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首页> 外文期刊>Medical hypotheses >Do dopaminergic gene polymorphisms affect mesolimbic reward activation of music listening response? Therapeutic impact on Reward Deficiency Syndrome (RDS).
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Do dopaminergic gene polymorphisms affect mesolimbic reward activation of music listening response? Therapeutic impact on Reward Deficiency Syndrome (RDS).

机译:多巴胺能基因多态性会影响音乐听觉反应的中脑边缘奖励激活吗?对奖励缺乏综合症(RDS)的治疗作用。

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摘要

Using fMRI, Menon and Levitin [9] clearly found for the first time that listening to music strongly modulates activity in a network of mesolimbic structures involved in reward processing including the nucleus accumbens (NAc) and the ventral tegmental area (VTA), as well as the hypothalamus, and insula, which are thought to be involved in regulating autonomic and physiological responses to rewarding and emotional stimuli. Importantly, responses in the NAc and VTA were strongly correlated pointing to an association between dopamine release and NAc response to music. Listing to pleasant music induced a strong response and significant activation of the VTA-mediated interaction of the NAc with the hypothalamus, insula, and orbitofrontal cortex. Blum et al. [10] provided the first evidence that the dopamine D2 receptor gene (DRD2) Taq 1 A1 allele significantly associated with severe alcoholism whereby the author's suggested that they found the first "reward gene" located in the mesolimbic system. The enhanced functional and effective connectivity between brain regions mediating reward, autonomic, and cognitive processing provides insight into understanding why listening to music is one of the most rewarding and pleasurable human experiences. However, little is known about why some people have a more or less powerful mesolimbic experience when they are listening to music. It is well-known that music may induce an endorphinergic response that is blocked by naloxone, a known opioid antagonist (Goldstein [19]). Opioid transmission in the NAc is associated with dopamine release in the VTA. Moreover, dopamine release in the VTA is linked to polymorphisms of the DRD2 gene and even attention-deficit hyperactivity disorder (ADHD), whereby carriers of the DRD2 A1 allele show a reduced NAc release of dopamine (DA). Thus it is conjectured that similar mechanisms in terms of adequate dopamine release and subsequent activation of reward circuitry by listening to music might also be affected by an individual's D2 density in the VTA mediated interaction of the NAc. It is therefore hypothesized that carriers of DRD2 A1 allele may respond significantly differently to carriers of the DRD2 A2 genotype. In this regard, carriers of the D2 A1 allele have a blunted response to glucose and monetary rewards. In contrast powerful D2 agonists like bromocryptine show a heightened activation of the reward circuitry only in DRD2 A1 allele carriers. If music causes a powerful activation in spite of the DRD2 A1 allele due to a strong DA neuronal release which subsequently impinges on existing D2 receptors, then it is reasonable to assume that music is a strong indirect D2 agonist (by virtue of DA neuronal release in the NAc) and may have important therapeutic applicability in Reward Deficiency Syndrome (RDS) related behaviors including Substance Use Disorder (SUD). Ross et al. [18] found that music therapy appears to be a novel motivational tool in a severely impaired inpatient sample of patients with co-occurring mental illness and addiction.
机译:Menon和Levitin [9]使用fMRI首次清楚地发现,听音乐强烈调节参与奖励处理的中边缘结构网络中的活动,该结构包括伏隔核(NAc)和腹侧被盖区(VTA),以及如下丘脑和岛突,它们被认为参与调节对奖励和情绪刺激的自主和生理反应。重要的是,NAc和VTA中的响应密切相关,表明多巴胺释放与NAc对音乐的响应之间存在关联。列出令人愉悦的音乐会引起强烈的反应,并显着激活VTA介导的NAc与下丘脑,岛突和眶额皮质的相互作用。 Blum等。 [10]提供了第一个证据表明多巴胺D2受体基因(DRD2)Taq 1 A1等位基因与严重酒精中毒显着相关,因此作者建议他们发现了第一个“奖励基因”位于中脑边缘系统。介导奖励,自主和认知过程的大脑区域之间增强的功能和有效连接性,使我们可以洞悉为什么听音乐是最有意义和令人愉快的人类体验之一。但是,对于为什么有些人在听音乐时会产生或多或少的中脑边缘体验,却知之甚少。众所周知,音乐可能会引起内啡肽反应,而纳洛酮是一种已知的阿片类药物拮抗剂(Goldstein [19])。 NAc中的阿片类药物传递与VTA中的多巴胺释放有关。此外,VTA中的多巴胺释放与DRD2基因的多态性甚至是注意力缺陷多动障碍(ADHD)相关,由此DRD2 A1等位基因的携带者显示出多巴胺(DA)的NAc释放减少。因此推测,在充分的多巴胺释放以及随后通过听音乐激活奖励电路方面,类似的机制也可能受到NAc在VTA介导的相互作用中个体D2密度的影响。因此,假设DRD2 A1等位基因的携带者可能对DRD2 A2基因型的携带者有明显不同的反应。在这方面,D2 A1等位基因的携带者对葡萄糖和金钱奖励的反应迟钝。相比之下,强效的D2激动剂(如溴隐亭)仅在DRD2 A1等位基因携带者中显示出奖励电路的增强激活。如果尽管DRD2 A1等位基因由于强DA神经元释放而引起音乐的强大激活,随后又影响现有D2受体,则可以合理地假设音乐是强间接D2激动剂(由于DA神经元释放(NAc),并且在包括物质使用障碍(SUD)在内的奖励不足综合症(RDS)相关行为中可能具有重要的治疗适用性。罗斯等。 [18]发现音乐疗法似乎是一种同时患有精神疾病和成瘾患者的住院患者严重受损的新型动机工具。

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