1. Fast inward currents mere elicited in freshly isolated sheep lympha
tic smooth muscle cells by depolarization from a holding potential of
-80 mV using the whole-cell patch-clamp technique. The currents activa
ted at voltages positive to -40 mV and peaked at 0 mV. 2. When sodium
chloride in the bathing solution was replaced isosmotically with choli
ne chloride inward currents were abolished at all potentials. 3. These
currents were very sensitive to tetrodotoxin (TTX). Peak current was
almost abolished at 1 mu M with half-maximal inhibition at 17 nM. 4. E
xamination of the voltage dependence of steady state inactivation show
ed ed that more than 90 % of the current was available at the normal r
esting potential of these cells (-60 mV). 5. The time course of recove
ry from inactivation was studied using a double-pulse protocol and sho
wed that recovery was complete within 100 ms with a time constant of r
ecovery of 20 ms. 6. Under current damp, action potentials were elicit
ed by depolarizing current pulses. These had a rapid upstroke and a sh
ort duration and could be blocked with 1 mu M TTX. 7. Spontaneous cont
ractions of isolated rings of sheep mesenteric lymphatic vessels were
abolished or significantly depressed by 1 mu M TTX.