Cardioprotective effects of iron chelator HAPI and ROS-activated boronate prochelator BHAPI against catecholamine-induced oxidative cellular injury
Jazyk angličtina Země Irsko Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
R01 GM084176
NIGMS NIH HHS - United States
PubMed
27744045
PubMed Central
PMC5134745
DOI
10.1016/j.tox.2016.10.004
PII: S0300-483X(16)30239-6
Knihovny.cz E-zdroje
- Klíčová slova
- BHAPI, Cardiotoxicity, Catecholamines, HAPI, Iron chelation, Prochelator,
- MeSH
- adrenalin antagonisté a inhibitory toxicita MeSH
- biokatalýza MeSH
- buněčné linie MeSH
- chelátory železa farmakologie MeSH
- glutathion metabolismus MeSH
- hydroxylový radikál metabolismus MeSH
- isoprenalin antagonisté a inhibitory toxicita MeSH
- kardiotonika farmakologie MeSH
- katecholaminy antagonisté a inhibitory toxicita MeSH
- krysa rodu Rattus MeSH
- kyseliny boronové farmakologie MeSH
- lidé MeSH
- membránový potenciál mitochondrií účinky léků MeSH
- oxidační stres účinky léků MeSH
- prekurzory léčiv farmakologie MeSH
- reaktivní formy kyslíku metabolismus MeSH
- semikarbazony farmakologie MeSH
- sloučeniny boru farmakologie MeSH
- železo chemie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- adrenalin MeSH
- chelátory železa MeSH
- glutathion MeSH
- hydroxylový radikál MeSH
- isoprenalin MeSH
- kardiotonika MeSH
- katecholaminy MeSH
- kyseliny boronové MeSH
- N'-(1-(2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyloxy)phenyl)ethylidene)isonicotinohydrazide MeSH Prohlížeč
- prekurzory léčiv MeSH
- reaktivní formy kyslíku MeSH
- semikarbazony MeSH
- sloučeniny boru MeSH
- železo MeSH
Catecholamines may undergo iron-promoted oxidation resulting in formation of reactive intermediates (aminochromes) capable of redox cycling and reactive oxygen species (ROS) formation. Both of them induce oxidative stress resulting in cellular damage and death. Iron chelation has been recently shown as a suitable tool of cardioprotection with considerable potential to protect cardiac cells against catecholamine-induced cardiotoxicity. However, prolonged exposure of cells to classical chelators may interfere with physiological iron homeostasis. Prochelators represent a more advanced approach to decrease oxidative injury by forming a chelating agent only under the disease-specific conditions associated with oxidative stress. Novel prochelator (lacking any iron chelating properties) BHAPI [(E)-Ń-(1-(2-((4-(4,4,5,5-tetramethyl-1,2,3-dioxoborolan-2-yl)benzyl)oxy)phenyl)ethylidene) isonicotinohydrazide] is converted by ROS to active chelator HAPI with strong iron binding capacity that efficiently inhibits iron-catalyzed hydroxyl radical generation. Our results confirmed redox activity of oxidation products of catecholamines isoprenaline and epinephrine, that were able to activate BHAPI to HAPI that chelates iron ions inside H9c2 cardiomyoblasts. Both HAPI and BHAPI were able to efficiently protect the cells against intracellular ROS formation, depletion of reduced glutathione and toxicity induced by catecholamines and their oxidation products. Hence, both HAPI and BHAPI have shown considerable potential to protect cardiac cells by both inhibition of deleterious catecholamine oxidation to reactive intermediates and prevention of ROS-mediated cardiotoxicity.
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