An Endogenous Ligand of Aryl Hydrocarbon Receptor 6-Formylindolo[3,2-b]Carbazole (FICZ) Is a Signaling Molecule in Neurogenesis of Adult Hippocampal Neurons.


Journal

Journal of molecular neuroscience : MN
ISSN: 1559-1166
Titre abrégé: J Mol Neurosci
Pays: United States
ID NLM: 9002991

Informations de publication

Date de publication:
May 2020
Historique:
received: 05 12 2019
accepted: 05 02 2020
pubmed: 11 2 2020
medline: 5 1 2021
entrez: 11 2 2020
Statut: ppublish

Résumé

Neurogenesis is a dynamic and physiologic developmental process that affects learning and hippocampal dependent memory. It is regulated by multi-cellular micro-environment and different types of transcription factors. The neurogenesis effects of endogenously activated aryl hydrocarbon receptor (AHR) by its endogenous ligand, 6-formylindolo[3,2-b] carbazole (FICZ), and its interactions with the Wnt/β-catenin signaling pathway were the main purpose of this study. In accordance, learning and hippocampus-dependent memory were examined. Male BALB/C mice received FICZ, CH223191, and XAV-939 in a single dose of 100 μg/kg, 1 mg/kg, and 5 mg/kg of body weight respectively via intraperitoneal (IP) injection. qRT-PCR for gene analyses and protein assay on the 7th and 28th days were performed. To assess the hippocampal dependent memory, they also underwent contextual fear conditioning on the 28th day after treatment. Our results showed that FICZ treatment led to elevation of the proneural transcription factors ASCL1 and Ngn2, immature neural marker DCX, differentiation neurons marker, NeuN, as well as β-catenin at mRNA and protein levels. We also indicated that hippocampal dependent memory and learning task were improved by FICZ treatment and impaired by the AHR and Wnt/ß-catenin inhibition. In this study for the first time, we demonstrated that the endogenous ligand of AHR, FICZ, has a positive effect on short- and long-term memory as well as learning skills. This ability is possibly mediated by the AHR-Wnt/ß-catenin cross-talk.

Identifiants

pubmed: 32040828
doi: 10.1007/s12031-020-01506-x
pii: 10.1007/s12031-020-01506-x
doi:

Substances chimiques

2-methyl-2H-pyrazole-3-carboxylic acid (2-methyl-4-o-tolylazophenyl)amide 0
6-formylindolo(3,2-b)carbazole 0
Ascl1 protein, mouse 0
Azo Compounds 0
Basic Helix-Loop-Helix Transcription Factors 0
Carbazoles 0
Dcx protein, mouse 0
Doublecortin Protein 0
Heterocyclic Compounds, 3-Ring 0
Nerve Tissue Proteins 0
Neurog2 protein, mouse 0
Pyrazoles 0
Receptors, Aryl Hydrocarbon 0
XAV939 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

806-817

Subventions

Organisme : Shiraz University of Medical Sciences
ID : Grant number: 15168

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Auteurs

Majid Keshavarzi (M)

Department of Pharmacology and Toxicology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.

Mohammad Javad Khoshnoud (MJ)

Department of Pharmacology and Toxicology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.

Ali Ghaffarian Bahraman (A)

Department of Pharmacology and Toxicology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.

Afshin Mohammadi-Bardbori (A)

Department of Pharmacology and Toxicology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran. toxicology@sums.ac.ir.

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Classifications MeSH