Literature DB >> 22186767

The effect of resveratrol on the prevention of cisplatin ototoxicity.

T Erdem1, Tuba Bayindir, A Filiz, M Iraz, E Selimoglu.   

Abstract

One of the most important adverse effects of cisplatin, a chemotherapeutic agent which is widely used in the treatment of cancer patients, is hearing loss. This has primarily been associated with the loss of inner ear hairy and spiral ganglion cells due to oxidative stress. Resveratrol is known to be an antioxidant agent, which has the theoretical potential of preventing cisplatin-related ototoxicity. This experimental study was approved by Animal Ethics Committee of Inonu University (2008-20) and supported by Inonu University Scientific Research Projects Support Fund (2009-17). Thirty-four 3-month-old Wistar albino female rats weighing 210-270 g were used in the study. The animals were allocated into four groups: in cisplatin group (Group A), a single dose of 12 mg/kg cisplatin was administered intraperitoneally to 10 rats; in cisplatin + resveratrol group (Group B), a single dose of 12 mg/kg cisplatin and 10 mg/kg resveratrol were administered intraperitoneally for 5 days to 10 rats; in resveratrol group (Group C), 10 mg/kg resveratrol was administered intraperitoneally for 5 days to seven rats and in control group (Group D), resveratrol solvent (5% alcohol-95% physiological saline) was administered intraperitoneally for 5 days to seven rats. Resveratrol administration has begun 1 day before cisplatin administration in the group treated with cisplatin and resveratrol combination. Distortion product otoacoustic emission (DPOAE) (Grason Stadler, Madison, USA) measurements were performed in the same ear of all rats (right ear) under general anesthesia at baseline, 1st and 5th days after drug administration. Statistically significant distortion product amplitude reductions were found in the cisplatin group at 1,418, 2,003, 3,363, 5,660, 8,003 and 9,515 Hz frequencies. Whereas in the cisplatin + resveratrol group, statistically significant difference was found between 1st and 5th day measurements only at 3,996 Hz frequency. No significant differences were noted between the measurements either in the resveratrol or in the control groups. According to these results, cisplatin-related ototoxicity has been greatly prevented by resveratrol use.

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Year:  2011        PMID: 22186767     DOI: 10.1007/s00405-011-1883-5

Source DB:  PubMed          Journal:  Eur Arch Otorhinolaryngol        ISSN: 0937-4477            Impact factor:   2.503


  22 in total

1.  Acute changes in cochlear potentials due to cisplatin.

Authors:  N Tsukasaki; C A Whitworth; L P Rybak
Journal:  Hear Res       Date:  2000-11       Impact factor: 3.208

2.  Cisplatin ototoxicity: involvement of iron and enhanced formation of superoxide anion radicals.

Authors:  N Dehne; J Lautermann; F Petrat; U Rauen; H de Groot
Journal:  Toxicol Appl Pharmacol       Date:  2001-07-01       Impact factor: 4.219

3.  Direct detection of ototoxicant-induced reactive oxygen species generation in cochlear explants.

Authors:  W J Clerici; K Hensley; D L DiMartino; D A Butterfield
Journal:  Hear Res       Date:  1996-09-01       Impact factor: 3.208

4.  Use of organotypic cultures of Corti's organ to study the protective effects of antioxidant molecules on cisplatin-induced damage of auditory hair cells.

Authors:  R D Kopke; W Liu; R Gabaizadeh; A Jacono; J Feghali; D Spray; P Garcia; H Steinman; B Malgrange; R J Ruben; L Rybak; T R Van de Water
Journal:  Am J Otol       Date:  1997-09

5.  The cochlear targets of cisplatin: an electrophysiological and morphological time-sequence study.

Authors:  Marjolein W M van Ruijven; John C M J de Groot; Sjaak F L Klis; Guido F Smoorenburg
Journal:  Hear Res       Date:  2005-07       Impact factor: 3.208

6.  Reversible cisplatin ototoxicity in the albino guinea pig.

Authors:  S F Klis; S J O'Leary; F P Hamers; J C De Groot; G F Smoorenburg
Journal:  Neuroreport       Date:  2000-02-28       Impact factor: 1.837

7.  Mechanism of cisplatin ototoxicity: antioxidant system.

Authors:  R Ravi; S M Somani; L P Rybak
Journal:  Pharmacol Toxicol       Date:  1995-06

8.  Direct effects of reactive oxygen species on cochlear outer hair cell shape in vitro.

Authors:  W J Clerici; D L DiMartino; M R Prasad
Journal:  Hear Res       Date:  1995-04       Impact factor: 3.208

9.  Ginkgo biloba extract (EGb 761) protects against cisplatin-induced ototoxicity in rats.

Authors:  Xinyan Huang; Craig A Whitworth; Leonard P Rybak
Journal:  Otol Neurotol       Date:  2007-09       Impact factor: 2.311

Review 10.  Comparative adverse effect profiles of platinum drugs.

Authors:  M J McKeage
Journal:  Drug Saf       Date:  1995-10       Impact factor: 5.606

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  18 in total

1.  Protective role of misoprostol against cisplatin-induced ototoxicity.

Authors:  Murat Doğan; Halil Polat; Mehmet Yaşar; Altan Kaya; Ali Bayram; Fatma Şenel; İbrahim Özcan
Journal:  Eur Arch Otorhinolaryngol       Date:  2016-04-06       Impact factor: 2.503

Review 2.  Innovative pharmaceutical approaches for the management of inner ear disorders.

Authors:  Umberto M Musazzi; Silvia Franzé; Francesco Cilurzo
Journal:  Drug Deliv Transl Res       Date:  2018-04       Impact factor: 4.617

3.  Comparison of the protective efficacy between intratympanic dexamethasone and resveratrol treatments against cisplatin-induced ototoxicity: an experimental study.

Authors:  Gökçe Simsek; Burak Mustafa Taş; Nuray Bayar Muluk; Musa Azman; Rahmi Kılıç
Journal:  Eur Arch Otorhinolaryngol       Date:  2019-09-17       Impact factor: 2.503

4.  The Protective Effect of Chrysin Against Cisplatin İnduced Ototoxicity in Rats.

Authors:  Mehmet Kelles; Mehmet Tan; M Tayyar Kalcioglu; Yuksel Toplu; Nazire Bulam
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  2013-11-28

5.  Protective effect of thymoquinone against cisplatin-induced ototoxicity.

Authors:  Mustafa Sagit; Ferhat Korkmaz; Alper Akcadag; Mehmet Akıf Somdas
Journal:  Eur Arch Otorhinolaryngol       Date:  2012-11-17       Impact factor: 2.503

6.  Protective role of bilberry extract against Cisplatin induced ototoxicity in rats.

Authors:  Zeliha Kapusuz; Mahmut Ozkırış; Mehtap Kala; Levent Saydam
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  2013-03-20

7.  Protective effects of resveratrol on cisplatin-dependent inner-ear damage in rats.

Authors:  Gökçe Simşek; Sibel Alicura Tokgoz; Erkan Vuralkan; Murat Caliskan; Omer Besalti; Istemihan Akin
Journal:  Eur Arch Otorhinolaryngol       Date:  2012-09-22       Impact factor: 2.503

8.  The protective role of molsidomine on the Cisplatin-induced ototoxicity.

Authors:  Yuksel Toplu; Hakan Parlakpinar; Emrah Sapmaz; Erkan Karatas; Alaattin Polat; Ahmet Kizilay
Journal:  Indian J Otolaryngol Head Neck Surg       Date:  2014-04-02

9.  Grape seed extract and resveratrol prevent 4-nitroquinoline 1-oxide induced oral tumorigenesis in mice by modulating AMPK activation and associated biological responses.

Authors:  Sangeeta Shrotriya; Alpna Tyagi; Gagan Deep; David J Orlicky; Joshua Wisell; Xiao-Jing Wang; Robert A Sclafani; Rajesh Agarwal; Chapla Agarwal
Journal:  Mol Carcinog       Date:  2013-11-14       Impact factor: 4.784

10.  Resveratrol attenuates CoCl2-induced cochlear hair cell damage through upregulation of Sirtuin1 and NF-κB deacetylation.

Authors:  Ping Wang; Bo Du; Wanzhong Yin; Xinrui Wang; Wei Zhu
Journal:  PLoS One       Date:  2013-11-21       Impact factor: 3.240

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