sure or maximum pressure at any doses tested. When AM251 was administered one voiding cycle before VDM11 administration, the increases in intercontraction intervals and threshold pressure induced by VDM11 administration alone were not seen. In contrast, when AM630 was administered before VDM11 administration, increases in intercontraction intervals and threshold pressure were still observed, as they were after VDM11 alone. CONCLUSIONS: These results suggest that anandamide transporters play an important role in the modulation of micturition reflex. Furthermore, these findings indicate that, in urethane-anesthetized rats, inhibition of the uptake of anandamide by VDM11 can inhibit the micturition reflex at least in part via activation of the CB1 receptor, but not the CB2 receptor. Thus, anandamide transporter inhibitors could be effective for the treatment of bladder dysfunction such as overactive bladder.