Fluoxetine induces proliferation and inhibits differentiation of hypothalamic neuroprogenitor cells in vitro

PLoS One. 2014 Mar 5;9(3):e88917. doi: 10.1371/journal.pone.0088917. eCollection 2014.

Abstract

A significant number of children undergo maternal exposure to antidepressants and they often present low birth weight. Therefore, it is important to understand how selective serotonin reuptake inhibitors (SSRIs) affect the development of the hypothalamus, the key center for metabolism regulation. In this study we investigated the proliferative actions of fluoxetine in fetal hypothalamic neuroprogenitor cells and demonstrate that fluoxetine induces the proliferation of these cells, as shown by increased neurospheres size and number of proliferative cells (Ki-67+ cells). Moreover, fluoxetine inhibits the differentiation of hypothalamic neuroprogenitor cells, as demonstrated by decreased number of mature neurons (Neu-N+ cells) and increased number of undifferentiated cells (SOX-2+ cells). Additionally, fluoxetine-induced proliferation and maintenance of hypothalamic neuroprogenitor cells leads to changes in the mRNA levels of appetite regulator neuropeptides, including Neuropeptide Y (NPY) and Cocaine-and-Amphetamine-Regulated-Transcript (CART). This study provides the first evidence that SSRIs affect the development of hypothalamic neuroprogenitor cells in vitro with consequent alterations on appetite neuropeptides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antidepressive Agents, Second-Generation / adverse effects
  • Antidepressive Agents, Second-Generation / pharmacology*
  • Cell Differentiation
  • Cell Proliferation
  • Cells, Cultured
  • Female
  • Fluoxetine / adverse effects
  • Fluoxetine / pharmacology*
  • Gene Expression / drug effects
  • Humans
  • Hypothalamus / cytology*
  • Hypothalamus / drug effects
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neural Stem Cells / drug effects*
  • Neural Stem Cells / metabolism
  • Neuropeptide Y / genetics
  • Neuropeptide Y / metabolism
  • Pregnancy
  • Pro-Opiomelanocortin / genetics
  • Pro-Opiomelanocortin / metabolism
  • Rats
  • Serotonergic Neurons / drug effects
  • Serotonergic Neurons / metabolism
  • Spheroids, Cellular / drug effects

Substances

  • Antidepressive Agents, Second-Generation
  • Nerve Tissue Proteins
  • Neuropeptide Y
  • cocaine- and amphetamine-regulated transcript protein
  • Fluoxetine
  • Pro-Opiomelanocortin

Grants and funding

This work was supported by grants from the Portuguese Foundation for Science and Technology, FEDER and COMPETE (PEst-C/SAU/LA0001/2013-2014; PTDC/SAU-FCF/099082/2008; PTDC/BIM-MED/0775/2012; SFRH/BD/30608/2006; SFRH/BPD/73942/2010; SFRH/BPD/78424/2011). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.