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P. 205

POSTER PRESENTATION / POSTER SUNUM



                                    Investigation of The Effect of Ursodeoxycholic Acid
                                  Against Liver Damage Induced by Imidacloprid in Rats


                     Yunus Emre BAŞAR                    Ebru YILDIRIM                Emine BAYDAN
                                          1,*
                                                                        2
                                                                                                      3
                                     Miyase Çınar                 Tuğçe ANTEPLİOĞLU
                                                                                       5
                                                  4

                            1 Kırıkkale University, Health Scineces Institude, Kırıkkale, TÜRKiYE
                 2 Kırıkkale University Veterinary Faculty Pharmacology and Toxicology Department ABD,
                                                     Kırıkkale, TÜRKiYE
           3 Ankara Üniversitesi Veterinary Faculty Pharmacology and Toxicology Department, Ankara, TÜRKiYE
                   4  Kırıkkale University Veterinary Faculty Biochenistry Department, Kırıkkale, TÜRKiYE
                    5 Kırıkkale University Veterinary Faculty Pathology Department, Kırıkkale, TÜRKiYE

               *Correspound Author: ynsmrbasar@gmail.com

                     In  this  study,  the  toxic  effects  of  imidacloprid  (İMD),  a  widely  used  neonicotinoid
               insecticide, on rat liver were evaluated and the potential protective effect of ursodeoxycholic
               acid  (UDCA)  against  this  toxicity  was  investigated  in  terms  of  biochemical,  and
               histopathological parameters. Forty male Wistar albino rats were used in the experiment.
               The rats were randomly divided into four groups as the control group (corn oil and 1% gum
               arabic administered orally by gavage), the UDCA only group (25 mg/kg/day, administered
               orally by gavage), the IMD only group (45 mg/kg/day, administered orally by gavage), and
               the  combined  group  (25  mg/kg/day  UDCA  and  45  mg/kg  İMD  administered  orally  by
               gavage). All treatments were performed for 30 days, and at the end of the treatments, blood
               and liver  tissue  samples were collected for  analysis. In  serum biochemical analyses, a
               statistically significant increase was observed in serum AST, ALT, GGT, triglyceride, urea, total
               cholesterol  and  total  bilirubin  levels  in  the  İMD  group compared to the control group.
               Additionally,  a  statistically  significant  decrease  was  detected  in  albumin  levels  of  İMD
               compared to control group (P<0.001). Statistically significant improvements were recorded
               in serum ALT, total bilirubin, triglyceride and urea levels in the group administered with UDCA
               (IMD+UDCA) compared to the IMD group. Histopathological evaluations revealed significant
               pathological findings of liver injury, such as hepatocyte degeneration, sinusoidal congestion,
               necrotic areas, and inflammatory cell infiltration, in the IMD treated group. In the IMD+UDCA
               group, the severity of these findings was reduced, and tissue integrity was largely preserved.
               In conclusion, it was determined that IMD caused biochemical and histopathological damage
               in the liver, while UDCA exhibited a significant protective effect against this toxicity. These
               findings suggest that UDCA may be used as a hepatoprotective agent in pesticide-induced
               liver injury.
               Keywords: Biochemistry, histopathology, imidacloprid, liver toxicity, rat, ursodeoxycholic acid
               Acknowledgement:  This  study  was  supported  by  Kırıkkale  University  Scientific  Research
               Projects Coordination Unit as master’s thesis project numbered 2024/62.



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