TY - JOUR
T1 - The neuroprotective effect of cannabidiol is enhanced by resveratrol and alpha-lipoic acid in social isolation
AU - Ricciardi, Federica
AU - Morace, Andrea Maria
AU - Limongelli, Rebecca
AU - Iannotta, Monica
AU - Boccella, Serena
AU - Fusco, Antimo
AU - Bonsale, Roozbe
AU - Perrone, Michela
AU - Infantino, Rosmara
AU - Di Martino, Emanuele
AU - Mattia, Consalvo
AU - Gargano, Francesca
AU - Trotta, Maria Consiglia
AU - Palazzo, Enza
AU - Maione, Sabatino
AU - Guida, Francesca
AU - Luongo, Livio
AU - Belardo, Carmela
N1 - Publisher Copyright:
Copyright © 2025 Ricciardi, Morace, Limongelli, Iannotta, Boccella, Fusco, Bonsale, Perrone, Infantino, Di Martino, Mattia, Gargano, Trotta, Palazzo, Maione, Guida, Luongo and Belardo.
PY - 2025
Y1 - 2025
N2 - Introduction: Post-traumatic stress disorder (PTSD) is a chronic psychiatric condition characterized by persistent cognitive and affective disturbances following exposure to severe trauma. In rodents, prolonged post-weaning social isolation is a well-established model of PTSD-like symptomatology. In this study, we investigated the behavioral effects of chronic cannabidiol (CBD) administration—either alone or in combination with two natural antioxidants, resveratrol (RES) and alpha-lipoic acid (ALA)in socially isolated mice. Methods: Male CD1 mice (n = 8) were isolated in individual cages from postnatal day 21 (PN21) and maintained in isolation for 30 days. They were then treated with CBD (2.5, 5, and 10 mg/kg), resveratrol (RES, 20 mg/kg), or alpha-lipoic acid (ALA, 10 mg/kg) for 15 days following social isolation. Results: While low-dose CBD (2.5 mg/kg) alone was ineffective, its combination with either RES or ALA restored the latency to the first attack and significantly reduced aggressive behavior, comparable to high-dose CBD (10 mg/kg). Similarly, combined treatments with RES or ALA markedly reduced immobility time in the tail suspension test, indicating antidepressant-like effects. In contrast, no significant anxiolytic effect was observed with the combinations in the hole-board test, suggesting a limited action on anxiety-like behavior. Discussion: These findings suggest that co-administration of CBD with RES or ALA exerts synergistic antidepressants and anti-aggressive effects in a PTSD-like model, potentially allowing for dose reduction of CBD. Further studies are warranted to explore the underlying molecular mechanisms.
AB - Introduction: Post-traumatic stress disorder (PTSD) is a chronic psychiatric condition characterized by persistent cognitive and affective disturbances following exposure to severe trauma. In rodents, prolonged post-weaning social isolation is a well-established model of PTSD-like symptomatology. In this study, we investigated the behavioral effects of chronic cannabidiol (CBD) administration—either alone or in combination with two natural antioxidants, resveratrol (RES) and alpha-lipoic acid (ALA)in socially isolated mice. Methods: Male CD1 mice (n = 8) were isolated in individual cages from postnatal day 21 (PN21) and maintained in isolation for 30 days. They were then treated with CBD (2.5, 5, and 10 mg/kg), resveratrol (RES, 20 mg/kg), or alpha-lipoic acid (ALA, 10 mg/kg) for 15 days following social isolation. Results: While low-dose CBD (2.5 mg/kg) alone was ineffective, its combination with either RES or ALA restored the latency to the first attack and significantly reduced aggressive behavior, comparable to high-dose CBD (10 mg/kg). Similarly, combined treatments with RES or ALA markedly reduced immobility time in the tail suspension test, indicating antidepressant-like effects. In contrast, no significant anxiolytic effect was observed with the combinations in the hole-board test, suggesting a limited action on anxiety-like behavior. Discussion: These findings suggest that co-administration of CBD with RES or ALA exerts synergistic antidepressants and anti-aggressive effects in a PTSD-like model, potentially allowing for dose reduction of CBD. Further studies are warranted to explore the underlying molecular mechanisms.
KW - aggressiveness
KW - antioxidant
KW - behavior and social isolation
KW - cannabidiol
KW - post traumatic stress disorder
UR - https://www.scopus.com/pages/publications/105021524305
U2 - 10.3389/fphar.2025.1676421
DO - 10.3389/fphar.2025.1676421
M3 - Article
AN - SCOPUS:105021524305
SN - 1663-9812
VL - 16
JO - Frontiers in Pharmacology
JF - Frontiers in Pharmacology
M1 - 1676421
ER -