A Nutraceutical Formulation Containing Brown Algae Reduces Hepatic Lipid Accumulation by Modulating Lipid Metabolism and Inflammation in Experimental Models of NAFLD and NASH.
Animals
C-Reactive Protein
/ metabolism
Dietary Supplements
Diglycerides
/ metabolism
Fatty Acid Synthases
Inflammation
/ metabolism
Interleukin-6
/ metabolism
Lipid Metabolism
Liver
Mice
Mice, Inbred C57BL
Models, Theoretical
Non-alcoholic Fatty Liver Disease
/ metabolism
Perilipin-2
/ metabolism
Peroxidase
/ metabolism
Phaeophyceae
/ metabolism
RNA, Messenger
/ metabolism
Rats
Seaweed
/ chemistry
Sterol Regulatory Element Binding Protein 1
/ genetics
Sterols
/ pharmacology
Tumor Necrosis Factor-alpha
/ metabolism
Ascophyllum nodosum
Fucus vesiculosus
NAFLD
NASH
algal extract
brown seaweed
steatosis
Journal
Marine drugs
ISSN: 1660-3397
Titre abrégé: Mar Drugs
Pays: Switzerland
ID NLM: 101213729
Informations de publication
Date de publication:
08 Sep 2022
08 Sep 2022
Historique:
received:
07
08
2022
revised:
30
08
2022
accepted:
05
09
2022
entrez:
22
9
2022
pubmed:
23
9
2022
medline:
28
9
2022
Statut:
epublish
Résumé
Recently, some preclinical and clinical studies have demonstrated the ability of brown seaweeds in reducing the risk factors for metabolic syndrome. Here, we analyzed the beneficial effect of a nutraceutical formulation containing a phytocomplex extracted from seaweeds and chromium picolinate in animal models of liver steatosis of differing severities (rats with non-alcoholic fatty liver disease (NAFLD) and its complication, non-alcoholic steatohepatitis (NASH)). This treatment led to a significant drop in hepatic fat deposition in both models (p < 0.01 vs. untreated animals), accompanied by a reduction in plasma inflammatory cytokines, such as interleukin 6, tumor necrosis factor α, and C reactive protein, and myeloperoxidase expression in liver tissue. Furthermore, a modulation of the molecular pathways involved in lipid metabolism and storage was demonstrated, since we observed the significant reduction of the mRNA levels of fatty acid synthase, diacylglycerol acyltransferases, the sterol-binding protein SREBP-1, and the lipid transporter perilipin-2, in both treated NAFLD and NASH rats in comparison to untreated ones. In conclusion, this nutraceutical product was effective in reducing liver steatosis and showed further beneficial effects on hepatic inflammation and glycemic control, which were particularly evident in rats characterized by a more severe condition, thus representing a therapeutic option for the treatment of NAFLD and NASH patients.
Identifiants
pubmed: 36135761
pii: md20090572
doi: 10.3390/md20090572
pmc: PMC9501409
pii:
doi:
Substances chimiques
Diglycerides
0
Interleukin-6
0
Perilipin-2
0
RNA, Messenger
0
Sterol Regulatory Element Binding Protein 1
0
Sterols
0
Tumor Necrosis Factor-alpha
0
C-Reactive Protein
9007-41-4
Peroxidase
EC 1.11.1.7
Fatty Acid Synthases
EC 2.3.1.85
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Aesculapius Farmaceutici (Italy)
Références
Biochimie. 2004 Nov;86(11):839-48
pubmed: 15589694
Drug Metab Rev. 2017 May;49(2):197-211
pubmed: 28303724
J Hepatol. 2016 Jun;64(6):1403-15
pubmed: 26867490
Nat Rev Gastroenterol Hepatol. 2017 Jun;14(6):343-355
pubmed: 28428634
Foods. 2021 Feb 19;10(2):
pubmed: 33669572
J Genet Genomics. 2022 Apr;49(4):269-278
pubmed: 34757037
Antioxidants (Basel). 2017 Jul 10;6(3):
pubmed: 28698499
Arch Biochem Biophys. 2018 Oct 1;655:1-11
pubmed: 30077544
Cell Death Dis. 2021 Oct 21;12(11):977
pubmed: 34675185
World J Gastroenterol. 2017 Nov 14;23(42):7519-7530
pubmed: 29204052
JHEP Rep. 2020 Oct 09;2(6):100192
pubmed: 33163950
Molecules. 2020 Sep 12;25(18):
pubmed: 32932674
Foods. 2022 Apr 25;11(9):
pubmed: 35563955
Nutrients. 2019 Jul 15;11(7):
pubmed: 31311123
Mar Drugs. 2019 Jul 24;17(8):
pubmed: 31344874
Int J Mol Sci. 2018 Mar 19;19(3):
pubmed: 29562725
Exp Cell Res. 2016 Jan 15;340(2):187-92
pubmed: 26515554
Mar Drugs. 2017 Feb 15;15(2):
pubmed: 28212301
J Diabetes Res. 2021 Sep 30;2021:3389316
pubmed: 34631894
J Agric Food Chem. 2009 May 13;57(9):3483-9
pubmed: 19338274
Biomedicines. 2021 Jun 17;9(6):
pubmed: 34204571
J Pharm Pharm Sci. 2012;15(1):141-83
pubmed: 22365095
Biometals. 2016 Oct;29(5):881-92
pubmed: 27497686
Nutrients. 2017 Sep 27;9(10):
pubmed: 28953222
Br J Nutr. 2013 Jul 28;110(2):197-205
pubmed: 23211098
J Trace Elem Med Biol. 2021 Jan;63:126656
pubmed: 33022485
Med Sci (Basel). 2018 Apr 18;6(2):
pubmed: 29669993
Foods. 2021 Jan 24;10(2):
pubmed: 33498824
Nature. 1997 Mar 20;386(6622):296-9
pubmed: 9069290
World J Gastrointest Pathophysiol. 2017 May 15;8(2):11-26
pubmed: 28573064
J Food Sci. 2010 Jun;75(5):H145-50
pubmed: 20629879
Front Immunol. 2018 Apr 13;9:754
pubmed: 29706967
Biomedicines. 2021 Apr 02;9(4):
pubmed: 33918467
World J Gastroenterol. 2014 Sep 28;20(36):12956-80
pubmed: 25278691
J Hepatol. 2014 Mar;60(3):633-42
pubmed: 24269473
Molecules. 2021 Jan 30;26(3):
pubmed: 33573121
Mol Cell Endocrinol. 2015 Dec 15;418 Pt 1:55-65
pubmed: 25724480
Circulation. 2005 Mar 22;111(11):1448-54
pubmed: 15781756
Biochem Biophys Res Commun. 2010 Jul 2;397(3):459-64
pubmed: 20513351
J Physiol Biochem. 2011 Dec;67(4):629-36
pubmed: 21847662
Biomedicines. 2020 Jul 21;8(7):
pubmed: 32708059
Mar Drugs. 2022 Mar 30;20(4):
pubmed: 35447916
Mar Drugs. 2020 May 22;18(5):
pubmed: 32456047
Atherosclerosis. 2013 May;228(1):198-202
pubmed: 23453352
Diabetes Care. 2004 Nov;27(11):2741-51
pubmed: 15505017
Eur J Gastroenterol Hepatol. 2021 Oct 1;33(10):1298-1306
pubmed: 32804855
Biol Trace Elem Res. 2019 Jan;187(1):192-201
pubmed: 29797206
Phytother Res. 2019 Mar;33(3):791-797
pubmed: 30714233
Mar Drugs. 2020 Jan 17;18(1):
pubmed: 31963560
Front Immunol. 2020 Aug 20;11:1893
pubmed: 32973784