Skip to main content
. 2021 Dec 16;12:797298. doi: 10.3389/fphar.2021.797298

TABLE 3.

Comprehensive information about the effects of myricetin in animal models Parkinson’s disease.

Pharmacological effect Object Drug administration Possible mechanisms References
Reverse 6-OHDA-induced decrease in dopamine contents in the striatum Rat *0.5 mg/ml Increase tyrosine hydroxylase expression and reduce iron-staining cells in the substantia nigra Ma et al. (2007)
*lateral cerebral ventricle injection
*7 days
Suppress rotenone-induced gait disturbance, muscular dys-coordination, memory impairment, dopaminergic neuronal degeneration, and dopamine reduction Drosophila *314 mM *Reduce TBARS levels and Bax expression Dhanraj et al. (2018)
*3 h before rotenone exposure *Increase GSH levels and Bcl-2 expression
*7 days
Attenuate MPP+-induced cell loss and nuclear condensation MES23.5 cells 50 μM Co-treatment *Restore mitochondrial transmembrane potential Zhang et al. (2011)
*Suppress reactive oxygen species production
Prevent rotenone-induced cell loss SH-SY5Y cells *50 μM *Suppress DNA fragmentation, lipid peroxidation, and the production of hydrogen peroxide and superoxide anion Molina-Jiménez et al. (2004)
*30 min before rotenone treatment
Alleviate rotenone-induced decreases in cell viability MES23.5 cells *1 μM *Suppress reactive oxygen species production Deng et al. (2021)
*24 h of pretreatment *Restore mitochondrial transmembrane potential
*Reduce hepcidin gene transcription
*Increase ferroportin 1 expression
Suppress the aggregation of the mutant α-synuclein (S87A) protein Cos-7 cells *10 μM Activate the ubiquitin-proteasome pathway Joshi et al. (2019)
*48 h