Protective Effect of Spirulina on Cisplatin-Induced Ototoxicity: A Functional and Histopathological Study

被引:1
作者
Tahir, Emel [1 ]
Buyuklu, Adnan Fuat [2 ]
Ocal, Fatma Ceyda Akin [3 ]
Gurgen, Seren Gulsen [4 ]
Sarsmaz, Hayrunnisa Yesil [5 ]
机构
[1] Ondokuz Mayis Univ, Dept Otorhinolaryngol, Sch Med, Samsun, Turkey
[2] Baskent Univ, Dept Otorhinolaryngol, Fac Med, Ankara, Turkey
[3] Univ Hlth Sci, Gulhane Traning & Res Hosp, Dept Otorhinolaryngol, Ankara, Turkey
[4] Celal Bayar Univ, Sch Vocat Hlth Serv, Dept Histol & Embryol, Manisa, Turkey
[5] Celal Bayar Univ, Fac Hlth Sci, Dept Histol & Embryol, Manisa, Turkey
关键词
cisplatin; ototoxicity; spirulina; antioxidants; hearing loss; auditory brain stem evoked responses; distortion product otoacoustic emissions; apoptosis; COCHLEA; HEARING;
D O I
10.5152/B-ENT.2022.21666
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective: The purpose of this study was to evaluate the protective effect of an antioxidant and anti-inflammatory agent, "spirulina," against cisplatin-induced ototoxicity in rats. Methods: Twenty-eight adult Sprague-Dawley rats were divided into 4 groups. Before drug administration, distortion product otoacoustic emission and auditory brainstem response tests were performed. Group 1 (n =7) received 1 mg of intraperitoneal saline. Group 2 (n=7) received a single dose of intraperitoneal cisplatin at 15 mg/kg/day. Group 3 (n=7) received oral spirulina at 1000 mg/kg/day for 10 days. Group 4 (n=7) received a single i.p. dose of cisplatin at 15 mg/kg/day, followed by 10 days of oral spirulina at 1000 mg/kg/day. The final distortion product otoacoustic emission and auditory brainstem response measurements were provided 10 days after the initial drug administration. Cochleas were removed, the histochemical examination was performed by caspase-3, caspase-9, and terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling methods. Results: Initially, there were no significant differences in distortion product otoacoustic emission and auditory brainstem response measurements between groups. Following cisplatin treatment, the mean difference in signal to noise ratio values was lower in the cisplatin + spirulina group compared to the cisplatin-only group. The increase in auditory brainstem response thresholds was more significant in the cisplatin-only group than in the cisplatin + spirulina group. Posttreatment auditory brainstem response latencies were prolonged in cisplatin and cisplatin + spirulina groups; however, a significant difference was obtained between these 2 groups. The cisplatin + spirulina group had a lower density of apoptotic cells than the cisplatin-only group. Conclusion: Spirulina has no adverse effects on cochlear functions and may provide some protection against cisplatin-induced ototoxicity.
引用
收藏
页码:34 / 43
页数:10
相关论文
共 36 条
  • [11] Evaluation of amifostine for protection against cisplatin-induced serious hearing loss in children treated for average-risk or high-risk medulloblastoma
    Gurney, James G.
    Bass, Johnnie K.
    Onar-Thomas, Arzu
    Huang, Jie
    Chintagumpala, Murali
    Bouffet, Eric
    Hassall, Tim
    Gururangan, Sridharan
    Heath, John A.
    Kellie, Stewart
    Cohn, Richard
    Fisher, Michael J.
    Panandiker, Atmaram Pai
    Merchant, Thomas E.
    Srinivasan, Ashok
    Wetmore, Cynthia
    Qaddoumi, Ibrahim
    Stewart, Clinton F.
    Armstrong, Gregory T.
    Broniscer, Alberto
    Gajjar, Amar
    [J]. NEURO-ONCOLOGY, 2014, 16 (06) : 848 - 855
  • [12] Vitamin E reduces cisplatin ototoxicity
    Kalkanis, JG
    Whitworth, C
    Rybak, LP
    [J]. LARYNGOSCOPE, 2004, 114 (03) : 538 - 542
  • [13] The protective effect of metformin against the noise-induced hearing loss
    Kesici, Guelin Gokcen
    Ocal, Fatma Ceyda Akin
    Gurgen, Seren Gulsen
    Erdem, Saban Remzi
    Ogus, Ersin
    Erbek, Hatice Seyra
    Ozluoglu, Levent Naci
    [J]. EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY, 2018, 275 (12) : 2957 - 2966
  • [14] C-phycocyanin from Limnothrix Species KNUA002 Alleviates Cisplatin-Induced Ototoxicity by Blocking the Mitochondrial Apoptotic Pathway in Auditory Cells
    Kim, Ye-Ri
    Do, Jeong-Mi
    Kim, Kyung Hee
    Stoica, Alexandra R.
    Jo, Seung-Woo
    Kim, Un-Kyung
    Yoon, Ho-Sung
    [J]. MARINE DRUGS, 2019, 17 (04):
  • [15] Investigation of Astaxanthin Effect on Cisplatin Ototoxicity in Rats by Using Otoacoustic Emission, Total Antioxidant Capacity, and Histopathological Methods
    Kinal, M. Emrah
    Tatlipinar, Arzu
    Uzun, Selami
    Keskin, Serhan
    Tekdemir, Emrah
    Ozbeyli, Dilek
    Akakin, Dilek
    [J]. ENT-EAR NOSE & THROAT JOURNAL, 2021, 100 (04) : NP198 - NP205
  • [16] Caffeic acid phenethyl ester ameliorated ototoxicity induced by cisplatin in rats
    Kizilay, A
    Kalcioglu, MT
    Ozerol, E
    Iraz, M
    Gulec, M
    Akyol, O
    Ozturan, O
    [J]. JOURNAL OF CHEMOTHERAPY, 2004, 16 (04) : 381 - 387
  • [17] Protection against cisplatin-induced nephrotoxicity by Spirulina in rats
    Krishna Mohan, Iyyapu
    Khan, Mahmood
    Chandra Shobha, Jagdish
    Umamaheswara Rao Naidu, Madireddy
    Prayag, Aruna
    Kuppusamy, Periannan
    Kumar Kutala, Vijay
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2006, 58 (06) : 802 - 808
  • [18] Renoprotective effect of Spirulina fusiformis on cisplatin-induced oxidative stress and renal dysfunction in rats
    Kuhad, Anurag
    Tirkey, Naveen
    Pilkhwal, Sangeeta
    Chopra, Kanwaljit
    [J]. RENAL FAILURE, 2006, 28 (03) : 247 - 254
  • [19] Protective Effect of Water Extracted Spirulina maxima on Glutamate-induced Neuronal Cell Death in Mouse Hippocampal HT22 Cell
    Lee, Hyeon Yong
    Ryu, Ga Hee
    Choi, Woon Yong
    Yang, Woo Seung
    Lee, Hyeon Woo
    Ma, Choong Je
    [J]. PHARMACOGNOSY MAGAZINE, 2018, 14 (54) : 242 - 247
  • [20] Salicylate protects hearing and kidney function from cisplatin toxicity without compromising its oncolytic action
    Li, GM
    Sha, SH
    Zotova, E
    Arezzo, J
    Van de Water, T
    Schacht, J
    [J]. LABORATORY INVESTIGATION, 2002, 82 (05) : 585 - 596