Literature DB >> 25382757

Evaluation of the selective glucocorticoid receptor agonist compound A for ototoxic effects.

Clemens Honeder1, Elisabeth Engleder, Hanna Schöpper, Markus Krause, Lukas David Landegger, Roberto Plasenzotti, Franz Gabor, Wolfgang Gstoettner, Christoph Arnoldner.   

Abstract

OBJECTIVES/HYPOTHESIS: To evaluate the selective glucocorticoid receptor agonist (SEGRA) compound A, a potential novel therapeutic for inner ear disorders, for ototoxic effects. STUDY
DESIGN: Laboratory animal study.
METHODS: Experimental guinea pigs were grouped as follows: Systemic application of compound A (1.5 mg/kg and 4.5 mg/kg; n = 6/group) and intratympanic application of compound A (1 mM and 10 mM; n = 6/group). Contralateral ears in topically treated animals served as controls. Hearing thresholds were determined by auditory brainstem response before and directly after the application of compound A, as well as on days 3, 7, 14, 21, and 28. At the end of the experiments, temporal bones were harvested for histological evaluation.
RESULTS: Systemic administration of compound A (1.5 mg/kg and 4.5 mg/kg) did not cause hearing threshold shifts, whereas the intratympanic injection (1 mM and 10 mM) resulted in a hearing loss. Histological analysis of the middle and inner ears after topical compound A application showed alterations in the tympanic membranes, the auditory ossicles, and the round window membranes, whereas spiral ganglion cells and hair cells were not affected.
CONCLUSION: SEGRAs such as compound A could provide novel therapeutic options for the treatment of inner ear disorders and reduce metabolic side effects. Whereas the intratympanic application of compound A resulted in a hearing loss, the systemic application of compound A merits evaluation for otoprotective effects in trauma models.
© 2014 The American Laryngological, Rhinological and Otological Society, Inc.

Entities:  

Keywords:  SEGRAs; Selective glucocorticoid receptor agonists; compound A; ototoxicity

Mesh:

Substances:

Year:  2014        PMID: 25382757      PMCID: PMC4885662          DOI: 10.1002/lary.25011

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


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