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DOI 10.1080/00016489.2026.2641822

Медицинская библиотека · Acta oto-laryngologica · 2026

The protective efficacy of rosmarinic acid in radiotherapy-induced ototoxicity.

Altıparmak Serkan, Özcan İbrahim, Kaya Altan, Aytekin Aynur, Karaman Hatice

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Аннотация

BACKGROUND

Radiotherapy-induced ototoxicity remains a significant clinical problem, and potential protective agents such as rosmarinic acid have gained increasing research interest.

OBJECTIVES

This study investigated the effectiveness of systemic and local rosmarinic acid administration in radiotherapy-induced ototoxicity using the auditory brainstem response (ABR), distortion product otoacoustic emission (DPOAE) test, and histopathological methods.

MATERIAL AND

METHODS

Sixty rats were included in the study. Seven groups were created, including control, radiotherapy-only, and combinations of radiotherapy with intratympanic or intraperitoneal rosmarinic acid, as well as a radiotherapy plus intratympanic saline group. ABR and DPOAE measurements were performed with all animals initially and at the end of the third week. The temporal bones of the decapitated rats were also fixed in formalin for histopathological measurements.

RESULTS

ABR thresholds increased significantly in the radiotherapy-only group (from 22.8 ± 3.1 to 45.4 ± 3.6 dB, p = 0.004) and the radiotherapy plus intratympanic saline group (from 24.6 ± 3.1 to 47.1 ± 3.6 dB, p = 0.005), while remaining stable in the other groups (p > 0.05). Correspondingly, DPOAE values decreased and histopathological damage scores were markedly higher in these two groups.

CONCLUSIONS AND SIGNIFICANCE: Rosmarinic acid protects against radiotherapy-induced ototoxicity when applied both systemically and locally, as confirmed by histopathological examination and objective audiological methods.

Для цитирования: Altıparmak Serkan, Özcan İbrahim, Kaya Altan, Aytekin Aynur, Karaman Hatice. The protective efficacy of rosmarinic acid in radiotherapy-induced ototoxicity.. Acta oto-laryngologica. 2026. DOI: 10.1080/00016489.2026.2641822.

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