It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Over the course of evolution, the amygdala (AMG) and medial frontal cortex (mPFC) network, involved in behavioral adaptation, underwent structural changes in the old-world monkey and human lineages. Yet, whether and how the functional organization of this network differs remains poorly understood. Using resting-state functional magnetic resonance imagery, we show that the functional connectivity (FC) between AMG nuclei and mPFC regions differs between humans and awake macaques. In humans, the AMG-mPFC FC displays U-shaped pattern along the corpus callosum: a positive FC with the ventromedial prefrontal (vmPFC) and anterior cingulate cortex (ACC), a negative FC with the anterior mid-cingulate cortex (MCC), and a positive FC with the posterior MCC. Conversely, in macaques, the negative FC shifted more ventrally at the junction between the vmPFC and the ACC. The functional organization divergence of AMG-mPFC network between humans and macaques might help understanding behavioral adaptation abilities differences in their respective socio-ecological niches.
A resting-state fMRI study in both humans and macaques suggest that the functional connectivity pattern between amygdala nuclei and the medial prefrontal cortex present similarities and differences that may explain differential behavioral adaptation.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details






1 Inserm, Stem Cell and Brain Research Institute U1208, Univ Lyon, Université Lyon 1, Bron, France (GRID:grid.7429.8) (ISNI:0000000121866389)
2 Inserm, Stem Cell and Brain Research Institute U1208, Univ Lyon, Université Lyon 1, Bron, France (GRID:grid.7429.8) (ISNI:0000000121866389); Inovarion, Paris, France (GRID:grid.7429.8)
3 Lyon Neuroscience Research Center (CRNL); Université Lyon 1, Integrative Multisensory Perception Action & Cognition Team (ImpAct), INSERM U1028, CNRS UMR5292, Bron, France (GRID:grid.461862.f) (ISNI:0000 0004 0614 7222)
4 CNRS UAR 3453, INSERM US7, Lyon 1 University, La Structure Fédérative de Recherche Santé Lyon-Est, Lyon, France (GRID:grid.7849.2) (ISNI:0000 0001 2150 7757); Centre d’Etude et de Recherche Multimodal et Pluridisciplinaire en Imagerie du Vivant (CERMEP), Bron, France (GRID:grid.420133.7) (ISNI:0000 0004 0639 301X)