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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
Language English Country Switzerland
Document type Journal Article, Review
Grant support
CC-0437-10-21-09-10
Consejo de Desarrollo Científico, Humanístico y Tecnológico (CONDES), University of Zulia
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
35328553
DOI
10.3390/ijms23063133
Knihovny.cz E-resources
- MeSH
- Atherosclerosis * metabolism MeSH
- Cardiovascular Diseases * drug therapy MeSH
- Docosahexaenoic Acids metabolism pharmacology therapeutic use MeSH
- Humans MeSH
- Inflammation Mediators metabolism MeSH
- Fatty Acids, Omega-3 * metabolism pharmacology therapeutic use MeSH
- Inflammation metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Review 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.
References provided by Crossref.org
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