It has been reported that thromboxane A2 (TXA2) and prostaglandin F2 (PGF2α) mediates inflammatory tachycardia by directly facilitating the automaticity of cardiac sinoatrial node preparations (Takayama et al, 2005). In this study, the action potential and membrane currents were recorded in isolated guinea-pig sinoatrial node cells and the ionic mechanisms underlying the positive chronotropic action of PGF2α and TXA2 were investigated by the patch clamp method. Both PGF2α and TXA2 increased the spontaneous firing frequency of isolated sinoatrial node cells, and this increase was partially blocked by 50 μM Ni2+. Under the voltage clamp condition, I-BOP, a selective agonist for TP receptor, increased the amplitude of low voltage-activated Ca2+ current with little affecting the high-threshold Ca2+ current, the delayed rectifier K+ current and the hyperpolarization-activated cation current. In the single channel recording, I-BOP increased the open probability of Ca2+ channels, which had tiny (-8pS) conductance and displayed rapid inactivation. The results indicate the functional role of T-type Ca2+ channel in the positive chronotropic action of PGF2α and TXA2. [J Physiol Sci. 2008;58 Suppl:S58]