In rats with unilateral 6-hydroxydopamine lesions in the nigrostriatal
pathway, injection of angiotensin II (2 nmol) into the unlesioned str
iatum elicited dose-related tight rotations ipsilateral to the lesion.
This rotation was suppressed by coadministration of the angiotensin A
T(1) receptor antagonist, losartan (2 nmol), which had no significant
effect when injected alone. Preadministration of the dopamine antagoni
st, haloperidol (2 mg/kg i.p.) completely blocked angiotensin II-induc
ed turning at doses of 0.3-3 nmol, and partially at 10 nmol. These res
ults further confirm the hypothesis that Ang II is intrinsically invol
ved in modulating dopamine release in the striatum, an effect which is
mediated predominantly by AT(1) receptors.