• Title of article

    The C60-Fullerene Porphyrin Adducts for Prevention of the Doxorubicin- Induced Acute Cardiotoxicity in Rat Myocardial Cells

  • Author/Authors

    Shetab Boushehri, Vahid Department of Toxicology and Pharmacology - Faculty of Pharmacy & Nanotechnology Research Center - Tehran University of Medical Sciences , Ostad, Nasser Department of Toxicology and Pharmacology - Faculty of Pharmacy & Nanotechnology Research Center - Tehran University of Medical Sciences , Sarkar, Saeed Research Center for Science and Technology in Medicine (RCSTIM) - Tehran University of Medical Sciences , Kuznetsov, Dmitry A N.N. Semenov Institute for Chemical Physics - Russian Academy of Sciences - Moscow - Russian Federation , Buchachenko, Anatoly L Department of Chemistry - M.V. Lomonosov Moscow State University - Moscow, Russian Federation , Orlova, Marina A Department of Anatomy - School of Medicine - Tehran University of Medical Sciences , Minaii, Bagher Department of Anatomy - School of Medicine - Tehran University of Medical Sciences , Kebriaeezadeh, Abbas Department of Toxicology and Pharmacology - Faculty of Pharmacy & Nanotechnology Research Center - Tehran University of Medical Sciences , Rezayat, Mahdi Department of Medical Nanotechnology - Tehran University of Medical Sciences

  • Pages
    9
  • From page
    342
  • To page
    350
  • Abstract
    This is a fullerene-based low toxic nanocationite designed for targeted delivery of the paramagnetic stable isotope of magnesium to the doxorubicin (DXR)-induced damaged heart muscle providing a prominent effect close to about 80% recovery of the tissue hypoxia symptoms in less than 24 hrs after a single injection (0.03 – 0.1 LD50). Magnesium magnetic isotope effect selectively stimulates the ATP formation in the oxygen-depleted cells due to a creatine kinase (CK) and mitochondrial respiratory chain-focusing “attack” of 25Mg2+ released by nanoparticles. These “smart nanoparticles” with membranotropic properties release the overactivating cations only in response to the intracellular acidosis. The resulting positive changes in the energy metabolism of heart cell may help to prevent local myocardial hypoxic (ischemic) disorders and, hence, to protect the heart muscle from a serious damage in a vast variety of the hypoxia-induced clinical situations including DXR side effects.
  • Keywords
    Fullerene nanoparticles , doxorubicin-induced cardiotoxicity , 25Mg2+ , mitochondrial dysfunctions
  • Journal title
    Astroparticle Physics
  • Serial Year
    2010
  • Record number

    2445897