Protective Role of Bilberry Extract Against Cisplatin Induced Ototoxicity in Rats

被引:10
作者
Kapusuz, Zeliha [1 ]
Ozkiris, Mahmut [1 ]
Kala, Mehtap [2 ]
Saydam, Levent [1 ]
机构
[1] Bozok Univ Med Fac, Dept Otolaryngol Head & Neck Surg, Yozgat, Turkey
[2] Tekden Med Ctr, Dept Pathol, Kayseri, Turkey
关键词
Cisplatin; Ototoxicity; Bilberry extract; ANTIOXIDANT ACTIVITY; ANTHOCYANINS;
D O I
10.1007/s12070-013-0642-x
中图分类号
R61 [外科手术学];
学科分类号
摘要
To investigate the potential preventive effect of bilberry extract in cisplatin-induced ototoxicity. Thirty-five 3-3.5-month healthy adult female Sprague-Dawley rats were randomly divided into three groups and treated as follows: Both, group 1 (n = 10) and group 2 (n = 15) subjects received a single dose of 12 mg/kg cisplatin intraperitoneally; while in group 2, bilberry extract was also administered via gavage feeding for 15 days. Group 3 (n = 10), received no cisplatin or bilberry extract. Baseline distortion product otoacoustic emissions testing were performed in all subjects prior to administration of any medication. The test was repeated at 15th day following administration of any medication. The distortion product otoacoustic emissions were evaluated at 1.5, 2, 3, 4, 5, 6, 7, 8, 10 and 12 kHz. Histopathological changes in the cochlea of rats were observed by light microscopy. There was no statistically significant difference in apical turn between three groups but there was a statistically significant difference in basal and mid turn external ciliated cells number. Stria vascularis changes were statistically significant between three groups. The median score for stria vascularis injury and spiral ganglion cells changes were significantly greater in group 1 than in group 2. The initial distortion product otoacoustic emissions measurement results gave similar statistically insignificant values in the three groups (p > 0.05). In contrast to initial measurements statistically significant differences were recorded between day 0 and 15 otoacoustic thresholds (p < 0.05). Bilberry extract group had a significantly higher DP-gram except for 1.5 and 2 kHz frequencies when compared to cisplatin group. The analyses of the results revealed statistically significant differences between two groups (p < 0.05), suggesting that bilberry extract had shown a protective effect against cisplatin ototoxicity. The results of our study revealed that treatment with bilberry extract affords significant protection to the cochlea from cisplatin toxicity and thus, oral experimental dose of bilberry extract administration may have a protective effect against cisplatin ototoxicity in rats.
引用
收藏
页码:339 / 344
页数:6
相关论文
共 26 条
[1]   Cisplatin-induced apoptotic cell death in Mongolian gerbil cochlea [J].
Alam, SA ;
Ikeda, K ;
Oshima, T ;
Suzuki, M ;
Kawase, T ;
Kikuchi, T ;
Takasaka, T .
HEARING RESEARCH, 2000, 141 (1-2) :28-38
[2]   Light microscopy study of cisplatin-induced ototoxicity in rats [J].
de Freitas, M. R. ;
de Castro Brito, G. A. ;
de Carvalho, J. V., Jr. ;
Gomes, R. M., Jr. ;
Barreto Martins, M. J. ;
de Albuquerque Ribeiro, R. .
JOURNAL OF LARYNGOLOGY AND OTOLOGY, 2009, 123 (06) :590-597
[3]   The effect of resveratrol on the prevention of cisplatin ototoxicity [J].
Erdem, T. ;
Bayindir, Tuba ;
Filiz, A. ;
Iraz, M. ;
Selimoglu, E. .
EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2012, 269 (10) :2185-2188
[5]   Roles of NADPH Oxidases in Cisplatin-Induced Reactive Oxygen Species Generation and Ototoxicity [J].
Kim, Hyung-Jin ;
Lee, Jeong-Han ;
Kim, Se-Jin ;
Oh, Gi Su ;
Moon, Hae-Dalma ;
Kwon, Kang-Beom ;
Park, Channy ;
Park, Byung Hyun ;
Lee, Ho-Kyun ;
Chung, Sang-Young ;
Park, Raekil ;
So, Hong-Seob .
JOURNAL OF NEUROSCIENCE, 2010, 30 (11) :3933-3946
[6]   Analysis of anthocyanin variation in wild populations of bilberry (Vaccinium myrtillus L.) in Finland [J].
Latti, Anja K. ;
Riihinen, Kaisu R. ;
Kainulainen, Pirjo S. .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2008, 56 (01) :190-196
[7]  
LAURELL G, 1991, J OTOLARYNGOL, V20, P158
[8]   Predicting cisplatin ototoxicity in children: the influence of age and the cumulative dose [J].
Li, Y ;
Womer, RB ;
Silber, JH .
EUROPEAN JOURNAL OF CANCER, 2004, 40 (16) :2445-2451
[9]   Reduction of acute cisplatin ototoxicity and nephrotoxicity in rats by oral administration of allopurinol and ebselen [J].
Lynch, ED ;
Gu, RD ;
Pierce, C ;
Kil, J .
HEARING RESEARCH, 2005, 201 (1-2) :81-89
[10]   Stimulatory effect of cyanidin 3-glycosides on the regeneration of rhodopsin [J].
Matsumoto, H ;
Nakamura, Y ;
Tachibanaki, S ;
Kawamura, S ;
Hirayama, M .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2003, 51 (12) :3560-3563