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呋塞米耳毒性:临床与实验方面

Furosemide ototoxicity: clinical and experimental aspects.

作者信息

Rybak L P

出版信息

Laryngoscope. 1985 Sep;95(9 Pt 2 Suppl 38):1-14. doi: 10.1288/00005537-198509010-00001.

Abstract

Furosemide is an ototoxic diuretic. Furosemide injection is followed by a rapid, but reversible decrease of the endocochlear potential and eighth nerve action potential with a more gradual decrease of the endolymph potassium concentration. In contrast to the reversible effects of furosemide alone on the cochlea, the combination of kanamycin with furosemide resulted in irreversible changes in cochlear function which were associated with elevated levels of kanamycin in the blood and perilymph of the experimental animals. There was a striking similarity between the blood level measured by high pressure liquid chromatography at the time of recovery of auditory function in experimental animals and the ototoxic blood levels proposed by others in clinical literature. These findings help to provide a pharmacologic basis for the clinical observation of furosemide-induced hearing loss.

摘要

呋塞米是一种耳毒性利尿剂。注射呋塞米后,内耳蜗电位和第八神经动作电位会迅速但可逆地降低,内淋巴钾浓度则会逐渐降低。与呋塞米单独对耳蜗的可逆作用相反,卡那霉素与呋塞米联合使用会导致耳蜗功能发生不可逆变化,这与实验动物血液和外淋巴中卡那霉素水平升高有关。实验动物听觉功能恢复时通过高压液相色谱法测得的血液水平与临床文献中其他人提出的耳毒性血液水平之间存在显著相似性。这些发现有助于为呋塞米所致听力损失的临床观察提供药理学依据。

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