Beaugard M E, Asakuma S, Snow J B
Arch Otolaryngol. 1981 Feb;107(2):104-9. doi: 10.1001/archotol.1981.00790380034008.
Chloramphenicol is not ototoxic if administered for systemic effect, but topical applications of it to the middle ear produce severe cochlear toxic effects. Ethacrynic acid potentiates the ototoxicity of aminoglycosides. Guinea pigs were administered chloramphenicol or kanamycin sulfate with ethacrynic acid to compare the ototoxicity of chloramphenicol and ethacrynic acid with the ototoxicity of kanamycin and ethacrynic acid. Preyer's reflex audiometry and measurement of the endocochlear dc potential, the cochlear microphonics, and the negative potential of the organ of Corti indicate that ethacrynic acid does not potentiate the ototoxicity of chloramphenicol. There is not even indirect evidence that the blood-cochlear barrier for chloramphenicol is altered by ethacrynic acid. Assuming that the ototoxicity of chloramphenicol and ethacrynic acid are similar for man and guinea pig, the combination of the administration of chloramphenicol and ethacrynic acid of systemic effect in dosages commonly used clinically should not produce greater ototoxicity than either agent administered alone.
氯霉素若用于全身作用则无耳毒性,但将其局部应用于中耳会产生严重的耳蜗毒性作用。依他尼酸会增强氨基糖苷类药物的耳毒性。给豚鼠施用氯霉素或硫酸卡那霉素与依他尼酸,以比较氯霉素和依他尼酸的耳毒性与卡那霉素和依他尼酸的耳毒性。普赖尔反射听力测定以及耳蜗内直流电位、耳蜗微音器电位和柯蒂氏器负电位的测量表明,依他尼酸不会增强氯霉素的耳毒性。甚至没有间接证据表明依他尼酸会改变氯霉素的血 - 耳蜗屏障。假设氯霉素和依他尼酸对人和豚鼠的耳毒性相似,那么在临床上常用剂量下将具有全身作用的氯霉素和依他尼酸联合使用,产生的耳毒性不应比单独使用任何一种药物更大。