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 in | Journal of the American College of Nutrition Vol. 39; no. 2; p. 163 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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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. |
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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 |
Author_xml | – sequence: 1 givenname: Juliana Paula surname: Bruch-Bertani fullname: Bruch-Bertani, Juliana Paula organization: Post Graduate Program in Gastroenterology and Hepatology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Brazil – sequence: 2 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 – sequence: 3 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 – sequence: 4 givenname: Larisse surname: Longo fullname: Longo, Larisse organization: Post Graduate Program in Gastroenterology and Hepatology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Brazil – sequence: 5 givenname: Raquel surname: Ayres fullname: Ayres, Raquel organization: Experimental Laboratory of Hepatology and Gastroenterology, Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Brazil – sequence: 6 givenname: Carolina Bortolin surname: Beskow fullname: Beskow, Carolina Bortolin organization: Post Graduate Program in Gastroenterology and Hepatology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Brazil – sequence: 7 givenname: Afonso Luis surname: Barth fullname: Barth, Afonso Luis organization: Research Laboratory on Bacterial Resistance (LABRESIS), Hospital de Clínicas de Porto Alegre (HCPA), Porto Alegre, Brazil – sequence: 8 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 – sequence: 9 givenname: Fábio surname: Meurer fullname: Meurer, Fábio organization: Post Graduate Program in Sustainable Development of Aquaculture, Universidade Federal do Paraná, Campus de Palotina, Paraná, Brazil – sequence: 10 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 – sequence: 11 givenname: Themis Reverbel surname: da Silveira fullname: da Silveira, Themis Reverbel organization: Post Graduate Program in Gastroenterology and Hepatology, Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, Brazil – sequence: 12 givenname: Mário Reis surname: Álvares-da-Silva fullname: Álvares-da-Silva, Mário Reis organization: Department of Internal Medicine, Gastroenterology and Hepatology Unit. School of Medicine, UFRGS. Gastroenterology and Hepatology Division, HCPA, Porto Alegre, Brazil – sequence: 13 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 |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31241423$$D View this record in MEDLINE/PubMed |
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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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