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Hepatoprotective Effect of Probiotic Lactic Acid Bacteria on Thioacetamide-Induced Liver Fibrosis in Rats

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dc.contributor.author Jantararussamee C.
dc.contributor.author Rodniem S.
dc.contributor.author Taweechotipatr M.
dc.contributor.author Showpittapornchai U.
dc.contributor.author Pradidarcheep W.
dc.date.accessioned 2022-03-10T13:16:56Z
dc.date.available 2022-03-10T13:16:56Z
dc.date.issued 2021
dc.identifier.issn 18671306
dc.identifier.other 2-s2.0-85085689121
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/17360
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-85085689121&doi=10.1007%2fs12602-020-09663-6&partnerID=40&md5=e51d30ddcb3a0b666800d8edd8c13759
dc.description.abstract Hepatic fibrosis is a reversible wound-healing response characterized by the accumulation of extracellular matrix. Probiotics have been used to prevent and treat various disorders. The aim of the present study was to investigate the hepatoprotective effects of probiotic lactic acid bacteria (mixture of Lactobacillus paracasei, Lactobacillus casei, and Weissella confusa) on thioacetamide (TAA)–induced liver fibrosis in rats. Thirty-five male Wistar rats were randomly divided into five groups: (1) control, (2) TAA, (3) TAA+probiotics, (4) TAA+silymarin, and (5) probiotics. Group 1 rats received a standard diet. In groups 2–4, fibrosis was induced by intraperitoneal injection of TAA (200 mg/kg BW) 3 times weekly for 8 consecutive weeks. Group 4 received TAA plus 100 mg/kg BW of silymarin 2 times weekly. Groups 3 and 5 were fed 109 CFU/mL viable microbial cells daily by gavage. The rats were sacrificed after 8 weeks of treatment. Liver tissues were collected immediately and processed for histopathological, lipid peroxidation, and Western blot analyses of TNF-α, TGF-β1, and α-SMA. Blood serum was collected to measure liver enzymes. Rats in the TAA groups suffered from hepatic injury (increased serum enzyme levels, liver inflammation, and increased concentration of TNF-α, TGF-β1, and α-SMA proteins) and extensive liver fibrosis. In contrast, TAA-treated rats receiving probiotics or silymarin had significantly lower serum enzyme levels, less inflammation, and less fibrosis. Liver damage was lower in the TAA+probiotics-treated group. Consumption of a mixture of probiotic lactic acid bacteria attenuates the development of liver fibrosis. © 2020, Springer Science+Business Media, LLC, part of Springer Nature.
dc.language en
dc.subject alanine aminotransferase
dc.subject alkaline phosphatase
dc.subject alpha smooth muscle actin
dc.subject aspartate aminotransferase
dc.subject malonaldehyde
dc.subject probiotic agent
dc.subject silymarin
dc.subject thioacetamide
dc.subject transforming growth factor beta1
dc.subject tumor necrosis factor
dc.subject thioacetamide
dc.subject animal experiment
dc.subject animal model
dc.subject animal tissue
dc.subject Article
dc.subject body weight
dc.subject cell infiltration
dc.subject controlled study
dc.subject hepatitis
dc.subject histopathology
dc.subject Lactobacillus casei
dc.subject Lactobacillus paracasei
dc.subject lipid peroxidation assay
dc.subject liver fibrosis
dc.subject liver injury
dc.subject liver necrosis
dc.subject liver protection
dc.subject liver weight
dc.subject male
dc.subject nonhuman
dc.subject oxidative stress
dc.subject polyacrylamide gel electrophoresis
dc.subject protein expression
dc.subject rat
dc.subject small intestine
dc.subject Weissella
dc.subject Weissella confusa
dc.subject Western blotting
dc.subject animal
dc.subject Lactobacillales
dc.subject liver cirrhosis
dc.subject metabolism
dc.subject pathology
dc.subject Wistar rat
dc.subject Animals
dc.subject Lactobacillales
dc.subject Liver Cirrhosis
dc.subject Male
dc.subject Rats
dc.subject Rats, Wistar
dc.subject Thioacetamide
dc.title Hepatoprotective Effect of Probiotic Lactic Acid Bacteria on Thioacetamide-Induced Liver Fibrosis in Rats
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Probiotics and Antimicrobial Proteins. Vol 13, No.1 (2021), p.40-50
dc.identifier.doi 10.1007/s12602-020-09663-6


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