Feeding High-Fat Diet Accelerates Development of Peripheral and Central Insulin Resistance and Inflammation and Worsens AD-like Pathology in APP/PS1 Mice
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
20-00546S
Czech Science Foundation
TN01000013
Technology Agency of the Czech Republic
RVO61388971, RVO67958523
Czech Academy of Sciences
LX22NP05104
EXCELES
CZ.02.2.69/18_053/0016940
European Regional Development Fund
PubMed
37686722
PubMed Central
PMC10490051
DOI
10.3390/nu15173690
PII: nu15173690
Knihovny.cz E-zdroje
- Klíčová slova
- APP/PS1, Alzheimer’s disease, amyloid-β, glucose intolerance, inflammation, insulin resistance, neuroinflammation, obesity, tau protein,
- MeSH
- Alzheimerova nemoc * etiologie MeSH
- amyloidní beta-protein MeSH
- diabetes mellitus 2. typu * MeSH
- dieta s vysokým obsahem tuků škodlivé účinky MeSH
- inzulinová rezistence * MeSH
- myši MeSH
- neurozánětlivé nemoci MeSH
- zánět MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- amyloidní beta-protein MeSH
Alzheimer's disease (AD) is a progressive brain disorder characterized by extracellular amyloid-β (Aβ) plaques, intracellular neurofibrillary tangles formed by hyperphosphorylated Tau protein and neuroinflammation. Previous research has shown that obesity and type 2 diabetes mellitus, underlined by insulin resistance (IR), are risk factors for neurodegenerative disorders. In this study, obesity-induced peripheral and central IR and inflammation were studied in relation to AD-like pathology in the brains and periphery of APP/PS1 mice, a model of Aβ pathology, fed a high-fat diet (HFD). APP/PS1 mice and their wild-type controls fed either a standard diet or HFD were characterized at the ages of 3, 6 and 10 months by metabolic parameters related to obesity via mass spectroscopy, nuclear magnetic resonance, immunoblotting and immunohistochemistry to quantify how obesity affected AD pathology. The HFD induced substantial peripheral IR leading to central IR. APP/PS1-fed HFD mice had more pronounced IR, glucose intolerance and liver steatosis than their WT controls. The HFD worsened Aβ pathology in the hippocampi of APP/PS1 mice and significantly supported both peripheral and central inflammation. This study reveals a deleterious effect of obesity-related mild peripheral inflammation and prediabetes on the development of Aβ and Tau pathology and neuroinflammation in APP/PS1 mice.
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