L-Ergothioneine slows the progression of age-related hearing loss in CBA/CaJ mice

IF 2.5 2区 医学 Q1 AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY Hearing Research Pub Date : 2024-04-02 DOI:10.1016/j.heares.2024.109004
Mark A. Bauer , Parveen Bazard , Alejandro A. Acosta , Nidhi Bangalore , Lina Elessaway , Mark Thivierge , Moksheta Chellani , Xiaoxia Zhu , Bo Ding , Joseph P. Walton , Robert D. Frisina
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Abstract

The naturally occurring amino acid, l-ergothioneine (EGT), has immense potential as a therapeutic, having shown promise in the treatment of other disease models, including neurological disorders. EGT is naturally uptaken into cells via its specific receptor, OCTN1, to be utilized by cells as an antioxidant and anti-inflammatory. In our current study, EGT was administered over a period of 6 months to 25–26-month-old CBA/CaJ mice as a possible treatment for age-related hearing loss (ARHL), since presbycusis has been linked to higher levels of cochlear oxidative stress, apoptosis, and chronic inflammation. Results from the current study indicate that EGT can prevent aging declines of some key features of ARHL. However, we found a distinct sex difference for the response to the treatments, for hearing – Auditory Brainstem Responses (ABRs) and Distortion Product Otoacoustic Emissions (DPOAEs). Males exhibited lower threshold declines in both low dose (LD) and high dose (HD) test groups throughout the testing period and did not display some of the characteristic aging declines in hearing seen in Control animals. In contrast, female mice did not show any therapeutic effects with either treatment dose. Further confirming this sex difference, EGT levels in whole blood sampling throughout the testing period showed greater uptake of EGT in males compared to females. Additionally, RT-PCR results from three tissue types of the inner ear confirmed EGT activity in the cochlea in both males and females. Males and females exhibited significant differences in biomarkers related to apoptosis (Cas-3), inflammation (TNF-a), oxidative stress (SOD2), and mitochondrial health (PGC1a).These changes were more prominent in males as compared to females, especially in stria vascularis tissue. Taken together, these findings suggest that EGT has the potential to be a naturally derived therapeutic for slowing down the progression of ARHL, and possibly other neurodegenerative diseases. EGT, while effective in the treatment of some features of presbycusis in aging males, could also be modified into a general prophylaxis for other age-related disorders where treatment protocols would include eating a larger proportion of EGT-rich foods or supplements. Lastly, the sex difference discovered here, needs further investigation to see if therapeutic conditions can be developed where aging females show better responsiveness to EGT.

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左旋麦角硫因可延缓 CBA/CaJ 小鼠老年性听力损失的进展
天然氨基酸--l-麦角硫因(EGT)作为一种疗法具有巨大的潜力,在治疗包括神经系统疾病在内的其他疾病模型方面已显示出前景。EGT 可通过其特异性受体 OCTN1 被细胞自然吸收,作为抗氧化剂和抗炎剂被细胞利用。在我们目前的研究中,我们给 25-26 个月大的 CBA/CaJ 小鼠注射了 6 个月的 EGT,作为治疗年龄相关性听力损失(ARHL)的一种可能方法,因为老花眼与较高水平的耳蜗氧化应激、细胞凋亡和慢性炎症有关。目前的研究结果表明,EGT 可以预防 ARHL 某些关键特征的衰老。然而,我们发现,在听力--听性脑干反应(ABRs)和失真产物耳声发射(DPOAEs)--的治疗反应方面,存在明显的性别差异。在整个测试期间,雄性小鼠在低剂量(LD)和高剂量(HD)测试组中都表现出较低的阈值下降,并且没有表现出对照组动物听力衰退的一些特征。相比之下,雌性小鼠在两种治疗剂量下均未显示出任何治疗效果。在整个测试期间,全血采样中的 EGT 水平显示,雄性小鼠对 EGT 的吸收量高于雌性小鼠,这进一步证实了性别差异。此外,来自内耳三种组织类型的 RT-PCR 结果证实,雄性和雌性耳蜗中都有 EGT 活性。男性和女性在与细胞凋亡(Cas-3)、炎症(TNF-a)、氧化应激(SOD2)和线粒体健康(PGC1a)相关的生物标志物方面表现出显著差异。综上所述,这些研究结果表明,EGT 有可能成为一种天然疗法,用于减缓 ARHL 以及其他神经退行性疾病的进展。EGT 在有效治疗老年男性老花眼的某些特征的同时,还可以被改造成其他老年相关疾病的一般预防药物,治疗方案将包括多吃富含 EGT 的食物或补充剂。最后,这里发现的性别差异还需要进一步研究,以确定是否可以开发出治疗条件,使衰老女性对 EGT 表现出更好的反应。
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来源期刊
Hearing Research
Hearing Research 医学-耳鼻喉科学
CiteScore
5.30
自引率
14.30%
发文量
163
审稿时长
75 days
期刊介绍: The aim of the journal is to provide a forum for papers concerned with basic peripheral and central auditory mechanisms. Emphasis is on experimental and clinical studies, but theoretical and methodological papers will also be considered. The journal publishes original research papers, review and mini- review articles, rapid communications, method/protocol and perspective articles. Papers submitted should deal with auditory anatomy, physiology, psychophysics, imaging, modeling and behavioural studies in animals and humans, as well as hearing aids and cochlear implants. Papers dealing with the vestibular system are also considered for publication. Papers on comparative aspects of hearing and on effects of drugs and environmental contaminants on hearing function will also be considered. Clinical papers will be accepted when they contribute to the understanding of normal and pathological hearing functions.
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