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Molecular biology of deafness in the Meniere's Model

梅尼埃模型中耳聋的分子生物学

基本信息

批准号：
7189009
负责人：
CLIFF A MEGERIAN
金额：
$ 7.25万
依托单位：
CASE WESTERN RESERVE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2005
资助国家：
美国
起止时间：
2005-03-01 至 2009-02-28
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7189009
关键词：
Acoustics Affect Affinity American Animal Model Animals Auditory Biochemical Biochemical Pathway Biological Calcium Cavia Cell Death Chromosome Pairing Cochlea Code Condition Dendrites Disease Ear Edema Electrons Endolymphatic Hydrops Enzymes Excitatory Amino Acid Receptors Excitatory Amino Acids Future GLAST Protein Gene Expression Genes Glutamate Receptor Glutamate-Ammonia Ligase Glutamatergic Agents Glutamates Glutamine Goals Grant Hair Cells Hearing Homeostasis Hyperacusis Injury Knowledge Labyrinth Lead Light Mediating Mediation Mediator of activation protein Medical Meniere&apos s Disease Messenger RNA Microscopic Modeling Molecular Molecular Biology Mus Neuronal Injury Neurons Nitric Oxide Operative Surgical Procedures Organ of Corti Pathogenesis Patients Pattern Perilymph Physiology Pilot Projects Play Proteins Radial Role Sensorineural Hearing Loss Severities Speech Discrimination Supporting Cell Symptoms Synapses Techniques Testing Thinking Tinnitus Tissue Sample Toxic effect Vertigo cell injury deafness excitotoxicity ganglion cell hearing impairment inner ear injury mRNA Expression neurotransmission prevent round window spiral ganglion therapy development

项目摘要

DESCRIPTION (provided by applicant): The goal for this project is to better understand the molecular biological changes that occur in the inner ear as a result of endolymphatic hydrops. Endolymphatic hydrops is a condition known to accompany Meniere's disease, a common disorder affecting millions of Americans. Meniere's disease causes both hearing loss and vertigo. Although vertigo has been shown to be controlled via numerous medical and surgical interventions, the hearing loss and subsequent deafness have no known treatment. This is in part due to the lack of knowledge regarding the exact mechanism of hearing loss in Meniere's related endolymphatic hydrops. Better understanding of the mechanisms of hydrops related hearing loss will be important in guiding the development of therapies to prevent such hearing loss. Glutamate and other excitatory amino acid (EAA) receptors are present in the mammalian inner ear and are thought to play a key role in normal hearing but are also implicated in excitotoxic injury when EAA levels are elevated. Neuronal findings have been described in the cochleas of patients with Meniere's disease and animal models of endolymphatic hydrops and these findings suggest that EAA toxicity may be playing an important role in the mediation of associated inner ear injury and subsequent hearing loss. The specific goals of the project include studies of a well-known model of surgically induced endolymphatic hydrops in the guinea pig. Once endolymphatic hydrops has been established, inner ear tissue samples will be collected and subjected to molecular biological techniques that allow for determination of whether messenger RNA levels of genes critical to EAA physiology .are up-regulated or down-regulated. This will provide clues to better understand the exact biochemical pathways that are activated in this condition and possibly provide new treatment strategies to be developed. It is expected that this project will lead to a larger grant in the future that explores and defines the entire cascade of biochemical changes accompanying Meniere's related endolymphatic hydrops and could someday provide better treatment alternatives to patients with Meniere's related hearing loss.

描述（由申请人提供）：本项目的目标是更好地了解内淋巴积水导致内耳发生的分子生物学变化。内淋巴积水是一种已知伴随梅尼埃病的病症，梅尼埃病是一种影响数百万美国人的常见疾病。梅尼埃病会导致听力损失和眩晕。虽然眩晕已被证明是通过许多医疗和手术干预控制，听力损失和随后的耳聋没有已知的治疗。这部分是由于缺乏关于梅尼埃相关的内淋巴积水中听力损失的确切机制的知识。更好地了解水肿相关性听力损失的机制将是重要的，指导治疗的发展，以防止这种听力损失。谷氨酸和其他兴奋性氨基酸（EAA）受体存在于哺乳动物内耳中，被认为在正常听力中发挥关键作用，但当EAA水平升高时也与兴奋性毒性损伤有关。在梅尼埃病患者和内淋巴积水动物模型的耳蜗中已经描述了神经元发现，这些发现表明EAA毒性可能在相关内耳损伤和随后的听力损失的介导中起重要作用。该项目的具体目标包括研究一个众所周知的豚鼠手术诱导内淋巴积水模型。一旦建立了内淋巴积水，将收集内耳组织样本并进行分子生物学技术，以确定对EAA生理学至关重要的基因的信使RNA水平是否上调或下调。这将提供线索，以更好地了解在这种情况下激活的确切生化途径，并可能提供新的治疗策略。预计该项目将在未来获得更大的资助，以探索和定义伴随梅尼埃相关内淋巴积水的整个生化变化级联，并有一天为梅尼埃相关听力损失患者提供更好的治疗选择。