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<title>The American Journal of Clinical Nutrition Volume 154 Issue 2 2024</title>
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<publisher>2024</publisher>
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<edition>Volume 154 Issue 2 2024</edition>
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<note>Background: &alpha;-Tocopherol (&alpha;T) deficiency causes several neurologic disorders, such as spinocerebellar ataxia, peripheral neuropathy, and
myopathy. Furthermore, decreased antibody production, impaired ex vivo T cell function, and elevated cytokine production are observed in
humans and mice with &alpha;T deficiency. Although modeling &alpha;T deficiency in animals is challenging, &alpha;T depletion can be more readily achieved
in &alpha;-tocopherol transfer protein-null (Ttpa-/-) mice than wild-type (WT) mice. Thus, the Ttpa-/- mouse model is a useful tool for studying
metabolic consequences of low &alpha;T status. Optimizing this mouse model and selecting the reliable indicators/markers of deficiency are still
needed.
Objective: Our objective was to assess whether &alpha;T depletion alters lipopolysaccharide (LPS)-induced inflammatory response in the brain
and/or grip strength used as a proxy for fatigue.
Methods: WT and Ttpa-/- weanling littermates (n 1&frasl;4 37&ndash;40/genotype) were fed an &alpha;T deficient diet ad libitum for 9 wk. Mice were then
injected with LPS (10 &mu;g/mouse) or saline (control) intraperitoneally and killed 4 h later. Concentrations of &alpha;T in diet and tissues were
measured via high-pressure liquid chromatography. Grip strength was evaluated via a grip strength meter apparatus 2 d before and 3.5 h
after LPS injection. Cerebellar and serum interleukin-6 (IL-6) concentrations were measured via enzyme-linked immunosorbent assay.
Results: &alpha;T concentrations in the liver, heart, and adipose tissue of WT mice were higher than Ttpa-/- mice. Although &alpha;T was detected in the
brain, muscle, and serum of WT mice, it was undetectable in these tissues of Ttpa-/- mice. Cerebellar and serum concentrations of IL-6 were
increased in LPS-treated groups but were not significantly affected by genotype. Grip strength was reduced in LPS-treated groups, an effect
that was more pronounced in Ttpa-/- mice.
Conclusions: Systemic LPS administration caused an acute inflammatory response with a concomitant decline in grip strength, especially in
Ttpa-/- mice. &alpha;T depletion appears to exacerbate reductions in grip strength brought on by systemic inflammation.
Keywords: vitamin E, RRR-&alpha;-tocopherol, Ttpa-null mouse, lipopolysaccharide, grip strength</note>
<subject authority=""><topic>Clinical Nutrition</topic></subject>
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