Article ; Online: Protective Mechanisms of Juncus effusus and Carbonized Juncus effusus against D-Galactosamine-Induced Acute Liver Injury in Mice.
Chemical & pharmaceutical bulletin
2024 Volume 72, Issue 3, Page(s) 280–285
Abstract: This study investigated the hepatoprotective effects of Juncus effusus (J. effusus) and Carbonized J. effusus against liver injury caused by D-galactosamine (D-GalN) in mice. J. effusus and Carbonized J. effusus were administered by gavage once daily ... ...
Abstract | This study investigated the hepatoprotective effects of Juncus effusus (J. effusus) and Carbonized J. effusus against liver injury caused by D-galactosamine (D-GalN) in mice. J. effusus and Carbonized J. effusus were administered by gavage once daily starting seven days before the D-GalN treatment. The results of the study indicated that J. effusus and Carbonized J. effusus suppressed the D-GalN-induced generation of serum alanine transaminase (ALT), aspartate aminotransferase (AST), hepatic malondialdehyde (MDA) and tumor necrosis factor-alpha (TNF-α) was observed. The values of superoxide dismutase (SOD) exhibited an increase. In addition, J. effusus and Carbonized J. effusus promoted the protein expression of nuclear factor erythroid 2-related factor 2 (Nrf2), NADPH quinone oxidoreductase-1 (NQO-1), heme oxygenase-1 (HO-1) as well as the mRNA expression of Nrf2, HO-1, NQO-1 and Glutamate cysteine ligase catalytic subunit (GCLC). The compressed Carbonized J. effusus demonstrated the optimum impact. These results suggest that J. effusus and Carbonized J. effusus protect against D-GalN-induced acute liver injury through the activation of the Nrf2 pathway. |
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MeSH term(s) | Animals ; Mice ; Alanine Transaminase/metabolism ; Alanine Transaminase/pharmacology ; Antioxidants/pharmacology ; Aspartate Aminotransferases/metabolism ; Aspartate Aminotransferases/pharmacology ; Chemical and Drug Induced Liver Injury/drug therapy ; Chemical and Drug Induced Liver Injury/metabolism ; Chemical and Drug Induced Liver Injury/pathology ; Galactosamine/toxicity ; Galactosamine/metabolism ; Lipopolysaccharides/pharmacology ; Liver ; NF-E2-Related Factor 2/metabolism ; Tumor Necrosis Factor-alpha/metabolism ; Plant Extracts/chemistry ; Plant Extracts/pharmacology |
Chemical Substances | Alanine Transaminase (EC 2.6.1.2) ; Antioxidants ; Aspartate Aminotransferases (EC 2.6.1.1) ; Galactosamine (7535-00-4) ; Lipopolysaccharides ; NF-E2-Related Factor 2 ; Tumor Necrosis Factor-alpha ; Plant Extracts |
Language | English |
Publishing date | 2024-02-07 |
Publishing country | Japan |
Document type | Journal Article |
ZDB-ID | 213307-6 |
ISSN | 1347-5223 ; 0009-2363 |
ISSN (online) | 1347-5223 |
ISSN | 0009-2363 |
DOI | 10.1248/cpb.c23-00578 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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