این سایت در حال حاضر پشتیبانی نمی شود و امکان دارد داده های نشریات بروز نباشند
Iranian Journal of Basic Medical Sciences، جلد ۲۹، شماره ۴، صفحات ۶۲۳-۶۳۳

عنوان فارسی
چکیده فارسی مقاله
کلیدواژه‌های فارسی مقاله

عنوان انگلیسی Mechanistic pathways and in silico modeling of gallic acid–mediated protection against doxorubicin-induced nephrotoxicity in rats
چکیده انگلیسی مقاله Objective(s): This study aimed to evaluate the protective effects of Gallic acid (GA) against (Doxorubicin) DOX-induced renal injury and to explore potential molecular interactions underlying its effects.Materials and Methods: Fifty male rats were randomly assigned to five groups: Control, DOX, GA50+DOX, GA100+DOX, and GA100. DOX was administered as a single intraperitoneal dose on day 8 (40 mg/kg), while GA was given orally at 50 or 100 mg/kg for 10 consecutive days. Renal tissues were collected on day 11 and analyzed for oxidative stress markers, pro- and anti-inflammatory cytokines, and the apoptotic marker caspase-3 via ELISA. Immunohistochemistry assessed Nrf-2 and HO-1 expression, and histopathology evaluated structural alterations. Molecular docking simulations were performed for DOX/topoisomerase IIα (PDB ID: 4FM9) and GA/TNF-α (PDB ID: 2AZ5).Results: GA significantly ameliorated DOX-induced oxidative stress, inflammatory cytokine imbalance, caspase-3 activation, and histological damage in a dose-dependent manner, while enhancing Nrf-2 and HO-1 expression. Docking analysis confirmed DOX binding to topoisomerase IIα and revealed strong GA–TNF-α binding affinity.Conclusion: GA exerts substantial renoprotective effects against DOX-induced nephrotoxicity by modulating oxidative, inflammatory, and apoptotic pathways. The agreement between in vivo findings and in silico modeling supports GA as a potential complementary agent to reduce chemotherapy-related renal injury.
کلیدواژه‌های انگلیسی مقاله Apoptosis, Doxorubicin, Gallic acid, Inflammation, Molecular docking, Nephrotoxicity, Oxidative stress

نویسندگان مقاله | Samet Teki̇n
Atatürk University, Faculty of Veterinary Medicine, Department of Physiology, 25000 Erzurum, Turkey


| Burak Çinar
Atatürk University, Faculty of Medicine, Department of Medical Pharmacology, 25000 Erzurum, Turkey


| Yusuf Dağ
Atatürk University, Faculty of Veterinary Medicine, Department of Physiology, 25000 Erzurum, Turkey


| Aslıhan Atasever
Atatürk University, Faculty of Veterinary Medicine, Department of Physiology, 25000 Erzurum, Turkey


| Merve Bolat
Atatürk University, Faculty of Veterinary Medicine, Department of Physiology, 25000 Erzurum, Turkey


| İsmail Bolat
Atatürk University, Faculty of Veterinary Medicine, Department of Pathology, 25000 Erzurum, Turkey


| Burak Batuhan Laçi̇n
Atatürk University, Faculty of Veterinary Medicine, Department of Physiology, 25000 Erzurum, Turkey


| Emin Şengül
Atatürk University, Faculty of Veterinary Medicine, Department of Physiology, 25000 Erzurum, Turkey


| Serkan Yıldırım
Atatürk University, Faculty of Veterinary Medicine, Department of Physiology, 25000 Erzurum, Turkey|Kyrgyzstan-Turkey Manas University, Faculty of Veterinary Medicine, Department of Pathology, 720007 Bishkek, Kyrgyzstan


| Mohamad Warda
Atatürk University, Faculty of Veterinary Medicine, Department of Physiology, 25000 Erzurum, Turkey|Cairo University, Faculty of Veterinary Medicine, Department of Biochemistry, 3753450 Giza, Egypt



نشانی اینترنتی https://ijbms.mums.ac.ir/article_27454.html
فایل مقاله فایلی برای مقاله ذخیره نشده است
کد مقاله (doi)
زبان مقاله منتشر شده en
موضوعات مقاله منتشر شده
نوع مقاله منتشر شده Original Article
برگشت به: صفحه اول پایگاه   |   نسخه مرتبط   |   نشریه مرتبط   |   فهرست نشریات