Literature DB >> 27842943

Raloxifene increases prefrontal activity during emotional inhibition in schizophrenia based on estrogen receptor genotype.

Jochen Kindler1, Cynthia Shannon Weickert2, Peter R Schofield3, Rhoshel Lenroot2, Thomas W Weickert4.   

Abstract

People with schizophrenia show decreased prefrontal cortex (PFC) activity during emotional response inhibition, a cognitive process sensitive to hormonal influences. Raloxifene, a selective estrogen receptor modulator, binds estrogen receptor alpha (ESR-α), improves memory, attention and normalizes cortical and hippocampal activity during learning and emotional face recognition in schizophrenia. Here, we tested the extent to which raloxifene restores neuronal activity during emotional response inhibition in schizophrenia. Since genetic variation in estrogen receptor alpha (ESR-1) determines cortical ESR-α production and correlates with cognition, we also predicted that genetic ESR-1 variation would differentially relate to increased cortical activity by raloxifene administration. Thirty people with schizophrenia participated in a thirteen-week randomized, double-blind, placebo-controlled, cross-over adjunctive treatment trial of raloxifene administered at 120mg/day. Effects of raloxifene on brain activation were assessed based on ESR-1 genotype using functional magnetic resonance imaging during emotional word inhibition. Raloxifene increased PFC activity during inhibition of response to negative words and the raloxifene related increased PFC activity was greater in patients homozygous for ESR-1 rs9340799 AA relative to G carriers. Comparison to 23 healthy controls demonstrated that PFC activity of people with schizophrenia receiving raloxifene was more similar to controls than to their own brain activity during placebo. Estrogen receptor modulation by raloxifene restores PFC activity during emotional response inhibition in schizophrenia and ESR-1 genotype predicts degree of increased neural activity in response to raloxifene. While these preliminary results require replication, they suggest the potential for personalized pharmacotherapy using ESR-1 and estrogen receptor targeting compounds in schizophrenia. Crown Copyright Â
© 2016. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Emotions; Estrogen receptor alpha; Inhibition; Magnetic resonance imaging; Raloxifene hydrochloride; Schizophrenia

Mesh:

Substances:

Year:  2016        PMID: 27842943     DOI: 10.1016/j.euroneuro.2016.10.009

Source DB:  PubMed          Journal:  Eur Neuropsychopharmacol        ISSN: 0924-977X            Impact factor:   4.600


  5 in total

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Authors:  Jochen Kindler; Frauke Schultze-Lutter; Martinus Hauf; Thomas Dierks; Andrea Federspiel; Sebastian Walther; Benno G Schimmelmann; Daniela Hubl
Journal:  Schizophr Bull       Date:  2018-01-13       Impact factor: 9.306

2.  Sex-Specific Associations of Androgen Receptor CAG Trinucleotide Repeat Length and of Raloxifene Treatment with Testosterone Levels and Perceived Stress in Schizophrenia.

Authors:  Samantha J Owens; Thomas W Weickert; Tertia D Purves-Tyson; Ellen Ji; Christopher White; Cherrie Galletly; Dennis Liu; Maryanne O'Donnell; Cynthia Shannon Weickert
Journal:  Mol Neuropsychiatry       Date:  2018-11-20

3.  Specificity proteins 1 and 4 in peripheral blood mononuclear cells in postmenopausal women with schizophrenia: a 24-week double-blind, randomized, parallel, placebo-controlled trial.

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Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  2018-08-30       Impact factor: 5.270

4.  Raloxifene Improves Cognition in Schizophrenia: Spurious Result or Valid Effect?

Authors:  Thomas W Weickert; Cynthia Shannon Weickert
Journal:  Front Psychiatry       Date:  2017-10-12       Impact factor: 4.157

5.  Prefrontal inhibition of neuronal Kv 7 channels enhances prepulse inhibition of acoustic startle reflex and resistance to hypofrontality.

Authors:  Jing Wang; Wenwen Yu; Qin Gao; Chuanxia Ju; KeWei Wang
Journal:  Br J Pharmacol       Date:  2020-09-17       Impact factor: 8.739

  5 in total

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