Signaling pathways regulating Homer1a expression: implications for antidepressant therapy

Tsvetan Serchov*, Rolf Heumann, Dietrich van Calker, Knut Biber

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

30 Citations (Scopus)
544 Downloads (Pure)

Abstract

Homer1a is upregulated by several different antidepressant measures, including non-pharmacological treatments, like sleep deprivation (SD) and electroconvulsive therapy (ECT) and antidepressant drugs, such as imipramine, fluoxetine and ketamine. Homer1a induction might thus be a crucial joint mechanism for antidepressant therapy in general. However, the upstream signaling pathways that regulate or induce Homer1a expression are still not well understood. The main focus of the present review is to offer an overview of the current knowledge about the potential role of Homer1a in depression and the signaling pathways responsible for Homer1a regulation. It is suggested here that a detailed characterization of the signaling mechanisms leading to Homer1a expression might provide novel therapeutic targets for antidepressant drug development.

Original languageEnglish
Pages (from-to)207-214
Number of pages8
JournalBiological Chemistry
Volume397
Issue number3
DOIs
Publication statusPublished - Mar-2016

Keywords

  • adenosine A(1) receptor
  • BDNF
  • depression
  • ERK pathway
  • Homer1a
  • Ras
  • METABOTROPIC GLUTAMATE RECEPTORS
  • POSTSYNAPTIC DENSITY PROTEINS
  • PYRAMIDAL CELL EXCITABILITY
  • ADENOSINE A(1) RECEPTORS
  • DEPRESSION-LIKE BEHAVIOR
  • ELEMENT-BINDING PROTEIN
  • SLEEP-DEPRIVATION
  • RAT-BRAIN
  • PHOSPHOLIPASE-C
  • RYANODINE RECEPTOR-TYPE-1

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