Shinozaki Sachiyo, Saito Motoaki, Kawatani Masahito
Department of Neurophysiology, Akita University School of Medicine, Akita, Japan.
Biomed Res. 2005 Feb;26(1):29-33. doi: 10.2220/biomedres.26.29.
Prostaglandins (PGs) are well known as one of the chemical mediators of inflammation. Nonsteroidal anti-inflammatory drugs (NSAIDs), PG synthesis inhibitors, are used for anti-nociception and/or anti-inflammation. We examine the effect of loxoprofen, an NSAID, on micturiton in acetic acid-induced bladder inflammation of the rats. In cystometrogram study with saline infusion into the urinary bladder, loxoprofen did not alter the interval of bladder contraction (IC, 107% of the control). IC was shortened by acetic acid infusion (65% of the control) and loxoprofen prolonged the IC (162% of acetic acid infused period). This prolonged IC was approximately same as the control. Loxoprofen did not alter the threshold pressure and the maximal voiding pressure. These data suggest that PGE2 might not play a part of normal micturition and may play a part of the micturition reflex during acetic acid infusion. That is, loxoprofen might be useful for pathological hyperreflex of the micturition.
前列腺素(PGs)作为炎症的化学介质之一广为人知。非甾体抗炎药(NSAIDs),即PG合成抑制剂,用于抗伤害感受和/或抗炎。我们研究了非甾体抗炎药洛索洛芬对大鼠醋酸诱导的膀胱炎症中排尿的影响。在向膀胱内注入生理盐水的膀胱压力描记图研究中,洛索洛芬未改变膀胱收缩间隔(IC,为对照组的107%)。注入醋酸可缩短IC(为对照组的65%),而洛索洛芬可延长IC(为注入醋酸时期的162%)。这种延长的IC与对照组大致相同。洛索洛芬未改变阈压力和最大排尿压力。这些数据表明,PGE2可能不参与正常排尿过程,而可能在注入醋酸期间参与排尿反射。也就是说,洛索洛芬可能对排尿的病理性反射亢进有用。