Possible Dose-Dependent Neuroprotective Effect of Ketamine in Brain in a Head Injury Model in Rats


Kılıç F. S.

EPHAR 2024, Athens, Yunanistan, 23 - 26 Haziran 2024, ss.23

  • Yayın Türü: Bildiri / Özet Bildiri
  • Basıldığı Şehir: Athens
  • Basıldığı Ülke: Yunanistan
  • Sayfa Sayıları: ss.23
  • Eskişehir Osmangazi Üniversitesi Adresli: Evet

Özet

Objective: In our study, we aimed to investigate the neuroprotective and anti-

inflammatory effects of ketamine, which has immunomodulatory effects, in an

experimental head injury model in rats.

Methods: The rats were divided into six groups (n: 6) as control, trauma and

ketamine-treated trauma (Trauma+10, Trauma+20, Trauma+40 and Trauma+60mg/kg

ketamine). Ketamine was administered intraperitoneally every day until the seventh

day after the trauma. Neurological examination was performed on the 24th, 48th hours

and seventh day after the trauma. Serum IL-1β, IL-10, TNF-α levels were measured at

the 24th hour and seventh day. On the seventh day the serum and brain levels of lipid

peroxidase (MDA), glutathione peroxidase, catalase, caspase-3 and serum levels of

AST, ALT, ALP, BUN, creatinine and LDH were studied. Hematoxylin-Eosin staining

was performed for histopathological evaluation of brain tissue and TUNEL staining

for apoptosis. Statistical analysis was performed by one-way and two-way analysis of

variance (ANOVA).

Results: Neurological examination scores were impaired in the ketamine

60mg/kg group (p<0.05) and a decrease in IL-1β levels was observed in the 40mg/kg

ketamine group (p<0.05) on the seventh day. Brain levels of glutathione peroxidase

were decreased at 60mg/kg ketamine dose compared to other doses (p<0.05). At the

dose of ketamine 60mg/kg, an increase in brain values of MDA were observed on the

seventh day (p<0.001). Necrosis was observed in histopathological examinations.

Conclusion: 60mg/kg ketamine dose had a negative effect on neurologic

examination scores, IL-1β, brain glutathione peroxidase and MDA levels. 40mg/kg

ketamine dose had a positive effect on IL-1β. No beneficial or harmful effects of

ketamine were observed at other doses. As the most important finding, ketamine, at

doses other than 60 mg/kg, played a protective role by preventing the worsening of

post-traumatic injuries.

Keywords: Traumatic Brain Injury, ketamine, neuroprotection, cytokines,

antioxidants