Table 1.
Neurodegenerative Disease |
Model | Effective Dose |
Mode of Administration | Major Outcomes | Reference | |
---|---|---|---|---|---|---|
Oil-Soluble CoQ10 | Alzheimer’s Disease | In-Vivo (Mice) | 10 g/kg diet | Oral | - Protection against neurotoxicity & oxidative stress - Mitochondrial stabilization - Reduced Aβ plaques - Improved cognitive performance |
Wadsworth 2008 [30] |
In-Vitro | 6.25 µM | Media Supplementation | Wadsworth 2008 [30] | |||
In-Vivo (Mice) | 0.4% or 2.4% | Oral | Dumont 2011 [35] | |||
In-Vitro | 10 µM | Media Supplementation | Sadli 2013 [33] | |||
Amyotrophic Lateral Sclerosis (ALS) | In-Vivo (Rats & Mice) | 200 mg/kg/ day | Oral | - Anti-oxidative effects - Preserved mitochondrial function - Increased lifespan |
Matthews 1998 [39] | |
In-Vivo (Mice) | 200 mg/kg/day (no effect) | Oral (Gavage) | Lucchetti 2013 [44] | |||
Frontotemporal Dementia | In-Vivo (Mice) | 0.5% of Diet | Oral | - Improved behaviour & survival | Elipenahli 2012 [50] | |
Huntington’s Disease | In-Vivo (Rats) | 200 mg/kg/day | Oral | - Improved motor performance & survival - Delayed weight loss - Prevented striatal neuron intranuclear inclusion formation - Slowed striatal neuron atrophy - Reduced HTT aggregate formation - Reduced oxidative damage |
Matthews 1998 [39] | |
In-Vivo (Mice) | 400 mg/kg/day | Oral | Ferrante 2002 [40] | |||
In-Vivo (Mice) | 0.2% of Diet | Oral | Stack 2006 [41] | |||
In-Vivo (Mice, Rats) | 1600–2000 mg/kg/day | Oral | Yang 2009 [24] | |||
In-Vivo (Mice) | 0.2% of Diet | Oral | Hickey 2012 [43] | |||
Machado-Joseph Disease | In-Vitro | 10 µM, 30 µM, 90 µM | Media Supplementation | - Improved cell viability & reduced apoptosis - Prevented ATX3 protein aggregation |
Lopes-Ramos 2016 [51] | |
Multiple-System Atrophy | In-Vitro | 25 µM | Media Supplementation | - Improved oxidative metabolism - Reduced apoptosis |
Nakamoto 2018 [53] | |
Parkinson’s Disease | In-Vivo (Mice) | 200 mg/kg/day | Oral | - Dopaminergic neurons saved in striatum and SNpc - Clearance of α-synuclein aggregates - Limited oxidative damage - Reduced pro-inflammatory cytokines |
Beal 1998 [21] | |
In-Vivo (Mice) | 200–1600 mg/kg/day | Oral | Cleren 2008 [22] | |||
In-Vivo (Mice) | 1% of Diet | Oral | Yang 2009 [24] | |||
In-Vivo (Drosophila) | 100 mg/mL (no effect) | Oral | Faust 2009 [25] | |||
In-Vivo (Rats) | 25 µg/mL | Intrastriatal Injection | Park 2020 [27] | |||
Ubisol-Q10 | Alzheimer’s Disease | In-Vitro | 50 µg/mL | Media Supplementation | - Inhibited oxidative stress - Upregulated autophagy - Maintained MMP - Reduced cell cycle arrest protein expression - Prevented SIPS onset - Inhibited apoptosis - Improved memory - Reduced hippocampal neurodegeneration - Cleared Aβ plaques - Increased astrocyte activity - Reduced microglial activity |
Ma 2014 [57] |
In-Vivo (Mice) | 6 mg/kg/day | Oral | Muthukumaran 2018 [58] | |||
In-Vivo (Mice) | 50 µg/mL | Oral | Vegh 2019 [59] | |||
In-Vitro | 50 µg/mL | Media Supplementation | Vegh 2019 [59] | |||
Parkinson’s Disease | In-Vivo (Rats) | 50 µg/mL | Oral | - Reduced oxidative stress - Maintained ATP generation - Stabilized mitochondrial membrane - Prevented loss of dopaminergic neurons - Activated pro -survival astrocytes - Ameliorated motor dysfunction |
Somayajulu-Nitu 2009 [60] | |
In-Vivo (Mice) | 6 mg/kg/day | Oral | Muthukumaran 2014 [61] | |||
In-Vivo (Rats) | 6 mg/kg/day | Oral | Muthukumaran 2014 [62] | |||
In-Vivo (Mice) | 3 mg/kg/day | Oral | Sikorska 2014 [63] |