Protective effects of quercetin against cyclophosphamide-induced hepatic and renal injury: histopathological and immunohistochemical evaluation of HSP70
Öz
Objective: Cyclophosphamide is a widely used alkylating agent in the treatment of various malignancies and autoimmune disorders; however, its clinical application is limited by its toxic effects on several organs, particularly the liver and kidneys. This study aimed to investigate the effects of cyclophosphamide-induced toxicity on histopathological alterations and HSP70 immunoreactivity in liver and kidney tissues, as well as to evaluate the potential protective effect of quercetin.
Methods: A total of 28 female Wistar albino rats weighing 250–350 g were randomly allocated into four experimental groups. At the end of the experimental period, liver and kidney tissues were collected, processed using routine histological procedures, and embedded in paraffin. Histopathological changes were evaluated using hematoxylin and eosin (H&E) staining, while HSP70 immunoreactivity was assessed by immunohistochemical analysis.
Results: Severe histopathological alterations were observed in the group III, whereas these changes were markedly attenuated in the group IV. In addition, HSP70 immunoreactivity was markedly reduced in the liver and kidney tissues of the group III compared with the group I. In contrast, HSP70 immunoreactivity in the group IV was comparable to that observed in the group I.
Conclusion: These results suggest that HSP70 may serve as a potential biomarker for the assessment of cyclophosphamide-induced hepatic and renal injury. Furthermore, quercetin appears to exert a protective effect against cyclophosphamide-induced tissue damage by preserving the cellular stress response, as evidenced by the maintenance of HSP70 immunoreactivity.
Anahtar Kelimeler
Destekleyen Kurum
Etik Beyan
Teşekkür
Kaynakça
- 1. Ziff OJ, Kotecha D. Digoxin: the good and the bad. Trends Cardiovasc Med. 2016;26(7):585-595.
- 2. Joglar JA, Chung MK, Armbruster AL et al. 2023 ACC/AHA/ACCP/HRS Guideline for the Diagnosis and Management of Atrial Fibrillation: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines. Circulation. 2024;149(1):e1-e156.
- 3. McDonagh TA, Metra M, Adamo M et al. 2023 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure. Eur Heart J. 2023;44:3627-3739.
- 4. Kapelios CJ, Lund LH, Benson L et al. Digoxin use in contemporary heart failure with reduced ejection fraction: an analysis from the Swedish Heart Failure Registry. Eur Heart J Cardiovasc Pharmacother. 2022;8(8):756-767.
- 5. Qamer SZ, Malik A, Bayoumi E et al. Digoxin use and outcomes in patients with heart failure with reduced ejection fraction. Am J Med. 2019;132(11):1311-1319.
- 6. Kanji S, MacLean RD. Cardiac glycoside toxicity: more than 200 years and counting. Crit Care Clin. 2012;28(4):527-535.
- 7. Biteker M, Başaran Ö, Dogan V et al. Real-life use of digoxin in patients with non-valvular atrial fibrillation: data from the RAMSES study. J Clin Pharm Ther. 2016;41(6):711-717.
- 8. Luca SA, Faur-Grigori AA, Văcărescu C et al. Reconsidering digoxin in atrial fibrillation: from historical controversy to physiologically guided and personalized rate control. Biomedicines. 2025;13(12):3098.
Ayrıntılar
Birincil Dil
İngilizce
Konular
Histoloji ve Embriyoloji
Bölüm
Araştırma Makalesi
Yazarlar
Şükran Aras
*
0000-0002-3267-5251
Türkiye
Ebru Karadağ Sarı
0000-0001-7581-6109
Türkiye
Kadriye Yılmaz
0009-0000-8942-6144
Türkiye
İsa Eliş
0000-0003-3212-7842
Türkiye
Mustafa Makav
0000-0003-1879-8180
Türkiye
Yayımlanma Tarihi
28 Eylül 2026
Gönderilme Tarihi
18 Ağustos 2026
Kabul Tarihi
23 Eylül 2026
Yayımlandığı Sayı
Yıl 2026 Cilt: 7 Sayı: 3