4.7 Article

Plant-Based Nutritional Supplementation Attenuates LPS-Induced Low-Grade Systemic Activation

Journal

Publisher

MDPI
DOI: 10.3390/ijms22020573

Keywords

diet; LPS; inflammation; metabolism; immune system

Funding

  1. National Institutes of Health [R01 ES016774-01, R21AG043718]
  2. VA Merit Award [I101RX001450]
  3. AHA SFRN grant [15SFDRN25710468]

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Plant-based nutritional supplementation can attenuate the progression of acute and chronic disorders by improving inflammatory responses and maintaining stable neurotransmitter levels. Experimentally induced inflammation by LPS affects glucose, insulin tolerance, and neurotransmitter levels.
Plant-based nutritional supplementation has been shown to attenuate and reduce mortality in the processes of both acute and chronic disorders, including diabetes, obesity, cardiovascular disease, cancer, inflammatory diseases, and neurological and neurodegenerative disorders. Low-level systemic inflammation is an important contributor to these afflictions and diets enriched in phytochemicals can slow the progression. The goal of this study was to determine the impact of lipopolysaccharide (LPS)-induced inflammation on changes in glucose and insulin tolerance, performance enhancement, levels of urinary neopterin and concentrations of neurotransmitters in the striatum in mouse models. Both acute and chronic injections of LPS (2 mg/kg or 0.33 mg/kg/day, respectively) reduced glucose and insulin tolerance and elevated neopterin levels, which are indicative of systemic inflammatory responses. In addition, there were significant decreases in striatal neurotransmitter levels (dopamine and DOPAC), while serotonin (5-HT) levels were essentially unchanged. LPS resulted in impaired execution in the incremental loading test, which was reversed in mice on a supplemental plant-based diet, improving their immune function and maintaining skeletal muscle mitochondrial activity. In conclusion, plant-based nutritional supplementation attenuated the metabolic changes elicited by LPS injections, causing systemic inflammatory activity that contributed to both systemic and neurological alterations.

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