Jeong M S, Lee J G
Department of Urology, Korea University College of Medicine, Seoul, Korea.
BJU Int. 2000 May;85(7):925-31. doi: 10.1046/j.1464-410x.2000.00572.x.
To elucidate the effects of alpha1- and alpha2-adrenoceptor antagonists on the micturition reflex induced by bladder distension in the anaesthetized rat at the peripheral and spinal level. Materials and methods Using continuous cystometry in 80 anaesthetized female Sprague-Dawley rats, changes in basal pressure (BaP), micturition pressure (MP), bladder capacity (BC), micturition volume (MV), interval of bladder contraction (frequency) and residual volume (RV) to the selective intra-arterial and intrathecal administration of drugs were monitored and analysed.
The intra-arterial administration of phentolamine, prazosin, doxazosin and tamsulosin significantly decreased the MP; doxazosin increased MV, BC, RV and frequency. MP was inhibited more by intra-arterial doxazosin than by prazosin or tamsulosin. Intrathecal phentolamine increased BaP, BC, RV and decreased MP and MV; tamsulosin decreased frequency and increased BC. Clonidine markedly increased BaP and frequency, whereas MV and BC were significantly lower; yohimbine increased MV, BC and decreased RV. Intra-arterial yohimbine significantly increased MV.
At the spinal level, the micturition reflex evoked by bladder distension was preferentially suppressed by phentolamine or yohimbine, suggesting the involvement of alpha2-adrenoceptors. In the periphery, alpha1-adrenoceptor blockers preferentially suppressed the reflex. We suggest that both alpha1- and alpha2-adrenoceptors play a role in the distension-evoked micturition reflex in the rat.
阐明α1和α2肾上腺素能受体拮抗剂在周围和脊髓水平对麻醉大鼠膀胱扩张诱发的排尿反射的影响。材料和方法:对80只麻醉的雌性Sprague-Dawley大鼠采用连续膀胱测压法,监测并分析选择性动脉内和鞘内给药后基础压力(BaP)、排尿压力(MP)、膀胱容量(BC)、排尿量(MV)、膀胱收缩间隔(频率)和残余尿量(RV)的变化。
动脉内给予酚妥拉明、哌唑嗪、多沙唑嗪和坦索罗辛可显著降低MP;多沙唑嗪增加MV、BC、RV和频率。动脉内给予多沙唑嗪对MP的抑制作用比哌唑嗪或坦索罗辛更强。鞘内给予酚妥拉明可增加BaP、BC、RV并降低MP和MV;坦索罗辛降低频率并增加BC。可乐定显著增加BaP和频率,而MV和BC显著降低;育亨宾增加MV、BC并降低RV。动脉内给予育亨宾显著增加MV。
在脊髓水平,膀胱扩张诱发的排尿反射优先被酚妥拉明或育亨宾抑制,提示α2肾上腺素能受体参与其中。在周围,α1肾上腺素能受体阻滞剂优先抑制该反射。我们认为α1和α2肾上腺素能受体在大鼠扩张诱发的排尿反射中均起作用。