4.7 Article

Selective Estrogen Receptor Modulation Increases Hippocampal Activity during Probabilistic Association Learning in Schizophrenia

Journal

NEUROPSYCHOPHARMACOLOGY
Volume 40, Issue 10, Pages 2388-2397

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/npp.2015.88

Keywords

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Funding

  1. University of New South Wales School of Psychiatry
  2. National Health and Medical Research Council [568807]
  3. Neuroscience Research Australia
  4. Schizophrenia Research Institute
  5. New South Wales Ministry of Health
  6. Macquarie Group Foundation
  7. Australian Schizophrenia Research Bank
  8. National Health and Medical Research Council of Australia
  9. Pratt Foundation
  10. Ramsay Health Care
  11. Viertal Charitable Foundation
  12. National Health and Medical Research Council (Australia) Senior Research Fellowship [1021970]
  13. Ian Scott Scholarship - Australian Rotary Health
  14. Swiss National fund (SSMBS, Advanced Postdoc Mobility) [P3SMP3 148381]
  15. South Eastern Sydney Local Health District
  16. NSW Institute of Psychiatry

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People with schizophrenia show probabilistic association learning impairment in conjunction with abnormal neural activity. The selective estrogen receptor modulator (SERM) raloxifene preserves neural activity during memory in healthy older men and improves memory in schizophrenia. Here, we tested the extent to which raloxifene modifies neural activity during learning in schizophrenia. Nineteen people with schizophrenia participated in a twelve-week randomized, double-blind, placebo-controlled, cross-over adjunctive treatment trial of the SERM raloxifene administered orally at 120 mg daily to assess brain activity during probabilistic association learning using functional magnetic resonance imaging (fMRI). Raloxifene improved probabilistic association learning and significantly increased fMRI BOLD activity in the hippocampus and parahippocampal gyrus relative to placebo. A separate region of interest confirmatory analysis in 21 patients vs 36 healthy controls showed a positive association between parahippocampal neural activity and learning in patients, but no such relationship in the parahippocampal gyrus of healthy controls. Thus, selective estrogen receptor modulation by raloxifene concurrently increases activity in the parahippocampal gyrus and improves probabilistic association learning in schizophrenia. These results support a role for estrogen receptor modulation of mesial temporal lobe neural activity in the remediation of learning disabilities in both men and women with schizophrenia.

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