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新型氨基糖苷类抗生素羟庆大霉素对豚鼠的耳毒性。

The ototoxicity of hydroxygentamicin, a new aminoglycoside antibiotic, in guinea pigs.

作者信息

Neidl M J, Liddell M R, Montenaro M J, Hawkins J E, Drobeck H P

出版信息

Fundam Appl Toxicol. 1981 Sep-Oct;1(5):395-402. doi: 10.1016/s0272-0590(81)80011-5.

Abstract

The comparative ototoxicity of hydroxygentamicin (Win 42,122-2), a new aminoglycosidic antibiotic, gentamicin and kanamycin was evaluated in guinea pigs by assessment of the Preyer (pinna) reflex response to pure tone frequencies ranging from 2.5 to 20.0 KHz, and by histologic examination of surface preparations of the organ of Corti. Daily subcutaneous administration of 80.0 mg/kg of gentamicin or 240.0 mg/kg of kanamycin to groups of six guinea pigs for 18 to 45 days resulted in loss of the Preyer reflex in all animals. The Preyer reflex was retained in 5 of 6 guinea pigs given 80.0 mg/kg/day of hydroxygentamicin for 77 days and in 6 of 6 guinea pigs given 160.0 mg/kg/day for the same period. Microscopic examination of cochleas from guinea pigs given gentamicin or kanamycin revealed extensive outer and inner hair cell loss in all animals. Cytocochleograms of 5 of 6 guinea pigs medicated with 160.0 mg/kg of hydroxygentamicin were comparable to those of the controls. In the sixth guinea pig there was a localized lesion involving all three rows of outer hair cells and some inner hair cells in the second turn. The results of this study indicated that hydroxygentamicin may be tolerated better than gentamicin in the guinea pig and therefore warrants further development as a new and less toxic aminoglycosidic antibiotic.

摘要

通过评估豚鼠对2.5至20.0千赫兹纯音频率的普雷耶(耳廓)反射反应,以及对柯蒂氏器表面制剂进行组织学检查,在豚鼠中评估了一种新的氨基糖苷类抗生素羟庆大霉素(Win 42,122 - 2)、庆大霉素和卡那霉素的相对耳毒性。对每组六只豚鼠每日皮下注射80.0毫克/千克庆大霉素或240.0毫克/千克卡那霉素,持续18至45天,导致所有动物的普雷耶反射消失。在给予80.0毫克/千克/天羟庆大霉素的6只豚鼠中,有5只在77天内保留了普雷耶反射;在同一时期给予160.0毫克/千克/天的6只豚鼠中,所有6只均保留了该反射。对给予庆大霉素或卡那霉素的豚鼠耳蜗进行显微镜检查发现,所有动物的外毛细胞和内毛细胞均有广泛损失。用160.0毫克/千克羟庆大霉素给药的6只豚鼠中,有5只的细胞耳蜗图与对照组相当。在第六只豚鼠中,有一个局部病变,累及第二圈的所有三排外毛细胞和一些内毛细胞。这项研究的结果表明,在豚鼠中,羟庆大霉素可能比庆大霉素耐受性更好,因此作为一种新的、毒性较小的氨基糖苷类抗生素值得进一步开发。

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