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Elevated levels of liver methylglyoxal and d ‐lactate in early‐stage hepatitis in rats
Author(s) -
Wang WenChuang,
Chou ChuKuang,
Chuang MingCheng,
Li YiChieh,
Lee JenAi
Publication year - 2018
Publication title -
biomedical chromatography
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.4
H-Index - 65
eISSN - 1099-0801
pISSN - 0269-3879
DOI - 10.1002/bmc.4039
Subject(s) - methylglyoxal , metabolite , chemistry , aspartate transaminase , medicine , ccl4 , lactate dehydrogenase , alanine transaminase , endocrinology , hepatitis , transaminase , biochemistry , carbon tetrachloride , enzyme , alkaline phosphatase , organic chemistry
Methylglyoxal (MGO) is highly cytotoxic and its levels are elevated in diabetes, nephropathy and atherosclerosis. However, it has never been studied in liver disease. For this reason, we aimed to assess the levels of MGO and its metabolite d ‐lactate in an early hepatitis model. Wistar rats were administered CCl 4 (0.75 mL/kg, i.p.) to induce hepatitis. In either CCl 4 ‐treated or untreated rats, alanine transaminase and aspartate transaminase levels did not change over the course of the study, indicating that significant liver damage did not occur following CCl 4 treatment. However, the levels of MGO and d ‐lactate were higher in the livers of CCl 4 ‐treated animals than in untreated animals (MGO: 128.2 ± 18.8 and 248.1 ± 64.9 μg/g protein, p < 0.01; d ‐lactate: 0.860 ± 0.040 and 1.293 ± 0.078 μmol/g protein, respectively p < 0.01). Furthermore, in untreated and treated animals, serum d ‐lactate levels were 57.65 ± 2.59 and 92.16 ± 16.69 μ m and urine d ‐lactate levels were 1.060 ± 0.007 and 1.555 ± 0.366 μmol/mg UCr, respectively ( p < 0.01). These data show that in this model of early‐stage liver damage, the levels of MGO and its metabolite d ‐lactate are elevated and that d ‐lactate could be useful as a reference marker for the early stage of hepatitis.