Seher Yılmaz, Caner Yatmaz, Furkan Büyükkal, Alev Cumbul, Işılay Öz, Mustafa Bülent Şerbetçioğlu
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All groups were subjected to auditory brainstem response assessments at 4 time points: pre-exposure (baseline), post-exposure day 1, day 7, and day 21. Both noise exposure and the Pycnogenol® treatment groups were exposed to 4 kHz narrowband noise at 120 dB SPL for 4 hours. Following sacrifice, histological and immunohistochemical evaluations were conducted on cochlear tissues. Statistical analyses were performed using SPSS software version 25 to determine significant differences between groups and across time points. Results: Outcome of this research shows that the auditory brainstem response thresholds and cochlear morphology between the experimental and control groups are significantly different from each other, suggesting that Pycnogenol® may have the potential to prevent NIHL loss in rats. Conclusion: Pycnogenol® shows potential in protecting against NIHL. However, further research, particularly at the molecular level, is necessary to better understand its therapeutic mechanisms and its specific impact on auditory metabolic processes.</p>","PeriodicalId":94238,"journal":{"name":"The journal of international advanced otology","volume":"21 1","pages":"1-7"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11843294/pdf/","citationCount":"0","resultStr":"{\"title\":\"Effect of Pycnogenol® on Noise-Induced Hearing Loss in Rats.\",\"authors\":\"Seher Yılmaz, Caner Yatmaz, Furkan Büyükkal, Alev Cumbul, Işılay Öz, Mustafa Bülent Şerbetçioğlu\",\"doi\":\"10.5152/iao.2025.241623\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Background: This study aims to elucidate the potential protective effects of Pycnogenol® against noise-induced hearing (NIHL) loss in a rat model. 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引用次数: 0
摘要
背景:本研究旨在阐明碧萝芷®对噪声性听力(NIHL)大鼠模型的潜在保护作用。方法:采用随机对照设计,研究碧萝芷®对大鼠NIHL的潜在保护作用。选取雄性Wistar白化大鼠25只,随机分为5组(每组5只):对照组生理盐水组、噪声暴露组、噪声+生理盐水组、仅服用碧萝芷®组、碧萝芷®治疗组,在噪声暴露后每天灌胃给予碧萝芷®40 mg/kg/d,连续7 d。所有组在4个时间点进行听觉脑干反应评估:暴露前(基线)、暴露后第1天、第7天和第21天。噪声暴露组和碧萝芷®处理组均暴露于120 dB SPL的4 kHz窄带噪声中4小时。牺牲后,对耳蜗组织进行组织学和免疫组化评价。采用SPSS软件版本25进行统计分析,以确定组间和跨时间点的显著差异。结果:本研究结果显示,实验组和对照组的听觉脑干反应阈值和耳蜗形态存在显著差异,提示碧萝芷®可能具有预防大鼠NIHL丢失的潜力。结论:碧萝芷®具有一定的抗NIHL作用。然而,进一步的研究,特别是在分子水平上,需要更好地了解其治疗机制及其对听觉代谢过程的具体影响。
Effect of Pycnogenol® on Noise-Induced Hearing Loss in Rats.
Background: This study aims to elucidate the potential protective effects of Pycnogenol® against noise-induced hearing (NIHL) loss in a rat model. Methods: This study employed a randomized controlled design to investigate the potential protective effects of Pycnogenol® against NIHL in a rat model. Twenty-five male Wistar albino rats were randomly assigned to 5 groups (n=5 per group): a control group receiving saline administration, a noise exposure group, a noise+saline receiving group, only Pycnogenol® receiving group, and finally, a Pycnogenol® treatment group receiving daily oral administration of Pycnogenol® at 40 mg/kg/day via gavage for 7 days following noise exposure. All groups were subjected to auditory brainstem response assessments at 4 time points: pre-exposure (baseline), post-exposure day 1, day 7, and day 21. Both noise exposure and the Pycnogenol® treatment groups were exposed to 4 kHz narrowband noise at 120 dB SPL for 4 hours. Following sacrifice, histological and immunohistochemical evaluations were conducted on cochlear tissues. Statistical analyses were performed using SPSS software version 25 to determine significant differences between groups and across time points. Results: Outcome of this research shows that the auditory brainstem response thresholds and cochlear morphology between the experimental and control groups are significantly different from each other, suggesting that Pycnogenol® may have the potential to prevent NIHL loss in rats. Conclusion: Pycnogenol® shows potential in protecting against NIHL. However, further research, particularly at the molecular level, is necessary to better understand its therapeutic mechanisms and its specific impact on auditory metabolic processes.