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Involvement of CB 1 and CB 2 receptors in neuroprotective effects of cannabinoids in experimental TDP-43 related frontotemporal dementia using male mice.
- Source :
-
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie [Biomed Pharmacother] 2024 May; Vol. 174, pp. 116473. Date of Electronic Publication: 2024 Mar 24. - Publication Year :
- 2024
-
Abstract
- Background: The elevation of endocannabinoid levels through inhibiting their degradation afforded neuroprotection in CaMKIIα-TDP-43 mice, a conditional transgenic model of frontotemporal dementia. However, which cannabinoid receptors are mediating these benefits is still pending to be elucidated.<br />Methods: We have investigated the involvement of the CB <subscript>1</subscript> and the CB <subscript>2</subscript> receptor using chronic treatments with selective ligands in CaMKIIα-TDP-43 mice, analysis of their cognitive deterioration with the Novel Object Recognition test, and immunostaining for neuronal and glial markers in two areas of interest in frontotemporal dementia.<br />Results: Our results confirmed the therapeutic value of activating either the CB <subscript>1</subscript> or the CB <subscript>2</subscript> receptor, with improvements in the animal performance in the Novel Object Recognition test, preservation of pyramidal neurons, in particular in the medial prefrontal cortex, and attenuation of glial reactivity, in particular in the hippocampus. In addition, the activation of both CB <subscript>1</subscript> and CB <subscript>2</subscript> receptors reduced the elevated levels of TDP-43 in the medial prefrontal cortex of CaMKIIα-TDP-43 mice, an effect exerted by mechanisms that are currently under investigation.<br />Conclusions: These data reinforce the notion that the activation of CB <subscript>1</subscript> and CB <subscript>2</subscript> receptors may represent a promising therapy against TDP-43-induced neuropathology in frontotemporal dementia. Future studies will have to confirm these benefits, in particular with one of the selective CB <subscript>2</subscript> agonists used here, which has been thoroughly characterized for clinical development.<br />Competing Interests: Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: CGC, ISG, LGT, CRC, JFR and EdL declare that they have no conflicts of interest, whereas MBW, PD and UG are employees of the company F. Hoffmann-La Roche Ltd.<br /> (Copyright © 2024 The Authors. Published by Elsevier Masson SAS.. All rights reserved.)
- Subjects :
- Animals
Male
Mice
Prefrontal Cortex drug effects
Prefrontal Cortex metabolism
Prefrontal Cortex pathology
Calcium-Calmodulin-Dependent Protein Kinase Type 2 metabolism
DNA-Binding Proteins metabolism
Mice, Inbred C57BL
Hippocampus drug effects
Hippocampus metabolism
Hippocampus pathology
Receptor, Cannabinoid, CB2 agonists
Receptor, Cannabinoid, CB2 metabolism
Neuroprotective Agents pharmacology
Mice, Transgenic
Receptor, Cannabinoid, CB1 metabolism
Receptor, Cannabinoid, CB1 agonists
Frontotemporal Dementia drug therapy
Frontotemporal Dementia metabolism
Frontotemporal Dementia pathology
Cannabinoids pharmacology
Disease Models, Animal
Subjects
Details
- Language :
- English
- ISSN :
- 1950-6007
- Volume :
- 174
- Database :
- MEDLINE
- Journal :
- Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
- Publication Type :
- Academic Journal
- Accession number :
- 38522237
- Full Text :
- https://doi.org/10.1016/j.biopha.2024.116473