4.5 Article

Different stressors produce excitation or inhibition of mesolimbic dopamine neuron activity: response alteration by stress pre-exposure

期刊

EUROPEAN JOURNAL OF NEUROSCIENCE
卷 35, 期 8, 页码 1312-1321

出版社

WILEY
DOI: 10.1111/j.1460-9568.2012.08038.x

关键词

amphetamine cross-sensitization; DA neuron population activity; prefrontal cortex; rat; ventral tegmental area

资金

  1. Johnson Johnson
  2. Lundbeck
  3. Pfizer
  4. GSK
  5. Puretech Ventures
  6. Merck
  7. Takeda
  8. Dainippon Sumitomo
  9. EMD Serrono
  10. United States Public Health Service [DA15408]

向作者/读者索取更多资源

Stressors can exert a wide variety of responses, ranging from adaptive responses to pathological changes; moreover, recent studies suggest that mild stressors can attenuate the response of a system to major stressful events. We have previously shown that 2-week exposure to cold, a comparatively mild inescapable stressor, induced a pronounced reduction in ventral tegmental area (VTA) dopamine (DA) neuron activity, whereas restraint stress increases DA neuron activity. However, it is not known if these stressors differentially impact the VTA in a region-specific manner, if they differentially impact behavioral responses, or whether the effects of such different stressors are additive or antagonistic with regard to their impact on DA neuron firing. To address these questions, single-unit extracellular recordings were performed in anesthetized control rats and rats exposed to chronic cold, and tested after delivery of a 2-h restraint session. Chronic cold stress strongly attenuated the number of DA neurons firing in the VTA, and this effect occurred primarily in the medial and central VTA regions that preferentially project to reward-related ventral striatal regions. Chronic cold exposure also prevented the pronounced increase in DA neuron population activity without affecting the behavioral sensitization to amphetamine produced by restraint stress. Taken together, these data show that a prolonged inescapable mild stressor can induce plastic changes that attenuate the DA system response to acute stress.

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