The present study investigated the effects of dopamine on chloride transport across cultured rat caudal epididymal epithelium. The results showed that dopamine induced a biphasic short-circuit current (Isc) in a concentration-dependent manner. The dopamine-induced response consisted of an initial rapid spike followed by a sustained phase. The alpha and beta adrenoreceptor inhibitors, phentolamine and propranolol, inhibited the initial spike and the sustained phase, respectively, suggesting a contribution of adrenergic receptors. The response was almost abolished by removing the extracellular Cl⁻, suggesting that the dopamine-induced short-circuit current is primarily a Cl⁻ current. The response was inhibited by the apical Cl⁻ channel blocker, diphenylamine-dicarboxylic acid, and the Ca² -activated Cl⁻ channel blocker, disulfonic acid stilbene, indicating that Cl⁻ may pass through two types of Cl⁻ channels on the apical side. Preloading monolayers with the intracellular Ca² chelator BAPTA/AM abolished the initial spike and greatly reduced the second phase in the Isc response to dopamine. Pretreating the monolayers with an adenylate cyclase inhibitor, MDL12330A, inhibited all of the second Isc response and part of the initial spike. Also, characteristics of the Cl⁻ currents induced by dopamine were observed in whole-cell patch-clamp recording. The increases of intracellular cAMP and Ca² induced by dopamine were also measured. The results suggest that extracellular dopamine activates Ca² -dependent and cAMP-dependent regulatory pathways, leading to activation of both Ca² -dependent and cAMP-dependent Cl⁻ conductances in epididymal epithelial cells.