Aspirin‐triggered lipoxin A4 inhibits atherosclerosis progression in apolipoprotein E−/− mice
MH Petri, A Laguna‐Fernandez… - British journal of …, 2017 - Wiley Online Library
British journal of pharmacology, 2017•Wiley Online Library
Background and Purpose Atherosclerosis is characterized by a chronic non‐resolving
inflammation in the arterial wall. Aspirin‐triggered lipoxin A4 (ATL) is a potent anti‐
inflammatory mediator, involved in the resolution of inflammation. However, the therapeutic
potential of immune targeting by means of ATL in atherosclerosis has not previously been
explored. The aim of the present study was to determine the effects of ATL and its receptor
Fpr2 on atherosclerosis development and progression in apolipoprotein E deficient …
inflammation in the arterial wall. Aspirin‐triggered lipoxin A4 (ATL) is a potent anti‐
inflammatory mediator, involved in the resolution of inflammation. However, the therapeutic
potential of immune targeting by means of ATL in atherosclerosis has not previously been
explored. The aim of the present study was to determine the effects of ATL and its receptor
Fpr2 on atherosclerosis development and progression in apolipoprotein E deficient …
Background and Purpose
Atherosclerosis is characterized by a chronic non‐resolving inflammation in the arterial wall. Aspirin‐triggered lipoxin A4 (ATL) is a potent anti‐inflammatory mediator, involved in the resolution of inflammation. However, the therapeutic potential of immune targeting by means of ATL in atherosclerosis has not previously been explored. The aim of the present study was to determine the effects of ATL and its receptor Fpr2 on atherosclerosis development and progression in apolipoprotein E deficient (ApoE−/−) mice.
Experimental Approach
ApoE−/− × Fpr2+/+ and ApoE−/− × Fpr2−/− mice were generated. Four‐week‐old mice fed a high‐fat diet for 4 weeks and 16‐week‐old mice fed chow diet received osmotic pumps containing either vehicle or ATL for 4 weeks. Atherosclerotic lesion size and cellular composition were measured in the aortic root and thoracic aorta. Lipid levels and leukocyte counts were measured in blood and mRNA was isolated from abdominal aorta and spleen.
Key Results
ATL blocked atherosclerosis progression in the aortic root and thoracic aorta of ApoE−/− mice. In addition, ATL reduced macrophage infiltration and apoptotic cells in atherosclerotic lesions. The mRNA levels of several cytokines and chemokines in the spleen and aorta were reduced by ATL, whereas circulating leukocyte levels were unchanged. The ATL‐induced athero‐protection was absent in ApoE−/− mice lacking the Fpr2 receptor.
Conclusion and Implications
ATL blocked atherosclerosis progression by means of an Fpr2‐mediated reduced local and systemic inflammation. These results suggest this anti‐inflammatory and pro‐resolving agent has therapeutic potential for the treatment of atherosclerosis.
Linked Articles
This article is part of a themed section on Targeting Inflammation to Reduce Cardiovascular Disease Risk. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.22/issuetoc and http://onlinelibrary.wiley.com/doi/10.1111/bcp.v82.4/issuetoc
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