4.5 Article

Acetate supplementation attenuates lipopolysaccharide-induced neuroinflammation

Journal

JOURNAL OF NEUROCHEMISTRY
Volume 117, Issue 2, Pages 264-274

Publisher

WILEY
DOI: 10.1111/j.1471-4159.2011.07198.x

Keywords

acetate; astrocytes; microglia; neuroinflammation; neurons; rats

Funding

  1. National Center for Research Resources (NCRR), a component of the National Institutes of Health (NIH) [P20RR17699-09]
  2. Direct For Biological Sciences
  3. Div Of Biological Infrastructure [1359243] Funding Source: National Science Foundation
  4. Div Of Biological Infrastructure
  5. Direct For Biological Sciences [0851869] Funding Source: National Science Foundation

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P>Glyceryl triacetate (GTA), a compound effective at increasing circulating and tissue levels of acetate was used to treat rats subjected to a continual 28 day intra-ventricular infusion of bacterial lipopolysaccharide (LPS). This model produces a neuroinflammatory injury characterized by global neuroglial activation and a decrease in choline acetyltransferase immunoreactivity in the basal forebrain. During the LPS infusion, rats were given a daily treatment of either water or GTA at a dose of 6 g/kg by oral gavage. In parallel experiments, free-CoA and acetyl-CoA levels were measured in microwave fixed brains and flash frozen heart, liver, kidney and muscle following a single oral dose of GTA. We found that a single oral dose of GTA significantly increased plasma acetate levels by 15 min and remained elevated for up to 4 h. At 30 min the acetyl-CoA levels in microwave-fixed brain and flash frozen heart and liver were increased at least 2.2-fold. The concentrations of brain acetyl-CoA was significantly increased between 30 and 45 min following treatment and remained elevated for up to 4 h. The concentration of free-CoA in brain was significantly decreased compared to controls at 240 min. Immunohistochemical and morphological analysis demonstrated that a daily treatment with GTA significantly reduced the percentage of reactive glial fibrillary acidic protein-positive astrocytes and activated CD11b-positive microglia by 40-50% in rats subjected to LPS-induced neuroinflammation. Further, in rats subjected to neuroinflammation, GTA significantly increased the number of choline acetyltransferase (ChAT)-positive cells by 40% in the basal forebrain compared to untreated controls. These data suggest that acetate supplementation increases intermediary short chain acetyl-CoA metabolism and that treatment is potentially anti-inflammatory and neuroprotective with regards to attenuating neuroglial activation and increasing ChAT immunoreactivity in this model.

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