Milan Stefek

Dr. Milan Stefek


Research Focus & Metrics

Academic Career Length

49Years (1978-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 September 2010 in Free Radical Research
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AAAgnieszka Augustyniak
Agnieszka Augustyniak
Grzegorz BartoszGrzegorz Bartosz
Grzegorz Bartosz
AČAna Čipak
Ana Čipak
GDGunars Duburs
Gunars Duburs
LHL'UBica Horáková
L'UBica Horáková
Neven ZarkovicNeven Zarkovic
Neven Zarkovic
The current understanding of the complex role of ROS in the organism and pathological sequelae of oxidative stress points to the necessity of comprehensive studies of antioxidant reactivities and interactions with cellular constituents. Studies of antioxidants performed within the COST B-35 action has concerned the search for new natural antioxidants, synthesis of new antioxidant compounds and evaluation and elucidation of mechanisms of action of both natural and synthetic antioxidants. Representative studies presented in the review concern antioxidant properties of various kinds of tea, the search for new antioxidants of herbal origin, modification of tocopherols and their use in combination with selenium and properties of two promising groups of synthetic antioxidants: derivatives of stobadine and derivatives of 1,4-dihydropyridine.

1 March 2004 in Journal of Diabetes and its Complications
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ZKZ Kyselova
Z Kyselova
MSMilan Stefek
Milan Stefek
VBV Bauer
V Bauer

1 September 2004 in Bioorganic & Medicinal Chemistry
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Journal Article
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LRLucia Račková
Lucia Račková
MMMagdaléna Májeková
Magdaléna Májeková
DKDaniela Košt’álová
Daniela Košt’álová
MSMilan Stefek
Milan Stefek

7 May 2013 in Free Radical Research
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Giancarlo AldiniGiancarlo Aldini
Giancarlo Aldini
Giulio VistoliGiulio Vistoli
Giulio Vistoli
MSMilan Stefek
Milan Stefek
NCN. Chondrogianni
N. Chondrogianni
TGTilman Grune
Tilman Grune
Grzegorz BartoszGrzegorz Bartosz
Grzegorz Bartosz
The advanced glycoxidation end products (AGEs) and lipoxidation end products (ALEs) contribute to the development of diabetic complications and of other pathologies. The review discusses the possibilities of counteracting the formation and stimulating the degradation of these species by pharmaceuticals and natural compounds. The review discusses inhibitors of ALE and AGE formation, cross-link breakers, ALE/AGE elimination by enzymes and proteolytic systems, receptors for advanced glycation end products (RAGEs) and blockade of the ligand–RAGE axis.

1 June 2003 in Neurochemical Research
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NUNuray Nuriye Ulusu
Nuray Nuriye Ulusu
MSMeral Sahilli
Meral Sahilli
AAAslihan Avci
Aslihan Avci
OCOrhan Canbolat
Orhan Canbolat
GOGülgün Ozansoy
Gülgün Ozansoy
ÇKÇimen Karasu
Çimen Karasu

12 December 2007 in Natural Product Research
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Journal Article
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LRLucia Račková
Lucia Račková
VJViera Jančinová
Viera Jančinová
MPMargita Petríková
Margita Petríková
KDKatarína Drábiková
Katarína Drábiková
RNRadomír Nosáľ
Radomír Nosáľ
MKMária Kováčová
Mária Kováčová
The antiradical activity, protective effect against lipid peroxidation of liposomal membrane, and inhibitory effect on whole blood reactive oxygen species (ROS) liberation of Glycyrrhiza glabra crude extract and glycyrrhizin, its major compound, were assessed. The liquorice extract showed significant activity in all the three assay systems used in a dose dependent manner. It displayed remarkable reactivity with free stable 1,1′-diphenyl-2-picrylhydrazyl (DPPH) radical, inhibitory efficacy in peroxidatively damaged unilamellar dioleoyl phosphatidylcholine (DOPC) liposomes, and inhibition of ROS chemiluminescence, generated by whole blood, induced by both receptor-bypassing stimuli (PMA) and receptor operating stimuli (Opz) in the ranking order of stimuli PMA> Opz. These activities may be attributed to phenolic antioxidants involving isoflavan derivatives, coumarins and chalcones. Nonetheless, triterpene saponin glycyrrhizin exhibited no efficacy in the system of DPPH reaction and peroxidation of liposomal membrane, and negligible inhibition of chemiluminescence generated by inflammatory cells. These results indicate that the mechanism of anti-inflammatory effect of glycyrrhizin most probably does not involve ROS and this major constituent is not responsible for the inhibition effects of liquorice extract on neutrophil functions.