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. 2017 Mar 22;125(3):365–384. doi: 10.1007/s00702-017-1708-9

Table 1.

Comparison between NHP models of PD highlighting key features for evaluation of CBTs for DA cell replacement

NHP PD model PD motor symptoms Nigrostriatal DA depletion Typical LIDs Synucleinopathy Comments
6-OHDA Yes Yes No Not reported Unilateral model. Requires multiple intracerebral stereotaxic injections to induce a stable lesion
MPTP systemic Yes Yes Yes Upregulation of a-syn Bilateral model. Needs to be individually titrated, and depending on dosing paradigm may require from one week to over a year to induce syndrome. PD symptoms may spontaneously recover
MPTP systemic+aging Yes Yes Yes Upregulation of α-syn, possible aggregates Same as MPTP systemic plus animals may require more intensive care post intoxication
MPTP ICA Yes Yes No Not reported Unilateral model. Requires surgical set up; Induces a stable and reproducible lesion
MPTP ICA+aging Yes Yes No Not reported Same as MPTP ICA except MPTP dose needs to be 2/3 of younger animals. Monkeys may require more intensive care post intoxication
Aged NHPs Yes Yes No Translocation of α-syn Not enough dopamine deficit to be responsive to l-DOPA treatment
Viral vector delivery of α-syn Yes (Common marmosets) Yes Unknown Overexpression of α-syn, aggregates Unilateral model. Requires intracerebral stereotaxic injections
Lewy body extracts No Yes Unknown Overexpression of α-syn, aggregates Unilateral model. Requires intracerebral stereotaxic injections
α-syn Transgenic Mild (Cynomolgus 1.5–2 years old) Unknown Unknown Unknown Bilateral model

6-OHDA 6 hydroxydopamine, α-syn alpha-synuclein, MPTP 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, ICA intracarotid artery, l -DOPA L-3,4-dihydroxyphenylalanine, LIDs l-DOPA induced dyskinesias