Kontani H, Nakagawa M, Sakai T
Department of Pharmacology, Hokuriku University, School of Pharmacy, Kanazawa, Japan.
Jpn J Pharmacol. 1992 Apr;58(4):339-46. doi: 10.1254/jjp.58.339.
We have developed an experimental urinary incontinence model in anesthetized female rabbits, in order to study the effects of alpha-adrenergic receptor agonists on it in vivo. Micturition was induced artificially by electrical stimulation of the abdomen of rabbits receiving a continuous infusion of glucose-free. Tyrode's solution into the urinary bladder. Alpha-1 adrenergic agonists, phenylephrine (1 mg/kg, i.v.) and the newly synthesized agent ST-1059 (1 mg/kg, i.v.) and its prodrug midodrine (10 mg/kg), which was intraduodenally administered, elevated the bladder pressure and arrested micturition induced by electrical stimulation. Prazosin (0.1 mg/kg, i.v.) inhibited these effects of phenylephrine. The effect of an alpha-2 agonist, clonidine (1 mg/kg, i.v.), on micturition induced by electrical stimulation was not clearly defined. This study demonstrates that alpha-1 adrenergic agonists can arrest artificially-induced micturition via urethral contraction. This method may be useful for evaluating the effect of a drug on urethral leakage in vivo.
我们在麻醉的雌性兔子身上建立了一个实验性尿失禁模型,以研究α-肾上腺素能受体激动剂在体内对其的影响。通过对持续输注无葡萄糖的Tyrode溶液到膀胱的兔子腹部进行电刺激来人工诱导排尿。α-1肾上腺素能激动剂苯肾上腺素(1毫克/千克,静脉注射)、新合成的药物ST-1059(1毫克/千克,静脉注射)及其前药米多君(10毫克/千克,十二指肠内给药)可升高膀胱压力并阻止电刺激诱导的排尿。哌唑嗪(0.1毫克/千克,静脉注射)可抑制苯肾上腺素的这些作用。α-2激动剂可乐定(1毫克/千克,静脉注射)对电刺激诱导的排尿的影响尚不明确。本研究表明,α-1肾上腺素能激动剂可通过尿道收缩阻止人工诱导的排尿。该方法可能有助于评估药物在体内对尿道漏尿的影响。