Ogurlu Mahmut, Celebi Erdivanli Ozlem, Tumkaya Levent, Ozgur Abdulkadir, Ozergin Coskun Zerrin, Terzi Suat, Demirci Munir, Dursun Engin
Department of Otorhinolaryngology, Recep Tayyip Erdogan University Medical Faculty, Rize, Turkey.
İslampaşa mahallesi, Recep Tayyip Erdoğan Üniversitesi Tıp Fakültesi Eğitim ve Araştırma Hastanesi, Kulak Burun Boğaz Anabilim Dalı, 53100, Rize, Türkiye.
Eur Arch Otorhinolaryngol. 2017 Feb;274(2):743-749. doi: 10.1007/s00405-016-4319-4. Epub 2016 Oct 20.
Thymoquinone has antioxidant properties. We hypothesized that thymoquinone may prevent or alleviate hearing loss induced by acoustic trauma. We aimed to study thymoquinone's effect on hearing function with distortion-product otoacoustic emissions and auditory brainstem response. Thirty adult Spraque Dawley rats were randomized into four groups following exposure to acoustic trauma for 4 h. Control group (n = 7) did not receive further treatment. Thymoquinone-20 (n = 8) and Thymoquinone-40 (n = 8) received 20 and 40 mg/kg of intraperitoneal thymoquinone, respectively. Corn-oil group (n = 7) received 1 ml of corn oil intraperitoneally. Hearing function of both ears was tested with distortion-product otoacoustic emission and auditory brainstem response before, and shortly after acoustic trauma, and 96 h following acoustic trauma. Post-trauma signal/noise ratios and wave V amplitude/latencies of all groups were significantly low compared with pre-trauma values, which indicate no preventive effect of thymoquinone. Rats in Thymoquinone-20 showed a significantly improved distortion-product otoacoustic emission and auditory brainstem response results at 4000 frequency and above in post-treatment tests (p < 0.05). Improvement in Thymoquinone-40 at the same frequencies was insignificantly inferior to Thymoquinone-20, yet superior to control and corn-oil groups (p < 0.05). We conclude that thymoquinone may not prevent acoustic trauma-induced hearing loss, however, at 20 mg/kg for 96 h, may repair the damage.
百里醌具有抗氧化特性。我们推测百里醌可能预防或减轻由声创伤引起的听力损失。我们旨在通过畸变产物耳声发射和听觉脑干反应来研究百里醌对听力功能的影响。30只成年Spraque Dawley大鼠在接受4小时声创伤后被随机分为四组。对照组(n = 7)未接受进一步治疗。百里醌-20组(n = 8)和百里醌-40组(n = 8)分别接受20毫克/千克和40毫克/千克的腹腔注射百里醌。玉米油组(n = 7)腹腔注射1毫升玉米油。在声创伤前、声创伤后不久以及声创伤后96小时,用畸变产物耳声发射和听觉脑干反应测试双耳的听力功能。与创伤前值相比,所有组创伤后的信号/噪声比和波V振幅/潜伏期均显著降低,这表明百里醌没有预防作用。百里醌-20组的大鼠在治疗后测试中,在4000赫兹及以上频率的畸变产物耳声发射和听觉脑干反应结果有显著改善(p < 0.05)。百里醌-40组在相同频率的改善略逊于百里醌-20组,但优于对照组和玉米油组(p < 0.05)。我们得出结论,百里醌可能无法预防声创伤引起的听力损失,然而,在20毫克/千克剂量下持续96小时,可能会修复损伤。