“…In fact, the racemic mixture of sVE is poor in the isomers that bind with high affinity the hepatic α-tocopherol binding protein of liver cells, i.e. primarily the 2R isomer of α-tocopherol and then the 3R isomer that corresponds to nVE ( Lauridsen et al., 2002 ; Traber and Head, 2021 ). These prevail on the other forms of the raceme in terms of cellular availability and transcriptional activity, and for the possibility to access the liver metabolism, including biotransformation pathways or incorporation into lipoprotein particles for tissue distribution ( Galli et al., 2007 ; Schubert et al., 2018 ), that are important intersection nodes for the effects of this vitamin and its metabolites to affect lipid metabolism, drug and xenobiotics detoxification, and inflammatory pathways ( Bartolini et al., 2017 ; Marinelli et al., 2020 ; Parker et al., 2004 ; Torquato et al., 2017 ; Willems et al., 2021 ).…”