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肥胖会改变时间敏感性,与促炎状态有关。

Altered temporal sensitivity in obesity is linked to pro-inflammatory state.

机构信息

Istituto Auxologico Italiano, I.R.C.C.S., Ospedale San Giuseppe, Piancavallo, Italy.

Department of Translational Medicine, Università del Piemonte Orientale 'A. Avogadro', Novara, Italy.

出版信息

Sci Rep. 2019 Oct 29;9(1):15508. doi: 10.1038/s41598-019-51660-5.

Abstract

Temporal sensitivity to multisensory stimuli has been shown to be reduced in obesity. We sought to investigate the possible role of the pro-inflammatory state on such alteration, considering the effect of the expression of markers, such as leptin and IL6, which are notably high in obesity. The performance of 15 male individuals affected by obesity and 15 normal-weight males was compared using two audiovisual temporal tasks, namely simultaneity judgment and temporal order judgment. Analyses of serum levels of inflammatory markers of leptin and IL6, and of neurotrophic factors of BDNF and S100SB were quantified. At the behavioral level we confirmed previous evidence showing poorer temporal sensitivity in obesity compared to normal-weight participants. Furthermore, leptin, that is a cytokine overexpressed in obesity, represented the best predictor of behavioral differences between groups in both tasks. The hypothesis we put forward is that the immune system, rather than overall cerebral dysfunction, might contribute to explain the altered temporal sensitivity in obesity. The present finding is discussed within the context of the role of cytokines on the brain mechanisms supporting temporal sensitivity.

摘要

已有研究表明,肥胖会导致对多感官刺激的时间敏感性降低。我们试图探讨这种变化可能与促炎状态有关,因为肥胖症患者体内的瘦素和白细胞介素 6(IL6)等标志物的表达水平显著升高。我们比较了 15 名肥胖男性和 15 名正常体重男性在两个视听时间任务(即同时性判断和时间顺序判断)中的表现。我们量化了血清中炎症标志物瘦素和白细胞介素 6(IL6)以及神经营养因子脑源性神经营养因子(BDNF)和 S100 钙结合蛋白 B(S100SB)的水平。在行为水平上,我们证实了之前的研究结果,即肥胖症患者的时间敏感性比正常体重参与者差。此外,瘦素是一种在肥胖症中过度表达的细胞因子,它是两种任务中组间行为差异的最佳预测因子。我们提出的假设是,免疫系统,而不是整体大脑功能障碍,可能有助于解释肥胖症患者时间敏感性的改变。本研究结果在细胞因子对支持时间敏感性的大脑机制的作用背景下进行了讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73b0/6820747/0d816f775981/41598_2019_51660_Fig1_HTML.jpg

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