Hepatoprotective Effect of Probiotic Lactobacillus rhamnosus GG Through the Modulation of Gut Permeability and Inflammasomes in a Model of Alcoholic Liver Disease in Zebrafish

Alcoholic liver disease (ALD) is among the leading causes of death from liver disease. Among the factors involved in its pathogenesis are inflammation and increased intestinal permeability. The aim of this study was to assess the effect of GG (LGG) on hepatic lipid accumulation, activation of inflam...

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Published inJournal of the American College of Nutrition Vol. 39; no. 2; p. 163
Main Authors Bruch-Bertani, Juliana Paula, Uribe-Cruz, Carolina, Pasqualotto, Amanda, Longo, Larisse, Ayres, Raquel, Beskow, Carolina Bortolin, Barth, Afonso Luis, Lima-Morales, Daiana, Meurer, Fábio, Tayguara Silveira Guerreiro, Gabriel, da Silveira, Themis Reverbel, Álvares-da-Silva, Mário Reis, Dall'Alba, Valesca
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LanguageEnglish
Published United States 17.02.2020
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Abstract Alcoholic liver disease (ALD) is among the leading causes of death from liver disease. Among the factors involved in its pathogenesis are inflammation and increased intestinal permeability. The aim of this study was to assess the effect of GG (LGG) on hepatic lipid accumulation, activation of inflammasomes, and gut permeability markers in experimental model of ALD with zebrafish. An experiment was conducted to assess the effective LGG dose capable of promoting intestinal colonization. Animals were divided into three groups (  = 64/group): ethanol group (E), ethanol + probiotic group (EP), and control group (C). Groups E and EP were exposed to 0.5% ethanol concentration for 28 days. At the end of this period, animals were euthanized, and livers were collected for Oil Red staining and assessment of the inflammasome system. Intestines were collected for evaluation of gut permeability markers. The dose of 1.55 × 10 UFC LGG/fish/d promoted intestinal colonization. Group EP presented lower hepatic lipid accumulation, lower expression, and higher expression when compared to group E. Supplementation with LGG was protective for hepatic steatosis in ALD model. In addition, LGG influenced the modulation of the inflammatory response and markers of gut permeability, improving the gut barrier structure.
AbstractList Alcoholic liver disease (ALD) is among the leading causes of death from liver disease. Among the factors involved in its pathogenesis are inflammation and increased intestinal permeability. The aim of this study was to assess the effect of GG (LGG) on hepatic lipid accumulation, activation of inflammasomes, and gut permeability markers in experimental model of ALD with zebrafish. An experiment was conducted to assess the effective LGG dose capable of promoting intestinal colonization. Animals were divided into three groups (  = 64/group): ethanol group (E), ethanol + probiotic group (EP), and control group (C). Groups E and EP were exposed to 0.5% ethanol concentration for 28 days. At the end of this period, animals were euthanized, and livers were collected for Oil Red staining and assessment of the inflammasome system. Intestines were collected for evaluation of gut permeability markers. The dose of 1.55 × 10 UFC LGG/fish/d promoted intestinal colonization. Group EP presented lower hepatic lipid accumulation, lower expression, and higher expression when compared to group E. Supplementation with LGG was protective for hepatic steatosis in ALD model. In addition, LGG influenced the modulation of the inflammatory response and markers of gut permeability, improving the gut barrier structure.
Author Bruch-Bertani, Juliana Paula
Álvares-da-Silva, Mário Reis
Dall'Alba, Valesca
Pasqualotto, Amanda
Uribe-Cruz, Carolina
Ayres, Raquel
Longo, Larisse
Lima-Morales, Daiana
Barth, Afonso Luis
Tayguara Silveira Guerreiro, Gabriel
Meurer, Fábio
da Silveira, Themis Reverbel
Beskow, Carolina Bortolin
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  givenname: Carolina
  surname: Uribe-Cruz
  fullname: Uribe-Cruz, Carolina
  organization: Post Graduate Program in Gastroenterology and Hepatology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Brazil
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  givenname: Amanda
  surname: Pasqualotto
  fullname: Pasqualotto, Amanda
  organization: Post Graduate Program in Gastroenterology and Hepatology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Brazil
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  givenname: Larisse
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  fullname: Barth, Afonso Luis
  organization: Research Laboratory on Bacterial Resistance (LABRESIS), Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Brazil
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  givenname: Daiana
  surname: Lima-Morales
  fullname: Lima-Morales, Daiana
  organization: Research Laboratory on Bacterial Resistance (LABRESIS), Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Brazil
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  givenname: Fábio
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  givenname: Gabriel
  surname: Tayguara Silveira Guerreiro
  fullname: Tayguara Silveira Guerreiro, Gabriel
  organization: Experimental Laboratory of Hepatology and Gastroenterology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Brazil
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  givenname: Themis Reverbel
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  givenname: Mário Reis
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  givenname: Valesca
  surname: Dall'Alba
  fullname: Dall'Alba, Valesca
  organization: Department of Nutrition. School of Medicine, UFRGS. Nutrition Division. Hospital de Clínicas de Porto Alegre, UFRGS. Porto Alegre, Brazil
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Keywords alcoholic liver disease
zebrafish
inflammasomes
Lactobacillus rhamnosus GG
probiotics
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Title Hepatoprotective Effect of Probiotic Lactobacillus rhamnosus GG Through the Modulation of Gut Permeability and Inflammasomes in a Model of Alcoholic Liver Disease in Zebrafish
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