Table 1.
Beneficial effects of the KD or ketone bodies in animal models.
| Disease | Animal model | Treatment | Outcome | References |
|---|---|---|---|---|
| Alzheimer's disease | 3xTgAD transgenic mouse | Diet supplemented with BHB | Reduced oxidized proteins and lipids | (7) |
| APP/PS1 and Tg4510 transgenic mice | KD for 3 months | Improved locomotor activity, no improvement in learning or change in amyloid or tau deposition | (8) | |
| 3xTgAD transgenic mouse | Ketosis induced by 2-deoxy-D-glucose | Reduced accumulation of Aβ and lowered oxidative stress | (9) | |
| PDGFB-APPSwInd transgenic mouse | BHB and ACA subcutaneous injections for 2 months | Reduced amyloid deposition, improved learning and memory and synaptic plasticity | (10) | |
| Epilepsy | adenosine A1 receptors (A1R)-/- and Adk-Tg mice | KD for 3 weeks | Reduced seizure frequency | (11) |
| Kcna1-/- mice | KD diet, BHB administration | Reduced spontaneous recurrent seizures | (12) | |
| 6-Hz induced seizure model and Kcna1-/-, mice | KD 2-14 days | Elevated seizure threshold, decreases seizure duration and frequency | (13) | |
| Glaucoma | DBA/2J mutant mouse with elevated intraocular pressure | KD for 8 weeks | Increased neuronal survival | (14) |
| NMDA-induced RGC death, rat | KD for 3 weeks | Increased RGC survival in juvenile not adults | (15) | |
| NMDA-induced RGC death, rat | Daily BHB or ACA intraperitoneal injection for 21 days | Increased RGC survival | (16) | |
| Blast pressure-induced ocular injury, mice | KD beginning 2 weeks prior to injury | Increased neuronal survival, decreased gliosis | (17) | |
| MS | Experimental autoimmune encephalomyelitis (EAE) mouse | KD up to 30 days | Increased spatial learning and memory, improved motor ability and reduced lesion size | (18) |
| Cuprizone-induced demyelination mouse | KD up to 35 days | Improved motor and behavioral deficits, increased mature oligodendrocytes and reduced hippocampal demyelination | (19) | |
| Parkinson's Disease | MPTP mouse | BHB infusions | Decreased dopaminergic neurons degeneration and reduced motor deficits | (20) |
| MPTP mouse | KD prior to injury | Improved motor function | (21) | |
| 6-OHDA rat | KD for 7 weeks | None | (2) | |
| 6-OHDA rat | KD for 2 weeks prior to and after injury | Increased neurons | (22) | |
| Retinal degeneration | rd10 model of retinitis pigmentosa, mouse | KD+low protein 1 week prior to disease onset | Increased retina function and thickness | (23) |
| Pde6a D670G model of retinitis pigmentosa, mouse | KD for 1 week | Improved retinal histology | (24) | |
| SCI | C5 spinal hemi-contusion, rats | KD initiated 2 weeks prior to injury | Motor recovery, reduced lesion size | (25) |
| Stroke | Endothelin-1 model of induced ischemia, rat | KD prior to injury | Improved mobility | (26) |
| Cardiac arrest-induced cerebral ischemia, rat | KD for 25 days prior to injury | Prevented neurodegeneration | (27) | |
| Middle cerebral artery occlusion, rat | Intravenous BHB administration after injury | Reduced cerebral infarct area and lower neurological deficits | (28) |