Endocochlear potential and furosemide

Active ingredient in the drug losartan
  • Furosemide is an ototoxic diuretic
  • The effective
  • 1 +/- 11
  • The endolymphatic potential b
  • A time-related reduction of the EP from the normal value a
  • 14, No
  • With loop diuretics the endocochlear DC potential decreased less in guinea pigs treated with kanamycin sulfate than it did in the control group

    2) recorded simultaneously

    On the other hand, each of these drugs also provides protection from a noise induced hearing loss if they are injected just before a noise exposure, probably as a result of the

    , 2011)

    We examined the effect of the cytosolic Ca(2+) concentration ([Ca(2+)](c)) in marginal cells on the asphyxia- or furosemide-induced decrease in the endocochlear potential (EP) by perfusing the endolymph with or without a Ca(2+) chelator or inhibitors of Ca(2+)-permeable channels or Ca(2+)-pump during transient asphyxia or intravenous administration of

    1970; 320 (4):359–372

    1) and MERG1a located in the intermediate Salicylic acid induces a reversible hearing loss since it binds to the motor protein prestin in the outer hair cells, reducing electromotility

    18)

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