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. 2022 Mar 15;23(6):3133. doi: 10.3390/ijms23063133

Table 3.

Specialized proresolving lipid mediators as a therapeutic target in atherosclerosis.

SPMs Author Methodology Results
RvE1 Hasturk et al.
[120]
39 rabbits with a dietary regimen for 13 weeks, were treated with topical RvE1 3 times per week. RvE1 decreased atherogenesis and C reactive protein levels (p < 0.05).
Salic et al.
[121]
80 ApoE*3Leiden mice who were fed with a high-fat diet were administered different doses of RvE1. High-dose and low-dose RvE1 reduce the size of the atherosclerotic lesion to the same degree (35%. p < 0.05).
Liu et al.
[94]
Male mice were fed with rodent food and treated with RvE1. RvE1 was generated from EPA with the aid of ASA.
RvD2 and MaR1 Viola et al.
[15]
ApoE -/- mice who were fed with a high-fat diet, were administered doses of RvD2 and MaR1. RvD2 and MaR1 were signs of atheromatous plaque stability.
Akagi et al.
[89]
Smooth muscle cells from the aorta of adult male mice received an intraperitoneal injection of RvD2 and MaR1. ASMC chemotaxis was reduced in 74% after treatment with RvD2 and MaR1.
ATL Petri et al.
[122]
Four mice who presented Fpr2 deficiency were fed with a high-fat diet for 4 weeks and later treated with ATL. ATL blocked the progression at the root of atherosclerosis.
RvD1 and PD1 Makino et al.
[123]
Male injured mice who were subjected to carotid artery angioplasty received 1 μg of RvD1 or PD1 intravenously. RvD1 and PD1 mitigated muscle cell proliferation, as well as leukocyte infiltration.
RvD1 and RvD2 Miyahara et al.
[57]
Cultures of human greater saphenous veins VSMC were isolated and treated with RvD1 and RvD2. RvD1 and RvD2 inhibited VSMC and monocyte proliferation, migration, and adhesion.
RvD1 Kain et al.
[114]
Male mice with coronary artery ligation were administered liposomes with RvD1 or Lipo-RvD1. RvD1 decreased macrophage density.
Orr et al.
[115]
0.5 g of EOR and BDA-RvD1 were given to mice. BDA-RvD1 was resistant to EOR and reduced neutrophil infiltration in the lungs.

Abbreviations: RvE1: Resolvin E1; RvD2: Resolvin E2; MaR1: Maresin 1; ATL: Aspirin Activated Lipoxin; Fpr2: Formyl peptide receptor 2; ASMC: Aortic smooth muscle cells; NFκB: Nuclear factor kappa B; ASA: aspirin; EPA: eicosapentaenoic acid; RvD1: Resolvin D1; RvD2: Resolvin D2; EOR: Eicosanoid oxidoreductase; BDA-RvD1: benzo-diacetylenic-17R-RvD1-methyl ester; VSMC: Vascular smooth muscle cells.