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Vitamin E sequestration by liver fat in humans
Pierre-Christian Violet, … , Maret G. Traber, Mark Levine
Pierre-Christian Violet, … , Maret G. Traber, Mark Levine
Published December 10, 2019
Citation Information: JCI Insight. 2020;5(1):e133309. https://doi.org/10.1172/jci.insight.133309.
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Clinical Medicine Hepatology Metabolism

Vitamin E sequestration by liver fat in humans

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Abstract

BACKGROUND We hypothesized that obesity-associated hepatosteatosis is a pathophysiological chemical depot for fat-soluble vitamins and altered normal physiology. Using α-tocopherol (vitamin E) as a model vitamin, pharmacokinetics and kinetics principles were used to determine whether excess liver fat sequestered α-tocopherol in women with obesity-associated hepatosteatosis versus healthy controls.METHODS Custom-synthesized deuterated α-tocopherols (d3- and d6-α-tocopherols) were administered to hospitalized healthy women and women with hepatosteatosis under investigational new drug guidelines. Fluorescently labeled α-tocopherol was custom-synthesized for cell studies.RESULTS In healthy subjects, 85% of intravenous d6-α-tocopherol disappeared from the circulation within 20 minutes but reappeared within minutes and peaked at 3–4 hours; d3- and d6-α-tocopherols localized to lipoproteins. Lipoprotein redistribution occurred only in vivo within 1 hour, indicating a key role of the liver in uptake and re-release. Compared with healthy subjects who received 2 mg, subjects with hepatosteatosis had similar d6-α-tocopherol entry rates into liver but reduced initial release rates (P < 0.001). Similarly, pharmacokinetics parameters were reduced in hepatosteatosis subjects, indicating reduced hepatic d6-α-tocopherol output. Reductions in kinetics and pharmacokinetics parameters in hepatosteatosis subjects who received 2 mg were echoed by similar reductions in healthy subjects when comparing 5- and 2-mg doses. In vitro, fluorescent-labeled α-tocopherol localized to lipid in fat-loaded hepatocytes, indicating sequestration.CONCLUSIONS The unique role of the liver in vitamin E physiology is dysregulated by excess liver fat. Obesity-associated hepatosteatosis may produce unrecognized hepatic vitamin E sequestration, which might subsequently drive liver disease. Our findings raise the possibility that hepatosteatosis may similarly alter hepatic physiology of other fat-soluble vitamins.TRIAL REGISTRATION ClinicalTrials.gov, NCT00862433.FUNDING National Institute of Diabetes and Digestive and Kidney Diseases and NIH grants DK053213-13, DK067494, and DK081761.

Authors

Pierre-Christian Violet, Ifechukwude C. Ebenuwa, Yu Wang, Mahtab Niyyati, Sebastian J. Padayatty, Brian Head, Kenneth Wilkins, Stacey Chung, Varsha Thakur, Lynn Ulatowski, Jeffrey Atkinson, Mikel Ghelfi, Sheila Smith, Hongbin Tu, Gerd Bobe, Chia-Ying Liu, David W. Herion, Robert D. Shamburek, Danny Manor, Maret G. Traber, Mark Levine

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Figure 3

Influence of liver fat on d6-α-tocopherol plasma concentrations: pharmacokinetics and kinetics in 10 healthy and 6 HS subjects.

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Influence of liver fat on d6-α-tocopherol plasma concentrations: pharmac...
(A) d6-α-Tocopherol 2 mg administered IV in healthy (●) or HS subjects (●) over 72 hours. (B–D) Initial rates of d6-α-tocopherol reappearance matched to patient status (C), to percentage liver fat by MRI (D). (E and F) Initial rates of d6-α-tocopherol reappearance to percentage body fat by DEXA in healthy (E) and HS (F) subjects. n = 6 for HS and n =10 for healthy cohorts. (A and B) Data represented as mean ± SEM. (C) Data represented as median.

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