Red Orange and Lemon Extract Ameliorates the Renal Oxidative Stress and Inflammation Induced by Ochratoxin A through the Modulation of Nrf2

Author:

Longobardi Consiglia1ORCID,Damiano Sara1ORCID,Fabroni Simona2ORCID,Montagnaro Serena1ORCID,Russo Valeria1,Vaccaro Emanuela1,Giordano Antonio34ORCID,Florio Salvatore1ORCID,Ciarcia Roberto1ORCID

Affiliation:

1. Department of Veterinary Medicine and Animal Productions, University of Naples Federico II, Via F. Delpino n.1, 80137 Naples, Italy

2. Council for Agricultural Research and Economics (CREA), Research Centre for Olive, Fruit and Citrus Crops, C.so Savoia n.190, 95024 Acireale, Italy

3. Sbarro Institute for Cancer Research and Molecular Medicine, Center of Biotechnology, College of Science and Technology, Temple University, Philadelphia, PA 19122, USA

4. Department of Medical Biotechnologies, University of Siena, 53100 Siena, Italy

Abstract

Background: The presence of ochratoxin A (OTA) in food and feed is a public health concern. OTA intoxication is caused by several mechanisms, one of which consists of the alteration of the antioxidant activity of the cell due to the oxidative stress (OS). In this context, the use of natural antioxidant substances could be a potential biological decontamination method of mitigating the negative outcomes induced by OTA. Methods: we aimed to investigate how a red orange and lemon extract (RLE), rich in anthocyanins, would affect OTA-treated rats. The current work sought to clarify the renal protective efficacy of RLE in an OTA-treated rat model (RLE (90 mg/kg b.w.); OTA (0.5 mg/kg b.w.)) by investigating, thorough Western blot analysis, the involvement of the Nuclear factor erythroid 2-related factor 2 (Nrf2) pathway. The OS parameters and inflammatory status were evaluated by spectrophotometry. The inflammatory infiltrates in the kidney were evaluated by immunohistochemical assays. Results and Conclusion: Our findings showed a significant increase in oxidative and inflammatory parameters after OTA exposure, while the OTA + RLE co-treatment counteracted both the inflammatory and OS damage through the modulation of the Nrf2 pathway.

Publisher

MDPI AG

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