Modulation of hippocampal theta oscillations and spatial memory by relaxin-3 neurons of the nucleus incertus

  1. Sherie Ma1,2,
  2. Francisco E. Olucha-Bordonau3,
  3. M. Akhter Hossain1,
  4. Feng Lin1,
  5. Chester Kuei4,
  6. Changlu Liu4,
  7. John D. Wade1,5,
  8. Steven W. Sutton4,
  9. Angel Nuñez6 and
  10. Andrew L. Gundlach1,7,8
  1. 1Howard Florey Institute, The University of Melbourne, Victoria 3010, Australia;
  2. 2Department of Medicine, The University of Melbourne, Austin Health, Heidelberg, Victoria 3084, Australia;
  3. 3Departamento de Anatomía y Embriología Humana, Facultad de Medicina, Universidad de Valencia, 46010 Valencia, Spain;
  4. 4Neuroscience Drug Discovery, Johnson & Johnson Pharmaceutical Research & Development, LLC, San Diego, California 92121, USA;
  5. 5Department of Chemistry, The University of Melbourne, Victoria 3010, Australia;
  6. 6Departamento de Anatomia, Histología y Neurociencia Facultad de Medicina, Universidad Autónoma de Madrid, 28029 Madrid, Spain;
  7. 7Department of Anatomy and Cell Biology, The University of Melbourne, Victoria 3010, Australia

    Abstract

    Hippocampal theta rhythm is thought to underlie learning and memory, and it is well established that “pacemaker” neurons in medial septum (MS) modulate theta activity. Recent studies in the rat demonstrated that brainstem-generated theta rhythm occurs through a multisynaptic pathway via the nucleus incertus (NI), which is the primary source of the neuropeptide relaxin-3 (RLN3). Therefore, this study examined the possible contribution of RLN3 to MS activity, and associated hippocampal theta activity and spatial memory. In anesthetized and conscious rats, we identified the ability of intraseptal RLN3 signaling to modulate neuronal activity in the MS and hippocampus and promote hippocampal theta rhythm. Behavioral studies in a spontaneous alternation task indicated that endogenous RLN3 signaling within MS promoted spatial memory and exploratory activity significantly increased c-Fos immunoreactivity in RLN3-producing NI neurons. Anatomical studies demonstrated axons/terminals from NI/RLN3 neurons make close contact with septal GABAergic (and cholinergic) neurons, including those that project to the hippocampus. In summary, RLN3 neurons of the NI can modulate spatial memory and underlying hippocampal theta activity through axonal projections to pacemaker neurons of the MS. NI/RLN3 neurons are highly responsive to stress and express corticotropin-releasing factor type-1 receptors, suggesting that the effects observed could be an important component of memory processing associated with stress responses.

    Footnotes

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