-
Je něco špatně v tomto záznamu ?
Krill Oil Supplementation Reduces Exacerbated Hepatic Steatosis Induced by Thermoneutral Housing in Mice with Diet-Induced Obesity
G. Sistilli, V. Kalendova, T. Cajka, I. Irodenko, K. Bardova, M. Oseeva, P. Zacek, P. Kroupova, O. Horakova, K. Lackner, A. Gastaldelli, O. Kuda, J. Kopecky, M. Rossmeisl
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
Grantová podpora
17-11027S
Czech Science Foundation
722619
H2020 Marie Skłodowska-Curie Actions
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
33572810
DOI
10.3390/nu13020437
Knihovny.cz E-zdroje
- MeSH
- bydlení zvířat MeSH
- dieta s vysokým obsahem tuků škodlivé účinky MeSH
- Euphausiacea MeSH
- fosfolipidy farmakologie MeSH
- fyziologie výživy zvířat MeSH
- inzulinová rezistence MeSH
- játra metabolismus MeSH
- modely nemocí na zvířatech MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- nealkoholová steatóza jater etiologie terapie MeSH
- obezita etiologie terapie MeSH
- potravní doplňky * MeSH
- rybí oleje farmakologie MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Preclinical evidence suggests that n-3 fatty acids EPA and DHA (Omega-3) supplemented as phospholipids (PLs) may be more effective than triacylglycerols (TAGs) in reducing hepatic steatosis. To further test the ability of Omega-3 PLs to alleviate liver steatosis, we used a model of exacerbated non-alcoholic fatty liver disease based on high-fat feeding at thermoneutral temperature. Male C57BL/6N mice were fed for 24 weeks a lard-based diet given either alone (LHF) or supplemented with Omega-3 (30 mg/g diet) as PLs (krill oil; ω3PL) or TAGs (Epax 3000TG concentrate; ω3TG), which had a similar total content of EPA and DHA and their ratio. Substantial levels of TAG accumulation (~250 mg/g) but relatively low inflammation/fibrosis levels were achieved in the livers of control LHF mice. Liver steatosis was reduced by >40% in the ω3PL but not ω3TG group, and plasma ALT levels were markedly reduced (by 68%) in ω3PL mice as well. Krill oil administration also improved hepatic insulin sensitivity, and its effects were associated with high plasma adiponectin levels (150% of LHF mice) along with superior bioavailability of EPA, increased content of alkaloids stachydrine and trigonelline, suppression of lipogenic gene expression, and decreased diacylglycerol levels in the liver. This study reveals that in addition to Omega-3 PLs, other constituents of krill oil, such as alkaloids, may contribute to its strong antisteatotic effects in the liver.
Institute of Pathology Medical University of Graz Neue Stiftingtalstraße 6 8010 Graz Austria
Institute of Physiology of the Czech Academy of Sciences Videnska 1083 14220 Prague 4 Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21019396
- 003
- CZ-PrNML
- 005
- 20220316092039.0
- 007
- ta
- 008
- 210728s2021 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3390/nu13020437 $2 doi
- 035 __
- $a (PubMed)33572810
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Sistilli, Gabriella $u Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic $u Department of Physiology, Faculty of Science, Charles University, Vinicna 7, 12844 Prague 2, Czech Republic
- 245 10
- $a Krill Oil Supplementation Reduces Exacerbated Hepatic Steatosis Induced by Thermoneutral Housing in Mice with Diet-Induced Obesity / $c G. Sistilli, V. Kalendova, T. Cajka, I. Irodenko, K. Bardova, M. Oseeva, P. Zacek, P. Kroupova, O. Horakova, K. Lackner, A. Gastaldelli, O. Kuda, J. Kopecky, M. Rossmeisl
- 520 9_
- $a Preclinical evidence suggests that n-3 fatty acids EPA and DHA (Omega-3) supplemented as phospholipids (PLs) may be more effective than triacylglycerols (TAGs) in reducing hepatic steatosis. To further test the ability of Omega-3 PLs to alleviate liver steatosis, we used a model of exacerbated non-alcoholic fatty liver disease based on high-fat feeding at thermoneutral temperature. Male C57BL/6N mice were fed for 24 weeks a lard-based diet given either alone (LHF) or supplemented with Omega-3 (30 mg/g diet) as PLs (krill oil; ω3PL) or TAGs (Epax 3000TG concentrate; ω3TG), which had a similar total content of EPA and DHA and their ratio. Substantial levels of TAG accumulation (~250 mg/g) but relatively low inflammation/fibrosis levels were achieved in the livers of control LHF mice. Liver steatosis was reduced by >40% in the ω3PL but not ω3TG group, and plasma ALT levels were markedly reduced (by 68%) in ω3PL mice as well. Krill oil administration also improved hepatic insulin sensitivity, and its effects were associated with high plasma adiponectin levels (150% of LHF mice) along with superior bioavailability of EPA, increased content of alkaloids stachydrine and trigonelline, suppression of lipogenic gene expression, and decreased diacylglycerol levels in the liver. This study reveals that in addition to Omega-3 PLs, other constituents of krill oil, such as alkaloids, may contribute to its strong antisteatotic effects in the liver.
- 650 _2
- $a fyziologie výživy zvířat $7 D000824
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a dieta s vysokým obsahem tuků $x škodlivé účinky $7 D059305
- 650 12
- $a potravní doplňky $7 D019587
- 650 _2
- $a modely nemocí na zvířatech $7 D004195
- 650 _2
- $a Euphausiacea $7 D033201
- 650 _2
- $a rybí oleje $x farmakologie $7 D005395
- 650 _2
- $a bydlení zvířat $7 D006799
- 650 _2
- $a inzulinová rezistence $7 D007333
- 650 _2
- $a játra $x metabolismus $7 D008099
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a myši inbrední C57BL $7 D008810
- 650 _2
- $a nealkoholová steatóza jater $x etiologie $x terapie $7 D065626
- 650 _2
- $a obezita $x etiologie $x terapie $7 D009765
- 650 _2
- $a fosfolipidy $x farmakologie $7 D010743
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Kalendova, Veronika $u Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic $u Department of Physiology, Faculty of Science, Charles University, Vinicna 7, 12844 Prague 2, Czech Republic
- 700 1_
- $a Cajka, Tomas $u Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic
- 700 1_
- $a Irodenko, Illaria $u Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic $u Department of Physiology, Faculty of Science, Charles University, Vinicna 7, 12844 Prague 2, Czech Republic
- 700 1_
- $a Bardova, Kristina $u Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic
- 700 1_
- $a Oseeva, Marina $u Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic $u Department of Physiology, Faculty of Science, Charles University, Vinicna 7, 12844 Prague 2, Czech Republic
- 700 1_
- $a Zacek, Petr $u Proteomics Core Facility, Faculty of Science, Charles University, Division BIOCEV, Prumyslova 595, 25250 Vestec, Czech Republic
- 700 1_
- $a Kroupova, Petra $u Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic
- 700 1_
- $a Horakova, Olga $u Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic
- 700 1_
- $a Lackner, Karoline $u Institute of Pathology, Medical University of Graz, Neue Stiftingtalstraße 6, 8010 Graz, Austria
- 700 1_
- $a Gastaldelli, Amalia $u Cardiometabolic Risk Unit, Institute of Clinical Physiology, National Research Council, Via Moruzzi 1, 56100 Pisa, Italy
- 700 1_
- $a Kuda, Ondrej $u Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic
- 700 1_
- $a Kopecky, Jan $u Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic
- 700 1_
- $a Rossmeisl, Martin $u Institute of Physiology of the Czech Academy of Sciences, Videnska 1083, 14220 Prague 4, Czech Republic $7 xx0270807
- 773 0_
- $w MED00189563 $t Nutrients $x 2072-6643 $g Roč. 13, č. 2 (2021)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/33572810 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20210728 $b ABA008
- 991 __
- $a 20220316092034 $b ABA008
- 999 __
- $a ok $b bmc $g 1690260 $s 1139842
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2021 $b 13 $c 2 $e 20210129 $i 2072-6643 $m Nutrients $n Nutrients $x MED00189563
- GRA __
- $a 17-11027S $p Czech Science Foundation
- GRA __
- $a 722619 $p H2020 Marie Skłodowska-Curie Actions
- LZP __
- $a Pubmed-20210728