Rapamycin Cannot Reduce Seizure Susceptibility in Infantile Rats with Malformations of Cortical Development Lacking mTORC1 Activation.


Journal

Molecular neurobiology
ISSN: 1559-1182
Titre abrégé: Mol Neurobiol
Pays: United States
ID NLM: 8900963

Informations de publication

Date de publication:
Dec 2022
Historique:
received: 25 04 2022
accepted: 04 09 2022
pubmed: 5 10 2022
medline: 2 11 2022
entrez: 4 10 2022
Statut: ppublish

Résumé

The mechanistic target of the rapamycin (mTOR) pathway is involved in cortical development. However, the efficacy of mTOR inhibitors in malformations of cortical dysplasia (MCD) outside of the tuberous sclerosis complex is unknown. We selected the MCD rat model with prenatal MAM exposure to test the efficacy of mTOR inhibitors in MCDs. We explored the early cortical changes of mTOR pathway protein expression in rats aged P15. We also monitored the early treatment effect of the mTOR inhibitor, rapamycin, on N-methyl-D-aspartate (NMDA)-induced spasms at P15 and their behavior in the juvenile stage. In vivo MR spectroscopy was performed after rapamycin treatment and compared with vehicle controls. There was no difference in mTORC1 pathway protein expression between MAM-exposed MCD rats and controls at P15, and prolonged treatment of rapamycin had no impact on NMDA-induced spasms despite poor weight gain. Prenatal MAM-exposed juvenile rats treated with rapamycin showed increased social approaching and freezing behavior during habituation. MR spectroscopy showed altered neurometabolites, including Gln, Glu+Gln, Tau, and Cr. Despite behavioral changes and in vivo neurometabolic alteration with early prolonged rapamycin treatment, rapamycin had no effect on spasms susceptibility in prenatal MAM-exposed infantile rats with MCD without mTORC1 activation. For MAM-exposed MCD rats without mTORC1 activation, treatment options outside of mTOR pathway inhibitors should be explored.

Identifiants

pubmed: 36194361
doi: 10.1007/s12035-022-03033-9
pii: 10.1007/s12035-022-03033-9
doi:

Substances chimiques

Sirolimus W36ZG6FT64
Mechanistic Target of Rapamycin Complex 1 EC 2.7.11.1
N-Methylaspartate 6384-92-5
TOR Serine-Threonine Kinases EC 2.7.11.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7439-7449

Subventions

Organisme : Ministry of Education
ID : NRF-2021R1A2C100447111

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Minyoung Lee (M)

Department of Pediatrics, University of Ulsan College of Medicine, Seoul, 05505, Korea.
Asan Medical Center, Asan Institute for Life Sciences, Seoul, 05505, Korea.

Eun-Jin Kim (EJ)

Department of Pediatrics, University of Ulsan College of Medicine, Seoul, 05505, Korea.
Asan Medical Center, Asan Institute for Life Sciences, Seoul, 05505, Korea.

Min-Jee Kim (MJ)

Department of Pediatrics, Asan Medical Center Children's Hospital, 88 Olympic-ro, Songpa-ku, Seoul, 05505, Korea.

Mi-Sun Yum (MS)

Department of Pediatrics, University of Ulsan College of Medicine, Seoul, 05505, Korea. misun.yum@gmail.com.
Department of Pediatrics, Asan Medical Center Children's Hospital, 88 Olympic-ro, Songpa-ku, Seoul, 05505, Korea. misun.yum@gmail.com.

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