胸腺醌对声创伤诱发的大鼠听力损失的影响

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Cureus Pub Date : 2024-10-23 eCollection Date: 2024-10-01 DOI:10.7759/cureus.72181
Mustafa Said Tekin, Abdullah Ayçiçek, Abdulkadir Bucak, Şahin Ulu, Erdoğan Okur
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引用次数: 0

摘要

背景 本研究旨在探讨胸腺醌(一种抗氧化剂)对声外伤诱发的大鼠听力损失的保护作用。材料和方法 本研究包括 32 只 Wistar Albino 大鼠,分为四组:对照组、声外伤组、胸腺醌 + 声外伤组和仅胸腺醌组,每组 8 只。对照组腹腔注射 0.5 毫升玉米油,连续 10 天。声创伤组暴露于 4 千赫 100 分贝的白噪声中 16 小时。胸腺醌+声学创伤组在声学创伤前两天和声学创伤后八天腹腔注射胸腺醌(10 毫克/千克)。仅胸腺醌组接受胸腺醌(10 毫克/千克)治疗 10 天。在治疗前后的第 1、4 和 10 天测量失真产物耳声发射 (DPOAE)。结果 在研究期间,对照组的 DPOAE 测量结果无明显变化。声波创伤组在创伤后第一天的 DPOAE 有明显下降,随后有所恢复。胸腺醌+声学创伤组在创伤后第一天的DPOAE没有明显下降,这表明胸腺醌具有保护作用。仅胸腺醌组的 DPOAE 测量结果也无明显变化,表明仅胸腺醌不会影响听力功能。结论 胸腺醌对声学创伤引起的大鼠听力损失有保护作用,创伤后稳定的DPOAE测量结果证明了这一点。这些研究结果表明,胸腺醌可通过减少耳蜗中的氧化应激来保护听力功能。要在人体中证实这些结果并优化剂量和治疗方案,还需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of Thymoquinone on Acoustic Trauma-Induced Hearing Loss in Rats.

Background The aim of this study was to investigate the protective effect of thymoquinone, an antioxidant, on hearing loss induced by acoustic trauma in rats. Material and methods This study included 32 Wistar Albino rats divided into four groups: control, acoustic trauma, thymoquinone + acoustic trauma, and thymoquinone only, with eight rats per group. The control group received 0.5 mL of corn oil intraperitoneally for 10 days. The acoustic trauma group was exposed to 100 dB white noise at 4 kHz for 16 hours. The thymoquinone + acoustic trauma group received thymoquinone (10 mg/kg) intraperitoneally for two days before acoustic trauma and eight days after acoustic trauma. The thymoquinone only group received thymoquinone (10 mg/kg) for 10 days. Distortion product otoacoustic emissions (DPOAEs) were measured before and after treatments on days 1, 4, and 10. Results In the control group, DPOAE measurements showed no significant change over the study period. The acoustic trauma group exhibited a significant decrease in DPOAE on the first day after trauma, followed by some recovery. The thymoquinone + acoustic trauma group showed no significant decrease in DPOAE on the first day post-trauma, suggesting a protective effect. The thymoquinone only group also indicated no significant change in DPOAE measurements, suggesting that thymoquinone alone did not affect hearing function. Conclusion Thymoquinone demonstrated a protective effect against acoustic trauma-induced hearing loss in rats, as evidenced by stable DPOAE measurements post-trauma. These findings suggest that thymoquinone may help preserve hearing function by reducing oxidative stress in the cochlea. Further studies are needed to confirm these results in humans and optimize dosage and treatment protocols.

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