This study extensively examined the role of a 5-HT 1A receptor in controlling voiding function in anesthetized male rats. A simultaneous recording of the intravesical pressure (IVP), external urethral sphincter (EUS)-electromyography (EMG), and urine flow rate (UFR) during continuous cystometry was used. 8-Hydroxy-2-(di-n-propylamino)-tetralin (8-OH-DPAT), a 5-HT 1A receptor agonist, significantly improved the voiding efficiency, as detected by increases in the evoked contraction amplitude, EUS burst period, and silent period, and decreases in the volume threshold, pressure threshold, and residual volume. Interestingly, the UFR during voiding was reduced by 8-OH-DPAT, as evidenced by decreases in the maximal UFR and mean UFRs of the voiding period, spike duration, and interspike interval. Conversely, treating rats with WAY-100635, a 5-HT1A antagonist, produced effects opposite to those produced by 8-OH-DPAT. These findings suggest that 8-OH-DPAT improved the voiding efficiency by enhancing the detrusor contractile ability and prolonging EUS burst period, which would compensate for the lower UFR, resulting from urethral smooth muscle contractions and longer EUS silent periods during voiding. The present study contributes to our understanding of the role of 5-HT1A receptors in controlling the urine flow rate in male rats. intravesical pressure; external urethral sphincter-electromyography; 8-hydroxy-2-(di-n-propylamino)-tetralin; WAY-100635; voiding efficiency SEROTONIN (5-HYDROXYTRYPTAMINE, 5-HT) comprises 14 structurally different 5-HT receptors in mammalian species, including seven subfamilies (5-HT 1 to 5-HT 7 ) (28). A number of 5-HT receptor subfamilies, particularly 5-HT 1A receptors, located at nerve terminals are involved in the function of the lower urinary tract (LUT) (38). Indeed, these 5-HT receptors-related nerve terminals are distributed in areas of the spinal cord containing afferent and efferent components of LUT neural control centers (8,15,19,24,38). Thus, 5-HT receptors appear to modulate all of the pathways involved in the control of reflex bladder and urethral sphincter activity, including the parasympathetic, sympathetic, and somatic pathways (13).The 5-HT 1A receptor is one of the most extensively investigated agents in functions of the LUT in various animal pharmacological experiments, including rats, guinea pigs, and cats (28). However, contradictory results have generated various interpretations of the functions of this receptor subtype in different animal species. Because the rat model has now gained greater popularity as the main species for investigating functions of the LUT, the effects of a 5-HT 1A receptor agonist on regulating urine storage and micturition reflexes have been extensively investigated in female rats (14, 20 -22, 35). However, few studies have explored these pharmacological effects in male animals. Moreover, our recent studies demonstrated that 8-OH-DPAT, a 5-HT 1A receptor agonist, elevated the urethral pressure (resistance) during the voiding reflex in male rats (1...