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March 6, 2026Kocatepe Veterinary Journal0 citationsOpen Access

Morin Reduces Ciprofloxacin-Induced Brain Damage by Regulating Oxidative Stress, Inflammation, and Histopathological Changes

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SASerpil AygörmezKafkas UniversityNANurhan AkarasAksaray UniversityEDElif DalkılınçAtatürk University

Key Points

  • This research aims to assess Morin's protective effects against brain damage induced by ciprofloxacin in rats.
  • Twenty-eight female rats were divided into four groups: control, Morin, CPFX, and CPFX+Morin.
  • Ciprofloxacin and Morin were administered daily for seven days.
  • Parameters for oxidative stress and inflammation were analyzed, along with histopathological evaluations.
  • Ciprofloxacin increased markers of oxidative stress and inflammation like NF-κB, MDA, TNF-α, and IL-1β.
  • Morin co-administration restored levels of antioxidant enzymes such as GPx, SOD, and CAT.
  • Histopathological analysis indicated reduced brain tissue damage when treated with Morin alongside ciprofloxacin.

Abstract

Ciprofloxacin (CPFX), one of the fluoroquinones, is an antibacterial antibiotic that is used in the treatment of urinary tract, respiratory, abdominal and gastrointestinal infections as well as having negative side effects on the central nervous system. Morin, a bioactive flavonoid, is an antioxidant with neuroprotective properties thanks to its many pharmacological properties. The protective effect off Morin against brain damage caused by CPFX, broad spectrum antibiotic, was investigated. Twentyeight female rats were divided into four groups as control, Morin, CPFX, CPFX+Morin. CPFX, Morin was administered once a day for seven days. Oxidative stress and inflammation parameters were analyzed to determine brain tissue damage and histopathological analysis was performed to determine tissue damage and structural changes. According to the findings obtained as a result of the analyses, CPFX increased nuclear factor kappa B (NF-B), malondialdehyde (MDA), tumor necrosis factor-alpha (TNF-α), and interleukin 1β (IL-1β) and decreased glutathione peroxidase (GPx), superoxide dismutase (SOD), catalase (CAT) and glutathione (GSH) in brain. Co-administration of CPFX with Morin increased GSH and GPx, SOD, CAT and decreased NF-B, MDA, TNF-α, IL-1β levels. According to findings, when evaluated together, it was found that CPFX caused damage in brain tissue by causing oxidative stress and inflammation and Morin as a supportive treatment reduced the damage in brain tissue by bringing these markers closer to normal.

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Cite This Study

Aygörmez et al. (2026) studied this question.

synapsesocial.com/papers/69aa70d6531e4c4a9ff5af70https://doi.org/10.30607/kvj.1702504
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