Table 2.
HDAC Inhibitors used in neurodegenerative disease models and their effect.
| HDAC inhibitors used | Effect of HDAC inhibitors treatment | References | ||
|---|---|---|---|---|
| Neurological Disease Models | ALS | Valproic acid, Trichostatin A 4-Phenyl Butyrate 4-Phenylbutyrate + Antioxidant Valproic acid + Lithiun 4-Phenybutyrate + Riluzole |
Reestablished CBP loss and histone hypoacetylation Suppressed motor neuronal death Improved motor function and survival of neurons |
Sugai et al., 2004; Ryu et al., 2005; Petri et al., 2006; Rouaux et al., 2007; Del Signore et al., 2009; Yoo and Ko, 2011 |
| AD | Sodium butyrate, Vorinostat 4-phenylbutyrate, Valproic acidNicotinamide, Tubastatin A ACY-125 |
Reestablished hypo acetylation Decreased Aβ plaque number and improved memory deficit Enhanced tubulin acetylation, reduced production and facilitated autophagic clearance of Aβ and hyperphosphorylated tau Reversed spatial memory deficits |
Fischer et al., 2007; Green et al., 2008; Kim et al., 2008; Qing et al., 2008; Guan et al., 2009; Ricobaraza et al., 2009; Noh and Seo, 2014; Zhang et al., 2014 | |
| SMA | Vorinostat, 4-Phenylbutyrate Nicotinamide |
Increased SMN2 expression Increase histone acetylation Improved survival and motor pathology Increased induced Bcl-2, Bcl-XL and BDNF |
Chang et al., 2001; Brichta et al., 2003; Sumner et al., 2003; Andreassi et al., 2004; Hahnen et al., 2006; Avila et al., 2007; Hauke et al., 2009; Riessland et al., 2010 | |
| HD | Vorinostat, Trichostatin A Sodium Butyrate 4-Phenylbutyrate HDACi 4b, Tubacin RGFP966 + Pimelic diphenylamine LBH589 |
Normalized striatal atrophy and degeneration Restored histone hypoacetylation and transcriptional dysfunction Increased vesicular transport of BDNF and improved motor performance and survival |
Steffan et al., 2001; Ferrante et al., 2003; Hockly et al., 2003; Bates et al., 2006; Dompierre et al., 2007; Sadri-Vakili et al., 2007; Pallos et al., 2008; Thomas et al., 2008 | |
| PD | Valproic acid, Tubastatin A 4-Phenyl Butyrate, M-275 Sodium Butyrate, Trichostatin A |
Reduction in dopaminergic death Increased acetylation of α-tubulin Increased GDNF and BDNF expression Improved sensorimotor reflexes and locomotor impairments |
Gardian et al., 2004; Chen et al., 2006; Kontopoulos et al., 2006; Wang et al., 2009; Lu et al., 2013; Wu et al., 2013; Choong et al., 2016; Pinho et al., 2016 | |
| MS | Trichostatin A, ITF2357 SAHA |
Reduction in spinal cord inflammatory infiltrates, demyelination and axonal loss increase in number of motor neurons in the ventral horn Improvement in neuronal pathology |
Camelo et al., 2005; Lillico et al., 2018; Sun et al., 2018 | |
HDAC, Histone deacetylases; ALS, Amyotropic Lateral Sclerosis; AD, Alzheimer's disease; SMA, Spinal Muscular Atrophy; HD, Huntington's disease; PD, Parkinson's disease; MS, Multiple Sclerosis; SAHA, suberoylanilide hydroxamic acid.