Renoprotective Effect of Taxifolin in Paracetamol-Induced Nephrotoxicity: Emerging Evidence from an Animal Model

Author:

Topal Ismail1,Özdamar Mustafa Yaşar2ORCID,Catakli Tulin3,Malkoc İsmail4ORCID,Hacimuftuoglu Ahmet5,Mamoulakis Charalampos6ORCID,Tsatsakis Aristidis7ORCID,Tsarouhas Konstantinos8ORCID,Tsitsimpikou Christina9,Taghizadehghalehjoughi Ali10ORCID

Affiliation:

1. Department of Pediatric Diseases, Medical Faculty, Erzincan University, 24000 Erzincan, Turkey

2. Department of Pediatric Surgery, Faculty of Medicine, Erzincan University, 24000 Erzincan, Turkey

3. Department of Pediatrics, Lokman Hekim Hospital, 06930 Ankara, Turkey

4. Department of Anatomy, Faculty of Medicine, Ataturk University, 25240 Erzurum, Turkey

5. Department of Medical Pharmacology, Medical Faculty, Duzce University, 81620 Duzce, Turkey

6. Department of Urology, University General Hospital of Heraklion, Medical School, University of Crete, 715 00 Heraklion, Greece

7. Department of Forensic Sciences and Toxicology, Faculty of Medicine, University of Crete, 71003 Heraklion, Greece

8. Department of Cardiology, University Hospital of Larissa, Terma Mezourlo, 413 34 Larissa, Greece

9. General Chemical State Laboratory of Greece, 11521 Athens, Greece

10. Department of Pharmacology, Faculty of Medicine, Seyh Edebali University, 11230 Biecik, Turkey

Abstract

Background: Taxifolin (TXF) is a flavonoid found abundantly in citrus/onion. Encouraging results on its renoprotective effect have been reported in a limited number of drug-induced nephrotoxicity animal models. The present study aimed to evaluate for the first time the potential renoprotective effects of TXF in a paracetamol (PAR)-induced nephrotoxicity rat model. Methods: Rats were divided into three equal groups (n = 6 animals per group). Group 1 (PAR group, PARG) received PAR diluted in normal saline by gavage (1000 mg/kg). Group 2 (TXF group, TXFG) received TXF diluted in normal saline by gavage (50 mg/kg) one hour after PAR administration. Group 3 (control group, CG) received normal saline. Twenty-four hours after PAR administration, all animals were sacrificed using high-dose anesthesia. Blood samples were collected and kidneys were removed. Results: The serum blood urea nitrogen, creatinine levels and serum malondialdehyde levels were significantly increased in the PARG. The serum glutathione peroxidase, glutathione reductase and total glutathione levels were significantly higher in the TXFG. At the same time, the kidneys of the PARG animals demonstrated tubular epithelium swelling, distension and severe vacuolar degeneration. The kidneys of the TXFG animals showed mildly dilated/congested blood vessels. Conclusions: The TXF renoprotective effects are promising in preventing PAR-induced nephrotoxicity, mainly through antioxidant activity, and warrant further testing in future studies.

Publisher

MDPI AG

Subject

General Medicine

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