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Specialized Proresolving Lipid Mediators: A Potential Therapeutic Target for Atherosclerosis
J. Salazar, D. Pirela, M. Nava, A. Castro, L. Angarita, H. Parra, S. Durán-Agüero, DM. Rojas-Gómez, N. Galbán, R. Añez, M. Chacín, A. Diaz, N. Villasmil, JB. De Sanctis, V. Bermúdez
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články, přehledy
Grantová podpora
CC-0437-10-21-09-10
Consejo de Desarrollo Científico, Humanístico y Tecnológico (CONDES), University of Zulia
NLK
Free Medical Journals
od 2000
Freely Accessible Science Journals
od 2000
PubMed Central
od 2007
Europe PubMed Central
od 2007
ProQuest Central
od 2000-03-01
Open Access Digital Library
od 2000-01-01
Open Access Digital Library
od 2007-01-01
Health & Medicine (ProQuest)
od 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
od 2000
PubMed
35328553
DOI
10.3390/ijms23063133
Knihovny.cz E-zdroje
- MeSH
- ateroskleróza * metabolismus MeSH
- kardiovaskulární nemoci * farmakoterapie MeSH
- kyseliny dokosahexaenové metabolismus farmakologie terapeutické užití MeSH
- lidé MeSH
- mediátory zánětu metabolismus MeSH
- omega-3 mastné kyseliny * metabolismus farmakologie terapeutické užití MeSH
- zánět metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
Cardiovascular disease (CVD) is a global public health issue due to its high morbidity, mortality, and economic impact. The implementation of innovative therapeutic alternatives for CVD is urgently required. Specialized proresolving lipid mediators (SPMs) are bioactive compounds derived from ω-3 and ω-6 fatty acids, integrated into four families: Lipoxins, Resolvins, Protectins, and Maresins. SPMs have generated interest in recent years due to their ability to promote the resolution of inflammation associated with the pathogeneses of numerous illnesses, particularly CVD. Several preclinical studies in animal models have evidenced their ability to decrease the progression of atherosclerosis, intimal hyperplasia, and reperfusion injury via diverse mechanisms. Large-scale clinical trials are required to determine the effects of SPMs in humans. This review integrates the currently available knowledge of the therapeutic impact of SPMs in CVD from preclinical and clinical studies, along with the implicated molecular pathways. In vitro results have been promising, and as such, SPMs could soon represent a new therapeutic alternative for CVD.
Citace poskytuje Crossref.org
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