A reliable and reproducible protocol for sound-evoked vestibular myogenic potentials in rattus norvegicus.

IF 2.6 3区 医学 Q2 BEHAVIORAL SCIENCES
Frontiers in Integrative Neuroscience Pub Date : 2023-09-05 eCollection Date: 2023-01-01 DOI:10.3389/fnint.2023.1236642
Federica M Raciti, Yasniary Morales, Hillary A Snapp, Suhrud M Rajguru
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引用次数: 0

Abstract

Introduction: Cervical vestibular evoked myogenic potentials (cVEMPs) provide an objective measure of the integrity of the sacculo-collic pathway leading to their widespread use as a clinical tool in the diagnostic vestibular test battery. Though the application of cVEMPs in preclinical models to assess vestibular function, as performed in relevant clinical populations, remains limited. The present study aimed to establish a rodent model of cVEMP with standardized methods and protocols, examine the neural basis of the responses, and characterize and validate important features for interpretation and assessment of vestibular function.

Methods: We compared air-conducted sound (ACS)-evoked VEMPs from the sternocleidomastoid muscles in naïve Brown Norway rats. A custom setup facilitated repeatable and reliable measurements which were carried out at multiple intensities with ACS between 1 and 16 kHz and over 7 days. The myogenic potentials were identified by the presence of a positive (P1)-negative (N1) waveform at 3-5 ms from the stimulus onset. Threshold, amplitude, and latency were compared with intensity- and frequency-matched responses within and between animals.

Results: cVEMP responses were repeatedly evoked with stimulus intensities between 50-100 dB SPL with excellent test-retest reliability and across multiple measurements over 7 days for all frequencies tested. Suprathreshold, cVEMP responses at 90 dB SPL for 6-10 kHz stimuli demonstrated significantly larger amplitudes (p < 0.01) and shorter latencies (p < 0.001) compared to cVEMP responses for 1-4 kHz stimuli. Latency of cVEMP showed sex-dependent variability, but no significant differences in threshold or amplitude between males and females was observed.

Discussion: The results provide a replicable and reliable setup, test protocol, and comprehensive characterization of cVEMP responses in a preclinical model which can be used in future studies to elucidate pathophysiological characteristics of vestibular dysfunctions or test efficacy of therapeutics.

Abstract Image

Abstract Image

Abstract Image

一种可靠且可重复的褐家鼠声音诱发前庭肌源电位方案。
引言:颈前庭诱发肌源性电位(cVEMP)提供了一种客观的囊-颈通路完整性的测量方法,因此被广泛用作诊断前庭测试组的临床工具。尽管cVEMP在临床前模型中评估前庭功能的应用,如在相关临床人群中进行的那样,仍然有限。本研究旨在用标准化的方法和方案建立cVEMP的啮齿动物模型,检查反应的神经基础,并表征和验证前庭功能解释和评估的重要特征。方法:我们比较了来自天真的Brown Norway大鼠胸锁乳突肌的空气传导声(ACS)诱发的VEMP。定制设置有助于在ACS介于1和16kHz之间的多个强度下并在7天内进行可重复和可靠的测量。肌源性电位通过在刺激开始后3-5毫秒出现阳性(P1)-阴性(N1)波形来识别。将阈值、振幅和潜伏期与动物内部和动物之间的强度和频率匹配反应进行比较。结果:cVEMP反应在刺激强度为50-100dB SPL的情况下被反复诱发,具有良好的重测可靠性,并且在7天内对所有测试频率进行多次测量。与对1-4kHz刺激的cVEMP反应相比,对6-10kHz刺激的90dB SPL的超折叠cVEMP响应表现出显著更大的振幅(p<0.01)和更短的潜伏期(p<0.001)。cVEMP的潜伏期表现出性别依赖性变异,但在阈值或振幅方面,男性和女性之间没有观察到显著差异。讨论:该结果提供了一个可复制和可靠的临床前模型中cVEMP反应的设置、测试方案和全面表征,可用于未来的研究,以阐明前庭功能障碍的病理生理特征或测试治疗效果。
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来源期刊
Frontiers in Integrative Neuroscience
Frontiers in Integrative Neuroscience Neuroscience-Cellular and Molecular Neuroscience
CiteScore
4.60
自引率
2.90%
发文量
148
审稿时长
14 weeks
期刊介绍: Frontiers in Integrative Neuroscience publishes rigorously peer-reviewed research that synthesizes multiple facets of brain structure and function, to better understand how multiple diverse functions are integrated to produce complex behaviors. Led by an outstanding Editorial Board of international experts, this multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Our goal is to publish research related to furthering the understanding of the integrative mechanisms underlying brain functioning across one or more interacting levels of neural organization. In most real life experiences, sensory inputs from several modalities converge and interact in a manner that influences perception and actions generating purposeful and social behaviors. The journal is therefore focused on the primary questions of how multiple sensory, cognitive and emotional processes merge to produce coordinated complex behavior. It is questions such as this that cannot be answered at a single level – an ion channel, a neuron or a synapse – that we wish to focus on. In Frontiers in Integrative Neuroscience we welcome in vitro or in vivo investigations across the molecular, cellular, and systems and behavioral level. Research in any species and at any stage of development and aging that are focused at understanding integration mechanisms underlying emergent properties of the brain and behavior are welcome.
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