Why the study?
Osteoarthritis can cause liver damage due to triggered systemic inflammatory reactions, and whether boric acid has a protective effect against osteoarthritis-induced liver damage required investigation.
Does boric acid protect against liver damage caused by systemic inflammatory reactions in rat models of knee osteoarthritis?
Does boric acid protect against liver damage caused by systemic inflammatory reactions in rat models of knee osteoarthritis?
Boric acid exhibits anti-inflammatory properties and protects liver tissue against systemic inflammatory reactions caused by osteoarthritis in a rat model.
Answers are grounded in this paper and cite their sources.
Does not support boric acid use in human OA; leaves open hepatoprotective effects for further study.
Osteoarthritis (OA) is a significant joint disease that can affect the health of individuals in many sectors. Although OA is primarily known as a joint disease in the field of health, it can also cause damage to organs such as the liver due to the systemic inflammatory reactions (SIRS) it triggers. Boric acid (BA), which has been the subject of many studies and has been shown to have anti-inflammatory, anti-apoptotic, antimicrobial, and anticancer properties, is widely used in various areas of the healthcare sector. In this study conducted for this purpose, the protective effect of BA against liver damage caused by OA was investigated. A total of 28 rats were divided into four groups, each consisting of 7 rats. Except for the control group, all animals were induced with monosodium iodoacetate (MIA) to develop OA, and then rats were administered doses of BA ranging 4 and 10 mg/kg for 21 days. In histopathological examinations, severe hepatitis and degenerative changes were observed in the liver tissue of the OA-induced group, while it was found that BA application reduced these damages dose-dependently. Similarly, in immunohistochemical analyses, it was observed that OA induction significantly increased the expression levels of TNF-α, IL-1β, iNOS, and MMP-13 in the liver, but in the groups treated with BA, this expression level significantly decreased depending on the dose. This study observed that BA exhibited anti-inflammatory properties and had a protective effect on liver tissue against SIRS caused by OA.
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Bolat et al. (2023) studied this question.
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