Velasco C, Guarneri L, Leonardi A, Testa R
Pharmaceutical R&D Division, Recordati SpA, Milano, Italy.
BJU Int. 2003 Jul;92(1):131-6. doi: 10.1046/j.1464-410x.2003.04281.x.
To evaluate the effect of the nonselective purinergic antagonist suramin and the alpha1-adrenergic antagonists, terazosin and BMY 7378, given intravenously or infused directly into the bladder during cystometry in conscious rats with bladder outlet obstruction induced by urethral ligation.
Cystometry was performed in conscious female rats recording bladder volume capacity (BVC), evaluated as the amount of saline infused between two voiding cycles, and micturition volume (MV). Changes in frequency and amplitude of spontaneous non-voiding bladder contractions (NVC) were also recorded. The effects of the intravenous administration of suramin (100 mg/kg), BMY 7378 (1 mg/kg), and terazosin (0.3 mg/kg) on NVC, BVC and MV were evaluated in obstructed rats with bladder infusion of saline. The effects of infravesical infusion of suramin (3-10 micromol/L), terazosin (1 micromol/L) and BMY 7378 (10 micromol/L) were also evaluated and compared with values observed in control rats during saline infusion into the bladder.
Intravenous injection with suramin had no effects on NVC, BVC and MV, but suramin infused into the bladder induced a consistent reduction in the amplitude of NVC (significantly different from matched control animals) with a tendency to reduce their frequency. BVC and MV were slightly but significantly decreased by infravesical infusion of suramin. In contrast, BMY 7378 and terazosin, given intravenously, were extremely potent at inhibiting the frequency and amplitude of the NVC, but were inactive on NVC when infused into bladder.
These findings confirm a role for alpha1-adrenergic receptors in bladder instability caused by bladder outlet obstruction. In addition, a purinergic neurotransmitter, presumably ATP, is shown to be involved.
评估非选择性嘌呤能拮抗剂苏拉明以及α1肾上腺素能拮抗剂特拉唑嗪和BMY 7378,在经尿道结扎诱导膀胱出口梗阻的清醒大鼠膀胱测压期间静脉注射或直接注入膀胱时的作用。
对清醒雌性大鼠进行膀胱测压,记录膀胱容量(BVC),以两个排尿周期之间注入的盐水量来评估,以及排尿量(MV)。还记录自发性非排尿膀胱收缩(NVC)的频率和幅度变化。在膀胱灌注生理盐水的梗阻大鼠中,评估静脉注射苏拉明(100 mg/kg)、BMY 7378(1 mg/kg)和特拉唑嗪(0.3 mg/kg)对NVC、BVC和MV的影响。还评估了膀胱下灌注苏拉明(3 - 10 μmol/L)、特拉唑嗪(1 μmol/L)和BMY 7378(10 μmol/L)的作用,并与在向膀胱灌注生理盐水的对照大鼠中观察到的值进行比较。
静脉注射苏拉明对NVC、BVC和MV无影响,但注入膀胱的苏拉明可使NVC的幅度持续降低(与匹配的对照动物有显著差异),且有降低其频率的趋势。膀胱下灌注苏拉明使BVC和MV略有但显著降低。相比之下,静脉注射BMY 7378和特拉唑嗪对抑制NVC的频率和幅度非常有效,但注入膀胱时对NVC无作用。
这些发现证实了α1肾上腺素能受体在膀胱出口梗阻引起的膀胱不稳定中的作用。此外,显示一种嘌呤能神经递质,可能是ATP,也参与其中。