Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Apr 24:9:394.
doi: 10.3389/fphys.2018.00394. eCollection 2018.

Flavonoids in Kidney Health and Disease

Affiliations
Review

Flavonoids in Kidney Health and Disease

Félix Vargas et al. Front Physiol. .

Abstract

This review summarizes the latest advances in knowledge on the effects of flavonoids on renal function in health and disease. Flavonoids have antihypertensive, antidiabetic, and antiinflammatory effects, among other therapeutic activities. Many of them also exert renoprotective actions that may be of interest in diseases such as glomerulonephritis, diabetic nephropathy, and chemically-induced kidney insufficiency. They affect several renal factors that promote diuresis and natriuresis, which may contribute to their well-known antihypertensive effect. Flavonoids prevent or attenuate the renal injury associated with arterial hypertension, both by decreasing blood pressure and by acting directly on the renal parenchyma. These outcomes derive from their interference with multiple signaling pathways known to produce renal injury and are independent of their blood pressure-lowering effects. Oral administration of flavonoids prevents or ameliorates adverse effects on the kidney of elevated fructose consumption, high fat diet, and types I and 2 diabetes. These compounds attenuate the hyperglycemia-disrupted renal endothelial barrier function, urinary microalbumin excretion, and glomerular hyperfiltration that results from a reduction of podocyte injury, a determinant factor for albuminuria in diabetic nephropathy. Several flavonoids have shown renal protective effects against many nephrotoxic agents that frequently cause acute kidney injury (AKI) or chronic kidney disease (CKD), such as LPS, gentamycin, alcohol, nicotine, lead or cadmium. Flavonoids also improve cisplatin- or methotrexate-induced renal damage, demonstrating important actions in chemotherapy, anticancer and renoprotective effects. A beneficial prophylactic effect of flavonoids has been also observed against AKI induced by surgical procedures such as ischemia/reperfusion (I/R) or cardiopulmonary bypass. In several murine models of CKD, impaired kidney function was significantly improved by the administration of flavonoids from different sources, alone or in combination with stem cells. In humans, cocoa flavanols were found to have vasculoprotective effects in patients on hemodialysis. Moreover, flavonoids develop antitumor activity against renal carcinoma cells with no toxic effects on normal cells, suggesting a potential therapeutic role in patients with renal carcinoma.

Keywords: acute kidney injury; arterial hypertension; chronic kidney disease; diabetes mellitus; flavonoids; kidney function; nephroprotection.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Flavonoid classes, their main subclasses and typical sources.
Figure 2
Figure 2
Effects of quercetin on sodium transporters in kidney tubules affect sodium balance.
Figure 3
Figure 3
Icariin together with mesenchymal stem cells (MSCs) improve a rat model of CKD.
Figure 4
Figure 4
Mechanisms through which flavonoids interfere with carcinogenesis mechanisms.
Figure 5
Figure 5
Flavonoids exert renoprotective actions due to their multiple beneficial properties, counteracting the deleterious effects of kidney injuries that can lead to chronic kidney disease.

References

    1. Ali B. H., Al Za'abi M., Adham S. A., Yasin J., Nemmar A., Schupp N. (2016). Therapeutic effect of chrysin on adenine-induced chronic kidney disease in rats. Cell. Physiol. Biochem. 38, 248–257. 10.1159/000438626 - DOI - PubMed
    1. Aoi W., Niisato N., Miyazaki H., Marunaka Y. (2004). Flavonoid-induced reduction of ENaC expression in the kidney of Dahl salt-sensitive hypertensive rat. Biochem. Biophys. Res. Commun. 315, 892–896. 10.1016/j.bbrc.2004.01.150 - DOI - PubMed
    1. Arab H. H., Mohamed W. R., Barakat B. M., Arafa-el S. A. (2016). Tangeretin attenuates cisplatin-induced renal injury in rats: impact on the inflammatory cascade and oxidative perturbations. Chem. Biol. Interact. 258, 205–213. 10.1016/j.cbi.2016.09.008 - DOI - PubMed
    1. Bagheri F., Gol A., Dabiri S., Javadi A. (2011). Preventive effect of garlic juice on renal reperfusion injury. Iran J. Kidney Dis. 5, 194–200. - PubMed
    1. Bai S., Huang Z. G., Chen L., Wang J. T., Ding B. P. (2013). Effects of felodipine combined with puerarin on ACE2-Ang (1-7)-Mas axis in renovascular hypertensive rat. Regul. Pept. 184, 54–61. 10.1016/j.regpep.2013.03.005 - DOI - PubMed