Literature DB >> 23001434

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

Gökçe Simşek1, Sibel Alicura Tokgoz, Erkan Vuralkan, Murat Caliskan, Omer Besalti, Istemihan Akin.   

Abstract

Cisplatin is a common chemotherapeutic agent used in many solid and hematologic malignancies. The main unwanted effect of cisplatin is ototoxicity, for which no standard treatment has been reported. The present study examined the protective efficacy of resveratrol on cisplatin-dependent ototoxicity through an experimental model. Fifteen rats were randomized into three groups. Group 1 (control group) (n = 5) received intraperitoneal (i.p.) 15 mg/kg cisplatin; group 2 (resveratrol group) (n = 5) received i.p. 100 mg/kg resveratrol, followed by i.p. 15 mg/kg cisplatin; group 3 (n = 5) served as a vehicle group and received i.p. 1 ml dimethyl sulfoxide. All rats underwent the auditory brainstem response (ABR) test before and 72 h after the treatment. Pretreatment ABR values of the groups were not significantly different. The pretreatment hearing threshold values of the groups were 30 ± 6.60 and 28.5 ± 5.29 dB in groups 1 and 2, respectively (p > 0.05). The post-ABR-I and post-ABR-IV values were, respectively, 1.41 ± 0.18 and 5.83 ± 0.16 ms in the control subjects and 1.19 ± 0.22 and 4.58 ± 0.27 ms in the study group. The ABR-I and ABR-IV durations in rats treated with resveratrol were significantly shorter (p < 0.01). A comparison of threshold values shows that the resveratrol-treated rats had significantly lower values than the control rats. After cisplatin injection, ABR I-IV intervals were compared among the groups. The ABR I-IV interval duration was 4.42 ± 0.16 ms in the control group, while the resveratrol-treated rats showed a significantly shorter ABR I-IV interval duration of 3.49 ± 0.27 ms (p < 0.001). Resveratrol attenuated cisplatin-dependent inner-ear damage, as shown by the ABR-I, ABR-IV, ABR I-IV interval, and hearing threshold values. Our results suggest that this natural antioxidant may be effectively used in reducing the unwanted effects of cisplatin on the ear physiology of patients, particularly those undergoing chemotherapy.

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Year:  2012        PMID: 23001434     DOI: 10.1007/s00405-012-2183-4

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


  21 in total

1.  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

2.  The electroreceptor organ of the catfish, Ictalurus melas, as a model for cisplatin-induced ototoxicity.

Authors:  R C Peters; P M Mommersteeg; P S Heijmen
Journal:  Neuroscience       Date:  1999       Impact factor: 3.590

3.  L-n-acetyl-cysteine protection against cisplatin-induced auditory neuronal and hair cell toxicity.

Authors:  J G Feghali; W Liu; T R Van De Water
Journal:  Laryngoscope       Date:  2001-07       Impact factor: 3.325

4.  Application of antioxidants and other agents to prevent cisplatin ototoxicity.

Authors:  L P Rybak; C Whitworth; S Somani
Journal:  Laryngoscope       Date:  1999-11       Impact factor: 3.325

5.  Effects of cadmium on the hearing system.

Authors:  H U Ozcaglar; B Agirdir; O Dinc; M Turhan; S Kilinçarslan; G Oner
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6.  Effect of protective agents against cisplatin ototoxicity.

Authors:  L P Rybak; K Husain; C Morris; C Whitworth; S Somani
Journal:  Am J Otol       Date:  2000-07

Review 7.  Oxidative stress and protective effects of polyphenols: comparative studies in human and rodent kidney. A review.

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8.  Mechanism of cisplatin ototoxicity: antioxidant system.

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

9.  The effects of L-carnitine on presbyacusis in the rat model.

Authors:  A Derin; B Agirdir; N Derin; O Dinç; K Güney; H Ozcaglar; S Kilinçarslan
Journal:  Clin Otolaryngol Allied Sci       Date:  2004-06

10.  Skin toxicity from external beam radiation therapy in breast cancer patients: protective effects of Resveratrol, Lycopene, Vitamin C and anthocianin (Ixor®).

Authors:  Rossella Di Franco; MariaGrazia Calvanese; Paola Murino; Roberto Manzo; Cesare Guida; Davide Di Gennaro; Caterina Anania; Vincenzo Ravo
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  10 in total

Review 1.  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

2.  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

Review 3.  Effect of intratympanic dimethyl sulphoxide (DMSO) in an in vivo model of cisplatin-related ototoxicity.

Authors:  A Roldán-Fidalgo; A Trinidad; A Rodríguez-Valiente; J R García-Berrocal; I Millán; M J Coronado; R Ramírez-Camacho
Journal:  Eur Arch Otorhinolaryngol       Date:  2014-03-08       Impact factor: 2.503

Review 4.  New treatment options for hearing loss.

Authors:  Ulrich Müller; Peter G Barr-Gillespie
Journal:  Nat Rev Drug Discov       Date:  2015-03-20       Impact factor: 84.694

5.  Effects of Spirulina on the functions and redox status of auditory system in senescence-accelerated prone-8 mice.

Authors:  Yin-Ching Chan; Juen-Haur Hwang
Journal:  PLoS One       Date:  2017-06-21       Impact factor: 3.240

6.  Polydatin activates the Nrf2/HO-1 signaling pathway to protect cisplatin-induced hearing loss in guinea pigs.

Authors:  Dafei Li; Haiyan Zhao; Piao Xu; Qiongping Lin; Tingting Zhao; Chubing Li; Zhong-Kai Cui; Guangyong Tian
Journal:  Front Pharmacol       Date:  2022-08-04       Impact factor: 5.988

7.  Protective effect of creatine on amikacin-induced ototoxicity.

Authors:  Emre Apaydın; Elif Dağlı; Sevinç Bayrak; Ekrem Said Kankılıç; Hasan Şahin; Aydın Acar
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8.  Inhibitory effects of epigenetic modulators and differentiation inducers on human medulloblastoma cell lines.

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Journal:  J Exp Clin Cancer Res       Date:  2013-05-14

9.  Enhanced inhibition of clonogenic survival of human medulloblastoma cells by multimodal treatment with ionizing irradiation, epigenetic modifiers, and differentiation-inducing drugs.

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10.  Resveratrol enhances cisplatin-induced apoptosis in human hepatoma cells via glutamine metabolism inhibition.

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Journal:  BMB Rep       Date:  2018-09       Impact factor: 4.778

  10 in total

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