1. Intracellular recordings were made from neurones in slices of rat s
triatum in vitro. 2. The forty-nine neurones studied were immunoreacti
ve for choline acetyltransferase and had the electrophysiological char
acteristics typical of large aspiny interneurones. 3. Focal stimulatio
n of the slice elicited a hyperpolarizing inhibitory postsynaptic pote
ntial in thirty-five neurones. This IPSP lasted 0.5-1 s and reversed p
olarity at a membrane potential which was dependent on the logarithm o
f the extracellular potassium concentration. 4. The IPSP was reversibl
y blocked by scopolamine and methoctramine, which has some selectivity
for the M-2 subtype of muscarinic receptor. It was unaffected by 6-cy
ano-7-nitroquinoxaline-2,3-dione (10 rho M), DL-2-amino-phosphonovaler
ic acid (30 mu M) and bicuculline (30 mu M). 5. Exogenous acetylcholin
e and muscarine also hyperpolarized the neurones, and this was blocked
by methoctramine but not by pirenzepine, which is an M-1 receptor-sel
ective antagonist. 6. The findings demonstrate that muscarinic IPSPs o
ccur in the central nervous system. The IPSP may mediate an 'autoinhib
ition' of striatal cholinergic neurone activity.