The Ameliorative Role of Lico A on Aflatoxin B 1 -Triggered Hepatotoxicity Partially by Activating Nrf2 Signal Pathway.

Aflatoxin B 1 (AFB 1 ) is one of the most harmful and toxic mycotoxins in foods and feeds, posing a serious health risk to both humans and animals, especially its hepatotoxicity. Nuclear factor-erythroid 2-related factor 2 (Nrf2), an important nuclear transcription factor, is generally recognized as a potential target for phytochemicals to ameliorate liver injury. The current study sought to elucidate the molecular processes by which licochalcone A (Lico A), a compound derived from Xinjiang licorice Glycyrrhiza inflate , protects against AFB 1 toxicity. In vivo , male wild-type (WT) and Nrf2 knockout (Nrf2 -/- ) C57BL/6 mice were orally administered AFB 1 at 1.5 mg/kg body weight (BW) with or without Lico A at 5 mg/kg. In vitro , AML12 cells were utilized to evaluate the protective effect and mechanism of Lico A against the AFB 1 -induced hepatotoxicity. Our findings demonstrated that AFB 1 caused severe hepatotoxicity, while Lico A treatment successfully relieved the toxicity. Meanwhile, Lico A effectively improved liver injury, inflammatory mediators, oxidative insults, apoptosis, liver fibrosis, and pyroptosis, which contributed to the inhibition of toll receptor 4 (TLR4)-NF-κB/MAPK and NOD-like receptors protein 3 (NLRP3)/caspase-1/GSDMD signaling pathway activation. Furthermore, Lico A was able to enhance the Nrf2 antioxidant signaling pathway. Intriguingly, Lico A still had a protective effect on AFB 1 -caused liver injury in mice via the inhibition of inflammation and pyroptosis, while apoptosis and liver fibrosis were blocked in the absence of Nrf2. To sum up, the present study first elucidated that Lico A ameliorated AFB 1 -induced hepatotoxic effects and its main mechanism involved the inhibitory effects on oxidative stress, apoptosis, liver fibrosis, inflammation, and pyroptosis, which might be partially dependent on the regulation of Nrf2. The work may enrich the role and mechanism of Lico A's resistance to liver injury caused by various factors, and its application is promising.