Curcumin alleviates AFB1-induced nephrotoxicity in ducks: regulating mitochondrial oxidative stress, ferritinophagy, and ferroptosis

Mycotoxin Res. 2023 Nov;39(4):437-451. doi: 10.1007/s12550-023-00504-3. Epub 2023 Oct 2.

Abstract

Aflatoxin B1 (AFB1), an extremely toxic mycotoxin that extensively contaminates feed and food worldwide, poses a major hazard to poultry and human health. Curcumin, a polyphenol derived from turmeric, has attracted great attention due to its wonderful antioxidant properties. Nevertheless, effects of curcumin on the kidneys of ducks exposed to AFB1 remain unclear. Additionally, the underlying mechanism between AFB1 and ferroptosis (based on excessive lipid peroxidation) has not been sufficiently elucidated. This study aimed to investigate the protective effects and potential mechanisms of curcumin against AFB1-induced nephrotoxicity in ducklings. The results indicated that curcumin alleviated AFB1-induced growth retardation and renal distorted structure in ducklings. Concurrently, curcumin inhibited AFB1-induced mitochondrial-mediated oxidative stress by reducing the expression levels of oxidative damage markers malondialdehyde (MDA) and 8-hydroxy-2 deoxyguanosine (8-OHdG) and improved the expression of mitochondria-related antioxidant enzymes and the Nrf2 pathway. Notably, curcumin attenuated iron accumulation in the kidney, inhibited ferritinophagy via the NCOA4 pathway, and balanced iron homeostasis, thereby alleviating AFB1-induced ferroptosis in the kidney. Collectively, our results suggest that curcumin alleviates AFB1-induced nephrotoxicity in ducks by inhibiting mitochondrial-mediated oxidative stress, ferritinophagy, and ferroptosis and provide new evidence for the mechanism of AFB1-induced nephrotoxicity in ducklings treated with curcumin.

Keywords: AFB1; Curcumin; Ferritinophagy; Ferroptosis; Mitochondrial oxidative stress.

MeSH terms

  • Aflatoxin B1 / metabolism
  • Aflatoxin B1 / toxicity
  • Animals
  • Antioxidants / metabolism
  • Antioxidants / pharmacology
  • Curcumin* / pharmacology
  • Ducks / metabolism
  • Ferroptosis*
  • Humans
  • Iron / pharmacology
  • Oxidative Stress

Substances

  • Antioxidants
  • Aflatoxin B1
  • Curcumin
  • Iron