RRC ID 39785
Author Michiels CF, Kurdi A, Timmermans JP, De Meyer GRY, Martinet W.
Title Spermidine reduces lipid accumulation and necrotic core formation in atherosclerotic plaques via induction of autophagy.
Journal Atherosclerosis
Abstract BACKGROUND AND AIMS:Spermidine is an endogenous biological polyamine that exhibits broad longevity-extending activities via the induction of autophagy. Because basal autophagy is atheroprotective during early atherosclerosis but dysfunctional in advanced plaques, the aim of the present study was to assess the potential beneficial effects of autophagy induction by spermidine on atherosclerotic plaque progression and composition.
METHODS:Apolipoprotein E-deficient (ApoE(-/-)) mice were fed a Western-type diet for 20 weeks with or without 5 mM spermidine in the drinking water.
RESULTS:(Immuno-)histochemical analysis of plaques in the aortic root, proximal ascending aorta and brachiocephalic artery showed that spermidine changed neither the size of the plaque nor its cellular composition. However, spermidine treatment significantly reduced necrotic core formation (6.6 ± 0.5% vs. 3.7 ± 0.5% in aortic root, p = 0.0008) and lipid accumulation inside the plaque (27 ± 3% vs. 17 ± 1% oil red O positivity in thoracic aorta, p = 0.017). In vitro experiments showed that macrophages, unlike vascular smooth muscle cells (VSMCs), were relatively insensitive to autophagy induction by spermidine. Along these lines, spermidine triggered cholesterol efflux in autophagy-competent VSMCs (5.7 ± 1.2% vs. 8.7 ± 0.2%, p = 0.0118), but not in autophagy-deficient Atg7(F/F)SM22α-Cre(+) VSMCs or macrophages. Analogous to the experiments in vitro, spermidine affected neither necrosis nor lipid load in plaques of Atg7(F/F)SM22α-Cre(+)ApoE(-/-) mice.
CONCLUSIONS:Spermidine inhibits lipid accumulation and necrotic core formation through stimulation of cholesterol efflux, albeit without changing plaque size or cellular composition. These effects, which are driven by autophagy in VSMCs, support the general idea that autophagy induction is potentially useful to prevent vascular disease.
Volume 251
Pages 319-327
Published 2016-8
DOI 10.1016/j.atherosclerosis.2016.07.899
PII S0021-9150(16)31200-X
PMID 27450786
MeSH Animals Atherosclerosis / drug therapy Autophagy* Cholesterol / chemistry Humans Lipids / chemistry* Macrophages / drug effects Male Mice Mice, Knockout, ApoE Myocytes, Smooth Muscle / metabolism Necrosis / drug therapy Necrosis / pathology* Plaque, Atherosclerotic / drug therapy Plaque, Atherosclerotic / pathology* Spermidine / therapeutic use*
IF 4.467
Times Cited 2
WOS Category CARDIAC & CARDIOVASCULAR SYSTEMS PERIPHERAL VASCULAR DISEASE
Resource
Mice GFP-LC3#53(RBRC00806)