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Combining Stress and Dopamine Based Models of Addiction: Towards a Psycho-Neuro-Endocrinological Theory of Addiction.

机译:结合压力和多巴胺为基础的成瘾模型:建立成瘾的心理神经内分泌学理论。

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The literature on the two main models of addiction (dopamine-based positive reinforcement and stress-based negative reinforcement models) have made many important contributions to understanding this brain disorder. However, rarely has there been a comprehensive critique of the limitations of both models. This article seeks to resolve theoretical issues inherent to each model, as well as propose a more comprehensive psycho-neuro-endocrinological theory of addiction which reconciles important elements of both. We suggest that there is not only direct interaction of dopaminergic and stress systems throughout the addiction cycle, from initial use, via the abusing stage, to the endpoint of addiction, but that this interaction is present prior to initial use. A combination of genetic factors and/or experiences of adversity may result in a stress-triggered sensitisation of dopaminergic networks which is present before the onset of substance use, which cannot be explained solely in terms of dopaminergic (positive) reinforcement. Rather these processes are best explained by an allostatic model which reconciles aspects of both models of addiction and shows how dopamine/stress interactions become increasingly pathological in the addiction cycle. Our model suggests that chronic stress eventually creates baseline hypodopaminergic activity, but also prompts dopaminergic hyperactivity in cue reactivity. This is the neural marker of allostatic mechanisms observed at endpoint addiction. We propose a multi-circuit explanation of how this cumulative effect of stress increasingly impacts on dopaminergic networks of reward, affect, attention, memory and behavioural control. This revised model provides a useful frame of reference for further research and ultimately clinical practice.
机译:关于成瘾的两种主要模型(基于多巴胺的正强化模型和基于压力的负强化模型)的文献为理解这种脑部疾病做出了许多重要贡献。但是,很少有关于这两种模型的局限性的全面批评。本文旨在解决每种模型固有的理论问题,并提出一种更全面的成瘾心理神经内分泌学理论,以兼顾两者的重要要素。我们建议不仅在整个成瘾周期中,从最初的使用到滥用阶段,直至成瘾的终点,都存在多巴胺能和压力系统的直接相互作用,而且这种相互作用在首次使用之前就存在。遗传因素和/或逆境经历的结合可能会导致多巴胺能网络出现应激触发的敏化作用,这种敏感性在物质使用开始之前就存在,这不能仅用多巴胺能(正)强化来解释。相反,这些过程最好用一个静力学模型来解释,该模型调和了两种成瘾模型的各个方面,并显示了多巴胺/应激相互作用在成瘾周期中如何变得越来越病理化。我们的模型表明,慢性应激最终会产生基线低多巴胺能活动,但也会提示提示反应性中多巴胺能过度活跃。这是在成瘾终点观察到的同种异体机制的神经标志。我们提出了一个多回路的解释,说明这种压力的累积效应如何逐渐影响奖励,影响,注意力,记忆和行为控制的多巴胺能网络。修订后的模型为进一步的研究和最终的临床实践提供了有用的参考框架。

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