4.7 Article

Hippocampal-Dorsolateral Prefrontal Coupling as a Species-Conserved Cognitive Mechanism: A Human Translational Imaging Study

期刊

NEUROPSYCHOPHARMACOLOGY
卷 40, 期 7, 页码 1674-1681

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/npp.2015.13

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资金

  1. German Ministry of Education and Research (BMBF) [01GQ1003B]
  2. German Science Foundation (DFG) [Du 354/6-1, Du 354/7-2]
  3. Alexza Pharmaceuticals
  4. AstraZeneca
  5. Bristol-Myers Squibb
  6. Defined Health
  7. Decision Resources
  8. Desitin Arzneimittel
  9. Elsevier
  10. F. Hoffmann-La Roche
  11. Gerson Lehrman Group
  12. Grupo Ferrer
  13. Les Laboratoires Servier
  14. Lilly Deutschland
  15. Lundbeck Foundation
  16. Outcome Sciences
  17. Outcome Europe
  18. PriceSpective
  19. Roche Pharma
  20. Abbott
  21. BASF
  22. GlaxoSmithKline
  23. Janssen- Cilag
  24. Lundbeck
  25. Pfizer Pharma
  26. Servier Deutschland

向作者/读者索取更多资源

Hippocampal-prefrontal cortex (HC-PFC) interactions are implicated in working memory (WM) and altered in psychiatric conditions with cognitive impairment such as schizophrenia. While coupling between both structures is crucial for WM performance in rodents, evidence from human studies is conflicting and translation of findings is complicated by the use of differing paradigms across species. We therefore used functional magnetic resonance imaging together with a spatial WM paradigm adapted from rodent research to examine HC-PFC coupling in humans. A PFC-parietal network was functionally connected to hippocampus (HC) during task stages requiring high levels of executive control but not during a matched control condition. The magnitude of coupling in a network comprising HC, bilateral dorsolateral PFC (DLPFC), and right supramarginal gyrus explained one-fourth of the variability in an independent spatial WM task but was unrelated to visual WM performance. HC-DLPFC coupling may thus represent a systems-level mechanism specific to spatial WM that is conserved across species, suggesting its utility for modeling cognitive dysfunction in translational neuroscience.

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