Aldosterone modulates blood homocysteine and cholesterol in coronary artery disease patients - a possible impact on atherothrombosis?
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
29303611
DOI
10.33549/physiolres.933668
PII: 933668
Knihovny.cz E-zdroje
- MeSH
- agregace trombocytů účinky léků MeSH
- aldosteron krev farmakologie MeSH
- cholesterol krev MeSH
- homocystein biosyntéza krev MeSH
- kolagen metabolismus MeSH
- kreatinin krev MeSH
- krysa rodu Rattus MeSH
- kyselina arachidonová metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- nadledviny účinky léků metabolismus MeSH
- nemoci koronárních tepen krev MeSH
- potkani Sprague-Dawley MeSH
- senioři MeSH
- sulfhydrylové sloučeniny krev MeSH
- techniky in vitro MeSH
- trombóza krev MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- aldosteron MeSH
- cholesterol MeSH
- homocystein MeSH
- kolagen MeSH
- kreatinin MeSH
- kyselina arachidonová MeSH
- sulfhydrylové sloučeniny MeSH
Aldosterone plays a key role in maintaining the homeostasis of the whole organism. Under some circumstances, aldosterone can contribute to the progression of cardiovascular diseases, including coronary artery disease. This study demonstrates that aldosterone associates negatively with some lipidogram parameters and positively with the concentration of homocysteine. These associations are characteristic for coronary artery disease and are not present in control subjects. The findings also indicate that in vitro aldosterone stimulates homocysteine production by rat adrenal glands, which may explain the associations observed with coronary artery disease. Moreover, we have found that aldosterone significantly modulates in vitro platelet reactivity to arachidonate and collagen - aldosterone increases the pro-aggregatory action of collagen, but decreases the pro-aggregatory potential of arachidonate. Therefore, the findings of these in vitro and ex vivo experiments indicate the existence of new pathways by which aldosterone modulates lipid- homocysteine- and platelet-dependent atherogenesis.
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