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Cannabinoid CB 2 receptors in primary sensory neurons are implicated in CB 2 agonist-mediated suppression of paclitaxel-induced neuropathic nociception and sexually-dimorphic sparing of morphine tolerance.
- Source :
-
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie [Biomed Pharmacother] 2024 Jul; Vol. 176, pp. 116879. Date of Electronic Publication: 2024 Jun 07. - Publication Year :
- 2024
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Abstract
- Cannabinoid CB <subscript>2</subscript> agonists show therapeutic efficacy without unwanted CB <subscript>1</subscript> -mediated side effects. The G protein-biased CB <subscript>2</subscript> receptor agonist LY2828360 attenuates the maintenance of chemotherapy-induced neuropathic nociception in male mice and blocks development of morphine tolerance in this model. However, the cell types involved in this phenomenon are unknown and whether this therapeutic profile is observed in female mice has never been investigated. We used conditional deletion of CB <subscript>2</subscript> receptors to determine the cell population(s) mediating the anti-allodynic and morphine-sparing effects of CB <subscript>2</subscript> agonists. Anti-allodynic effects of structurally distinct CB <subscript>2</subscript> agonists (LY2828360 and AM1710) were present in paclitaxel-treated CB <subscript>2</subscript> <superscript>f/f</superscript> mice and in mice lacking CB <subscript>2</subscript> receptors in CX3CR1 expressing microglia/macrophages (CX3CR1 <superscript>CRE/+</superscript> ; CB <subscript>2</subscript> <superscript>f/f</superscript> ), but were absent in mice lacking CB <subscript>2</subscript> receptors in peripheral sensory neurons (Advillin <superscript>CRE/+</superscript> ; CB <subscript>2</subscript> <superscript>f/f</superscript> ). The morphine-sparing effect of LY28282360 occurred in a sexually-dimorphic manner, being present in male, but not female, mice. LY2828360 treatment (3 mg/kg per day i.p. x 12 days) blocked the development of morphine tolerance in male CB <subscript>2</subscript> <superscript>f/f</superscript> and CX3CR1 <superscript>CRE/+</superscript> ; CB <subscript>2</subscript> <superscript>f/f</superscript> mice with established paclitaxel-induced neuropathy but was absent in male (or female) Advillin <superscript>CRE/+</superscript> ; CB <subscript>2</subscript> <superscript>f/f</superscript> mice. Co-administration of morphine with a low dose of LY2828360 (0.1 mg/kg per day i.p. x 6 days) reversed morphine tolerance in paclitaxel-treated male CB <subscript>2</subscript> <superscript>f/f</superscript> mice, but not Advillin <superscript>CRE/+</superscript> ; CB <subscript>2</subscript> <superscript>f/f</superscript> mice of either sex. LY2828360 (3 mg/kg per day i.p. x 8 days) delayed, but did not prevent, the development of paclitaxel-induced mechanical or cold allodynia in either CB <subscript>2</subscript> <superscript>f/f</superscript> or CX3CR1 <superscript>CRE/+</superscript> ; CB <subscript>2</subscript> <superscript>f/f</superscript> mice of either sex. Our findings have potential clinical implications.<br />Competing Interests: Declaration of Competing Interest The authors have no financial/personal interest or belief that could affect the objectivity of this manuscript. Dr. Hohmann is a consultant for Anagin Inc.<br /> (Copyright © 2024 The Authors. Published by Elsevier Masson SAS.. All rights reserved.)
- Subjects :
- Animals
Male
Female
Mice
Nociception drug effects
Mice, Inbred C57BL
Sex Characteristics
Mice, Knockout
Cannabinoid Receptor Agonists pharmacology
Paclitaxel
Receptor, Cannabinoid, CB2 agonists
Receptor, Cannabinoid, CB2 metabolism
Receptor, Cannabinoid, CB2 genetics
Morphine pharmacology
Sensory Receptor Cells drug effects
Sensory Receptor Cells metabolism
Drug Tolerance physiology
Neuralgia chemically induced
Neuralgia drug therapy
Neuralgia metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1950-6007
- Volume :
- 176
- Database :
- MEDLINE
- Journal :
- Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
- Publication Type :
- Academic Journal
- Accession number :
- 38850666
- Full Text :
- https://doi.org/10.1016/j.biopha.2024.116879