H. Huddart et Rb. Hill, IONIC DEPENDENCY OF MEMBRANE-POTENTIAL AND AUTORHYTHMICITY IN THE ATRIUM OF THE WHELK BUSYCON CANALICULATUM, General pharmacology, 27(5), 1996, pp. 819-825
1. Calcium-free media usually caused a cessation of all electrical and
mechanical activity of the Busycon atrium. Where any electrical activ
ity survived, the action potential consisted of a pre- and plateau-lik
e potential devoid of the usual terminal spike. 2. High Ca salines ind
uced tonic force, membrane depolarization and reduction in generation
of spontaneous action potentials. The Ca ionophore A23187 enhanced con
tractions and the SR CaATPase inhibitor cyclopiazonic acid induced sli
ght depolarization, tonic contractures and increased action potential
firing. 3. The inorganic Ca antagonist Co2+ was without effect on the
preparations, although the lanthanide Gd3+ inhibited contractions and
spontaneous action potentials as well as inducing membrane potential d
epolarization. 4. The organic Ca entry-blocker nifedipine enhanced bot
h spontaneous action potential amplitude and the phasic contractions t
hey generated. 5. High K salines considerably depolarized atrial prepa
rations with accompanying large tonic contractures and suppression of
action potentials. The K channel-blocker 4AP enhanced action potential
amplitude with slight increase in contractions, and TEA depolarized t
he atrium, and enhanced action potentials and rhythmic contractions. 6
. Sodium-free salines strongly hyperpolarized atrial preparations and
abolished spontaneous action potentials and, on washout, the membrane
potential became temporarily unstable. In 2 preparations, low chloride
and chloride-free media induced significant membrane potential hyperp
olarization. 7. It is concluded that, in the atrium, the resting membr
ane potential is largely determined by the transmembrane K gradient, b
ut with significant conductances to Na and Cl though probably not Ca.
The action potential spike appears to be a Ca-dependent event and the
plateau-like phase may be a Na-dependent event.