-
Je něco špatně v tomto záznamu ?
Feeding High-Fat Diet Accelerates Development of Peripheral and Central Insulin Resistance and Inflammation and Worsens AD-like Pathology in APP/PS1 Mice
A. Mengr, V. Strnadová, Š. Strnad, V. Vrkoslav, H. Pelantová, M. Kuzma, T. Comptdaer, B. Železná, J. Kuneš, MC. Galas, A. Pačesová, L. Maletínská
Jazyk angličtina Země Švýcarsko
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
NLK
Free Medical Journals
od 2009
PubMed Central
od 2009
Europe PubMed Central
od 2009
ProQuest Central
od 2009-01-01
Open Access Digital Library
od 2009-01-01
Open Access Digital Library
od 2009-01-01
Health & Medicine (ProQuest)
od 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2009
PubMed
37686722
DOI
10.3390/nu15173690
Knihovny.cz E-zdroje
- 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
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.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc23016516
- 003
- CZ-PrNML
- 005
- 20231026105746.0
- 007
- ta
- 008
- 231013s2023 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3390/nu15173690 $2 doi
- 035 __
- $a (PubMed)37686722
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Mengr, Anna $u Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo nám. 2, Prague 6, 166 10 Prague, Czech Republic
- 245 10
- $a Feeding High-Fat Diet Accelerates Development of Peripheral and Central Insulin Resistance and Inflammation and Worsens AD-like Pathology in APP/PS1 Mice / $c A. Mengr, V. Strnadová, Š. Strnad, V. Vrkoslav, H. Pelantová, M. Kuzma, T. Comptdaer, B. Železná, J. Kuneš, MC. Galas, A. Pačesová, L. Maletínská
- 520 9_
- $a 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.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a myši $7 D051379
- 650 12
- $a Alzheimerova nemoc $x etiologie $7 D000544
- 650 12
- $a inzulinová rezistence $7 D007333
- 650 _2
- $a neurozánětlivé nemoci $7 D000090862
- 650 _2
- $a dieta s vysokým obsahem tuků $x škodlivé účinky $7 D059305
- 650 12
- $a diabetes mellitus 2. typu $7 D003924
- 650 _2
- $a zánět $7 D007249
- 650 _2
- $a amyloidní beta-protein $7 D016229
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Strnadová, Veronika $u Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo nám. 2, Prague 6, 166 10 Prague, Czech Republic
- 700 1_
- $a Strnad, Štěpán $u Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo nám. 2, Prague 6, 166 10 Prague, Czech Republic $1 https://orcid.org/0000000207692420
- 700 1_
- $a Vrkoslav, Vladimír $u Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo nám. 2, Prague 6, 166 10 Prague, Czech Republic $1 https://orcid.org/0000000251268360
- 700 1_
- $a Pelantová, Helena $u Institute of Microbiology of the Czech Academy of Sciences, Vídeňská 1083, Prague 4, 142 20 Prague, Czech Republic $1 https://orcid.org/0000000225237413
- 700 1_
- $a Kuzma, Marek $u Institute of Microbiology of the Czech Academy of Sciences, Vídeňská 1083, Prague 4, 142 20 Prague, Czech Republic
- 700 1_
- $a Comptdaer, Thomas $u University of Lille, Inserm, CHU Lille, CNRS, LilNCog-Lille Neuroscience & Cognition, F-59000 Lille, France
- 700 1_
- $a Železná, Blanka $u Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo nám. 2, Prague 6, 166 10 Prague, Czech Republic
- 700 1_
- $a Kuneš, Jaroslav $u Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo nám. 2, Prague 6, 166 10 Prague, Czech Republic $u Institute of Physiology of the Czech Academy of Sciences, Vídeňská 1083, Prague 4, 142 20 Prague, Czech Republic
- 700 1_
- $a Galas, Marie-Christine $u University of Lille, Inserm, CHU Lille, CNRS, LilNCog-Lille Neuroscience & Cognition, F-59000 Lille, France
- 700 1_
- $a Pačesová, Andrea $u Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo nám. 2, Prague 6, 166 10 Prague, Czech Republic
- 700 1_
- $a Maletínská, Lenka $u Institute of Organic Chemistry and Biochemistry of the Czech Academy of Sciences, Flemingovo nám. 2, Prague 6, 166 10 Prague, Czech Republic
- 773 0_
- $w MED00189563 $t Nutrients $x 2072-6643 $g Roč. 15, č. 17 (2023)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/37686722 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20231013 $b ABA008
- 991 __
- $a 20231026105740 $b ABA008
- 999 __
- $a ok $b bmc $g 2000183 $s 1202878
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2023 $b 15 $c 17 $e 20230823 $i 2072-6643 $m Nutrients $n Nutrients $x MED00189563
- GRA __
- $a 20-00546S $p Czech Science Foundation
- GRA __
- $a TN01000013 $p Technology Agency of the Czech Republic
- GRA __
- $a RVO61388971, RVO67958523 $p Czech Academy of Sciences
- GRA __
- $a LX22NP05104 $p EXCELES
- GRA __
- $a CZ.02.2.69/18_053/0016940 $p European Regional Development Fund
- LZP __
- $a Pubmed-20231013