4.4 Article

Circulating Plasma and Exosomal microRNAs as Indicators of Drug-Induced Organ Injury in Rodent Models

Journal

BIOMOLECULES & THERAPEUTICS
Volume 25, Issue 4, Pages 367-373

Publisher

KOREAN SOC APPLIED PHARMACOLOGY
DOI: 10.4062/biomolther.2016.174

Keywords

miRNAs; Exosomes; Liver-specific injury; N-acetyl cysteine; Biomarkers

Funding

  1. National Research Foundation of Korea (NRF) - Korea government [2014R1A5A2009242]
  2. Intramural Fund of the National Institute on Alcoholism and Alcohol Abuse, NIH, USA
  3. Korean Biomedical Scientist Fellowship Program Award by the Korean Research Institute of Bioscience and Biotechnology
  4. National Research Foundation of Korea [2014R1A5A2009242] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study was performed to evaluate whether microRNAs (miRNAs) in circulating exosomes may serve as biomarkers of drug induced liver, kidney, or muscle-injury. Quantitative PCR analyses were performed to measure the amounts of liver-specific miRNAs (miR-122, miR-192, and miR-155), kidney-specific miR-146a, or muscle-specific miR-206 in plasma and exosomes from mice treated with liver, kidney or muscle toxicants. The levels of liver-specific miRNAs in circulating plasma and exosomes were elevated in acetaminophen-induced liver injury and returned to basal levels by treatment with antioxidant N-acetyl-cysteine. Circulating miR-146a and miR-206 were increased in cisplatin-induced nephrotoxicity and bupivacaine-induced myotoxicity, respectively. Taken together, these results indicate that circulating plasma and exosomal miRNAs can be used as potential biomarkers specific for drug-induced liver, kidney or muscle injury.

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