Table 3.
Role of purinoreceptors in experimental models and patients with Alzheimer's disease (AD) and Parkinson's disease (PD).
R Sample | P2X7 receptor | A2A receptor | Reference |
---|---|---|---|
Transgenic mouse model of AD (brain slices) | Upregulated | — | [169] |
| |||
Microglia from AD patients Human microglia treated with amyloid-beta peptide in vitro Rat hippocampus after amyloid-beta peptide injection |
Upregulated | — | [170] |
| |||
Transgenic mouse model of AD | Inhibition of P2X7R decreased the number of hippocampal amyloid plaques | — | [171] |
| |||
Human macrophages and microglia preactivated with amyloid-beta peptide | P2X7R stimulation enhanced secretion of proinflammatory cytokines | — | [172, 173] |
| |||
Rats injected with 6-OHDA | — | Inhibition of A2AR improved motor performance and cognition | [174] |
| |||
Rats injected with haloperidol (DA antagonist) | — | Inhibition of A2AR reversed locomotor suppression and tremulous jaw movements | [174, 175] |
Alzheimer's disease (AD), P2X7 receptors (P2X7R), adenosine A2A receptor (A2AR), 6-hydroxydopamine (6-OHDA), and dopamine (DA).