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1.
Mar Drugs ; 20(9)2022 Sep 08.
Artigo em Inglês | MEDLINE | ID: mdl-36135761

RESUMO

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.


Assuntos
Hepatopatia Gordurosa não Alcoólica , Phaeophyceae , Alga Marinha , Animais , Proteína C-Reativa/metabolismo , Suplementos Nutricionais , Diglicerídeos/metabolismo , Ácido Graxo Sintases , Inflamação/metabolismo , Interleucina-6/metabolismo , Metabolismo dos Lipídeos , Fígado , Camundongos , Camundongos Endogâmicos C57BL , Modelos Teóricos , Hepatopatia Gordurosa não Alcoólica/metabolismo , Perilipina-2/metabolismo , Peroxidase/metabolismo , Phaeophyceae/metabolismo , RNA Mensageiro/metabolismo , Ratos , Alga Marinha/química , Proteína de Ligação a Elemento Regulador de Esterol 1/genética , Esteróis/farmacologia , Fator de Necrose Tumoral alfa/metabolismo
2.
Mar Drugs ; 18(1)2020 Jan 17.
Artigo em Inglês | MEDLINE | ID: mdl-31963560

RESUMO

The Asian coastal communities have used the brown seaweeds Fucus vesiculosus and Ascophyllum nodosum since ancient times. Recently, some in vitro and in vivo studies have demonstrated their abilities in reducing risk factors for metabolic syndrome. Here, we analyzed the protective effect of a phytocomplex extracted from these seaweeds on the deposition of fat in the liver after the administration of a high-fat diet (HFD) to rats for five weeks. The administration of F. vesiculosus and A. nodosum led to significant reductions in microvescicular steatosis and plasma biochemical and lipid parameters, such as alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), total and conjugated bilirubin, and triglycerides. Furthermore, the postprandial glycemic peak was delayed and significantly reduced (p < 0.01) by the algal extract administration. In conclusion, this extract is effective in reducing microvescicular steatosis and improving glycemic control, thereby lowering the risk of nonalcoholic fatty liver disease, obesity, and diabetes, diseases related to the consumption of fat and sugar-enriched diets.


Assuntos
Ascophyllum/química , Dieta Redutora/efeitos adversos , Fucus/química , Fígado/efeitos dos fármacos , Hepatopatia Gordurosa não Alcoólica/induzido quimicamente , Hepatopatia Gordurosa não Alcoólica/tratamento farmacológico , Extratos Vegetais/farmacologia , Alanina Transaminase/metabolismo , Animais , Aspartato Aminotransferases/metabolismo , Glicemia/efeitos dos fármacos , Dieta Hiperlipídica/efeitos adversos , Fígado/metabolismo , Masculino , Hepatopatia Gordurosa não Alcoólica/metabolismo , Período Pós-Prandial/efeitos dos fármacos , Ratos , Ratos Wistar , Alga Marinha/química , Triglicerídeos/metabolismo
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