Protective Effect of Quercetin 3- O -Glucuronide against Cisplatin Cytotoxicity in Renal Tubular Cells

• Published in: Molecules (Basel, Switzerland) Switzerland), 2022-02, Vol.27 (4), p.1319
• Main Authors: Muñoz-Reyes, Daniel, Casanova, Alfredo G, González-Paramás, Ana María, Martín, Ángel, Santos-Buelga, Celestino, Morales, Ana I, López-Hernández, Francisco J, Prieto, Marta
• Format: Article
• Language: English
• Subjects: Animals; Apoptosis; Bioavailability; Biocompatibility; Cell division; Cell Line; Cell lines; Cells, Cultured; Chemotherapy; Chromatography, High Pressure Liquid; Cisplatin; Cisplatin - adverse effects; Cisplatin - pharmacology; Creatinine; cytoprotection; Cytoprotection - drug effects; Cytotoxicity; Drug dosages; Epithelial Cells - drug effects; Evaluation; Flavonoids; Glomerular Filtration Rate; High-performance liquid chromatography; Kidney Function Tests - methods; Kidney Tubules - cytology; Kidney Tubules - drug effects; Kinases; Light microscopy; Liquid chromatography; Metabolites; nephrotoxicity; Optical microscopy; Oral administration; Plasma; Prophylaxis; Protective Agents - pharmacology; Quercetin; Quercetin - analogs & derivatives; Quercetin - pharmacology; quercetin 3-O-glucuronide; Rats; Rutin; Small intestine; Urine
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules27041319

Quercetin, a flavonoid with promising therapeutic potential, has been shown to protect from cisplatin nephrotoxicity in rats following intraperitoneal injection, but its low bioavailability curtails its prospective clinical utility in oral therapy. We recently developed a micellar formulation (P-quercetin) with enhanced solubility and bioavailability, and identical nephroprotective properties. As a first aim, we herein evaluated the oral treatment with P-quercetin in rats, which displayed no nephroprotection. In order to unravel this discrepancy, quercetin and its main metabolites were measured by HPLC in the blood and urine after intraperitoneal and oral administrations. Whilst quercetin was absorbed similarly, the profile of its metabolites was different, which led us to hypothesize that nephroprotection might be exerted in vivo by a metabolic derivate. Consequently, we then aimed to evaluate the cytoprotective capacity of quercetin and its main metabolites (quercetin 3- -glucoside, rutin, tamarixetin, isorhamnetin and quercetin 3- -glucuronide) against cisplatin toxicity, in HK-2 and NRK-52E tubular cell lines. Cells were incubated for 6 h with quercetin, its metabolites or vehicle (pretreatment), and subsequently 18 h in cotreatment with 10-300 μM cisplatin. Immediately after treatment, cell cultures were subject to the MTT technique as an index of cytotoxicity and photographed under light microscopy for phenotypic assessment. Quercetin afforded no direct cytoprotection and quercetin-3- -glucuronide was the only metabolite partially preventing the effect of cisplatin in cultured tubule cells. Our results identify a metabolic derivative of quercetin contributing to its nephroprotection and prompt to further explore exogenous quercetin-3- -glucuronide in the prophylaxis of tubular nephrotoxicity.