From: The multifaceted role of ferroptosis in infection and injury and its nutritional regulation in pigs
Nutrients | Models | Mechanisms | References |
---|---|---|---|
Selenium | DON-induced intestinal injury in mice | Increase levels of GPX4 and 4-HNE by activating PI3K/AKT pathway | [64] |
Selenium | Cerebral I/R injury in MCAO model mice and OGD/R model of N2a cells | Upregulate expression of Mfn1 to alleviate oxidative stress and ferroptosis by promoting mitochondrial fusion | [65] |
Selenium | Autism spectrum disorder model mice | Inhibit ferroptosis by regulating Nrf2/GPX4 pathway | [66] |
Selenium | Hemorrhagic stroke model mice and HT22 murine hippocampal cells | Augment the transcription of GPX4 via coordinated activation of the transcription factors TFAP2c and Sp1 | [67] |
Glycine | Diquat-induced intestinal injury in pigs | Upregulate expression of SLC7A11 and GPX4, and downregulate expression of TFR1 in ileum | [68] |
Glycine | Diquat-induced hepatic injury in pigs | Downregulate expression of TFR1 | [69] |
L-citrulline | Iron overload-induced intestine injury in mice and IPEC-J2 cells | Downregulate expression of TFR, FTH, and NCOA4; Improve oxidative stress by regulating AMPK signaling pathway | [54] |
Fish skin gelatin peptides and Gly-Pro-Ala peptide | DON-induced toxicity in mice and IPEC-J2 cells | Inhibit ROS and MDA production and enhance antioxidant enzyme activity by promoting Nrf2 migration | [70] |
Lentil peptides | Anemic Caco-2 cells | Downregulate expression of DMT1 and TFR | [71] |
Vitamin E | T cell-specific Gpx4-deficient mice with acute lymphocytic choriomeningitis virus and Leishmania major parasite infections | Upregulate expression of GPX4 | [72] |
Vitamin EÂ | Mice | Deplete liver iron stores by suppressing Nrf2 and enhance iron efflux by upregulating expression of liver FPN | [73] |
Vitamin EÂ | Mice with conditional deletion of Gpx4 in hepatocytes along with lacking Txnrd1 and selenocysteine tRNA in hepatocytes | Inhibit lipid peroxidation | [74] |
Holly polyphenols | Diquat-induced hepatic and intestinal injury in pigs | Upregulate expression of GPX4 and SLC7A11 and downregulate expression of TFR | |
Hesperidin | DON-induced intestinal injury in pigs | Exert protective effects on intestinal epithelium barrier and mitochondria via inhibiting ER-mitochondrial calcium transfer mediated by IP3Rs | [76] |
Quercetin | DON-induced intestinal injury in mice | Decrease the levels of TFR, ACSL4, and 4-HNE, and increase the expression of FTH1, SLC7A11, GPX4, FPN1, and FSP1 | [77] |
Resveratrol | Intestinal I/R mice model and Caco-2 hypoxia-reoxygenation model | Activate SIRT3/FoxO3a pathway, increase the expression of SOD2 and catalase, and inhibit ROS generation | [78] |
Resveratrol | DON-exposed HepG2 cells | Activate SLC7A11-GSH-GPX4 signaling pathway | [79] |
Lycopene | Mycotoxins (ZEN + DON + AFB1)-induced intestinal injury in mice | Downregulate expression of TFR1, FTH1, and SLC3A2 | [80] |
Lycopene | Atrazine-induced hippocampus injury in mice | Upregulate expression of Nrf2 and SLC7A11 | [81] |
Glycyrrhetinic acid | DON-induced hepatic damage in mice and AML12 cells | Inhibit NCOA4 signaling pathway | [82] |
Epigallocatechin gallate | Iron overload-induced hepatic damage in mice | Elevate antioxidant capacity by increasing Nfr2 and GPX4 expression and attenuate iron metabolism disorders by upregulating FTH and FTL expression | [83] |
Astragalus polysaccharide | DSS-induced colitis in mice, and RSL3-stimulated Caco-2 cells | Decrease expression of FTH and FTL and the levels of MDA, GSH, and iron load via inhibiting Nrf2/HO-1 pathway | [84] |