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首页> 外文期刊>Frontiers in Psychology >An Affective Neuroscience Framework for the Molecular Study of Internet Addiction
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An Affective Neuroscience Framework for the Molecular Study of Internet Addiction

机译:互联网成瘾分子研究的情感神经科学框架

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Internet addiction represents an emerging global health issue. Increasing efforts have been made to characterize risk factors for the development of Internet addiction and consequences of excessive Internet use. During the last years, classic research approaches from psychology considering personality variables as vulnerability factor, especially in conjunction with neuroscience approaches such as brain imaging, have led to coherent theoretical conceptualizations of Internet addiction. Although such conceptualizations can be valuable aid, the research field is currently lacking a comprehensive framework for determining brain-based and neurochemical markers of Internet addiction. The present work aims at providing a framework on the molecular level as a basis for future research on the neural and behavioral level, in order to facilitate a comprehensive neurobiological model of Internet addiction and its clinical symptomatology. To help establish such a molecular framework for the study of Internet addiction, we investigated in N = 680 participants associations between individual differences in tendencies toward Internet addiction measured by the Generalized Problematic Internet Use Scale-2 (GPIUS-2) and individual differences in primary emotional systems as assessed by the Affective Neuroscience Personality Scales (ANPS). Regression analysis revealed that the ANPS scales FEAR and SADNESS were the ANPS scales most robustly positively linked to several (sub)scales of the GPIUS-2. Also the scales SEEKING, CARE and PLAY explain variance in some of the GPIUS-2 subscales. As such, these scales are negatively linked to the GPIUS-2 subscales. As the ANPS has been constructed on substantial available brain data including an extensive molecular body with respect to evolutionary highly conserved emotional circuitry in the ancient mammalian brain, the present study gives first ideas on putative molecular mechanisms underlying different facets of Internet addiction as derived from associations between tendencies toward Internet addiction and individual differences in primary emotional systems. For example, as SADNESS is linked to the overall GPIUS-2 score, and the neuropeptide oxytocin is known to downregulate SADNESS, it is conceivable that the neuropeptide might play a role in Internet addition on the molecular level. Our findings provide a theoretical framework potentially illuminating the molecular underpinnings of Internet addiction. Finally, we also present data on the ANPS and smartphone addiction at the end of the paper. Similar to the reported associations between the ANPS and the GPIUS-2, these correlations might provide an initial outline for a framework guiding future studies that aim to address the molecular basis of smartphone addiction.
机译:网络成瘾代表了一个新兴的全球健康问题。人们已经做出了越来越多的努力来表征互联网成瘾发展的风险因素以及过度使用互联网的后果。在过去的几年中,心理学的经典研究方法将人格变量视为易受伤害因素,尤其是与诸如大脑成像之类的神经科学方法相结合,已经导致了有关网络成瘾的理论概念的形成。尽管这样的概念化可以提供有价值的帮助,但是当前研究领域缺乏用于确定网络成瘾的基于大脑和神经化学标志物的综合框架。本工作旨在提供分子水平的框架,作为将来在神经和行为水平研究的基础,以促进互联网成瘾及其临床症状的综合神经生物学模型。为了帮助建立这样一个用于研究网络成瘾的分子框架,我们在N = 680名参与者中进行了调查,该问题由广义问题互联网使用量表2(GPIUS-2)衡量的网络成瘾倾向的个体差异与初级个体的个体差异之间的关联情感系统由情感神经科学人格量表(ANPS)评估。回归分析显示,ANPS量表的FEAR和SADNESS是与GPIUS-2的几个(子)量表最有力的正相关的ANPS量表。 SEEKING,CARE和PLAY量表也解释了某些GPIUS-2子量表的方差。因此,这些量表与GPIUS-2子量表负相关。由于ANPS已建立在大量可用的大脑数据上,包括关于古代哺乳动物大脑中进化高度保守的情感电路的广泛分子体,因此本研究就基于关联的互联网成瘾的不同方面所推定的分子机制提出了第一个思路网络成瘾倾向与主要情绪系统的个体差异之间的关系。例如,由于SADNESS与总GPIUS-2得分相关,并且已知神经肽催产素下调SADNESS,因此可以想象,神经肽可能在分子水平上在Internet添加中发挥作用。我们的发现提供了可能阐明互联网成瘾的分子基础的理论框架。最后,我们还在本文结尾处提供了有关ANPS和智能手机成瘾的数据。与已报道的ANPS和GPIUS-2之间的关联相似,这些关联可能为指导未来研究的框架提供了初步轮廓,该研究旨在解决智能手机成瘾的分子基础。

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