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几种治疗药物对哺乳动物前庭功能的影响:美克洛嗪、地西泮和 JNJ7777120。

Effects of Several Therapeutic Agents on Mammalian Vestibular Function: Meclizine, Diazepam, and JNJ7777120.

机构信息

Department of Special Education and Communication Disorders, University of Nebraska-Lincoln, 301 Barkley Memorial Center, Lincoln, NE, 68583-0738, USA.

Department of Otolaryngology, University of Rochester, Rochester, NY, 14642, USA.

出版信息

J Assoc Res Otolaryngol. 2021 Oct;22(5):527-549. doi: 10.1007/s10162-021-00803-5. Epub 2021 May 19.

Abstract

Management of vestibular dysfunction may include treatment with medications that are thought to act to suppress vestibular function and reduce or eliminate abnormal sensitivity to head motions. The extent to which vestibular medications act centrally or peripherally is still debated. In this study, two commonly prescribed medications, meclizine and diazepam, and a candidate for future clinical use, JNJ7777120, were evaluated for their effects on short latency compound action potentials generated by the peripheral vestibular system and corresponding central neural relays (i.e., vestibular sensory-evoked potentials, VsEPs). The effects of the selected drugs developed slowly over the course of two hours in the mouse. Findings indicate that meclizine (600 mg/kg) and diazepam (> 60 mg/kg) can act on peripheral elements of the vestibular maculae whereas diazepam also acts most effectively on central gravity receptor circuits to exert its suppressive effects. The novel pharmacological agent JNJ7777120 (160 mg/kg) acts in the vestibular periphery to enhance macular responses to transient stimuli (VsEPs) while, hypothetically, suppressing macular responses to sustained or slowly changing stimuli.

摘要

前庭功能障碍的治疗方法可能包括使用药物治疗,这些药物被认为可以抑制前庭功能,减少或消除对头部运动的异常敏感性。前庭药物在中枢或外周起作用的程度仍存在争议。在这项研究中,评估了两种常用的药物,即甲磺酸倍他司汀和地西泮,以及一种有希望用于未来临床应用的候选药物 JNJ7777120,评估它们对由外周前庭系统和相应中枢神经中继(即前庭感觉诱发电位,VsEPs)产生的短潜伏期复合动作电位的影响。在小鼠中,所选药物的作用在两小时的过程中缓慢发展。研究结果表明,甲磺酸倍他司汀(600mg/kg)和地西泮(>60mg/kg)可作用于前庭斑的外周成分,而地西泮还可有效地作用于重力受体中枢回路以发挥其抑制作用。新型药理学药物 JNJ7777120(160mg/kg)在外周前庭中起作用,可增强对瞬态刺激的黄斑反应(VsEPs),同时,假设抑制对持续或缓慢变化的刺激的黄斑反应。

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