Abstract |
TJN-101, which is a lignan component isolated from schisandra fruits, inhibits hepatotoxic chemicals-induced liver injuries. In this study, effects of TJN-101 on immunologically induced liver injuries were investigated in vivo and in vitro. When a small dose of lipopolysaccharide was injected into mice previously injected with heat-killed Propionibacterium acnes, most of the animals died with acute hepatic failure which was produced by cytotoxic factors from activated adherent cells, and liver cells were injured by antibody-dependent cell-mediated cytotoxic (ADCC) reaction or activated macrophages in vitro. TJN-101 reduced the mortality of the mice with acute hepatic failure dose-dependently. Histologically, necrosis was suppressed by the treatment of TJN-101, but infiltration of non-specific inflammatory cells was not. TJN-101 inhibited the isolated liver cell injuries induced by ADCC reaction or activated macrophages in vitro. These results suggest that TJN-101 can be markedly protective against immunological liver injuries.
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Authors | Y Ohkura, Y Mizoguchi, Y Sakagami, K Kobayashi, S Yamamoto, S Morisawa, S Takeda, M Aburada |
Journal | Japanese journal of pharmacology
(Jpn J Pharmacol)
Vol. 44
Issue 2
Pg. 179-85
(Jun 1987)
ISSN: 0021-5198 [Print] Japan |
PMID | 3656775
(Publication Type: Journal Article)
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Chemical References |
- Cyclooctanes
- Dioxoles
- Lignans
- Lipopolysaccharides
- Polycyclic Compounds
- Proteins
- schizandrol B
- Aspartate Aminotransferases
- Alanine Transaminase
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Topics |
- Alanine Transaminase
(blood)
- Animals
- Antibody-Dependent Cell Cytotoxicity
(drug effects)
- Aspartate Aminotransferases
(blood)
- Cyclooctanes
- Dioxoles
- Guinea Pigs
- Lignans
- Lipopolysaccharides
(antagonists & inhibitors)
- Liver Diseases
(drug therapy, immunology, pathology)
- Macrophage Activation
(drug effects)
- Male
- Mice
- Mice, Inbred BALB C
- Polycyclic Compounds
(pharmacology)
- Proteins
(metabolism)
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