Mesolimbic novelty processing in older adults

被引:53
作者
Bunzeck, Nico
Schuetze, Hartmut
Stallforth, Sabine
Kaufmann, Joern
Duezel, Sandra
Heinze, Hans-Jochen
Duezel, Emrah
机构
[1] UCL, Dept Psychol, London WC1N 3AR, England
[2] Otto Von Guericke Univ, Dept Neurol 2, D-39120 Magdeburg, Germany
[3] Otto Von Guericke Univ, Ctr Adv Imaging, D-39120 Magdeburg, Germany
关键词
fMRI; hippocampus; mesolimbic system; novelty; substantia; nigra/VTA;
D O I
10.1093/cercor/bhm020
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Normal aging is associated with neuronal loss in the dopaminergic midbrain (substantia nigra/ventral tegmental area, SN/VTA), a region that has recently been implicated in processing novel stimuli as part of a mesolimbic network including the hippocampus. Here, we quantified age-related structural degeneration of the mesolimbic system using magnetization transfer ratio (MTR) and correlated it with mesolimbic hemodynamic responses (HRs) to stimulus novelty. Twenty-one healthy older adults between 55 and 77 years performed a visual oddball paradigm allowing to distinguish mesolimbic HRs to novelty from rareness, negative emotional valence, and targetness using functional magnetic resonance imaging. The HRs in the right SN/VTA and the right hippocampus to novelty were positively correlated both with the SN/VTA MTR and hippocampus MTR but not amygdala MTR. However, the HR of the amygdala to negative emotional valence correlated with the amygdala MTR but not with the MTR in SN/VTA or the hippocampus. The results establish a structure-function relationship in support of a hippocampal-SN/VTA loop of mesolimbic novelty processing by showing that the hemodynamic activation in SN/VTA and hippocampus for novelty is selectively affected by age-related degeneration of these structures.
引用
收藏
页码:2940 / 2948
页数:9
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