Literature DB >> 20544535

Protection of mouse heart against hypoxic damage by AMP deaminase inhibition.

T Borkowski1, E M Slominska, C Orlewska, S Chlopicki, P Siondalski, M H Yacoub, R T Smolenski.   

Abstract

Clinical observation in patients with heart disease indicates that reduced activity of AMP deaminase could be protective in heart failure and ischemic heart disease. This study evaluated the effect of 3-[2-(3-carboxy-4-bromo-5,6,7,8-tetrahydronaphthyl)ethyl]-3,6,7,8-tetrahydroimidazo [4,5-d][1,3]diazepin-8-ol, an AMP deaminase inhibitor (AMPDI) in the mouse heart subjected to hypoxia. ApoE/LDLR knock-out mice were subjected to reduced oxygen tension in breathing air. AMPDI was infused before hypoxia in the treated group. We observed amelioration of elcetrocardiographic changes during hypoxia in the treated group that are consistent with a protective effect.

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Year:  2010        PMID: 20544535     DOI: 10.1080/15257771003741364

Source DB:  PubMed          Journal:  Nucleosides Nucleotides Nucleic Acids        ISSN: 1525-7770            Impact factor:   1.381


  2 in total

1.  Alterations in Metabolites Associated with Hypoxemia in Neonates and Infants with Congenital Heart Disease.

Authors:  Jelena Klawitter; Jesse Davidson; Evan Pagano; Benjamin Frank; James Jaggers; Mark Twite; Tracy T Urban
Journal:  Congenit Heart Dis       Date:  2020-09-07       Impact factor: 2.007

Review 2.  AMP deaminase 1 gene polymorphism and heart disease-a genetic association that highlights new treatment.

Authors:  Ryszard T Smolenski; Iwona Rybakowska; Jacek Turyn; Paweł Romaszko; Magdalena Zabielska; Anne Taegtmeyer; Ewa M Słomińska; Krystian K Kaletha; Paul J R Barton
Journal:  Cardiovasc Drugs Ther       Date:  2014-04       Impact factor: 3.727

  2 in total

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