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通过疾病状态检测新型耳毒素及耳毒性的增强作用。

Detecting Novel Ototoxins and Potentiation of Ototoxicity by Disease Settings.

作者信息

Coffin Allison B, Boney Robert, Hill Jordan, Tian Cong, Steyger Peter S

机构信息

Washington State University Vancouver, Vancouver, WA, United States.

Rewire Neuro, Portland, OR, United States.

出版信息

Front Neurol. 2021 Aug 17;12:725566. doi: 10.3389/fneur.2021.725566. eCollection 2021.

Abstract

Over 100 drugs and chemicals are associated with permanent hearing loss, tinnitus, and vestibular deficits, collectively known as ototoxicity. The ototoxic potential of drugs is rarely assessed in pre-clinical drug development or during clinical trials, so this debilitating side-effect is often discovered as patients begin to report hearing loss. Furthermore, drug-induced ototoxicity in adults, and particularly in elderly patients, may go unrecognized due to hearing loss from a variety of etiologies because of a lack of baseline assessments immediately prior to novel therapeutic treatment. During the current pandemic, there is an intense effort to identify new drugs or repurpose FDA-approved drugs to treat COVID-19. Several potential COVID-19 therapeutics are known ototoxins, including chloroquine (CQ) and lopinavir-ritonavir, demonstrating the necessity to identify ototoxic potential in existing and novel medicines. Furthermore, several factors are emerging as potentiators of ototoxicity, such as inflammation (a hallmark of COVID-19), genetic polymorphisms, and ototoxic synergy with co-therapeutics, increasing the necessity to evaluate a drug's potential to induce ototoxicity under varying conditions. Here, we review the potential of COVID-19 therapies to induce ototoxicity and factors that may compound their ototoxic effects. We then discuss two models for rapidly detecting the potential for ototoxicity: mammalian auditory cell lines and the larval zebrafish lateral line. These models offer considerable value for pre-clinical drug development, including development of COVID-19 therapies. Finally, we show the validity of screening for ototoxic potential using a computational model that compares structural similarity of compounds of interest with a database of known ototoxins and non-ototoxins. Preclinical screening at , and levels can provide an earlier indication of the potential for ototoxicity and identify the subset of candidate therapeutics for treating COVID-19 that need to be monitored for ototoxicity as for other widely-used clinical therapeutics, like aminoglycosides and cisplatin.

摘要

超过100种药物和化学物质与永久性听力损失、耳鸣和前庭功能障碍有关,统称为耳毒性。在临床前药物开发或临床试验期间,很少评估药物的耳毒性潜力,因此这种使人衰弱的副作用往往是在患者开始报告听力损失时才被发现。此外,由于在开始新的治疗之前缺乏基线评估,成人尤其是老年患者因各种病因导致的听力损失,药物性耳毒性可能未被识别。在当前的大流行期间,人们正在加紧努力寻找新的药物或重新利用美国食品药品监督管理局(FDA)批准的药物来治疗COVID-19。几种潜在的COVID-19治疗药物是已知的耳毒素,包括氯喹(CQ)和洛匹那韦-利托那韦,这表明有必要确定现有药物和新药物的耳毒性潜力。此外,一些因素正成为耳毒性的增强剂,如炎症(COVID-19的一个特征)、基因多态性以及与联合治疗药物的耳毒性协同作用,这增加了在不同条件下评估药物诱发耳毒性潜力的必要性。在这里,我们综述了COVID-19治疗药物诱发耳毒性的潜力以及可能加剧其耳毒性作用的因素。然后,我们讨论了两种快速检测耳毒性潜力的模型:哺乳动物听觉细胞系和斑马鱼幼体侧线。这些模型为临床前药物开发,包括COVID-19治疗药物的开发,提供了相当大的价值。最后,我们展示了使用计算模型筛选耳毒性潜力的有效性,该模型将感兴趣的化合物与已知耳毒素和非耳毒素数据库进行结构相似性比较。在细胞、组织和动物水平进行临床前筛选,可以更早地表明耳毒性的潜力,并确定治疗COVID-19的候选治疗药物中需要像对其他广泛使用的临床治疗药物(如氨基糖苷类和顺铂)一样监测耳毒性的子集。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22f1/8418111/049b2f81e540/fneur-12-725566-g0001.jpg

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