Department of Clinical Psychology, VU University Amsterdam, van der Boechorststraat 1, NL-1081 BT Amsterdam, The Netherlands.
School of Social and Behavioral Sciences, Tilburg University, Warandelaan 2, 5037 AB Tilburg, The Netherlands.
Pharmacol Biochem Behav. 2014 Apr;119:39-48. doi: 10.1016/j.pbb.2013.07.015. Epub 2013 Aug 1.
The present article advances a neurobiological model of the reciprocal associations between social attachment and drug abuse, and social attachment and chronic stress, as overlapping systems are involved in stress coping and social attachment. In terms of coping, responding to a novel stressor or challenge involves initial novelty processing and activation of learning mechanisms that allow habituation to the stressor through familiarization. Similarly, social attachments are initially formed by being attracted by rewarding properties of an as-yet novel individual, and subsequently developing feelings of attachment towards the familiarized individual. Attachment and familiarization increase the availability of "internal working models" for the control of behavior and emotion, which may explain why secure attachments are associated with increased resilience in the face of stress, accompanied by less reactive reward responding (i.e., increased resilience against drug addiction). The present article seeks to illuminate the role of the neuropeptide oxytocin, which may be involved in the overlapping mechanisms of stable attachment formation and stress coping by shifting processing from novelty and reward seeking to appreciation of familiarity. Oxytocin may accomplish this by facilitating a ventral-to-dorsal shift in activation in corticostriatal loops, which produces a shift from a reactive reward drive (wanting) to stable appreciation of familiar social aspects ("liking" or "loving"). The authors suggest that through dopaminergic, serotonergic and endogenous opioid mechanisms, oxytocin is involved in shifting the balance between wanting and liking in corticostriatal loops by facilitating consolidation of social information from ventral reactive reward systems to dorsal internal working models that aid in prospectively selecting optimal actions in the future, increasing resilience in the face of stress and addiction.
本文提出了一个神经生物学模型,用于研究社交依恋和药物滥用、社交依恋和慢性应激之间的相互关联,因为重叠系统涉及应激应对和社交依恋。在应对方面,对新的应激源或挑战的反应涉及初始的新奇处理和激活学习机制,使个体通过熟悉化来适应应激源。同样,社交依恋最初是通过被尚未熟悉的个体的奖励属性所吸引而形成的,然后对熟悉的个体产生依恋感。依恋和熟悉感增加了行为和情绪控制的“内部工作模型”的可用性,这可以解释为什么安全的依恋与面对压力时的增强弹性有关,同时伴随着反应性奖励反应的减少(即,增强对成瘾的抵抗力)。本文旨在阐明神经肽催产素的作用,催产素可能通过将处理过程从新奇和奖励寻求转移到熟悉感的欣赏,参与到稳定的依恋形成和应激应对的重叠机制中。催产素可以通过促进皮质纹状体回路中的腹侧到背侧的激活转移来实现这一点,这会导致从反应性奖励驱动(想要)到稳定的熟悉社交方面的欣赏(“喜欢”或“爱”)的转变。作者认为,通过多巴胺能、5-羟色胺能和内源性阿片肽机制,催产素通过促进从腹侧反应性奖励系统到背侧内部工作模型的社交信息的巩固,参与到皮质纹状体回路中想要和喜欢之间的平衡的转变,从而有助于在未来前瞻性地选择最佳行动,增加面对压力和成瘾时的弹性。