In vitro and in vivo effects of lutein against cisplatin-induced ototoxicity

被引:16
|
作者
Roldan-Fidalgo, A. [1 ]
Martin Saldana, S. [2 ]
Trinidad, A. [1 ]
Olmedilla-Alonso, B. [3 ]
Rodriguez-Valiente, A. [1 ]
Garcia-Berrocal, J. R. [1 ]
Ramirez-Camacho, R. [1 ]
机构
[1] Univ Autonoma Madrid, Dept Otorhinolaryngol, Hosp Puerta de Hierro Majadahonda, Madrid, Spain
[2] Puerta de Hierro Hosp, Fdn Biomed Res, Madrid, Spain
[3] CSIC, Inst Food Sci Technol & Nutr, Madrid, Spain
关键词
Cisplatin; Lutein; Ototoxicity; HEI-OC1; Rat; OXIDATIVE STRESS; MACULAR PIGMENT; CAROTENOIDS; EXPRESSION; ZEAXANTHIN; DISEASE; MODEL;
D O I
10.1016/j.etp.2016.01.003
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Introduction: Cisplatin is a commonly prescribed drug that produces ototoxicity as a side effect. Lutein is a carotenoid with antioxidant and anti-inflammatory properties previously tested for eye, heart and skin diseases but not evaluated to date in ear diseases. Aim: To evaluate the protective effects of lutein on HEI-OC1 auditory cell line and in a Wistar rat model of cisplatin ototoxicity. Materials and Methods: In vitro study: Culture HEI-OC1 cells were exposed to lutein (2.5-100 mu M) and to 25 mu M cisplatin for 24 h. In vivo study: Twenty eight female Wistar rats were randomized into three groups. Group A (n = 8) received intratympanic lutein (0.03 mL) (1 mg/mL) in the right ear and saline solution in the left one to determine the toxicity of lutein. Group B (n = 8) received also intraperitoneal cisplatin (10 mg/kg) to test the efficacy of lutein against cisplatin ototoxicity. Group C (n = 12) received intratympanic lutein (0.03 mL) (1 mg/mL) to quantify lutein in cochlear fluids (30 min, 1 h and 5 days after treatment). Hearing function was evaluated by means of Auditory Steady-State Responses before the procedure and 5 days after (groups A and B). Morphological changes were studied by. confocal laser scanning microscopy. Results: In vitro study: Lutein significantly reduced the cisplatin-induced cytotoxicity in the HEI-OC1 cells when they were pre-treated with lutein concentrations of 60 and 80 mu M. In vivo study: Intratympanic lutein (1 mg/mL) application showed no ototoxic effects. However it did not achieve protective effect against cisplatin-induced ototoxicity in Wistar rats. Conclusions: Although lutein has shown beneficial effects in other pathologies, the present study only obtained protection against cisplatin ototoxicity in culture cells, but not in the in vivo model. The large molecule size, the low dose administered, and restriction to diffusion in the inner ear could account for this negative result. (C) 2016 Elsevier GmbH. All rights reserved.
引用
收藏
页码:197 / 204
页数:8
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