4.6 Article

Plasma microRNA profiles distinguish lethal injury in acetaminophen toxicity: A research study

Journal

WORLD JOURNAL OF GASTROENTEROLOGY
Volume 18, Issue 22, Pages 2798-2804

Publisher

BAISHIDENG PUBL GRP CO LTD
DOI: 10.3748/wjg.v18.i22.2798

Keywords

Plasma microRNA; Hepatotoxicity; Acetaminophen; Drug-induced liver injury; Alanine aminotransferase

Funding

  1. PHS [DK075635]
  2. McNeil Consumer Healthcare, a division of McNeil-PCC Inc.

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AIM: To investigate plasma microRNA (miRNA) profiles indicative of hepatotoxicity in the setting of lethal acetaminophen (APAP) toxicity in mice. METHODS: Using plasma from APAP poisoned mice, either lethally (500 mg/kg) or sublethally (150 mg/kg) dosed, we screened commercially available murine microRNA libraries (SABiosciences, Qiagen Sciences, MD) to evaluate for unique miRNA profiles between these two dosing parameters. RESULTS: We distinguished numerous, unique plasma miRNAs both up- and downregulated in lethally compared to sublethally dosed mice. Of note, many of the greatest up- and downregulated miRNAs, namely 574-5p, 466g, 466f-3p, 375, 29c, and 148a, have been shown to be associated with asthma in prior studies. Interestingly, a relationship between APAP and asthma has been previously well described in the literature, with an as yet unknown mechanism of pathology. There was a statistically significant increase in alanine anninotransferase levels in the lethal compared to sublethal APAP dosing groups at the 12 h time point (P < 0.001). There was 90% mortality in the lethally compared to sublethally dosed mice at the 48 h time point (P = 0.011). CONCLUSION: We identified unique plasma miRNAs both up- and downregulated in APAP poisoning which are correlated to asthma development. (C) 2012 Baishideng. All rights reserved.

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