2022
DOI: 10.1089/can.2022.0090
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Cannabidiol Protects Striatal Neurons by Attenuating Endoplasmic Reticulum Stress

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Cited by 2 publications
(3 citation statements)
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“…Additionally, CBD demonstrated the neuroprotective effect on endoplasmic reticulum stress in STHdhQ7/Q7 striatal cells. CBD pretreatment increased cell viability and the gene expression of the pro-survival chaperone GRP78 and the neurotrophic factor MANF, while decreasing the expression of pro-apoptotic markers such as BIM and caspase-12, indicating that CBD may protect against endoplasmic reticulum stress-induced cell death [87]. CBD demonstrated anti-inflammatory and antinociceptive effects in conditions induced by zymosan.…”
Section: Role Of Cannabis Compounds In Neurological and Systemic Infl...mentioning
confidence: 93%
“…Additionally, CBD demonstrated the neuroprotective effect on endoplasmic reticulum stress in STHdhQ7/Q7 striatal cells. CBD pretreatment increased cell viability and the gene expression of the pro-survival chaperone GRP78 and the neurotrophic factor MANF, while decreasing the expression of pro-apoptotic markers such as BIM and caspase-12, indicating that CBD may protect against endoplasmic reticulum stress-induced cell death [87]. CBD demonstrated anti-inflammatory and antinociceptive effects in conditions induced by zymosan.…”
Section: Role Of Cannabis Compounds In Neurological and Systemic Infl...mentioning
confidence: 93%
“…The modulation of these quantifiable molecular markers of AD by CBD and its precursor CBDA were further translated into AD-relevant changes in cell viability in vitro, and physiological and cognitive-behavioural changes in vivo [133][134][135][136][137][138][139]141,143,144,146,[148][149][150]152,154]. Multiple investigations revealed that CBD did not display neurotoxicity at physiologically relevant doses, while also increasing the viability of SH-SY5Y cells and mouse cortical neurons and striatal-derived STHdh Q7/Q7 cells compared to cells treated only with neurotoxic compounds, such as Aβ 1-42 and t-BHP [133,134,137,141]. Patel et al also showed that STHdh Q7/Q7 cells pre-treated with CBD exhibited increased pro-survival markers of the unfolded protein response (UPR) at the mRNA and protein level, while decreasing mRNA expression of pro-apoptotic genes Bcl-2-like protein 11 (BIM) and caspase-12 [141].…”
Section: Cannabidiol As a Potential Treatment For Alzheimer's Diseasementioning
confidence: 99%
“…Multiple investigations revealed that CBD did not display neurotoxicity at physiologically relevant doses, while also increasing the viability of SH-SY5Y cells and mouse cortical neurons and striatal-derived STHdh Q7/Q7 cells compared to cells treated only with neurotoxic compounds, such as Aβ 1-42 and t-BHP [133,134,137,141]. Patel et al also showed that STHdh Q7/Q7 cells pre-treated with CBD exhibited increased pro-survival markers of the unfolded protein response (UPR) at the mRNA and protein level, while decreasing mRNA expression of pro-apoptotic genes Bcl-2-like protein 11 (BIM) and caspase-12 [141]. Although some studies reported that the treatment of rodent models of AD with CBD alone had no effect on AD-related pathologies or cognition, many reported opposite findings [147,148].…”
Section: Cannabidiol As a Potential Treatment For Alzheimer's Diseasementioning
confidence: 99%