4.5 Article

Radioprotective effect of melatonin against radiotherapy-induced cerebral cortex and cerebellum damage in rat

Journal

INTERNATIONAL JOURNAL OF RADIATION BIOLOGY
Volume 97, Issue 3, Pages 348-355

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/09553002.2021.1864047

Keywords

Radiotherapy; flattening filter free; melatonin; brain; histopathology; biochemistry

Funding

  1. Scientific Research Projects Grants Unit, University of Health Sciences Turkey, Istanbul, Turkey [2019/055]

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The study shows that melatonin has a radioprotective effect against early brain damage caused by different dose rate beams, improving histopathological and biochemical parameters. However, there is no significant difference between low and high dose rate beams in terms of their effects on the brain. Further studies are needed to clarify the radiobiological uncertainties of different dose rates on various tissues.
Purpose The present study aims to investigate the radioprotective effect of melatonin (MEL) against early period brain damage caused by different dose rate beams in the experimental rat model. Materials and methods Forty-eight Sprague Dawley rats were randomly divided into six groups; the control, only melatonin, low dose rate-radiotherapy (LDR-RT), high dose rate-radiotherapy (HDR-RT) groups and (LDR-RT) + MEL and (HDR-RT) + MEL radiotherapy plus melatonin groups. Each rat administered melatonin was given a dose of 10 mg/kg through intraperitoneal injection, 15 minutes before radiation exposure. The head and neck region of each rat in only radiotherapy and radiotherapy plus melatonin groups was irradiated with a single dose of 16 Gy in LDR-RT and HDR-RT beams. Rats in all groups were examined for histopathology and biochemistry analysis 10 days after radiotherapy. Results Comparing the findings for LDR-RT and HDR-RT only radiotherapy groups and the control group, there was a statistically significant difference in histopathological and biochemical parameters, however, melatonin administered in radiotherapy plus melatonin groups contributed improving these parameters (p < .05). There was no statistically significant difference between LDR-RT and HDR-RT beams (p > .05). Conclusions It was concluded that melatonin applied before LDR-RT and HDR-RT radiotherapy protected early period radiotherapy-induced brain damage. The effects of clinically low and high dose beams on the cerebral cortex and cerebellum were investigated histopathologically for the first time. HDR beams can be safely applied in brain radiotherapy. However, more experimental rat and clinical studies are needed to explain the radiobiological uncertainties about the clinic dose rate on different cancerous and healthy tissues.

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