-
Something wrong with this record ?
Cardio- and Neurometabolic Adipobiology: Consequences and Implications for Therapy
J. Frohlich, GN. Chaldakov, M. Vinciguerra
Language English Country Switzerland
Document type Journal Article, Review
Grant support
Project 856871 - TRANSTEM
H2020 Research Infrastructures
Project MAGNET (No. CZ.02.1s01/0.0/0.0/15_003/0000492
European Research Development Fund
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
33923652
DOI
10.3390/ijms22084137
Knihovny.cz E-resources
- MeSH
- Adipokines metabolism MeSH
- Molecular Targeted Therapy methods MeSH
- Humans MeSH
- Metabolic Syndrome drug therapy metabolism MeSH
- Neurodegenerative Diseases drug therapy metabolism MeSH
- Neuropeptides metabolism MeSH
- Nerve Growth Factors metabolism MeSH
- Signal Transduction MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
Studies over the past 30 years have revealed that adipose tissue is the major endocrine and paracrine organ of the human body. Arguably, adiopobiology has taken its reasonable place in studying obesity and related cardiometabolic diseases (CMDs), including Alzheimer's disease (AD), which is viewed herein as a neurometabolic disorder. The pathogenesis and therapy of these diseases are multiplex at basic, clinical and translational levels. Our present goal is to describe new developments in cardiometabolic and neurometabolic adipobiology. Accordingly, we focus on adipose- and/or skeletal muscle-derived signaling proteins (adipsin, adiponectin, nerve growth factor, brain-derived neuroptrophic factor, neurotrophin-3, irisin, sirtuins, Klotho, neprilysin, follistatin-like protein-1, meteorin-like (metrnl), as well as growth differentiation factor 11) as examples of metabotrophic factors (MTFs) implicated in the pathogenesis and therapy of obesity and related CMDs. We argue that these pathologies are MTF-deficient diseases. In 1993 the "vascular hypothesis of AD" was published and in the present review we propose the "vasculometabolic hypothesis of AD." We discuss how MTFs could bridge CMDs and neurodegenerative diseases, such as AD. Greater insights on how to manage the MTF network would provide benefits to the quality of human life.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21018822
- 003
- CZ-PrNML
- 005
- 20210830100411.0
- 007
- ta
- 008
- 210728s2021 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3390/ijms22084137 $2 doi
- 035 __
- $a (PubMed)33923652
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Frohlich, Jan $u International Clinical Research Center, St. Anne's University Hospital, 656 91 Brno, Czech Republic
- 245 10
- $a Cardio- and Neurometabolic Adipobiology: Consequences and Implications for Therapy / $c J. Frohlich, GN. Chaldakov, M. Vinciguerra
- 520 9_
- $a Studies over the past 30 years have revealed that adipose tissue is the major endocrine and paracrine organ of the human body. Arguably, adiopobiology has taken its reasonable place in studying obesity and related cardiometabolic diseases (CMDs), including Alzheimer's disease (AD), which is viewed herein as a neurometabolic disorder. The pathogenesis and therapy of these diseases are multiplex at basic, clinical and translational levels. Our present goal is to describe new developments in cardiometabolic and neurometabolic adipobiology. Accordingly, we focus on adipose- and/or skeletal muscle-derived signaling proteins (adipsin, adiponectin, nerve growth factor, brain-derived neuroptrophic factor, neurotrophin-3, irisin, sirtuins, Klotho, neprilysin, follistatin-like protein-1, meteorin-like (metrnl), as well as growth differentiation factor 11) as examples of metabotrophic factors (MTFs) implicated in the pathogenesis and therapy of obesity and related CMDs. We argue that these pathologies are MTF-deficient diseases. In 1993 the "vascular hypothesis of AD" was published and in the present review we propose the "vasculometabolic hypothesis of AD." We discuss how MTFs could bridge CMDs and neurodegenerative diseases, such as AD. Greater insights on how to manage the MTF network would provide benefits to the quality of human life.
- 650 _2
- $a adipokiny $x metabolismus $7 D054392
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a metabolický syndrom $x farmakoterapie $x metabolismus $7 D024821
- 650 _2
- $a cílená molekulární terapie $x metody $7 D058990
- 650 _2
- $a neurotrofní faktory $x metabolismus $7 D009414
- 650 _2
- $a neurodegenerativní nemoci $x farmakoterapie $x metabolismus $7 D019636
- 650 _2
- $a neuropeptidy $x metabolismus $7 D009479
- 650 _2
- $a signální transdukce $7 D015398
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a přehledy $7 D016454
- 700 1_
- $a Chaldakov, George N $u Department of Anatomy and Cell Biology and Research Institute of the Medical University, 9002 Varna, Bulgaria $u Department of Translational Stem Cell Biology, Research Institute of the Medical University, 9002 Varna, Bulgaria
- 700 1_
- $a Vinciguerra, Manlio $u International Clinical Research Center, St. Anne's University Hospital, 656 91 Brno, Czech Republic $u Department of Translational Stem Cell Biology, Research Institute of the Medical University, 9002 Varna, Bulgaria
- 773 0_
- $w MED00176142 $t International journal of molecular sciences $x 1422-0067 $g Roč. 22, č. 8 (2021)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/33923652 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20210728 $b ABA008
- 991 __
- $a 20210830100411 $b ABA008
- 999 __
- $a ok $b bmc $g 1689801 $s 1139268
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 22 $c 8 $e 20210416 $i 1422-0067 $m International journal of molecular sciences $n Int J Mol Sci $x MED00176142
- GRA __
- $a Project 856871 - TRANSTEM $p H2020 Research Infrastructures
- GRA __
- $a Project MAGNET (No. CZ.02.1s01/0.0/0.0/15_003/0000492 $p European Research Development Fund
- LZP __
- $a Pubmed-20210728