Systemic administration of a dopamine D2 receptor blocker, haloperidol, but
not vehicle, significantly increased the number of c-Fos-immunoreactive ne
urons in the globus pallidus (GP) in rats. Dual immunohistochemistry, a com
bination of c-Fos immunohistochemistry and retrograde tracing experiments w
ith cholera toxin B (ChB), revealed that a subset, of the c-Fos-immunoreact
ive GP neurons was pallidostriatal feedback neurons. Lesioning of the subth
alamic nucleus (STN) by local infection of ibotenic acid inhibited the halo
peridol-induced c-Fos expression in the GP neurons, suggesting that the act
ivation of GP neurons is a result of increased excitatory drives from the S
TN. Therefore, the present findings are evidence of the existence of the su
bthalamo-pallido-striatal axis as a feedback system in the internal circuit
s of the basal ganglia. NeuroReport 12:3795-3798 (C) 2001 Lippincott Willia
ms & Wilkins.