RRC ID 58769
著者 Krishnan M, Hwang JS, Kim M, Kim YJ, Seo JH, Jung J, Ha E.
タイトル β-hydroxybutyrate Impedes the Progression of Alzheimer's Disease and Atherosclerosis in ApoE-Deficient Mice.
ジャーナル Nutrients
Abstract β-hydroxybutyrate (β-OHB) has been shown to exert an anti-inflammatory activity. Apolipoprotein-E (ApoE) is strongly associated with atherosclerosis and Alzheimer's disease (AD). This study aimed to explore the therapeutic effect of β-OHB in the brain and the aorta of high-fat diet (HFD)-fed ApoE-deficient mice. We found in Apo-E deficient mice that β-OHB attenuated lipid deposition in the choroid plexus (ChP) and decreased amyloid plaque in the substantia nigra pars compacta. We also found decreased CD68-positive macroglia infiltration of the ChP in β-OHB-treated ApoE-deficient mice. β-OHB treatment ameliorated IgG extravasation into the hippocampal region of the brain. In vitro study using ChP mice cell line revealed that β-OHB attenuated oxidized low-density lipoprotein-induced ApoE-specific differentially expressed inflammatory ChP genes. Treatment with β-OHB reduced aortic plaque formation without affecting blood lipid profiles and decreased serum production of resistin, a well-established risk factor for both AD and atherosclerosis. Thus, the current study suggests and describes the therapeutic potential of β-OHB for the treatment of AD and atherosclerosis.
巻・号 12(2)
公開日 2020-2-13
DOI 10.3390/nu12020471
PII nu12020471
PMID 32069870
PMC PMC7071244
MeSH 3-Hydroxybutyric Acid / pharmacology* Alzheimer Disease / drug therapy* Alzheimer Disease / etiology Animals Anti-Inflammatory Agents / pharmacology* Aorta / drug effects Apolipoproteins E / deficiency Atherosclerosis / drug therapy* Atherosclerosis / etiology Brain / drug effects Diet, High-Fat Disease Models, Animal Disease Progression Male Mice Mice, Inbred C57BL Mice, Knockout Plaque, Amyloid
IF 4.546
引用数 0
リソース情報
ヒト・動物細胞 ECPC-4(RCB1287)