4.3 Article

Whole-Brain Mapping of Neuronal Activity in the Learned Helplessness Model of Depression

期刊

FRONTIERS IN NEURAL CIRCUITS
卷 10, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fncir.2016.00003

关键词

C-fos expression; serial two-photon tomography; Positron-emission tomography; learned helplessness; depression

资金

  1. Brain AMP
  2. Behavior Research Foundation (NARSAD) Young Investigator Award
  3. Charles A. Dana Fellowship
  4. Rossi Family Funds (MM)
  5. U.S. Department of Energy [LDRD-07-096]
  6. Simons Foundation
  7. NIH

向作者/读者索取更多资源

Some individuals are resilient, whereas others succumb to despair in repeated stressful situations. The neurobiological mechanisms underlying such divergent behavioral responses remain unclear. Here, we employed an automated method for mapping neuronal activity in search of signatures of stress responses in the entire mouse brain. We used serial two-photon tomography to detect expression of c-FosGFP - a marker of neuronal activation - in c-fosGFP transgenic mice subjected to the learned helplessness (LH) procedure, a widely used model of stress-induced depression-like phenotype in laboratory animals. We found that mice showing helpless behavior had an overall brain-wide reduction in the level of neuronal activation compared with mice showing resilient behavior, with the exception of a few brain areas, including the locus coeruleus, that were more activated in the helpless mice. In addition, the helpless mice showed a strong trend of having higher similarity in whole-brain activity profile among individuals, suggesting that helplessness is represented by a more stereotypic brain-wide activation pattern. This latter effect was confirmed in rats subjected to the LH procedure, using 2-deoxy-2[18F]fluoro-D-glucose positron emission tomography to assess neural activity. Our findings reveal distinct brain activity markings that correlate with adaptive and maladaptive behavioral responses to stress, and provide a framework for further studies investigating the contribution of specific brain regions to maladaptive stress responses.

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