Medizinische Universität Graz - Research portal

Logo MUG Resarch Portal

Selected Publication:

SHR Neuro Cancer Cardio Lipid Metab Microb

Bognar, Z; Kalai, T; Palfi, A; Hanto, K; Bognar, B; Mark, L; Szabo, Z; Tapodi, A; Radnai, B; Sarszegi, Z; Szanto, A; Gallyas, F; Hideg, K; Sumegi, B; Varbiro, G.
A novel SOD-mimetic permeability transition inhibitor agent protects ischemic heart by inhibiting both apoptotic and necrotic cell death.
Free Radic Biol Med. 2006; 41(5): 835-848. Doi: 10.1016/j.freeradbiomed.2006.06.004
Web of Science PubMed FullText FullText_MUG

 

Co-authors Med Uni Graz
Radnai Balazs
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
In ischemia-reperfusion injuries, elevated calcium and reactive oxygen species (ROS) induce mitochondrial permeability transition (mPT), which plays a pivotal role in mediating damages and cell death. Inhibition of mPT decreases necrotic cell death; however, during reperfusion, the continuous production of ROS may contribute to the temporary opening of the pore and thus the onset of the delayed apoptotic cell death. Based on amiodarone structure, we developed the first SOD-mimetic mPT inhibitor (HO-3538) that can eliminate ROS in the microenvironment of the permeability pore. In isolated mitochondria, HO-3538 inhibited mPT and the release of proapoptotic mitochondrial proteins. It had a ROS scavenging effect and antiapoptotic effect in a cardiomyocyte line and it diminished release of mitochondrial proapoptotic proteins. Furthermore, HO-3538 significantly enhanced the recovery of mitochondrial energy metabolism and functional cardiac parameters; decreased infarct size, lipid peroxidation, and protein oxidation; and suppressed necrotic as well as apoptotic cell death pathways in Langendorff-perfused hearts. In these respects it was somewhat superior to its two constituents, amiodarone and a pyrrol-derivative free radical scavenger. These data suggest that the SOD-mimetic mPT inhibitors are ideal candidates for drug development for the alleviation of postinfarct myocardial injuries.
Find related publications in this database (using NLM MeSH Indexing)
Amiodarone - analogs & derivatives Amiodarone - pharmacology
Animals -
Apoptosis -
Cytochromes c - metabolism
Humans -
Ischemia - pathology
Jurkat Cells -
Magnetic Resonance Spectroscopy -
Mice -
Mitochondria - metabolism
Myocardial Infarction - pathology
Necrosis - pathology
Rats -
Rats, Wistar -
Reperfusion Injury -
Superoxide Dismutase - metabolism

Find related publications in this database (Keywords)
mitochondrial permeability transition
ROS
ischemia-reperfusion
Langendorff-perfused hearts
NMR
apoptosis
necrosis
© Med Uni GrazImprint