Maggi C A, Giuliani S, Giachetti A, Meli A
Pharmacology Department, A. Menarini Pharmaceuticals, Florence, Italy.
Eur J Pharmacol. 1990 May 31;181(1-2):105-9. doi: 10.1016/0014-2999(90)90250-a.
We studied the effect of MK-801, a potent non-competitive NMDA receptor antagonist, on the micturition reflex in anesthetized rats. Pretreatment with MK-801 (0.1-1 mg/kg i.v.) dose dependently increased the bladder capacity and reduced the micturition contraction. The ability of MK-801 to inhibit bladder voiding was confirmed in additional experiments in which the compound (30-50 micrograms/kg i.v.) transiently suppressed established bladder voiding produced by continuous bladder filling. MK-801 (1 microM) did not affect nerve-mediated contractions of the rat bladder or inhibit the response to capsaicin. These findings provide pharmacological evidence for an involvement of NMDA receptors in the micturition reflex pathways.
我们研究了强效非竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂MK-801对麻醉大鼠排尿反射的影响。静脉注射MK-801(0.1 - 1毫克/千克)进行预处理,可剂量依赖性地增加膀胱容量并减少排尿收缩。在另外的实验中证实了MK-801抑制膀胱排尿的能力,在这些实验中,该化合物(静脉注射30 - 50微克/千克)可短暂抑制由持续膀胱充盈产生的已建立的膀胱排尿。MK-801(1微摩尔)不影响大鼠膀胱的神经介导收缩,也不抑制对辣椒素的反应。这些发现为NMDA受体参与排尿反射通路提供了药理学证据。