BDNF or vehicle were administered by unilateral supranigral infusion in nor
mal and chronically lesioned MPTP-treated common marmosets (Callithrix jacc
hus) for four weeks and locomotor activity, disability and response to apom
orphine were assessed with nigral TH, GFAP and GAD immunoreactivity and str
iatal [H-3]mazindol autoradiography. Selective contraversive orientation an
d ipsilateral neglect evolved in MPTP-treated marmosets receiving BDNF with
no significant difference in disability or locomotor activity when compare
d to the vehicle-infused group. Apomorphine produced an ipsiversive rotatio
nal bias in BDNF-treated animals. In normal animals infused with BDNF contr
alateral neglect, ipsiversive turning, postural instability and ataxia rapi
dly evolved. In MPTP-treated marmosets BDNF caused increased ipsilateral st
riatal [H-3]mazindol binding with increased somatic size and staining inten
sity in GAD-immunoreactive cells and a 10-20% loss of nigral TH-immunoreact
ive cells with increased GFAP staining. In normal common marmosets, both ve
hicle and BDNF infusion decreased nigral TH-immunoreactivity. Chronic supra
nigral infusion of BDNF alters motor behaviour and spatial attention in MPT
P-treated marmosets which may reflect altered function in residual nigral d
opaminergic neurons and brainstem GABAergic neurons and in normal animals p
roduces behavioural and histological signs of nigrostriatal hypofunction.