TABLE 1.
Current therapeutic strategies against mitochondrial dysfunction in neurodegenerative diseases.
Compound name | Advantages | Disadvantages | References |
---|---|---|---|
Minocycline | Antioxidant properties | Clinical trials do not confirm neuroprotective effects | Investigators (2006), Quintero et al. (2006), Antonenko et al. (2010), Howard et al. (2020) |
Reduces mitochondrial calcium overloading | |||
Easily penetrate the blood-brain barrier | |||
Polyphenols (Curcumin and Resveratrol) | Antioxidants properties | Poor absorption and low bioavailability | Quintero et al. (2006), Sandoval-Acuna et al. (2014), Naoi et al. (2019), Pannu and Bhatnagar (2019) |
Induce mitochondrial biogenesis | |||
Vitamins (A, B3, D, E) | Antioxidant properties | Daily dosage and controversial results | Etminan et al. (2005), Hiller et al. (2018), Marie et al. (2021) |
Coenzyme Q10 (CoQ10) | An enhancer of the electron transport chain activity | Therapeutic benefits are associated with high doses (2.4 g/day) | Shults et al. (2002) |
Monoamine oxidase B inhibitors | Inhibitors of dopamine metabolism | Adverse effects, including confusion and hallucinations | Guay (2006), Carradori et al. (2016) |
Prevents free oxidative radical formation | |||
Creatine | Promotes mitochondrial ATP production | Clinical trials do not confirm neuroprotective effects | Matthews et al. (1999), Investigators (2006), Investigators (2008) |
Mitoquinone (MitoQ) | Protection against oxidative damage by inhibiting lipid peroxidation | Clinical trials do not confirm neuroprotective effects | Doughan and Dikalov (2007), Snow et al. (2010), Aimaiti et al. (2021) |