit, Department of Psychiatry, Medical University Innsbruck, Innsbruck, Austria.

出版信息

Pharmacology. 2007;80(2-3):65-119. doi: 10.1159/000103923. Epub 2007 Jun 14.

Abstract

Escalation of drug use, a hallmark of drug dependence, has traditionally been interpreted as reflecting the development of tolerance to the drug's effects. However, on the basis of animal behavioral data, several groups have recently proposed alternative explanations, i.e. that such an escalation of drug use might not be based on (1) tolerance, but rather be indicative of (2) sensitization to the drug's reinforcing effect, (3) reward allostasis, (4) an increase in the incentive salience of drug-associated stimuli, (5) an increase in the reinforcing strength of the drug reinforcer relative to alternative reinforcers, or (6) habit formation. From the pharmacological perspective, models 1-3 allow predictions about the change in the shape of drug dose-effect curves that are based on mathematically defined models governing receptor-ligand interaction and signal transduction. These predictions are tested in the present review, which also describes the other currently championed models for drug use escalation and other components of apparent 'reinforcement' (in its original meaning, like 'tolerance' or 'sensitization', a purely descriptive term). It evaluates the animal experimental approaches employed to support or prove the existence of each of the models and reinforcement components, and recapitulates the clinical evidence, which strongly suggests that escalation of drug use is predominantly based on an increase in the frequency of intoxication events rather than an increase in the dose taken at each intoxication event. Two apparent discrepancies in animal experiments are that (a) sensitization to overall reinforcement has been found more often for psychostimulants than for opioids, and that (b) tolerance to the reinforcing and other effects has been observed more often for opioids than for cocaine. These discrepancies are resolved by the finding that cocaine levels seem to be more tightly regulated at submaximum reinforcing levels than opioid levels are. Consequently, animals self-administering opioids are more likely to expose themselves to higher above-threshold doses than animals self-administering psychostimulants, rendering the development of tolerance to opioids more likely than tolerance to psychostimulants. The review concludes by making suggestions on how to improve the current behavioral experimental approaches.

摘要

药物使用量增加是药物依赖的一个标志,传统上被解释为反映了对药物作用耐受性的发展。然而,基于动物行为学数据,一些研究团队最近提出了其他解释,即这种药物使用量的增加可能并非基于(1)耐受性,而是表明(2)对药物强化作用的敏化、(3)奖赏稳态、(4)与药物相关刺激的动机显著性增加、(5)相对于其他强化物,药物强化物的强化强度增加,或者(6)习惯形成。从药理学角度来看,模型1 - 3允许基于控制受体 - 配体相互作用和信号转导的数学定义模型,对药物剂量 - 效应曲线形状的变化进行预测。本综述对这些预测进行了检验,还描述了目前其他支持药物使用量增加及明显“强化”(按其原始含义,如“耐受性”或“敏化”,是一个纯粹的描述性术语)其他成分的模型。它评估了用于支持或证明每个模型及强化成分存在的动物实验方法,并概括了临床证据,这些证据有力地表明药物使用量增加主要是基于中毒事件频率的增加,而非每次中毒事件所服用剂量的增加。动物实验中存在两个明显的差异:(a)相较于阿片类药物,精神兴奋剂对整体强化的敏化现象更常见;(b)相较于可卡因,阿片类药物对强化及其他效应的耐受性更常见。可卡因水平在次最大强化水平下似乎比阿片类药物水平受到更严格的调节,这一发现解决了这些差异。因此,与自我给药精神兴奋剂的动物相比,自我给药阿片类药物的动物更有可能使自己暴露于高于阈值的更高剂量,使得阿片类药物耐受性的发展比精神兴奋剂耐受性的发展更有可能。综述最后就如何改进当前行为实验方法提出了建议。

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