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  • Montecucco, Fabrizio  (2)
  • 1
    In: Arteriosclerosis, Thrombosis, and Vascular Biology, Ovid Technologies (Wolters Kluwer Health), Vol. 32, No. suppl_1 ( 2012-05)
    Abstract: Elevated endocannabinoid levels are linked with the development of atherosclerotic vascular disease and coronary circulatory dysfunction in obese individuals, a precursor of coronary artery disease. However, it remains unclear whether endocannabinoid levels represent a risk factor or diagnostic biomarker for acute atherosclerotic vascular events. So far, a causal role of increased endocannabinoid levels in atherosclerotic plaque vulnerability and occurrence of acute clinical events has not been investigated. Here, we studied the involvement of fatty acid amide hydrolase (FAAH) deficiency, the major enzyme responsible for endocannabinoid anandamide degradation, in atherosclerotic plaque vulnerability. We interbred apolipoprotein E-deficient (ApoE-/-) mice with FAAH -/- mice to generate ApoE-/-FAAH -/- mice and measured serum levels of anandamide and related FAAH metabolites palmitoyl- and oleoylethanolamide. We assessed atherosclerosis in ApoE -/- and ApoE-/-FAAH -/- mice after 5, 10 and 15 weeks on high cholesterol diet (HCD; 1.25% cholesterol). Levels of FAAH metabolites anandamide, palmitoyl- and oleoylethanolamide were 1.4 to 2-fold higher in FAAH-/-ApoE-/-mice. FAAH deficiency attenuated atherosclerotic plaque size increase (by ∼50% in thoraco-abdominal aortas after 15 weeks HCD; n=7-10; P=0.007), but plaques had significantly lower content of smooth muscle cells (36% less after 10 weeks HCD in aortic sinuses; n=10-15; P=0.01) and increased matrix metalloproteinase MMP-9 expression (by 73%; P=0.049). There was no difference in macrophage content, but a 65% increase in neutrophil infiltrates (P=0.0007) in aortic sinus plaques from ApoE-/-FAAH -/- mice compared to ApoE -/- controls. This was accompanied by 1.9-fold increased chemokine CXCL1 mRNA levels (P =0.004) in mouse aortas. CXCL1 expression was confirmed by immunostaining which revealed colocalization with lesional macrophages. MMP-9 mainly colocalized with neutrophils rather than macrophages (correlation coefficient r: 0.6529; P=0.006). Increased levels of endocannabinoid anandamide and related FAAH metabolite levels are associated with the development of smaller atherosclerotic plaques with more vulnerable phenotype.
    Type of Medium: Online Resource
    ISSN: 1079-5642 , 1524-4636
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2012
    detail.hit.zdb_id: 1494427-3
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  • 2
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2013
    In:  Arteriosclerosis, Thrombosis, and Vascular Biology Vol. 33, No. 2 ( 2013-02), p. 215-223
    In: Arteriosclerosis, Thrombosis, and Vascular Biology, Ovid Technologies (Wolters Kluwer Health), Vol. 33, No. 2 ( 2013-02), p. 215-223
    Abstract: Endocannabinoid levels are elevated in human and mouse atherosclerosis, but their causal role is not well understood. Therefore, we studied the involvement of fatty acid amide hydrolase (FAAH) deficiency, the major enzyme responsible for endocannabinoid anandamide degradation, in atherosclerotic plaque vulnerability. Methods and Results— We assessed atherosclerosis in apolipoprotein E–deficient (ApoE –/– ) and ApoE –/– FAAH –/– mice. Before and after 5, 10, and 15 weeks on high-cholesterol diet, we analyzed weight, serum cholesterol, and endocannabinoid levels, and atherosclerotic lesions in thoracoabdominal aortas and aortic sinuses. Serum levels of FAAH substrates anandamide, palmitoylethanolamide (PEA), and oleoylethanolamide (OEA) were 1.4- to 2-fold higher in case of FAAH deficiency. ApoE –/– FAAH –/– mice had smaller plaques with significantly lower content of smooth muscle cells, increased matrix metalloproteinase-9 expression, and neutrophil content. Circulating and bone marrow neutrophil counts were comparable between both genotypes, whereas CXC ligand1 levels were locally elevated in aortas of FAAH-deficient mice. We observed enhanced recruitment of neutrophils, but not monocytes, to large arteries of ApoE –/– mice treated with FAAH inhibitor URB597. Spleens of ApoE –/– FAAH –/– mice had reduced CD4+FoxP3+regulatory T-cell content, and in vitro stimulation of splenocytes revealed significantly elevated interferon-γ and tumor necrosis factor-α production in case of FAAH deficiency. Conclusion— Increased anandamide and related FAAH substrate levels are associated with the development of smaller atherosclerotic plaques with high neutrophil content, accompanied by an increased proinflammatory immune response.
    Type of Medium: Online Resource
    ISSN: 1079-5642 , 1524-4636
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2013
    detail.hit.zdb_id: 1494427-3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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