2005
DOI: 10.1161/01.atv.0000184760.95957.d6
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Impact of Short-Term Administration of High-Density Lipoproteins and Atorvastatin on Atherosclerosis in Rabbits

Abstract: Objective-This study investigates effects of short-term administration of high-density lipoproteins (HDL) and a statin on atherosclerosis in cholesterol-fed rabbits. Effects of HDL apolipoprotein and phospholipid composition have also been investigated. Methods and Results-Aortic atherosclerosis was established over 17 weeks in 46 rabbits by balloon denudation and cholesterol feeding. During the past 5 days of the cholesterol-feeding period, animals received: (1) no treatment; (2)

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Cited by 145 publications
(93 citation statements)
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References 45 publications
(30 reference statements)
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“…Elevation of HDL-C, via infusion of HDL [12] or transgenic expression of apoA-I [18], results in a reduction of macrophages and chemokines within established atherosclerotic lesions. This was further supported by the recent report that infusion of small amounts of reconstituted or native HDL, without an increase in systemic HDL-C levels, rapidly reduces lesion size ( Figure 4) and increases the ratio of smooth muscle cells to macrophages ( Figure 5) in a model of established atherosclerotic plaque, induced by aortic balloon denudation in the cholesterol-fed rabbit [38]. This suggests that the quality of HDL that is administered, rather than the systemic level of HDL-C achieved, is of particular importance in potential remodelling of established atherosclerotic plaque and its proclivity to result in clinical ischaemia.…”
Section: Anti-inflammatory Propertiessupporting
confidence: 68%
“…Elevation of HDL-C, via infusion of HDL [12] or transgenic expression of apoA-I [18], results in a reduction of macrophages and chemokines within established atherosclerotic lesions. This was further supported by the recent report that infusion of small amounts of reconstituted or native HDL, without an increase in systemic HDL-C levels, rapidly reduces lesion size ( Figure 4) and increases the ratio of smooth muscle cells to macrophages ( Figure 5) in a model of established atherosclerotic plaque, induced by aortic balloon denudation in the cholesterol-fed rabbit [38]. This suggests that the quality of HDL that is administered, rather than the systemic level of HDL-C achieved, is of particular importance in potential remodelling of established atherosclerotic plaque and its proclivity to result in clinical ischaemia.…”
Section: Anti-inflammatory Propertiessupporting
confidence: 68%
“…The antioxidative function of apoA-I was corroborated by the finding that recombinant HDL containing only apoA-I and 1-palmitoyl-2-oleoylphosphatidylcholine (POPC) was as effective as native HDL in preventing LDL oxidation. In addition, in vivo studies have demonstrated that apoA-I can act as an antioxidative, anti-inflammatory, and anti-atherosclerotic agent (Nicholls et al 2005a, b;Paszty et al 1994). This further underlines a key antioxidant role for the HDL major protein apoA-I (Zerrad-Saadi et al 2009).…”
Section: Mechanisms Under Physiological Conditionsmentioning
confidence: 95%
“…Studies of HDL infusions into cholesterol-fed rabbits indicate that HDL upregulates endothelial cell thrombomodulin, which is an additional anticoagulant factor. 22 Therefore the reduction of HDL maybe one of the initiating factors for pulmonary arterial trunk embolism. As reported by Yang et al, 23 the level of HDL became elevated in VTE patients after heparin therapy.…”
Section: Discussionmentioning
confidence: 99%