-
Something wrong with this record ?
Direct effects of (-)-epicatechin and procyanidin B2 on the respiration of rat heart mitochondria
DM. Kopustinskiene, A. Savickas, D. Vetchý, R. Masteikova, A. Kasauskas, J. Bernatoniene,
Language English Country United States
Document type Journal Article
NLK
Free Medical Journals
from 2013
PubMed Central
from 2013
Europe PubMed Central
from 2013
ProQuest Central
from 2013
Open Access Digital Library
from 2001-01-01
Open Access Digital Library
from 2012-12-04
Open Access Digital Library
from 2013-01-01
CINAHL Plus with Full Text (EBSCOhost)
from 2013-01-01
Medline Complete (EBSCOhost)
from 2013-01-01
Health & Medicine (ProQuest)
from 2013
Wiley-Blackwell Open Access Titles
from 2001
ROAD: Directory of Open Access Scholarly Resources
from 2013
PubMed
25811024
DOI
10.1155/2015/232836
Knihovny.cz E-resources
- MeSH
- Adenosine Diphosphate pharmacology MeSH
- Biflavonoids chemistry pharmacology MeSH
- Cell Respiration drug effects MeSH
- Cytochromes c metabolism MeSH
- Catechin chemistry pharmacology MeSH
- Rats MeSH
- Oxidation-Reduction MeSH
- Proanthocyanidins chemistry pharmacology MeSH
- Mitochondria, Heart drug effects metabolism MeSH
- Substrate Specificity drug effects MeSH
- Succinates metabolism MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
Flavonol (-)-epicatechin and its derived dimer procyanidin B2, present in high amounts in cocoa products, have been shown to exert beneficial effects on the heart and cardiovascular system; however, their mechanism of action has not been fully elucidated. We studied effects of (-)-epicatechin and procyanidin B2 on the oxidative phosphorylation of isolated rat heart mitochondria. (-)-Epicatechin and procyanidin B2 had stimulating effect (up to 30% compared to control) on substrate-driven (State 2) mitochondrial respiration. Their effect was dependent on the respiratory substrates used. (-)-Epicatechin at higher concentrations (from 0.27 µg/mL) significantly decreased (up to 15%) substrate- and ADP-driven (State 3) mitochondrial respiration in case of pyruvate and malate oxidation only. Procyanidin B2 (0.7-17.9 ng/mL) inhibited State 3 respiration rate up to 19%, the most profound effect being expressed with succinate as the substrate. (-)-Epicatechin at concentrations of 0.23 µg/mL and 0.46 µg/mL prevented loss of the cytochrome c from mitochondria when substrate was succinate, supporting the evidence of membrane stabilizing properties of this flavonol. Thus, both (-)-epicatechin and procyanidin B2 directly influenced mitochondrial functions and the observed effects could help to explain cardiometabolic risk reduction ascribed to the consumption of modest amounts of cocoa products.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc16000193
- 003
- CZ-PrNML
- 005
- 20160122104937.0
- 007
- ta
- 008
- 160108s2015 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1155/2015/232836 $2 doi
- 035 __
- $a (PubMed)25811024
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Kopustinskiene, Dalia M $u Department of Pharmaceutical Technology and Social Pharmacy, Medical Academy, Lithuanian University of Health Sciences, Eiveniu 4, LT-50161 Kaunas, Lithuania.
- 245 10
- $a Direct effects of (-)-epicatechin and procyanidin B2 on the respiration of rat heart mitochondria / $c DM. Kopustinskiene, A. Savickas, D. Vetchý, R. Masteikova, A. Kasauskas, J. Bernatoniene,
- 520 9_
- $a Flavonol (-)-epicatechin and its derived dimer procyanidin B2, present in high amounts in cocoa products, have been shown to exert beneficial effects on the heart and cardiovascular system; however, their mechanism of action has not been fully elucidated. We studied effects of (-)-epicatechin and procyanidin B2 on the oxidative phosphorylation of isolated rat heart mitochondria. (-)-Epicatechin and procyanidin B2 had stimulating effect (up to 30% compared to control) on substrate-driven (State 2) mitochondrial respiration. Their effect was dependent on the respiratory substrates used. (-)-Epicatechin at higher concentrations (from 0.27 µg/mL) significantly decreased (up to 15%) substrate- and ADP-driven (State 3) mitochondrial respiration in case of pyruvate and malate oxidation only. Procyanidin B2 (0.7-17.9 ng/mL) inhibited State 3 respiration rate up to 19%, the most profound effect being expressed with succinate as the substrate. (-)-Epicatechin at concentrations of 0.23 µg/mL and 0.46 µg/mL prevented loss of the cytochrome c from mitochondria when substrate was succinate, supporting the evidence of membrane stabilizing properties of this flavonol. Thus, both (-)-epicatechin and procyanidin B2 directly influenced mitochondrial functions and the observed effects could help to explain cardiometabolic risk reduction ascribed to the consumption of modest amounts of cocoa products.
- 650 _2
- $a adenosindifosfát $x farmakologie $7 D000244
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a biflavonoidy $x chemie $x farmakologie $7 D044946
- 650 _2
- $a katechin $x chemie $x farmakologie $7 D002392
- 650 _2
- $a buněčné dýchání $x účinky léků $7 D019069
- 650 _2
- $a cytochromy c $x metabolismus $7 D045304
- 650 _2
- $a srdeční mitochondrie $x účinky léků $x metabolismus $7 D008929
- 650 _2
- $a oxidace-redukce $7 D010084
- 650 _2
- $a proantokyanidiny $x chemie $x farmakologie $7 D044945
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a substrátová specifita $x účinky léků $7 D013379
- 650 _2
- $a sukcináty $x metabolismus $7 D013386
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Savickas, Arunas $u Department of Pharmaceutical Technology and Social Pharmacy, Medical Academy, Lithuanian University of Health Sciences, Eiveniu 4, LT-50161 Kaunas, Lithuania.
- 700 1_
- $a Vetchý, David $u Department of Pharmaceutics, University of Veterinary and Pharmaceutical Sciences Brno, Palackeho 1/3, 612 42 Brno, Czech Republic.
- 700 1_
- $a Masteikova, Ruta $u Department of Pharmaceutics, University of Veterinary and Pharmaceutical Sciences Brno, Palackeho 1/3, 612 42 Brno, Czech Republic.
- 700 1_
- $a Kasauskas, Arturas $u Department of Biochemistry, Medical Academy, Lithuanian University of Health Sciences, Kaunas, A. Mickeviciaus 9, LT-44307 Kaunas, Lithuania.
- 700 1_
- $a Bernatoniene, Jurga $u Department of Pharmaceutical Technology and Social Pharmacy, Medical Academy, Lithuanian University of Health Sciences, Eiveniu 4, LT-50161 Kaunas, Lithuania.
- 773 0_
- $w MED00182164 $t BioMed research international $x 2314-6141 $g Roč. 2015, č. - (2015), s. 232836
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/25811024 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20160108 $b ABA008
- 991 __
- $a 20160122105057 $b ABA008
- 999 __
- $a ok $b bmc $g 1102474 $s 924399
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2015 $b 2015 $c - $d 232836 $e 20150224 $i 2314-6141 $m BioMed research international $n Biomed Res Int $x MED00182164
- LZP __
- $a Pubmed-20160108