ObjectiveThe arteries of aged spontaneously hypertensive rats (SHR) exhibit spontaneous electrical activity together with membrane depolarization. Vascular eicosanoid production is increased in SHR, which is further accelerated with aging. We tested the hypothesis that eicosanoids are involved in spontaneous electrical activity, membrane depolarization or both in mesenteric arteries of aged SHR.Design and methodsMembrane potentials were recorded with microelectrodes from the mesenteric arteries of aged (24 months and older) SHR, aged Wistar–Kyoto (WKY) rats and adult (6- to 8-month-old) SHR.ResultsThe membrane potential was less negative in aged SHR (−38.5 ± 0.9 mV) than in either aged WKY rats or adult SHR (−49.8 ± 0.5 and −47.2 ± 0.6 mV, respectively;P< 0.05 for both). Spontaneous electrical activity (5–20 mV, 1–7/min) was present only in arteries of aged SHR. Spontaneous electrical activity was not affected by phentolamine, atropine or tetrodotoxin, but was abolished by indomethacin, a cyclooxygenase inhibitor, and ONO-3708, a thromboxane A2/prostaglandin H2receptor antagonist. Furthermore, indomethacin and ONO-3708 hyperpolarized the membrane by about 5 mV in aged SHR but not in the other two groups. Spontaneous electrical activity was enhanced by a thromboxane A2analog and prostaglandin H2, and was abolished by a Ca2+antagonist, nicardipine, and Ca2+-free solution.ConclusionsThese findings suggest that cyclooxygenase-dependent eicosanoids contribute importantly to both spontaneous electrical activity and membrane depolarization, presumably through activation of the thromboxane A2/prostaglandin H2receptor, in mesenteric arteries of aged SHR, and that spontaneous electrical activity is mediated by a Ca2+influx through voltage-dependent Ca2+channels.