4.7 Article

Anti-Depressant Fluoxetine Reveals its Therapeutic Effect Via Astrocytes

Journal

EBIOMEDICINE
Volume 32, Issue -, Pages 72-83

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ebiom.2018.05.036

Keywords

Astrocytes; Fluoxetine; ATP; Adenosine; Vesicular nucleotide transporter; BDNF

Funding

  1. JSPS [3507, 25116512, 25117003, 16H04669, 18H05121]
  2. Japan Agency for Medical Research and Development (AMED)-CREST [15652227]
  3. JST CREST [14532115]
  4. Takeda Science Foundation
  5. The Kurata Grants [1305]
  6. Takahashi Industrial and Economic Research Foundation [040]
  7. SENSHIN Medical Research Foundation

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Although psychotropic drugs act on neurons and glial cells, how glia respond, and whether glial responses are involved in therapeutic effects are poorly understood. Here, we show that fluoxetine (FLX), an anti-depressant, mediates its anti-depressive effect by increasing the gliotransmission of ATP. FLX increased ATP exocytosis via vesicular nucleotide transporter (VNUT). FLX-induced anti-depressive behavior was decreased in astrocyteselective VNUT-knockout mice or when VNUT was deleted in mice, but it was increased when astrocyteselective VNUT was overexpressed in mice. This suggests that VNUT-dependent astrocytic ATP exocytosis has a critical role in the therapeutic effect of FLX. Released ATP and its metabolite adenosine act on P2Y11 and adenosine A2b receptors expressed by astrocytes, causing an increase in brain-derived neurotrophic factor in astrocytes. These findings suggest that in addition to neurons, FLX acts on astrocytes and mediates its therapeutic effects by increasing ATP gliotransmission. (C) 2018 The Authors. Published by Elsevier B.V.

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