eISSN: 1897-4295
ISSN: 1734-9338
Advances in Interventional Cardiology/Postępy w Kardiologii Interwencyjnej
Current issue Archive Manuscripts accepted About the journal Editorial board Abstracting and indexing Subscription Contact Instructions for authors
SCImago Journal & Country Rank
vol. 15
Original paper

Local intravascular delivery of low-density-lipoprotein cholesterol corresponds with increased intimal thickening in a healthy porcine coronary model. A prelude to development of a model of atherosclerosis

Piotr P. Buszman
Bartłomiej Orlik
Krzysztof P. Milewski
Tomasz Roleder
Michał Jelonek
Filip Polczyk
Frank D. Kolodgie
Maciej Jankowski
Renu Virmani
Paweł E. Buszman

Adv Interv Cardiol 2019; 15, 1 (55): 81–90
Online publish date: 2019/04/04
Article file
- Local intravascular.pdf  [0.62 MB]
Get citation
JabRef, Mendeley
Papers, Reference Manager, RefWorks, Zotero


We aimed to evaluate the vascular response to local, intramural delivery of human, highly atherogenic lipids into domestic swine (DS). A total of 24 coronary artery segments of 10 DS were enrolled. Following balloon injury (POBA), segments were assigned to local delivery of 2 ml of human LDL (n = 9), 0.9% NaCl (control, n = 7) or to POBA alone. Following 28 days, optical coherence tomography (OCT), virtual histology IVUS (VH-IVUS) and NIRS spectroscopy were performed and vessel segments harvested for evaluation. At 28 days the % area stenosis in OCT was highest in the LDL group (23.6 ±13 vs. 10.8 ±7 vs. 8.1 ±7%; p = 0.02).


Large animal coronary artery models of in-stent restenosis and local drug delivery play an important role in development and validation of novel intravascular technologies and therapies such as vascular stents, scaffolds or drug-coated balloons. They have been validated mainly for drug release kinetics as well as safety by evaluation of healing and biocompatibility [1, 2]. On the other hand, the evaluation of efficacy and translation into the clinical setting has been limited, mainly due to a lack of underlying atherosclerotic lesions. Currently, multiple models of coronary artery disease exist, indicating the possibility of creating thin cap fibroatheromas [38]. These models however have multiple disadvantages. Most are based on small laboratory animals, not eligible for testing of human prototype devices. Additionally, the reproducibility, plaque volume, breeding time and cost are not satisfactory. Therefore, with the advances in transcatheter technologies, local delivery methods of lipoproteins supported by high cholesterol diet in large animals have been proposed [911] which resulted in positively remodeled, atheromatous but non-occlusive lesions 8–10 weeks following injury. These experiments however were based on high-cholesterol fed diet animals and/or familial hypercholesterolemic swine. Therefore, the independent role of direct cholesterol injection into the vessel wall is unknown.


Herein, we sought to evaluate the vascular response after local injection of highly atherogenic human low-density lipoprotein (LDL) in a normocholesterolemic domestic swine coronary model with anticipation of creation of a normocholesterolemic, reproducible model of occlusive atherosclerotic lesions.

Material and methods

Study design

After 7-day acclimation, using standard percutaneous techniques, under general anesthesia, coronary angiography with live quantitative analysis (QCA) was performed. One, medial segment of each main coronary artery (LAD, LCx, RCA) without side branches was chosen for the baseline procedure.

Following triple, 130% balloon overstretch injury (POBA), eligible coronary segments were randomized to three groups: (1) the study group with local delivery of 2 ml of human LDL from apheresis (LDL group); (2) the control group with delivery of 0.9% NaCl; and (3) the reference group (POBA alone group).

After 28 days of follow-up, control angiography was performed as well as multi-modality intravascular imaging with optical coherence tomography (OCT), virtual histology IVUS (VH-IVUS) and NIRS spectroscopy. Subsequently, the animals were euthanized and the vessel segments were harvested for independent pathological analysis.

Study device

The solutions were infused into the arterial wall with a modified, triple circumferential micro-needle catheter (Peregrine, Ablative Solutions, San Jose, CA, USA). The standard Peregrine catheter is approved for renal denervation procedures, in which it is used for peri-adventitial alcohol delivery and nerve ablation. The main advantages of these system, such as full proper targeting with full circumferential coverage, efficiency and controlled deployment, have been proved in preclinical studies [12]. In this study, we used a modified Peregrine catheter with a system enabling only short, 1–2 mm micro-needle deployment, sufficient to inject solution into the arterial wall instead of the peri-adventitial space (Figure 1).

Figure 1

Intramural injection of studied solutions utilizing modified circumferential, triple needle delivery catheter (Peregrine, ASI)


Solution – LDL isolation

Low-density lipoprotein (LDL) was isolated from apheresis waste fluid, obtained from patients with familial hypercholesterolemia undergoing LDL apheresis at the 1st Chair and Clinic of Cardiology, Medical University of Gdansk, by sequential density gradient ultracentrifugation using an ultracentrifuge Beckman Coulter Optima TLX-120 equipped with a fixed angle TLA-100.3 with slow acceleration and deceleration. LDL-apheresis fluid was distributed to 3.5-ml polycarbonate centrifuge tubes and a discontinuous density gradient was made by overlaying the apheresis solution (2.1 ml) with solution containing NaCl, 10 mg/dl EDTA and 1 mM NaOH (density, d = 1.006 g/ml). The tubes were ultracentrifuged at 100 000 rpm for 1 h at 4°C. The upper fraction was discharged and the lower fraction was mixed with 16.7% NaCl in the ratio 1 : 1. The high density-adjusted fraction was then centrifuged at 100 000 rpm for 2.5 h at 16°C after which the LDL fraction was collected from the top of the tube (d < 1.063 g/ml). The fraction containing LDL was desalted by running the samples over a Sephadex G-10 column (GE Healthcare) and filtered through a 0.20-µm pore-size syringe filter (Corning). Finally, sucrose at a final concentration of 10% was added and samples were placed at –80°C. the LDL concentration was evaluated in a series of samples to confirm the reproducibility of the solutions.

Experimental procedures

The study protocol has been accepted by the Local Ethics Committee for animal research. All animals received the standard of care outlined in the study protocol and in accordance with the act of animal welfare and the Principles of Care of Laboratory Animals [13]. Swine were fasted overnight before intravascular procedures. All pigs were pre-medicated with atropine (0.5 mg), then sedated with intramuscular ketamine hydrochloride (20 mg/kg) and xylazine (2 mg/kg), intubated and anesthetized with an intravenous propofol bolus (20–40 mg) followed by a continuous infusion (2–4 mg/kg/h). The electrocardiogram and blood pressure were continuously monitored during the whole procedure. Arterial access was obtained via the carotid artery utilizing cut-down technique and insertion of a 7 Fr sheath. Anticoagulation with heparin was achieved (3,000–10,000 U) to maintain a coagulation time ≥ 250 s. Following coronary angiography and live QCA analysis, one proximal segment, with diameter of 3–4 mm of each main coronary artery, was chosen for triple balloon dilation (POBA) at an inflation pressure sufficient to achieve 130% overstretch (balloon-artery ratio). Subsequently, in previously prepared segments, using a modified micro-needle catheter, the LDL solution or 0.9% NaCl was injected into the arterial wall. In the reference group, procedures were stopped after POBA. Finally, coronary angiography was performed.

After 28 days of follow-up, under general anesthesia as described above, terminal angiography with QCA, OCT and VH-IVUS was performed. Then all animals were sacrificed with pentobarbital overdose. Their coronary arteries were excised, perfused with formalin solution and then isolated for further histopathological analysis.

Quantitative coronary analysis (QCA)

Angiography of coronary arteries was performed using a General Electric Innova angiographic unit. A renal, short shaft 7 Fr guiding catheter was used to perform coronary angiography, balloon injury and the needle catheter delivery. QCA analysis was performed in a blinded fashion using QAngio XA Software version (Medis Medical Imaging Systems) from two contralateral projections. The baseline and 28-day follow-up minimal lumen diameters (MLD) and reference vessel diameters (RVD) were taken using the guiding catheter as a standard for measurement for calibration. Subsequently, the balloon-to-artery ratio was calculated. Percent diameter stenosis (%DS) at follow-up was calculated as: [1 – (MLD/RVD)] × 100%. Late lumen loss was calculated as MLD at baseline minus MLD at follow-up.

Histological analysis

Following vessel harvesting, studied segments were immersed in normal buffered formalin 10% (NBF) and were sent to an independent laboratory for pathological analysis (CVPath, Gaithersburg, MA, USA). All vessel segments were trimmed at three levels each (proximal, middle and distal), processed, embedded in paraffin, sectioned twice serially and the resulting sections were stained with hematoxylin and eosin (H + E) and Movat’s Pentachrome (MP) for evaluation. All sections were analyzed using a scoring system, and the following parameters were calculated: the vessel wall injury, neointima maturity, neointima fibrin, adventitial, media or mural inflammation, endothelialization, the encroachment of the thrombus on the vascular lumen, media hypocellularity, adventitial fibrosis.

There were noted other morphological features such as inflammatory cell type distribution, mural avulsion, endothelium erosion (terminal or artifact), mineralization, media fibrosis, neointima/media/adventitia – necrosis, neointimal vascularization, pre-aneurysmal dilation, occlusion, media smooth muscle cell vacuolation, leukocyte margination, foam cells, media free lipids, hemosiderin/hemorrhage, laceration/dissection, plaque calcification, fibrous plaque. For these parameters, semi-quantitative scoring at each section level was evaluated as follows: 0 – not present; 1 – present, but minimal feature; 2 – notable feature, mild; 3 – prominent feature that does not disrupt tissue architecture and is not overwhelming, moderate; 4 – overwhelming feature or feature that effaces or disrupts tissue architecture, severe.

Intravascular imaging

OCT image analysis

The OCT image analysis scrutinized serial cross-sectional images of the vessel, at 1 mm intervals, using CAAS Intravascular 2.0 software (Pie Medical Imaging BV, Netherlands). The region of interest (ROI) for OCT, IVUS and NIRS analysis was the location of the vessel’s injury performed at the index procedure. Plaque composition was analyzed according to previously validated criteria for OCT. In brief, signal-rich homogeneous plaques were classified as fibrous, signal-poor regions with diffuse borders were classified as lipid, signal-poor regions with well-defined borders were classified as calcified plaques, and signal-poor regions with visible media were classified as layered neointima. In addition, the presence of both plaque rupture and/or luminal thrombus was noted during OCT analysis.

Cross-sectional area (CSA), minimal and maximal diameter, and lumen eccentricity ((maximal diameter-minimal diameter)/maximal diameter) of the vessel were measured every 1 mm. The smallest CSA in one segment was taken as the OCT-defined minimal CSA. The OCT reference lumen area was estimated as the largest CSA within 5 mm proximally or distally – the region of interest (ROI) in the scanned coronary segment.

NIRS image analysis

The NIRS map analysis was performed using CAAS Intravascular 2.0 software (Pie Medical Imaging BV, Netherlands). The NIRS measurements are demonstrated as a color-coded, red-yellow scaled NIRS map. Each pixel on the NIRS map represents the probability the presence of an atherosclerotic lipid core. Red pixels correspond to low and yellow pixels correspond to a high probability of lipid core. Pixels with insufficient data (e.g. caused by guidewire shadowing) appear as black.

The NIRS map analysis allows calculation of the lipid core burden index (LCBI). The LCBI is estimated by dividing yellow pixels by all pixels (excluding black ones) within the analyzed pullback compartment and are expressed per mill (‰). In the present study the maximal LCBI was estimated in 4 mm pullback compartments for every analyzed ROI (max LCBI4mm).

IVUS image analysis

Quantitative grey-scale IVUS measurements were performed every one millimeter in scanned coronary segments using CAAS Intravascular 2.0 software (Pie Medical Imaging BV, Netherlands). Cross-sectional images were quantified for lumen CSA, external elastic lamina (EEM) CSA, plaque and media CSA, plaque burden, plaque area, and plaque volume. The eccentricity of the lumen and EEM CSA was measured as ((maximal diameter-minimal diameter)/maximal diameter). The IVUS reference lumen area was estimated as the largest CSA within 5 mm located proximally or distally to the ROI in one analyzed coronary segment.

VH-IVUS analysis

The VH-IVUS analysis was performed at the site of maximum plaque burden within the analyzed ROI. The necrotic core (NC), dense calcium (DC), fibrous fatty (FF) and fibrous tissue (FI) were detected according to previously validated criteria. The VH-IVUS analysis was performed using the Volcano S5 Imaging System.

Statistical analysis

Normally distributed parametric data are expressed as average and standard deviation, and as median and interquartile range (IQR) in cases of skewed distribution. When equal variance and normality were observed, one-way analysis of variance (ANOVA) and Student-Newman-Keuls post-ANOVA tests were used to test for differences in variables between stent types. When either the equal variance test or the normality test failed, the Kruskal-Wallis test (with Dunn’s method for post-hoc group comparison) was conducted.


Study flowchart

A study flowchart is presented in Figure 2. A total of 10 domestic swine, mean age 3–4 months and average weight of 35–45 kg, were included. Six segments were excluded due to vessel size (n = 3) and in three cases due to tortuous anatomy delivery of the catheter was not possible. Following randomization 9, 7 and 8 segments were allocated to LDL, 0.9% NaCl and POBA groups respectively. There were no periprocedural deaths. All animals survived to terminal follow-up.

Figure 2

Study flow chart


Quantitative coronary angiography

The QCA data are presented in Table I. The baseline vessel reference diameters, balloon diameters and the injury expressed as balloon-to-artery ratios were comparable between groups. At 28-day follow-up no occlusive stenosis (< 50% DS) was found in any of the vessels and the minimal lumen diameters were similar among groups. Late lumen loss was comparable between groups.

Table I

Quantitative coronary angiography at baseline and follow-up

ParameterPOBA (n = 8) Mean ± SDLDL (n = 9) Mean ± SD0.9% NaCl (n = 7) Mean ± SDP-value
 Minimal lumen diameter [mm]2.48 ±0.32.42 ±0.22.61 ±0.40.46
 Vessel reference diameter [mm]2.67 ±0.42.58 ±0.22.77 ±0.30.48
 Balloon diameter [mm]3.17 ±0.23.10 ±0.23.30 ±0.20.30
 Balloon-to-artery ratio1.29 ±0.21.30 ±0.21.22 ±0.20.68
 Minimal lumen diameter [mm]2.35 ±0.42.36 ±0.42.48 ±0.30.77
 Vessel reference diameter [mm]2.53 ±0.42.61 ±0.52.75 ±0.20.55
 Percent area stenosis (%)14.45 ±6.618.11 ±6.518.57 ±11.00.58
 Percent diameter stenosis (%)7.36 ±3.69.57 ±3.69.96 ±6.50.53
 Late lumen loss [mm]0.13 ±0.40.29 ±0.90.12 ±0.40.82

Optical coherence tomography

The results of the intravascular imaging are presented in Table II and highlighted in Figure 3. The minimal lumen diameters and areas were lowest in the LDL group, although not significantly statistically. The vessel stenosis was highest in the LDL group as represented by the percent area (%AS) and diameter stenosis (%DS); it was 2- and 3-fold higher compared to the saline and POBA groups respectively (p = 0.02).

Table II

Intravascular ultrasound (IVUS) volumetric, planimetric and near-infra red spectroscopy analysis (NIRS). Optical coherence tomography (OCT) volumetric and planimetric parameters

ParameterPOBA (n = 8) Mean ± SDLDL (n = 9) Mean ± SD0.9% NaCl (n = 7) Mean ± SDP-value
Optical coherence tomography:
 Minimal lumen area [mm2]5.54 ±1.14.31 ±2.46.66 ±2.70.15
 Minimal lumen diameter (average)2.61 ±0.32.26 ±0.72.86 ±0.70.17
 Lumen volume151.3 ±43143 ±72159 ±600.89
 Minimal lumen diameter2.34 ±0.21.98 ±0.62.60 ±0.70.13
 % Diameter stenosis12.35 ±11.935.97 ±20.816.42 ±13.20.02
 %AS (MLD based)8.13 ±7.823.67 ±13.710.80 ±8.70.02
 Lesion length20.95 ±4.221.84 ±4.318.60 ±1.80.34
Intravascular ultrasound and NIRS:
 Lumen volume [mm3]180.6 ±101165.6 ±71198.2 ±600.72
 Lipid core burden index (LCBI, NIRS)2.8 ±7000.35
 Minimal lumen plaque burden32.3 ±1238.8 ±1928.6 ±170.45
 Plaque area3.1 ±24.2 ±32.9 ±10.43
 Plaque volume NIRS’55.6 ±4568.5 ±4145.0 ±110.46
 Lumen eccentricity NIRS’
Figure 3

Morphometric lesion evaluation in optical coherence tomography

*P < 0.05 LDL vs. POBA and LDL vs. NaCl.


Intravascular ultrasound with NIRS and VH

The plaque burden expressed as plaque volume and area was highest in the LDL group, but there was no statistically significant difference between groups. Similarly, lumen volume was lowest in the study group but without significant differences between groups.

The analysis with near infrared spectroscopy did not show any meaningful signs of lipids in any of the groups as represented by the minimal or zero value of the lipid core burden index.

The virtual histopathology on the other hand showed a differentiated lesion composition including fibrous, fibro-fatty and necrotic core tissue, without any differences between groups (Figure 4).

Figure 4

Plaque composition in virtual histology IVUS

FI – fibrous tissue, FF – fibrofatty tissue, NC – necrotic core.


Representative corresponding cross sections in intravascular imaging and pathology are presented in Figure 5.

Figure 5

Representative, corresponding images of vessel cross sections in pathology and multimodal intravascular imaging modalities. From left to right: pathology, OCT, NIRS with IVUS, VH-IVUS


Pathological evaluation

No histologic differences were noted across test and control groups except a tendency toward higher percent area stenosis in the LDL group (Figure 5). The main finding was varying degrees of balloon injury with the typical SMC/proteoglycan-rich lesions observed in most sections, which were considered a fibrotic ‘sclerotic’ response to varying degrees of underlying balloon injury. There was only rare evidence of macrophage foam cells and general absence of necrotic core formation or other relevant attributes of atherosclerosis. Inflammation, when present, consisted of lymphocytes, macrophages, and giant cells, and was generally confined to areas of deep injury involving the outer media, adventitia, and peri-adventitial space (Figure 6). Occasional vessels with moderate to severe balloon injury showed lymphoid aggregates with granulomatous-type reactions with notable giant cells mainly in the adventitial or peri-adventitial. Less frequently, eosinophils and plasma cells were also present. A summary of qualitative pathological analysis is presented in Table III.

Table III

Pathological evaluation

ParameterPOBA (n = 8)LDL (n = 9)0.9% NaCl (n = 7)P-value
 Lumen area1.000.7–1.30.810.6–1.10.910.5–1.50.57
 IEL area1.931.3–2.11.561.2–2.21.511.0–2.20.97
 Med area1.931.6––2.81.991.7–2.70.97
 EEL area3.872.8–4.63.723.0–5.03.922.8–5.10.97
 Neointimal area0.60.4–1.10.970.4–1.30.550.3–0.60.72
 Med Inj Score1.601.1––3.11.800.9–2.00.22
 % Stenosis17.2011.7–24.033.014–4519.04–240.14
Qualitative analysis:
 Free cholesterol0.000.0–––0.0
 Necrotic core0.000.0–––0.0
 T cells0.000.0–––0.0

[i] IEL – internal elastic lamina, Med. – medial layer area, EEL – external elastic lamina.

Figure 6

LDL injection – low (Movat pentachrome) and respective high power (H&E) stained sections show severe arterial balloon injury and restenosis consisting mainly of SMCs and proteoglycan matrix. There are isolated areas of lymphohistiocytic inflammation, including a few giant cells in the deep media, adventitia, and peri-adventitial space (blue arrows)



In the current study, we aimed to develop a reproducible and predictable model of atherosclerosis in a healthy swine model by means of injection of highly saturated human LDL cholesterol into the coronary artery vessel wall. Following 28 days of observation, multiple intravascular imaging modalities were performed to assess the vascular response. Following in-vivo imaging, vessels were harvested for independent pathological analysis. The results showed higher degrees of stenosis in intravascular ultrasound and optical coherence tomography in the group where LDL cholesterol was injected. In the pathological evaluation the SMC/proteoglycan-rich lesions were observed in most sections and were considered as a fibrotic ‘sclerotic’ response to varying degrees of underlying balloon injury, with some evidence of macrophage foam cells and general absence of necrotic core formation or other relevant attributes of mature atherosclerosis. A tendency toward increased area of stenosis caused by neointimal thickening was observed, thus confirming the intravascular imaging findings. Similarly, previous studies have questioned the validation of the VH-IVUS with pathological evaluation [10].

Multiple reports have been published previously in which the authors anticipated induction of a local atherosclerotic process either with utilization of familial hypercholesterolemic swine or increased cholesterol diet [10, 14]. Both of these models produce advanced atheromas, with lipid pools and necrotic cores, but they mostly induce positive vascular remodeling rather than negative, and the location of these lesions is unpredictable and uncontrollable. Therefore, with the advances in endovascular catheter technologies, local, intramural injection of concentrated lipid solutions has been proposed by Granada et al. [9, 11, 15]. These results have shown various degrees of atherosclerosis progression, but still no significant stenotic or occlusive lesions were induced. Furthermore, it was impossible to discriminate the independent effect of local injection of cholesterol from generalized hypercholesterolemia. Therefore, in the current study we aimed to evaluate the independent vascular response to cholesterol injection. Moreover, for the first time highly saturated human LDL from apheresis was chosen as a solution and a novel, triple microneedle catheter instead of one needle catheter. To reduce the bias of local vascular injury with balloon and needle injection a placebo controlled group was included. The results showed that in the saturated LDL group injection, vessel stenosis was highest (36% DS), as shown in OCT evaluation. Therefore, although not significant or occlusive, these lesions can be considered as moderate severity. In pathology, the groups did not differ with regard to tissue composition and consisted mainly of excessive neointimal formation with a trend toward highest neointimal area in the study group. The morphometric calculation in post-mortem pathology sections however is not reliable, due to lack of blood pressure and tissue contractility; therefore in-vivo intravascular imaging provides better vessel morphometric evaluation.

The mechanism of increased neointimal thickening after LDL injection is unclear. We hypothesize that the higher stenosis and neointimal hyperplasia, with SMC and proteoglycan rich lesions, which were observed after LDL injection could be a similar process to intimal thickening in humans. Such a lesion (AHA type III) represents the early stage of atherosclerotic lesion development in humans found during autopsies [16, 17]. Although we did not see lipid pools, typical for pathological intimal thickening (PIT), we believe that this reaction is a footprint after early lipid injection into the vessel wall which initiated the inflammation and excessive neointimal hyperplasia as a consequence. The lack of lipid pools is most likely caused by only single delivery of cholesterol and fast porcine metabolism. Most likely earlier follow-up would have shown lipid deposits. Also, an alternative approach of repeated LDL administration or long-term retention could lead to an immune response which could in turn contribute to more rapid plaque formation. This hypothesis seems to be proven by the latest paper by Nakagawa and Nakashima, who reported that pathologic intimal thickening in human atherosclerosis is formed by accumulation of plasma-derived lipids and dispersion of intimal smooth muscle cells [17]. To fully prove this, further studies and evidence are required.

Validation of the current model with intravascular implantable and drug-eluting devices is required. Furthermore, achieving long-term intramural lipid retention should be attempted to provide continuous inflammation, and further and non-reversible development of atherosclerotic lesions.


This paper has been funded by the National Science Center Grant No. 2013/11/D/N25/0382 Poland. Supplementary funding has been provided from the Adamed Scientific Grant.

Conflict of interest

The authors declare no conflict of interest.



Schwartz RS, Edelman E, Virmani R, et al. , authors. Drug-eluting stents in preclinical studies: updated consensus recommendations for preclinical evaluation. Circ Cardiovasc Interv. 2008. 1:p. 143–53


Schwartz RS, Edelman ER, Carter A, et al. , authors. Preclinical evaluation of drug-eluting stents for peripheral applications: recommendations from an expert consensus group. Circulation. 2004. 110:p. 2498–505


Buja LM, Kita T, Goldstein JL, et al. , authors. Cellular pathology of progressive atherosclerosis in the WHHL rabbit. An animal model of familial hypercholesterolemia. Arteriosclerosis. 1983. 3:p. 87–101


Reddick RL, Zhang SH, Maeda N , authors. Atherosclerosis in mice lacking apo E. Evaluation of lesional development and progression. Arterioscler Thromb. 1994. 14:p. 141–7


Schwartz SM, Galis ZS, Rosenfeld ME, Falk E , authors. Plaque rupture in humans and mice. Arterioscler Thromb Vasc Biol. 2007. 27:p. 705–13


Shiomi M, Fan J , authors. Unstable coronary plaques and cardiac events in myocardial infarction-prone Watanabe heritable hyperlipidemic rabbits: questions and quandaries. Curr Opin Lipidol. 2008. 19:p. 631–6


Shiomi M, Ito T, Tsukada T, et al. , authors. Cell compositions of coronary and aortic atherosclerotic lesions in WHHL rabbits differ. An immunohistochemical study. Arterioscler Thromb. 1994. 14:p. 931–7


Zadelaar S, Kleemann R, Verschuren L, et al. , authors. Mouse models for atherosclerosis and pharmaceutical modifiers. Arterioscler Thromb Vasc Biol. 2007. 27:p. 1706–21


Granada JF, Moreno PR, Burke AP, et al. , authors. Endovascular needle injection of cholesteryl linoleate into the arterial wall produces complex vascular lesions identifiable by intravascular ultrasound: early development in a porcine model of vulnerable plaque. Coron Artery Dis. 2005. 16:p. 217–24


Granada JF, Wallace-Bradley D, Win HK, et al. , authors. In vivo plaque characterization using intravascular ultrasound-virtual histology in a porcine model of complex coronary lesions. Arterioscler Thromb Vasc Biol. 2007. 27:p. 387–93


Tellez A, Schuster DS, Alviar C, et al. , authors. Intramural coronary lipid injection induces atheromatous lesions expressing proinflammatory chemokines: implications for the development of a porcine model of atherosclerosis. Cardiovasc Revasc Med. 2011. 12:p. 304–11


Fischell TA, Vega F, Raju N, et al. , authors. Ethanol-mediated perivascular renal sympathetic denervation: preclinical validation of safety and efficacy in a porcine model. EuroIntervention. 2013. 9:p. 140–7


Institute of Laboratory Animal Resources NRC , author. Principles of Care of Laboratory Animals. NIH Publication. 1996. p. 85–23


Hasler-Rapacz J, Ellegren H, Fridolfsson AK, et al. , authors. Identification of a mutation in the low density lipoprotein receptor gene associated with recessive familial hypercholesterolemia in swine. Am J Med Genet. 1998. 76:p. 379–86


van Vlijmen BJ, van den Maagdenberg AM, Gijbels MJ, et al. , authors. Diet-induced hyperlipoproteinemia and atherosclerosis in apolipoprotein E3-Leiden transgenic mice. J Clin Invest. 1994. 93:p. 1403–10


Kolodgie FD, Burke AP, Nakazawa G, Virmani R , authors. Is pathologic intimal thickening the key to understanding early plaque progression in human atherosclerotic disease? Arterioscler Thromb Vasc Biol. 2007. 27:p. 986–9


Nakagawa K, Nakashima Y , authors. Pathologic intimal thickening in human atherosclerosis is formed by extracellular accumulation of plasma-derived lipids and dispersion of intimal smooth muscle cells. Atherosclerosis. 2018. 274:p. 235–42

Copyright: © 2019 Termedia Sp. z o. o. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
Quick links
© 2020 Termedia Sp. z o.o. All rights reserved.
Developed by Bentus.
PayU - płatności internetowe