Signaling pathways regulating Homer1a expression: implications for antidepressant therapy

Biol Chem. 2016 Mar;397(3):207-14. doi: 10.1515/hsz-2015-0267.

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antidepressive Agents / pharmacology
  • Antidepressive Agents / therapeutic use
  • Brain-Derived Neurotrophic Factor / metabolism
  • Carrier Proteins / genetics*
  • Carrier Proteins / metabolism
  • Depression / drug therapy
  • Depression / genetics
  • Depression / metabolism*
  • Depressive Disorder / drug therapy
  • Depressive Disorder / genetics
  • Depressive Disorder / metabolism
  • Gene Expression Regulation* / drug effects
  • Homer Scaffolding Proteins
  • Humans
  • Receptor, Adenosine A1 / metabolism
  • Signal Transduction* / drug effects
  • ras Proteins / metabolism

Substances

  • Antidepressive Agents
  • Brain-Derived Neurotrophic Factor
  • Carrier Proteins
  • Homer Scaffolding Proteins
  • Receptor, Adenosine A1
  • ras Proteins