Journal article
γ Peptide Nucleic Acid-Based miR-122 Inhibition Rescues Vascular Endothelial Dysfunction in Mice Fed a High-Fat Diet
Journal of medicinal chemistry, Vol.65(4), pp.3332-3342
02/24/2022
DOI: 10.1021/acs.jmedchem.1c01831
PMCID: PMC8883473
PMID: 35133835
Appears in UI Libraries Support Open Access
Abstract
The blood levels of microRNA-122 (miR-122) is associated with the severity of cardiovascular disorders, and targeting it with efficient and safer miR inhibitors could be a promising approach. Here, we report the generation of a γ-peptide nucleic acid (γPNA)-based miR-122 inhibitor (γP-122-I) that rescues vascular endothelial dysfunction in mice fed a high-fat diet. We synthesized diethylene glycol-containing γP-122-I and found that its systemic administration counteracted high-fat diet (HFD)-feeding-associated increase in blood and aortic miR-122 levels, impaired endothelial function, and reduced glycemic control. A comprehensive safety analysis established that γP-122-I affects neither the complete blood count nor biochemical tests of liver and kidney functions during acute exposure. In addition, long-term exposure to γP-122-I did not change the overall adiposity, or histology of the kidney, liver, and heart. Thus, γP-122-I rescues endothelial dysfunction without any evidence of toxicity
and demonstrates the suitability of γPNA technology in generating efficient and safer miR inhibitors.
Details
- Title: Subtitle
- γ Peptide Nucleic Acid-Based miR-122 Inhibition Rescues Vascular Endothelial Dysfunction in Mice Fed a High-Fat Diet
- Creators
- Ravinder Reddy Gaddam - University of IowaKarishma Dhuri - University of ConnecticutYoung-Rae Kim - University of IowaJulia S Jacobs - Roy J. and Lucille A. Carver College of MedicineVikas Kumar - University of ConnecticutQiuxia Li - University of IowaKaikobad Irani - University of IowaRaman Bahal - University of ConnecticutAjit Vikram - Roy J. and Lucille A. Carver College of Medicine
- Resource Type
- Journal article
- Publication Details
- Journal of medicinal chemistry, Vol.65(4), pp.3332-3342
- DOI
- 10.1021/acs.jmedchem.1c01831
- PMID
- 35133835
- PMCID
- PMC8883473
- NLM abbreviation
- J Med Chem
- ISSN
- 0022-2623
- eISSN
- 1520-4804
- Publisher
- American Chemical Society
- Grant note
- DOI: 10.13039/100000968, name: American Heart Association, award: 18CDA34080125, 828081
- Language
- English
- Date published
- 02/24/2022
- Academic Unit
- Cardiovascular Medicine; Radiation Oncology; Fraternal Order of Eagles Diabetes Research Center; Internal Medicine
- Record Identifier
- 9984313094402771
Metrics
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