Martine Hamann
University of Leicester, UK
Scientific Tracks Abstracts: J Mol Genet Med
Tinnitus, the pathological percept of phantom sound, is a highly prevalent disorder, affecting 10 to 15% of the population worldwide. Tinnitus can be triggered by prolonged exposure to loud noise damaging cochlear hair cells and introducing excitability changes in the auditory brainstem. There is no sensitive biomarker for diagnosis or early detection of tinnitus. MicroRNAs are approximately 22-nt RNA segments that are involved in the regulation of protein expression primarily by binding to one or more target sites on an mRNA transcript and inhibiting translation. MicroRNAs are highly stable and have been recently described as powerful biomarkers in a wide range of diseases. The study aims at identifying microRNAs present during tinnitus, assessed in CBA mice using the gapprepulse inhibition of the acoustic startle reflex, a broadly applied paradigm to study changes in neural processing related to tinnitus. We demonstrate selective gap detection deficits in CBA mice 3-4 weeks following acoustic over-exposure and identify specific modulation of microRNA levels in the brainstem and blood in those tinnitus positive CBA mice. Using the database DIANA-TarBase v7.0, we show that most regulated microRNAs (e.g. miR-128-3p, miR-140-5p, miR-151-5p and miR-204-5p) are involved in fatty acid metabolism and steroid signaling. The present results have important implications toward understanding tinnitus pathophysiology and designing novel pharmacotherapies targeting the function of those microRNAs.
Martine Hamann is an Associate Professor of Neurosciences in Department of Neurosciences, Psychology and Behavior at University of Leicester, UK. She completed her Graduation and PhD in Neurosciences at University of Strasbourg (France) and Centre Medical Universitaire (Geneva, Switzerland). She has completed her Post-doctoral studies at University College London. Her research focuses on Understanding cellular mechanisms associated to hearing loss and tinnitus in pre-clinical models, and aims at identifying markers to prevent and/or target those auditory deficits.
Email: mh86@le.ac.uk
Molecular and Genetic Medicine received 3919 citations as per Google Scholar report