4.4 Article

A method for intracochlear drug delivery in the mouse

Journal

JOURNAL OF NEUROSCIENCE METHODS
Volume 150, Issue 1, Pages 67-73

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jneumeth.2005.05.017

Keywords

mouse; inner ear; CNQX; salicylate; cochlea; drug delivery; cochleostomy

Funding

  1. NIDCD NIH HHS [R21 DC04983, R01 DC03401-07, R01 DC00767, P30 DC0052009] Funding Source: Medline
  2. PHS HHS [DLH-543157] Funding Source: Medline

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The confluence of two rapidly emerging research arenas - development of mouse models of human deafness and inner ear drug therapy for treatment and prevention of hearing loss - provides an opportunity for unprecedented approaches to study and treat deafness. Toward such goals, we have developed a method for intracochlear drug delivery in the mouse. The bulla was exposed using a ventral approach and the stapedial artery cauterized. An opening made into the inferior-medial aspect of the bulla, where the basal cochlear wall fuses with tympanic bulla, provided direct access to the scala tympani without separately opening the bulla or elevating auditory response thresholds. Cochlear responses, assayed by frequency-specific effects on ABRs and DPOAEs, were stable with infusion (1 mu l/h) of an artificial perilymph solution (80 min). The glutamate receptor antagonist, CNQX (100 mu M; 175 min), reduced ABR responses without affecting DPOAEs. Salicylate (5 mM; 165 min) altered both. Both drugs had greatest effects at high frequencies, but distributed throughout the cochlea and were reversible. The safe delivery of drugs into the cochlea by this approach has immediate application in the study and treatment of various forms of human hearing loss that can be modeled in the mouse. (c) 2005 Elsevier B.V. All rights reserved.

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