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Serum miR‐122 and miR‐192 as biomarkers of intrinsic and idiosyncratic acute hepatotoxicity: A quantitative real‐time polymerase chain reaction study in adult albino rats

Journal of Biochemical and Molecular Toxicology • 2019
العودة
معلومات البحث
المؤلفون Madboly AG, Alhusseini NF, Abd El Rahman SM, El Gazzar WB and Idris AMM
الكلمات المفتاحية biomarkers, hepatotoxicity, idiosyncratic, intrinsic, miR‐122, miR‐192, real‐time polymerase chain reaction
المجلة العلمية Journal of Biochemical and Molecular Toxicology
الناشر © 2019 Wiley Periodicals, Inc.
المجلد 33
العدد 7
الصفحات 1-9
publication.type International
رابط البحث Not Available
المواد المرفقة Not Available
الملخص
miR‐122 and miR‐192 were investigated as indicators of toxic liver injury caused by acetaminophen, but their role in idiosyncratic toxic liver injury remains controversial.
So, this work aimed to assess and compare the expressions of miR‐122 and miR‐192 in two different types of toxic liver injury (intrinsic [acetaminophen] and idiosyncratic [diclofenac]). Forty male adult Wistar albino rats were divided into equal five groups,
in which serum liver enzymes; microRNAs (miRNAs) expressions (miR‐122 and
miR‐192) and histopathological findings were studied. The present study showed that
(1) miR‐122 and miR‐192 are good serum biomarkers of toxic liver injury whatever its
etiology, as their serum levels exhibited a significantly earlier increase and earlier
return to normal baseline levels as compared to serum aminotransferase levels;
(2) miR‐122 is more specific than miR‐192; and (3) both serum levels of miR‐122 and
miR‐192 showed non‐significant differences in relation to the type of toxic liver
injury.