Journals / KBB-Forum / 2003 / Cilt: 2 - Sayı: 1

Aminoglikozit içeren kulak damlalarının neden olduğu ototoksisiteden bir spin trap'le (PBN) korunma: Kronik etkiler

Protection against aminoglycoside otic drop-induced ototoxicity by a spin trap (PBN): Chronic effects

Journal
KBB-Forum
Pages
17–23
DOI
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

Conclusion: These findings suggest that free radical mediated events are partially responsible for, and that DPOAEs are very sensitive to, AD induced chronic ototoxicity in guinea pigs.

📌 3 Key Takeaways

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Objective & Hypothesis:Objectives: To investigated the long-term spin trap protection against aminoglycoside otic drop-induced ototoxicity.
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Key Findings & Data:Material and Methods: We evaluated the ability of intraperitoneal α-phenyl-tert-butyl-nitrone (PBN) or 0.9% saline applications to reduce the chronic effects of topical aminoglycoside otic drops (AD) or artificial perilymph (PER) treatment on cochlear microphonic (CM), compound action potential (CAP) and 2F1-F2 distortion product otoacoustic emission (DPOAEs) sensitivities in three groups of guinea pigs. (n=5/group): a) saline+PER (controls), b) saline+AD and c) PBN+AD.
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Conclusion & Impact:Conclusion: These findings suggest that free radical mediated events are partially responsible for, and that DPOAEs are very sensitive to, AD induced chronic ototoxicity in guinea pigs.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Modeller · teorik · Polimiksin B

Abstract

Objectives: To investigated the long-term spin trap protection against aminoglycoside otic drop-induced ototoxicity. Material and Methods: We evaluated the ability of intraperitoneal &#945;-phenyl-tert-butyl-nitrone (PBN) or 0.9% saline applications to reduce the chronic effects of topical aminoglycoside otic drops (AD) or artificial perilymph (PER) treatment on cochlear microphonic (CM), compound action potential (CAP) and 2F1-F2 distortion product otoacoustic emission (DPOAEs) sensitivities in three groups of guinea pigs. (n=5/group): a) saline+PER (controls), b) saline+AD and c) PBN+AD. Results: Relative to control values, saline+AD group mean CM and CAP values were severely degraded at all frequencies (p<.05). PBN+AD group mean losses were significantly (p<.05) smaller than those of the saline+AD group for CAP and CM at 8, 12, 16 and 24 kHz, indicating that PBN provided protection against topical AD induced damage. Mean 2F1-F2 DPOAE values decreased to below background levels at all frequencies in groups receiving ADs, irrespective of PBN treatment. Conclusion: These findings suggest that free radical mediated events are partially responsible for, and that DPOAEs are very sensitive to, AD induced chronic ototoxicity in guinea pigs.

Özet

Amaç: Aminoglikozit içeren kulak damlalarının (AD) neden olduğu ototoksisitenin engellenmesinde spin trapl’erin uzun süreli koruyucu etkisini araştırmak. Yöntem ve Gereçler: Topikal aminoglikozid kulak damlaları (AD) ve yapay perilenf(PER) tedavisinin kohlear mikrofonik (CM), birleşik aksiyon potansiyeli (CAP) ve 2F1-F2 distorsiyon product otoakustik emisyon(DPOAE) sensitiviteleri üzerindeki kronik etkilerinin intraperitoneal α-phenyl-tert-butyl-nitrone (PBN) ve %0.9 NaCl (saline) uıygulaması ile azalıp azalmadığını 3 guinea pig grubu üzerinde araştırdık (n=5/grup):a)saline + PER;b)saline+AD; c) PBN +AD. Bulgular: Kontrol değerleriyle karşılaştırıldığında,saline+AD grubunun ortalama CM ve CAP değerleri bütün frekanslarda ileri derecede azalmıştı (p<.05). CAP ve CM için, PBN+AD grubundaki ortalama kayıplar saline+AD grubundan 8,12,16 ve 24 kHz’de belirgin olarak daha azdı, ve ve bu durum PBN’nin topikal AD’nin oluşturduğu hasarı önlediğini gösteriyordu. Bütün frekanslardaki ortalama 2F1-F2 DPOAE değerleri, AD alan bütün gruplarda PBN tedavisinden bağımsız olarak ilk değerlerinin altına indi. Sonuç: Bu bulgular, serbest radikaller aracılığıyla oluşan olayların guinea pig’lerde AD tarafından meydana getirilen ototoksisiteden kısmen sorumlu olduğunu ve DPOAE’lerin bu ototoksisiteye karşı çok duyarlı olduğunu desteklemektedir.

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Cite This Article

TUNCEL, Ü., AYGENÇ, E., CLERICI, W. (2003). Aminoglikozit içeren kulak damlalarının neden olduğu ototoksisiteden bir spin trap'le (PBN) korunma: Kronik etkiler. KBB-Forum, Cilt: 2 - Sayı: 1, 17–23. https://ajindex.com/articles/209396

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References (16)

  1. Meyerhoff WL, Morzono T, Shaddock LC, Wright CG, Shea DA, Sikora MA. Tympanostomy tubes and otic drops. Laryngoscope 1983
  2. [ Abstract ] 2) Morzano T. Toxicity of ototopical drugs: animal modeling. Ann Otol Rhinol Laryngol 1990
  3. [ Abstract ] 3) Roland PS. Clinical ototoxicity of topical antibiotic drops. Otolaryngol Head Neck Surg 1994
  4. [ Abstract ] 4) Lundy LB, Graham MD. Ototoxicity and ototopical medications: a survery of otolaryngologists. Am J Otol 1993
  5. [ Abstract ] 5) Barlow DW, Duckert LG, Kreig CS, Gates GA. Ototoxicity of topical otomicrobial agents. Acta Otolaryngol ( Stockh) 1995
  6. [ Abstract ] 6) Ravi R, Somani SM, Rybak LP. Mechanism of cisplatin ototoxicity: Antioxidant system. Pharmacol Toxicol 1995
  7. [ Abstract ] 7) Garetz SL, Altschuler RA, Schacht J. Attenuation of gentamicin ototoxicity by glutathione in the guinea pig in vivo. Hear Res 1994
  8. [ Abstract ] 8) Garetz SL, Rhee DJ, Schacht J. Sulfhydryl compounds and antioxidants inhibit cytotoxicity to outer hair cells of a gentamicin metabolite in vitro. Hear Res 1994
  9. [ Abstract ] 9) Clerici WJ, Hensley K, DiMartino DL, Butterfield DA. Direct detection of ototoxicant-induced reactive oxygen species generation in cochlear explants. Hear Res 1996
  10. [ Abstract ] 10) Tuncel U, Clerici WJ, Jones RO. Differential ototoxicities induced by lead acetate and tetraethyl lead. Hear Res 2002
  11. [ Abstract ] 11) Clerici WJ, DiMartino DL, Prasad MR. Direct effects of reactive oxygen species on cochlear outer hair cell shape in vitro. Hear Res 1995
  12. [ Abstract ] 12) Clerici WJ, Yang L. Direct effects of intraperilymphatic reactive oxygen generation on cochlear potentials. Hear Res 1996
  13. [ Abstract ] 13) Clerici WJ, Hensley K, DiMartino DL, Butterfield DA. Direct determination of reactive oxygen species generation by ototoxicants using electron paramagnetic resonance spectroscopy. Assoc Res Otolaryngol abstr. 1995
  14. Carney JM, Floyd RA. Protection against oxidative damage to CNS by á- phenyl-tert-butyl-nitrone (PBN) and other spin-trapping agents: a novel series of nonlipid free radical scavengers. J Mol Neurosci 1991
  15. [ Abstract ] 15) Hester TO, Jones, RO, Clerici WJ. Protection against aminoglycoside otic drop-induced ototoxicity by a spin trap (PBN): I. Acute effects. Otolaryngol Head Neck Surg 1998
  16. [ Abstract ] 16) Ikeda K, Morizono T, Juhn SK