Chemoprotective effect of Fumaria parviflora L. extract against vincristine induced hepatotoxicity in male rats

Authors

  • Malakijoo, Noorolhoda Pharmaceutical Research Center, Faculty of Pharmacy and Pharmaceutical Sciences, Tehran Medical Sciences, Islamic Azad University, Tehran-Iran ,MSc Toxicology student, Faculty of Pharmacy and Pharmaceutical Sciences, Tehran Medical Sciences, Islamic Azad University (IAUPS), Tehran, Iran
  • Mousavi, Zahra Department of Pharmacology and Toxicology, Faculty of Pharmacy and Pharmaceutical Sciences, Tehran Medical Sciences, Islamic Azad University (IAUPS), Tehran, Iran,Herbal pharmacological Research Center, Faculty of Medicine, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran
  • Rezaeikia, Zahra MSc student, Department of Chemistry, Collage of Science, Damghan Branch, Islamic Azad University, Damghan-Iran.وPharmaceutical Research Center, Faculty of Pharmacy and Pharmaceutical Sciences, Tehran Medical Sciences, Islamic Azad University, Tehran-Iran
  • Saeidi-Sar, Sakineh Department of Chemistry, Collage of Science, Damghan Branch, Islamic Azad University, Damghan-Iran
Abstract:

Background: Hepatoprotective effects of Fumaria parviflora have been approved in pharmaceutical and chemical toxicity models. Given the importance of the vincristine- induced hepatotoxicity during chemotherapy, the aim of this study was to investigate the potential hepatoprotective effects of F. parviflora extract on vincristine induced toxicity in adult male rats. Materials and methods: In this experimental study, the rats (n=42) were divided into 7 groups: 1) Sham group, 2) vehicle group, 3) vincristine group (VCR) (0.5 mg/kg, i.p.), 4) F. parviflora extract (300 mg/kg, p.o.), 5) F. parviflora extract (500 mg/kg, p.o.), 6) Pretreatment group: F. parviflora extract (300mg/kg for 10 days, p.o.) + VCR (0.5 mg/kg, i.p.) on 9th and 10th days of the experiment, and 7) Pretreatment group: F. parviflora extract (500mg/kg for 10 days, p.o.) +VCR (0.5 mg/kg, i.p.) on 9th and 10th days of the experiment. Serum values of AST, ALT, ALP and malondialdehyde (MDA) were measured. Data were analyzed by one way ANOVA using prism software. Results: F. parviflora extract with dose of 500 mg/kg markedly decreased ALT hepatic enzyme level caused by vincristine (P<0.01). In addition, the dose of 300 mg/kg could not decrease the elevated liver enzymes, including ALP, ALT and AST and also MDA levels. Conclusion: Hepatoprotective effects of F. parviflora extract were not considerable in pretreatment groups. Keywords: F. parviflora, vincristine, Hepatotoxicity, Rat.

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Journal title

volume 29  issue 2

pages  125- 130

publication date 2019-06

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