Literature DB >> 19340354

Complex porcine model of atherosclerosis: induction of early coronary lesions after long-term hyperlipidemia without sustained hyperglycemia.

Sandra Artinger1, Carolin Deiner, Christoph Loddenkemper, Peter L Schwimmbeck, Heinz-Peter Schultheiss, Klaus Pels.   

Abstract

BACKGROUND: The incidence of coronary artery disease (CAD) is still increasing in industrialized countries and it is even higher in diabetic patients. For experimental studies investigating the pathophysiology of CAD, the use of an animal model comparable with the pathological situation in patients is crucial.
OBJECTIVE: To develop a model of advanced coronary atherosclerosis with induction of hyperlipidemia and hyperglycemia in domestic pigs.
METHODS: Six pigs were fed a standard pig chow (controls), two were fed a 2% cholesterol and 17% coconut fat diet (Chol group), and two pigs received a 4% cholesterol and 17% coconut fat diet combined with streptozotocin (STZ) injections to induce diabetes (High Chol+STZ group). Serum lipid and plasma glucose values were analyzed, and histochemical staining for morphometric analysis and immunohistochemistry were performed.
RESULTS: Pigs on the hyperlipidemic diet had elevated mean (+/- SD) serum lipid levels (total cholesterol 5.05+/-1.45 mmol/L [Chol] and 5.03+/-2.41 mmol/L [High Chol+STZ] versus 2.09+/-0.23 mmol/L [controls]). Histopathological evaluation revealed an initial stage of coronary atherosclerosis. None of the STZ-treated pigs showed a sustained elevation of plasma glucose (mean glucose before STZ injection was 5.11+/-0.94 mmol/L and thereafter was 6.03+/-2.39 mmol/L) or a decline in pancreatic beta cells.
CONCLUSIONS: The current data suggest that the domestic porcine model is not suitable to create severe CAD using an atherogenic diet in combination with STZ injections for experimental interventional vascular research. This may be due to different STZ sensitivities among species. However, hyperlipidemia induced early pathological lesions in coronary arteries resembling initial stages of atherosclerosis without severe luminal narrowing.

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Year:  2009        PMID: 19340354      PMCID: PMC2706769          DOI: 10.1016/s0828-282x(09)70068-6

Source DB:  PubMed          Journal:  Can J Cardiol        ISSN: 0828-282X            Impact factor:   5.223


  26 in total

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3.  Dyslipidemia and vascular dysfunction in diabetic pigs fed an atherogenic diet.

Authors:  J L Dixon; J D Stoops; J L Parker; M H Laughlin; G A Weisman; M Sturek
Journal:  Arterioscler Thromb Vasc Biol       Date:  1999-12       Impact factor: 8.311

4.  Effects of reducing LDL and increasing HDL with gemfibrozil in experimental coronary lesion development and thrombotic risk.

Authors:  C P Palazón; J Alfón; P Gaffney; M Berrozpe; T Royo; L Badimon
Journal:  Atherosclerosis       Date:  1998-02       Impact factor: 5.162

5.  Enhanced coronary vasa vasorum neovascularization in experimental hypercholesterolemia.

Authors:  H M Kwon; G Sangiorgi; E L Ritman; C McKenna; D R Holmes; R S Schwartz; A Lerman
Journal:  J Clin Invest       Date:  1998-04-15       Impact factor: 14.808

6.  Streptozotocin-induced diabetes in large animals (pigs/primates): role of GLUT2 transporter and beta-cell plasticity.

Authors:  Denis Dufrane; Mathieu van Steenberghe; Yves Guiot; Rose-Marie Goebbels; Alain Saliez; Pierre Gianello
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7.  Diabetes-induced accelerated atherosclerosis in swine.

Authors:  R G Gerrity; R Natarajan; J L Nadler; T Kimsey
Journal:  Diabetes       Date:  2001-07       Impact factor: 9.461

8.  Dietary induced atherogenesis in swine. Morphology of the intima in prelesion stages.

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Review 10.  Oxidation of low density lipoproteins in the pathogenesis of atherosclerosis.

Authors:  P Holvoet; D Collen
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