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Th2 cytokine‐mediated methimazole‐induced acute liver injury in mice
Author(s) -
Kobayashi Masanori,
Higuchi Satonori,
Ide Mika,
Nishikawa Satomi,
Fukami Tatsuki,
Nakajima Miki,
Yokoi Tsuyoshi
Publication year - 2012
Publication title -
journal of applied toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.784
H-Index - 87
eISSN - 1099-1263
pISSN - 0260-437X
DOI - 10.1002/jat.2731
Subject(s) - methimazole , liver injury , cytokine , medicine , immunology , pharmacology , thyroid
Drug‐induced liver injury (DILI) is a major safety concern in drug development and clinical practice. The pathogenesis of DILI usually involves the participation of the parent drug or metabolites that either affect cellular function or elicit an immune response. However, the mechanisms leading to DILI are unknown in most cases. Methimazole (MTZ) is used as an antithyroid drug and is well known to have induced liver injuries such as cholestatic hepatitis in a small number of human cases. Immune‐mediated reactions were also suggested to play a role in MTZ‐induced acute liver injury, but the mechanism underlying this process has not been elucidated. To address this issue, we measured plasma aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels, hepatic glutathione levels, hepatic expression of CD4 + Th cell‐related transcriptional factors, cytokines and chemokines, plasma interleukin (IL)‐4 levels and histopathological changes in the liver following MTZ (450 mg kg −1 , p.o.) administration in mice. The hepatic expression of mRNA for Th2 cell‐related factors, such as GATA‐binding protein, macrophage inflammatory protein‐2 (MIP‐2) and plasma IL‐4 levels, as well as plasma AST and ALT levels, was significantly increased in mice treated with MTZ. These changes were markedly enhanced by pre‐treatment with L‐buthionine sulfoximine (3 mmol kg −1 , i.p.) and MTZ (15 mg kg −1 , p.o.). Neutralization of IL‐4 using a monoclonal anti‐mouse IL‐4 antibody (100 µg/mouse, single i.p.) suppressed the hepatotoxic effect of MTZ. In conclusion, this report is the first to demonstrate that Th2 cytokine‐mediated immune responses are involved in MTZ‐induced acute liver injury in mice. Copyright © 2012 John Wiley & Sons, Ltd.