Journals / Cukurova Medical Journal / 2019 / Cilt: 44 - Sayı: 2

Efficacy of adrenomedullin on cisplatin ototoxicity in rats

Ratlarda cisplatin ototoksisitesinde adrenomedüllinin etkinliği

Pages
642–652
Publication Date
2019-06-30
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In the Distortion product-evoked otoacoustic emission (DPOAE) measurements, the between-day differences at 16000 frequency in the cisplatin + intraperitoneal adrenomedullin group were accepted as statistically significantConclusion: Adrenomedullin, which is a strong vasodilator and antioxidant, was found to have a protective effect against cisplatin ototoxicity in the cochlea.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Purpose: The aim of this study was to evaluate the efficacy of adrenomedullin on damage associated with cisplatin ototoxicity created in an experimental animal model.Materials and Methods: A total of 32 Wistar Albino rats were separated into 4 groups of 8.
📊
Key Findings & Data:To the rats in Group 1 (control), 1% acetic acid was administered intraperitoneally and intratympanically, to Group 2, cisplatin (10mg/kg/2 days) + intratympanic acetic acid, to Group 3, cisplatin + intraperitoneal adrenomedullin (12 µg/kg) and to Group 4, cisplatin +0.1- 0.3ml intratympanic adrenomedullin (12 µg/kg).
💡
Conclusion & Impact:In the Distortion product-evoked otoacoustic emission (DPOAE) measurements, the between-day differences at 16000 frequency in the cisplatin + intraperitoneal adrenomedullin group were accepted as statistically significantConclusion: Adrenomedullin, which is a strong vasodilator and antioxidant, was found to have a protective effect against cisplatin ototoxicity in the cochlea.
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:Adrenomedüllin · cisplatin · kohlea

Abstract

Purpose: The aim of this study was to evaluate the efficacy of adrenomedullin on damage associated with cisplatin ototoxicity created in an experimental animal model.Materials and Methods: A total of 32 Wistar Albino rats were separated into 4 groups of 8. To the rats in Group 1 (control), 1% acetic acid was administered intraperitoneally and intratympanically, to Group 2, cisplatin (10mg/kg/2 days) + intratympanic acetic acid, to Group 3, cisplatin + intraperitoneal adrenomedullin (12 µg/kg) and to Group 4, cisplatin +0.1- 0.3ml intratympanic adrenomedullin (12 µg/kg). The drugs were administered on the first 5 days and signal-to-noise ratio (SNR) measurements of the auditory brainstem response (ABR) and distortion product otoacoustic emissions (DPOAE) were made on days 0, 5 and 15. The rats were sacrificed and serum and ear tissue samples were taken for histopathological examination and examination of oxidative stress levels.Results: A statistically significant difference was determined in the cisplatin+intratympanic adrenomedullin group in the Auditory brain-stem response (ABR) measurements on days 0, 5 and 15 . In the Distortion product-evoked otoacoustic emission (DPOAE) measurements, the between-day differences at 16000 frequency in the cisplatin + intraperitoneal adrenomedullin group were accepted as statistically significantConclusion: Adrenomedullin, which is a strong vasodilator and antioxidant, was found to have a protective effect against cisplatin ototoxicity in the cochlea.

Özet

Amaç: Bu çalışmanın amacı daha önce hiç çalışılmamış olan adrenomedüllinin deneysel hayvan modelinde oluşturulan cisplatin ototoksisitesine bağlı hasarı üzerindeki etkinliğini değerlendirmektir. Gereç ve Yöntem: 32 wistar albino rat 4 gruba ayrıldı. Grup 1 kontrol grubu intraperitoneal ve intratimpanik %1 asedik asit verilen, grup 2 cisplatin (10 mg/kg/ 2 gün)+ intratimpanik asedik asit verilen, grup 3 cisplatin + intraperitoneal adrenomedüllin (12mikrogr/kg) verilen, grup 4 cisplatin + 0,1-0,3 ml intratimpanik (12mikrogr/kg) adrenomedüllin verilen grup olarak her bir grupta rastgele 8 rat olacak şekilde düzenlendi. İlk 5 gün ilaç uygulamaları yapıldı. ABR ve DPOAE deki sinyal gürültü oranları (SNR) 0. 5. ve 15. gün ölçümleri yapıldı. Ratlar sakrifiye edildi, histopatolojik inceleme, serum ve kulak doku örneklerinde oksidatif stres düzeyleri çalışıldı. Bulgular: İşitsel uyarılmış beyinsapı potansiyelleri (ABR) ölçümlerinde C+IT ADM grubunun 0. gün 5. gün ve 15. gün değerleri arasındaki farklılık istatistiksel olarak anlamlı olarak değerlendirilmiştir. Distorsiyon ürünü otoakustik emisyon (DPOAE) ölçümlerine göre 16000 hz frekanstaki cisplatin + intraperitoneal adrenomedüllin grubundaki günler arasındaki farklılık istatistiksel olarak anlamlı olarak kabul edilmiştir Sonuç: Güçlü bir vazodilatattör ve antioksidan olan adrenomedüllinin cisplatin ototoksisistesinde kokleayı koruyucu etkisinin olduğu bulundu.

🔖

Cite This Article

BİLAL, N., KURUTAŞ, E. B., BAHAR, A. Y., BİLAL, B., SARICA, S., ORHAN, İ., DOĞANER, A., GÜNGÖR, M. (2019). Efficacy of adrenomedullin on cisplatin ototoxicity in rats. Cukurova Medical Journal, Cilt: 44 - Sayı: 2, 642–652. https://ajindex.com/articles/56459

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (14)

  1. Rabik CA, Dolan ME, Molecular mechanisms of resistance and toxicity associated with platinating agents, Cancer Treat Rev. 2007;33: 9–23
  2. Daldal A, Odabasi O, Serbetcioglu B, The protective effect of intratympanic dexamethasone on cisplatininduced ototoxicity in guinea pigs, Otolaryngol Head Neck Surg.2007;137:747-52
  3. Sockalingam R, Freeman S, Cherny TL, Sohmer H, Effect of high-dose cisplatin on auditory brainstem responses and otoacoustic emissions in laboratory animals, Am J Otol. 2000;21:521–27
  4. Kirisci M, Oktar GL, Ozogul C, Oyar EO, Akyol SN, Demirtas CY, Arslan M, Effect of adrenomedullin and vascular endothelial growth factor on ischemia/reperfusion injury in sceletal muscle in rats, J Surg Res. 2013;185:56-63
  5. Wimalawansa SJ, Amylin calcitonin gene-related peptide, calcitonin, and adrenomedullin: a peptide superfamily, Crit Rev Neurobiol. 1997;11:167–239
  6. Hinson JP, Kapas S, Smith DM, Adrenomedullin, a multifunctional regulatory peptide, Endocr Rev. 2000;21:138–67
  7. Nishikimi T, Kitamura K, Saito Y, Shimada K, Ishimitsu T, Takamiya M, Kangawa K, Matsuo H, Eto T, Omae T, Clinical studies on the sites of production and clearance of circulating adrenomedullin in human subjects, Hypertension. 1994;24:600–4. 8. de Freitas MR, de Castro Brito GA, de Carvalho JV Jr, Gomes RM Jr, Barreto Martins MJ, de Albuquerque Ribeiro R, Light microscopy study of cisplatin-induced ototoxicity in rats, J Laryngol Otol. 2009;123:590–7
  8. Fridovich I, Superoxide dismutase, Adv Enzymol. 1974;41:35-97
  9. Beutler E, Red Cell Metabolism: A Manual of Biochemical Methods, 3rd edn., New York, Grune and Stratton Inc. 1984
  10. Ohkawa H, Ohishi N, Tagi K, Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction, Anal Biochem. 1979;95:351-8
  11. Yoshimoto T, Fukai N, Sato R, Sugiyama T, Ozawa N, Shichiri M, Hirata Y, Antioxidant effect of adrenomedullin on angiotensin II-induced reactive oxygenspecies generation in vascular smooth muscle cells, Endocrinology. 2004;145:3331-7
  12. Shimosawa T, Shibagaki Y, Ishibashi K, Kitamura K, Kangawa K, Kato S, Ando K, Fujita T, Adrenomedullin, an endogenous peptide, counteracts cardiovascular damage, Circulation. 2002;105:106
  13. Bekmez Bilmez ZE, Aydin S, Sanli A, Altintoprak N, Demir MG, Atalay Erdoğan B, Kösemihal E, Oxytocin as a protective agent in cisplatin-induced ototoxicity, Cancer Chemother Pharmacol. 2016;77:875-9
  14. Yumusakhuylu AC, Yazici M, Sari M, Binnetoglu A, Kosemihal E, Akdas F, S