-
Something wrong with this record ?
The influence of microbial isoflavonoid specific metabolites on platelets and transition metals iron and copper
T. Migkos, L. Applová, P. Horký, V. Tvrdý, J. Karlíčková, K. Macáková, M. Hrubša, MC. Catapano, M. Tomanek, M. Pour, P. Mladěnka,
Language English Country Germany
Document type Journal Article
- MeSH
- Platelet Aggregation drug effects MeSH
- Aspirin pharmacology MeSH
- Biological Availability MeSH
- Equol metabolism MeSH
- Phenols metabolism MeSH
- Isoflavones metabolism pharmacology MeSH
- Humans MeSH
- Copper metabolism MeSH
- Blood Platelets drug effects MeSH
- Iron metabolism MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
BACKGROUND: Isoflavonoids seem to possess positive cardiovascular and other beneficial effects in humans. HYPOTHESIS: Their low bioavailability, however, indicates that small isoflavonoid metabolites formed by human microflora can significantly contribute to these activities. STUDY DESIGN: Testing antiplatelet activity ex vivo in human blood and interaction with transition metals in vitro. METHODS: The effect on platelet aggregation induced by different triggers (arachidonic acid, collagen, ADP, TRAP-6), and interactions with transition metals (iron and copper chelation/reduction) were evaluated against four isoflavonoid-specific metabolites: S-equol; O-desmethylangolensin; 2-(4-hydroxyphenyl) propionic acid (HPPA); and 4-ethylphenol. RESULTS: S-equol, 4-ethylphenol and O-desmethylangolensin blocked platelet aggregation induced by arachidonic acid and collagen. S-equol even matched the potency of acetylsalicylic acid in the case of collagen, which is the most physiological inducer of aggregation. Moreover, their effects in general seemed to be biologically relevant and attainable at achievable plasma concentrations, with the exception of HPPA which was ineffective. While only O-desmethylangolensin mildly chelated iron and copper, all four compounds markedly reduced cupric ions. Their direct free radical scavenging effects seem to have little clinical relevance. CONCLUSION: This study has shown that S-equol, O-desmethylangolensin and 4-ethylphenol, arising from isoflavonoid intake, can have biologically relevant effects on platelet aggregation.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20006275
- 003
- CZ-PrNML
- 005
- 20221018085005.0
- 007
- ta
- 008
- 200511s2019 gw f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.phymed.2019.152974 $2 doi
- 035 __
- $a (PubMed)31181402
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a gw
- 100 1_
- $a Migkos, Thomas $u Department of Pharmacology and Toxicology, Faculty of Pharmacy in Hradec Králové, Charles University, Akademika Heyrovského 1203, Hradec Králové 500 05, Czech Republic.
- 245 14
- $a The influence of microbial isoflavonoid specific metabolites on platelets and transition metals iron and copper / $c T. Migkos, L. Applová, P. Horký, V. Tvrdý, J. Karlíčková, K. Macáková, M. Hrubša, MC. Catapano, M. Tomanek, M. Pour, P. Mladěnka,
- 520 9_
- $a BACKGROUND: Isoflavonoids seem to possess positive cardiovascular and other beneficial effects in humans. HYPOTHESIS: Their low bioavailability, however, indicates that small isoflavonoid metabolites formed by human microflora can significantly contribute to these activities. STUDY DESIGN: Testing antiplatelet activity ex vivo in human blood and interaction with transition metals in vitro. METHODS: The effect on platelet aggregation induced by different triggers (arachidonic acid, collagen, ADP, TRAP-6), and interactions with transition metals (iron and copper chelation/reduction) were evaluated against four isoflavonoid-specific metabolites: S-equol; O-desmethylangolensin; 2-(4-hydroxyphenyl) propionic acid (HPPA); and 4-ethylphenol. RESULTS: S-equol, 4-ethylphenol and O-desmethylangolensin blocked platelet aggregation induced by arachidonic acid and collagen. S-equol even matched the potency of acetylsalicylic acid in the case of collagen, which is the most physiological inducer of aggregation. Moreover, their effects in general seemed to be biologically relevant and attainable at achievable plasma concentrations, with the exception of HPPA which was ineffective. While only O-desmethylangolensin mildly chelated iron and copper, all four compounds markedly reduced cupric ions. Their direct free radical scavenging effects seem to have little clinical relevance. CONCLUSION: This study has shown that S-equol, O-desmethylangolensin and 4-ethylphenol, arising from isoflavonoid intake, can have biologically relevant effects on platelet aggregation.
- 650 _2
- $a Aspirin $x farmakologie $7 D001241
- 650 _2
- $a biologická dostupnost $7 D001682
- 650 _2
- $a trombocyty $x účinky léků $7 D001792
- 650 _2
- $a měď $x metabolismus $7 D003300
- 650 _2
- $a equol $x metabolismus $7 D060754
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a železo $x metabolismus $7 D007501
- 650 _2
- $a isoflavony $x metabolismus $x farmakologie $7 D007529
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a fenoly $x metabolismus $7 D010636
- 650 _2
- $a agregace trombocytů $x účinky léků $7 D010974
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Applová, Lenka $u Department of Pharmacology and Toxicology, Faculty of Pharmacy in Hradec Králové, Charles University, Akademika Heyrovského 1203, Hradec Králové 500 05, Czech Republic. $7 xx0277670
- 700 1_
- $a Horký, Pavel $u Department of Inorganic and Organic Chemistry, Faculty of Pharmacy in Hradec Králové, Charles University, Akademika Heyrovského 1203, Hradec Králové 500 05, Czech Republic; Department of Social and Clinical Pharmacy, Faculty of Pharmacy in Hradec Králové, Charles University, Zborovská 2089, Hradec Králové 500 05, Czech Republic.
- 700 1_
- $a Tvrdý, Václav $u Department of Pharmacology and Toxicology, Faculty of Pharmacy in Hradec Králové, Charles University, Akademika Heyrovského 1203, Hradec Králové 500 05, Czech Republic.
- 700 1_
- $a Karlíčková, Jana $u Department of Pharmaceutical Botany, Faculty of Pharmacy in Hradec Králové, Charles, Akademika Heyrovského 1203, Hradec Králové 500 05, Czech Republic.
- 700 1_
- $a Macáková, Kateřina $u Department of Pharmaceutical Botany, Faculty of Pharmacy in Hradec Králové, Charles, Akademika Heyrovského 1203, Hradec Králové 500 05, Czech Republic.
- 700 1_
- $a Hrubša, Marcel $u Department of Pharmacology and Toxicology, Faculty of Pharmacy in Hradec Králové, Charles University, Akademika Heyrovského 1203, Hradec Králové 500 05, Czech Republic.
- 700 1_
- $a Catapano, Maria Carmen $u Department of Pharmacology and Toxicology, Faculty of Pharmacy in Hradec Králové, Charles University, Akademika Heyrovského 1203, Hradec Králové 500 05, Czech Republic.
- 700 1_
- $a Tomanek, Magdalena $u Institute of Chemistry, Department of Theoretical Chemistry, University of Silesia in Katowice, Faculty of Mathematics, Physics and Chemistry, Bankowa 14, Katowice 40-007, Poland.
- 700 1_
- $a Pour, Milan $u Department of Inorganic and Organic Chemistry, Faculty of Pharmacy in Hradec Králové, Charles University, Akademika Heyrovského 1203, Hradec Králové 500 05, Czech Republic.
- 700 1_
- $a Mladěnka, Přemysl $u Department of Pharmacology and Toxicology, Faculty of Pharmacy in Hradec Králové, Charles University, Akademika Heyrovského 1203, Hradec Králové 500 05, Czech Republic. Electronic address: mladenkap@faf.cuni.cz.
- 773 0_
- $w MED00003830 $t Phytomedicine $x 1618-095X $g Roč. 62, č. - (2019), s. 152974
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31181402 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20200511 $b ABA008
- 991 __
- $a 20221018085002 $b ABA008
- 999 __
- $a ok $b bmc $g 1525133 $s 1096331
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 62 $c - $d 152974 $e 20190528 $i 1618-095X $m Phytomedicine $n Phytomedicine $x MED00003830
- LZP __
- $a Pubmed-20200511