Tianeptine antagonizes the reduction of PV+ and GAD67 cells number in dorsal hippocampus of socially isolated rats.


Journal

Progress in neuro-psychopharmacology & biological psychiatry
ISSN: 1878-4216
Titre abrégé: Prog Neuropsychopharmacol Biol Psychiatry
Pays: England
ID NLM: 8211617

Informations de publication

Date de publication:
08 03 2019
Historique:
received: 30 07 2018
revised: 08 10 2018
accepted: 23 10 2018
pubmed: 28 10 2018
medline: 26 3 2019
entrez: 28 10 2018
Statut: ppublish

Résumé

Adult male rats exposed to chronic social isolation (CSIS) show depressive- and anxiety-like behaviors and reduce the numbers of parvalbumin-positive (PV+) interneurons in the dorsal hippocampus. We aimed to determine whether tianeptine (Tian), administered during the last three weeks of a six-week-social isolation (10 mg/kg/day), may reverse CSIS-induced behavioral changes and antagonize the CSIS-induced reduction in the number of PV+ interneurons. We also studied whether Tian affects the GABA-producing enzyme GAD67+ cells, in Stratum Oriens (SO), Stratum Pyramidale (SP), Stratum Radiatum (SR) and Stratum Lacunosum Moleculare (LM) of CA1-3, as well as in molecular layer-granule cell layer (ML-GCL) and Hilus (H) of the dentate gyrus (DG). CSIS-induced reduction in the number of PV+ cells was layer/subregion-specific with the greatest decrease in SO of CA2. Reduction in the number of PV+ cells was significantly higher than GAD67+ cells, indicating that PV+ cells are the main target following CSIS. Tian reversed CSIS-induced behavior phenotype and antagonized the reduction in the number of PV+ and GAD67+ cells in all subregions. In controls, Tian led to an increase in the number of PV+ and GAD67+ cells in SP of all subregions and PV+ interneurons in ML-GCL of DG, while treatment during CSIS, compared to CSIS alone, resulted with an increase of PV+ interneurons in SO and SP CA1, SP CA2/CA3 and ML-GCL DG with simultaneous increase in GAD67+ cells in all CA1, LM CA2, SO/SR/LM CA3. Data show that Tian offers protection from CSIS via modulation of the dorsal hippocampal GABAergic system.

Identifiants

pubmed: 30367961
pii: S0278-5846(18)30581-5
doi: 10.1016/j.pnpbp.2018.10.013
pii:
doi:

Substances chimiques

Anti-Anxiety Agents 0
Antidepressive Agents, Tricyclic 0
Parvalbumins 0
Thiazepines 0
tianeptine 0T493YFU8O
Glutamate Decarboxylase EC 4.1.1.15
glutamate decarboxylase 1 EC 4.1.1.15

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

386-399

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Ivana Perić (I)

Vinča Institute of Nuclear Sciences, Laboratory for molecular biology and endocrinology, University of Belgrade, Serbia.

Andrijana Stanisavljević (A)

Vinča Institute of Nuclear Sciences, Laboratory for molecular biology and endocrinology, University of Belgrade, Serbia.

Dragos Inta (D)

Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany; Department of Psychiatry (UPK), University of Basel, Switzerland.

Peter Gass (P)

Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

Undine E Lang (UE)

Department of Psychiatry (UPK), University of Basel, Switzerland.

Stefan Borgwardt (S)

Department of Psychiatry (UPK), University of Basel, Switzerland.

Dragana Filipović (D)

Vinča Institute of Nuclear Sciences, Laboratory for molecular biology and endocrinology, University of Belgrade, Serbia. Electronic address: dragana@vinca.rs.

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Classifications MeSH