TY - JOUR
T1 - Specialized Proresolving Lipid Mediators
T2 - A Potential Therapeutic Target for Atherosclerosis
AU - Salazar, Juan
AU - Pirela, Daniela
AU - Nava, Manuel
AU - Castro, Ana
AU - Angarita, Lissé
AU - Parra, Heliana
AU - Durán-Agüero, Samuel
AU - Rojas-Gómez, Diana Marcela
AU - Galbán, Néstor
AU - Añez, Roberto
AU - Chacín, Maricarmen
AU - Diaz, Andrea
AU - Villasmil, Nelson
AU - De Sanctis, Juan Bautista
AU - Bermúdez, Valmore
N1 - Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/3/1
Y1 - 2022/3/1
N2 - 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.
AB - 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.
KW - Atherosclerosis
KW - Inflammation
KW - Intimal hyperplasia
KW - Reperfusion injury
KW - Resolution
KW - Specialized proresolving mediators
UR - http://www.scopus.com/inward/record.url?scp=85126101722&partnerID=8YFLogxK
U2 - 10.3390/ijms23063133
DO - 10.3390/ijms23063133
M3 - Review article
AN - SCOPUS:85126101722
SN - 1661-6596
VL - 23
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 6
M1 - 3133
ER -