Brummett R E, Bendrick T, Himes D
J Clin Pharmacol. 1981 Nov-Dec;21(11):628-36. doi: 10.1002/j.1552-4604.1981.tb05675.x.
The ototoxicity of bumetanide and furosemide was compared in Topeka strain guinea pigs pretreated with kanamycin. The animals, anesthetized with pentobarbital, received a single dose of 400 mg/kg kanamycin subcutaneously and the diuretics via indwelling catheter in the jugular vein 2 hours later. Ototoxic drug effects were determined by measuring the electrophysiological responses of the cochlea to sound stimuli and by determining the presence or absence of cochlear sensory hair cells from the organ of Corti. Both bumetanide and furosemide produced permanent alteration of cochlear activity in the kanamycin-pretreated animals. The ototoxic effect of bumetanide is five times that of furosemide on a milligram-for-milligram basis. The ototoxic potential of bumetanide is one eighth that of furosemide when the doses are adjusted for diuretic potency difference between the two diuretics.
在预先用卡那霉素处理的托皮卡品系豚鼠中,比较了布美他尼和呋塞米的耳毒性。动物用戊巴比妥麻醉,皮下注射400mg/kg卡那霉素单剂量,2小时后通过颈静脉留置导管给予利尿剂。通过测量耳蜗对声音刺激的电生理反应以及确定柯蒂氏器中是否存在耳蜗感觉毛细胞来确定耳毒性药物的作用。布美他尼和呋塞米在预先用卡那霉素处理的动物中均产生了耳蜗活动的永久性改变。以毫克为单位计算,布美他尼的耳毒性作用是呋塞米的五倍。当根据两种利尿剂之间的利尿效力差异调整剂量时,布美他尼的耳毒性潜力是呋塞米的八分之一。