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Published on: March 16, 2018
The protective effect of intraperitoneal medical ozone preconditioning and treatment on hepatotoxicity induced by
Arif Aslaner1, Tuğrul Çakır1, Betül Çelik2
1Department of General Surgery, Antalya Education and Research Hospital Antalya, Turkey.
Abstract:
The aim of this study is to determine the effects of medical ozone preconditioning and treatment on the methotrexate acute induced hepatotoxicity in rats that has not reports elsewhere. Eighteen rats were randomly assigned into three equal groups; control, Mtx and Mtx with ozone. Hepatotoxicity was performed with a single dose of 20 mg/kg Mtx to group 2 and group 3 at the fifteenth day. The medical ozone preconditioning was administered intraperitonealy in group 3 for fifteen days and more five days after inducing Mtx. The other rats of the group 1 and 2 received saline injection. At the twentyfirst day the blood and the liver tissue samples were obtained to measure the levels of liver enzymes ALT and AST, proinflamatory cytokines TNF-α, IL-1β, malondialdehyde, glutathione and myeloperoxidase. And the histolopatological examination was evaluated for injury score. In our study Mtx administration caused a significant increase on the liver enzymes ALT and AST, the tissue MDA and MPO activity and significant decrease in the tissue GSH. Moreover the both pro-inflammatory cytokines were significantly increased in the Mtx group. Medical ozone preconditioning and treatment reversed all these biochemical parameters and histopathological changes of the hepatotoxicity induced by Mtx. We conclude that medical ozone ameliorates Mtx induced hepatotoxicity in rats.
Insights
Medical ozone effectively protected rats against methotrexate-induced liver damage. Ozone therapy reversed elevated liver enzymes and inflammatory markers, demonstrating its therapeutic potential for drug-induced hepatotoxicity.
Area of Science:
- Toxicology
- Pharmacology
- Biochemistry
Background:
- Methotrexate (MTX) is a chemotherapy agent known to cause significant liver toxicity.
- Hepatotoxicity induced by MTX presents challenges in clinical management, necessitating protective strategies.
- The potential of medical ozone as a protective agent against drug-induced liver injury requires investigation.
Purpose of the Study:
- To investigate the protective effects of medical ozone preconditioning and treatment on methotrexate-induced hepatotoxicity in a rat model.
- To evaluate the biochemical and histopathological alterations in liver tissue following MTX administration and ozone intervention.
Main Methods:
- Eighteen rats were divided into control, MTX-induced hepatotoxicity, and MTX with ozone groups.
- Hepatotoxicity was induced by a single dose of 20 mg/kg MTX.
- Medical ozone was administered intraperitoneally as preconditioning and treatment in the ozone group.
- Liver enzymes (ALT, AST), inflammatory cytokines (TNF-α, IL-1β), oxidative stress markers (MDA, GSH), and myeloperoxidase (MPO) were measured.
- Histopathological examination assessed liver injury scores.
Main Results:
- MTX administration significantly increased liver enzymes (ALT, AST), MDA, MPO activity, and pro-inflammatory cytokines (TNF-α, IL-1β), while decreasing GSH levels.
- Medical ozone preconditioning and treatment significantly reversed these biochemical changes induced by MTX.
- Histopathological examination revealed that ozone therapy ameliorated MTX-induced liver damage.
Conclusions:
- Medical ozone demonstrates significant hepatoprotective effects against acute methotrexate-induced liver injury in rats.
- Ozone therapy effectively mitigates oxidative stress and inflammation associated with MTX hepatotoxicity.
- These findings suggest medical ozone as a potential therapeutic strategy for managing MTX-induced liver damage.
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