Anxiolytic and Anti-depressive Like Effects of Translocator Protein (18 kDa) Ligand YL-IPA08 in a Rat Model of Postpartum Depression.
Animals
Anti-Anxiety Agents
/ therapeutic use
Antidepressive Agents
/ therapeutic use
Anxiety Disorders
/ drug therapy
Carrier Proteins
/ genetics
Depression, Postpartum
/ drug therapy
Female
Gene Expression
/ drug effects
Hippocampus
/ drug effects
Imidazoles
/ therapeutic use
Ligands
Open Field Test
/ drug effects
Prefrontal Cortex
/ drug effects
Pregnanolone
/ metabolism
Progesterone
/ metabolism
Pyridines
/ therapeutic use
Rats, Sprague-Dawley
Receptors, GABA-A
/ genetics
Neurosteroid
Postpartum depression
Translocator protein (18 kDa)
YL-IPA08
Journal
Neurochemical research
ISSN: 1573-6903
Titre abrégé: Neurochem Res
Pays: United States
ID NLM: 7613461
Informations de publication
Date de publication:
Aug 2020
Aug 2020
Historique:
received:
30
01
2020
accepted:
15
04
2020
revised:
19
03
2020
pubmed:
10
5
2020
medline:
4
6
2021
entrez:
9
5
2020
Statut:
ppublish
Résumé
Translocator protein 18 kDa (TSPO) is mainly distributed in the outer mitochondrial membrane of steroid-synthesizing cells in the central and peripheral nervous systems. It mediates cholesterol transportation across the phospholipid membrane, which is a prerequisite for neurosteroid synthesis. Though the ligand of TSPO has clinical value in the diagnosis and treatment of neuropsychiatric disorders, the pharmacological study of TSPO for anti-postpartum depression has not been reported. In this study, the classical method of reproductive hormone withdrawal was used to construct a rat model of postpartum depression (PPD). The effect of YL-IPA08, a new ligand compound of TSPO, on PPD was evaluated using multiple behavioral tests at progressive time points. Additionally, real-time quantitative PCR, Western-blotting and an enzyme linked immunosorbent assay were conducted to elucidate the potential molecular mechanism of such effect. We report that the levels of TSPO and neurosteroids in the hippocampus and prefrontal cortex were significantly decreased in PPD rats compared to healthy controls. After 3 weeks of drug treatment, the levels of TSPO and neurosteroids in the hippocampus of PPD rats were increased, and anxiety and depressive like behaviors were alleviated. Meanwhile, compared with sertraline treatment, a positive control in this study, YL-IPA08 treatment had a shorter onset time. Our results suggest that the anxiolytic and anti-depressive activity of YL-IPA08 has significant value in the treatment of PPD and that TSPO may be a potential new target for the treatment of PPD.
Identifiants
pubmed: 32383026
doi: 10.1007/s11064-020-03036-9
pii: 10.1007/s11064-020-03036-9
doi:
Substances chimiques
Anti-Anxiety Agents
0
Antidepressive Agents
0
Carrier Proteins
0
Imidazoles
0
Ligands
0
N-ethyl-N-(2-pyridinylmethyl)-2-(3,4-chlorophenyl)-7-methylimidazo(1,2-a)pyridine-3-acetamide
0
Pyridines
0
Receptors, GABA-A
0
Tspo protein, rat
141440-82-6
Progesterone
4G7DS2Q64Y
Pregnanolone
BXO86P3XXW
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1746-1757Subventions
Organisme : National Natural Science Foundation of China
ID : 817010172