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Borolatonin limits cognitive deficit and neuron loss while increasing proBDNF in ovariectomised rats.

Authors :
Barrón-González M
Rivera-Antonio AM
Jarillo-Luna RA
Santiago-Quintana JM
Levaro-Loquio D
Pérez-Capistran T
Guerra-Araiza CH
Soriano-Ursúa MA
Farfán-García ED
Source :
Fundamental & clinical pharmacology [Fundam Clin Pharmacol] 2024 Aug; Vol. 38 (4), pp. 730-741. Date of Electronic Publication: 2024 Feb 29.
Publication Year :
2024

Abstract

Background: Borolatonin is a potential therapeutic agent for some neuronal diseases such as Alzheimer's disease (AD). Its administration exerts ameliorative effects such as those induced by the equimolar administration of melatonin in behavioral tests on male rats and in neuronal immunohistochemistry assays.<br />Objective: In this study, motivated by sex differences in neurobiology and the incidence of AD, the ability of borolatonin to induce changes in female rats was assessed.<br />Methods: Effects of borolatonin were measured by the evaluation of both behavioral and immunohistopathologic approaches; additionally, its ability to limit amyloid toxicity was determined in vitro.<br />Results: Surprisingly, behavioral changes were similar to those reported in male rats, but not those evaluated by immunoassays regarding neuronal survival; while pro-brain-derived neurotrophic factor (BDNF) immunoreactivity and the limitation of toxicity by amyloid in vitro were observed for the first time.<br />Conclusion: Borolatonin administration induced changes in female rats. Differences induced by the administration of borolatonin or melatonin could be related to the differences in the production of steroid hormones in sex dependence. Further studies are required to clarify the possible mechanism and origin of differences in disturbed memory caused by the gonadectomy procedure between male and female rats.<br /> (© 2024 Société Française de Pharmacologie et de Thérapeutique. Published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1472-8206
Volume :
38
Issue :
4
Database :
MEDLINE
Journal :
Fundamental & clinical pharmacology
Publication Type :
Academic Journal
Accession number :
38423984
Full Text :
https://doi.org/10.1111/fcp.12997