Skip to main content

The apolipoprotein A-I mimetic peptide, ETC-642, reduces chronic vascular inflammation in the rabbit

Abstract

Background

High-density lipoproteins (HDL) and their main apolipoprotein, apoA-I, exhibit anti-inflammatory properties. The development of peptides that mimic HDL apolipoproteins offers a promising strategy to reduce inflammatory disease. This study aimed to compare the anti-inflammatory effects of ETC-642, an apoA-I mimetic peptide, with that of discoidal reconstituted HDL (rHDL), consisting of full-length apoA-I complexed with phosphatidylcholine, in rabbits with chronic vascular inflammation.

Results

New Zealand White rabbits (n = 10/group) were placed on chow supplemented with 0.2% (w/w) cholesterol for 6-weeks. The animals received two infusions of saline, rHDL (8 mg/kg apoA-I) or ETC-642 (30 mg/kg peptide) on the third and fifth days of the final week. The infusions of rHDL and ETC-642 were able to significantly reduce cholesterol-induced expression of intracellular cell adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) in the thoracic aorta (p < 0.05). When isolated rabbit HDL was pre-incubated with human coronary artery endothelial cells (HCAECs), prior to stimulation with TNF-α, it was found that HDL from ETC-642 treated rabbits were more effective at inhibiting the TNF-α-induced increase in ICAM-1, VCAM-1 and p65 than HDL isolated from saline treated rabbits (p < 0.05). There were, however, no changes in HDL lipid composition between treatment groups.

Conclusions

Infusion of ETC-642 causes anti-inflammatory effects that are comparable to rHDL in an animal model of chronic vascular inflammation and highlights that apoA-I mimetic peptides present a viable strategy for the treatment of inflammatory disease.

Background

An increase in the endothelial cell expression of adhesion molecules such as vascular cell adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1) is characteristic of the initial inflammatory response triggered by endothelial damage or dysfunction [1]. Elevated expression of adhesion molecules promotes the recruitment and trans-endothelial migration of circulating monocytes into the artery wall, eventually leading to the development of atherosclerosis [1].

The anti-inflammatory properties of high-density lipoproteins (HDL) are well established [2]. In vitro studies have demonstrated that reconstituted (rHDL), containing apolipoprotein (apo) A-I (the main apolipoprotein constituent of HDL) complexed with phospholipids, inhibit the expression of VCAM-1 and ICAM-1 in human umbilical vein endothelial cells [36]. Consistent with this, in vivo studies in rabbits also show that lipid free apoA-I and rHDL reduce the expression of arterial VCAM-1 and ICAM-1 in the peri-arterial cuff model of acute inflammation [3, 7, 8]. Due to their potent anti-inflammatory properties, both HDL and apoA-I have immense therapeutic potential, but despite this there is currently no translated use to clinic.

The limiting factor in the therapeutic usefulness of apoA-I is its relatively large size of 243 amino acids, thereby making its synthesis difficult. This has lead to the development of apoA-I mimetic peptides that are much shorter in length (18-22 peptides) and able to be readily synthesized on a large scale, but still exhibit the same beneficial properties as HDL and full-length apoA-I. For example, infusions of mimetic peptides reduce atherosclerotic lesion size, improve endothelial dysfunction and also inhibit VCAM-1 and ICAM-1 expression in vitro and in vivo[913]. The apoA-I mimetic peptide used in our study, ETC-642, consists of a 22-amino acid synthetic amphipathic peptide complexed with sphingomyelin and 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) [14, 15]. Recent studies have found that ETC-642 is as effective as rHDL at suppressing acute inflammation in the rabbit peri-arterial collar model [16]. The anti-inflammatory effects of ETC-642 on chronic inflammation are, however, currently unknown.

Accordingly, this study has investigated the effect of ETC-642 on low-grade chronic vascular inflammation, in cholesterol-fed New Zealand White (NZW) rabbits [17, 18]. We find that ETC-642 reduced the expression of VCAM-1 and ICAM-1 in the rabbit thoracic aorta to a similar extent as rHDL containing full-length apoA-I. These studies highlight the efficacy and therapeutic potential of mimetic peptides in the treatment of inflammation and cardiovascular disease.

Results

Effects of the dietary intervention on plasma lipids

The concentrations of plasma total cholesterol, HDL cholesterol and non-HDL are presented in Table 1. Consumption of a chow diet supplemented with 0.2% cholesterol for 6 weeks significantly increased total cholesterol concentrations (~3 fold) in all treatment groups (p < 0.01). At sacrifice, there were no differences in plasma total cholesterol between the control animals and those receiving infusions of rHDL or ETC-642.

Table 1 Effects of saline, rHDL and ETC-642 infusions on plasma lipid levels in NZW rabbits

HDL cholesterol levels were not altered after six weeks of cholesterol feeding. Treatment with rHDL or ETC-642 did not change HDL cholesterol levels, compared to saline infused rabbits, at the time of sacrifice.

Non-HDL cholesterol levels were significantly increased (p < 0.05) with cholesterol feeding in rabbits injected with saline (22-fold), rHDL (9-fold) or ETC-642 (8.5 fold) (p < 0.05 for all). However, at the time of sacrifice there were no significant differences in non-HDL cholesterol concentrations between treatment groups.

Effect of rHDL and ETC-642 on chronic vascular inflammation

The ability of rHDL and ETC-642 to reduce cholesterol-induced inflammation in the thoracic aorta was determined by measuring endothelial ICAM-1 and VCAM-1 expression (Figure 1). After six weeks of cholesterol feeding endothelial ICAM-1 expression was at readily detectable levels in rabbits infused with saline. In rabbits infused with rHDL, ICAM-1 expression was reduced by 58% (p < 0.05). The ETC-642 infusions were as effective as rHDL and reduced endothelial ICAM-1 expression by 53% (p < 0.05). Endothelial VCAM-1 expression was increased to detectable levels following 6 weeks of cholesterol feeding. Two infusions of rHDL or ETC-642 in the final week of cholesterol feeding were found to reduce VCAM-1 by 73% and 76% respectively (p < 0.05).

Figure 1
figure 1

ETC-642 reduces endothelial adhesion molecule expression. Panel A: Immunohistochemical staining for ICAM-1 and VCAM-1 in representative thoracic aortic sections from cholesterol-fed NZW rabbits (n = 10 animals/group) infused with either saline, rHDL (8 mg/kg apoA-I) or ETC-642 (30 mg/kg peptide). Panel B: Endothelial expression of ICAM-1 and VCAM-1 were quantified as described in "Materials and Methods". Results are expressed as mean ± SEM. *p < 0.05 and **p < 0.01, compared to saline-infused animals.

After six weeks of cholesterol feeding there were no signs of fatty streak formation and therefore macrophages were not detected in the immuno-histochemically stained thoracic aortic sections.

Effect of ETC-642 on the anti-inflammatory properties and composition of rabbit HDL

HDL were isolated from the rabbits that were infused with saline, rHDL and ETC-642 and assessed for their ability to inhibit TNF-α-induced expression of ICAM-1 and VCAM-1 in HCAECs (Figure 2). As expected, stimulation of HCAECs with TNF-α increased ICAM-1 (17.2 fold) and VCAM-1 (50.6 fold) mRNA levels, compared to un-stimulated control cells (p < 0.001). When the cells were pre-incubated for 24 hrs with rHDL, the TNF-α-mediated increase in ICAM-1 and VCAM-1 mRNA levels was reduced by 35.5 ± 19.4% (p < 0.05) and 73.8 ± 8.4% (p < 0.001), respectively. We found that pre-incubation of cells with HDL from ETC-642 injected rabbits, caused reductions in TNF-α-induced ICAM-1 (17.4 ± 3.0%) and VCAM-1 (27.1 ± 15.0%) mRNA levels (p < 0.05). HCAECs incubated with HDL isolated from rabbits injected with saline and rHDL also expressed lower levels of ICAM-1 and VCAM-1 mRNA, compared to TNF-α stimulated controls, but these reductions did not reach statistical significance.

Figure 2
figure 2

The effect of isolated rabbit HDL on adhesion molecule expression and NF-κB activation in HCAECs. HCAECs were pre-incubated for 24 hrs with rHDL or HDL isolated from the plasma of rabbits injected with either saline, rHDL or ETC-642 (n = 10), then stimulated with TNF-α (1 ng/ml) for 5 hrs. ICAM-1, VCAM-1 and p65 mRNA levels were quantified as described in "Materials and Methods". Results expressed as mean ± SEM from triplicate in vitro experiments. *p < 0.05 and **p < 0.01, compared to TNF-α stimulated control cells.

Changes in the mRNA levels of p65, the active subunit of NF-κB, were also measured, as it is a known regulator of ICAM-1 and VCAM-1 expression. Stimulation of HCAECs with TNF-α increased p65 mRNA levels (1.5 fold), compared to un-stimulated control cells (p < 0.01). When cells were pre-incubated for 24 hrs with rHDL, the TNF-α-mediated increase in p65 mRNA levels was reduced by 36.0 ± 13.4% (p < 0.05). We found that pre-incubation of cells with HDL from rabbits injected with saline and ETC-642 caused reduced TNF-α-induced p65 mRNA levels, by 21.4 ± 10.8% and 31.0 ± 4.3% respectively (p < 0.05). Pre-incubation with HDL from the rabbits that received rHDL did not inhibit p65 mRNA levels.

Infusion of rHDL or ETC-642 did not significantly affect the composition of HDL. The relative concentrations of phospholipid, unesterified cholesterol, cholesterol ester and triglyceride were not statistically different from what was observed for HDL isolated from rabbits infused with saline (Table 2).

Table 2 Effects of saline, rHDL and ETC-642 infusions on HDL composition

Discussion

The development of apoA-I mimetic peptides has provided much therapeutic promise for the treatment of inflammatory and cardiovascular diseases. ETC-642 is a 22 amino acid peptide that mimics the structure of the amphipathic α-helices of apoA-I when combined with lipids. We therefore compared its ability to inhibit chronic vascular inflammation in cholesterol-fed rabbits, with that of rHDL (containing apoA-I and PLPC). We find, for the first time, that the mimetic peptide ETC-642 inhibits adhesion molecule expression in this model. Furthermore, HDL isolated from rabbits injected with ETC-642 displays more potent anti-inflammatory properties than HDL isolated from rabbits injected with saline or rHDL.

Increased expression of adhesion molecules VCAM-1 and ICAM-1, represent the earliest vasculature alteration following the initiation of an atherogenic diet [17, 18]. Using a cholesterol-fed rabbit model, vascular inflammation develops gradually via a process that is somewhat comparable to early human lesion development [17]. In this model we have demonstrated that infusions of rHDL were able to significantly attenuate cholesterol-induced aortic expression of VCAM-1 and ICAM-1. These findings support the numerous in vitro studies that demonstrate the anti-inflammatory properties of rHDL and in vivo studies showing that rHDL and apoA-I inhibit acute vascular inflammation [3, 6, 13, 19]. Furthermore, this study shows for the first time that the mimetic peptide ETC-642 can inhibit adhesion molecule expression in a model of chronic vascular inflammation. Our findings are also consistent with previous studies that have used ETC-642 and shown that it inhibits the development of similar inflammatory pathologies such as acute inflammation in the carotid artery in the rabbit peri-arterial collar model [16], cholesterol-induced aortic valve stenosis [20] and atherosclerosis in apoE-/- mice [21].

The beneficial cardio-protective properties of HDL have been attributed to their ability to efflux cholesterol from cells, including endothelial cells [22, 23]. Several studies have demonstrated that apoA-I mimetic peptides are also able to stimulate cholesterol efflux [13, 24]. For example, infusions of ETC-642 transiently elevate cholesterol levels in rats and humans [20, 25], indicating enhanced mobilization of cell cholesterol into the plasma. Enhanced cholesterol efflux may provide a mechanism for the anti-inflammatory effects of ETC-642, as has been demonstrated by other mimetic peptides [13]. In the current study, however, we found that ETC-642 had no effect on plasma total cholesterol or HDL cholesterol concentrations at the time of sacrifice. The reason for this is likely to be that the final ETC-642 injection was 48 hours prior to sacrifice. As the cholesterol elevating properties of ETC-642 occur within 45 minutes after infusion [20], the lack of change at 48 h post-infusion is therefore to be expected [16]. This may also explain why HDL composition did not change following rHDL and ETC-642 infusions and confirms our recent work, which showed that injection of lipid free apoA-I and rHDL increased HDL phospholipid, unesterified cholesterol and cholesterol ester levels at 5 minutes, but not at 6 h after infusion [26].

Despite the lack of apparent compositional change in rabbit HDL between treatment groups, the HDL from rabbits infused with ETC-642 appeared to exert more potent anti-inflammatory effects ex vivo in HCAECs than the HDL from rabbits injected with saline or rHDL. Recent proteomic studies have identified multiple proteins that co-isolate with human HDL [27, 28], including for example antioxidants, protease inhibitors and growth factors. These HDL-associated proteins are likely to impart some of the beneficial physiological effects of HDL [27]. Changes in the presence of these HDL-associated proteins are also likely to alter HDL function. It is possible that whilst the ETC-642 infusions did not significantly alter the relative amounts of phospholipids, unesterified cholesterol, esterified cholesterol or triglycerides, it may have changed the protein composition of the rabbit HDL in a way that increased their anti-inflammatory properties. Interestingly, the HDL from ETC-642 injected mice were also able to reduce the protein levels of the active subunit of NF-κB, p65. This reduction in p65 provides a possible mechanism for the reductions in both VCAM-1 and ICAM-1 as they are both regulated via activation of the NF-κB pathway [29, 30]. This is also consistent with a number of studies showing that HDL and rHDL reduce NF-κB activation and the expression of p65 [6, 13, 31].

The current study demonstrated that infusions of rHDL and ETC-642 inhibit the initial inflammatory response. This suggests that rHDL and ETC-642 may also attenuate the next stages of atherosclerotic lesion development. In support of this, previous work by our group and others has demonstrated that rHDL reduces lesion size and macrophage content in rabbits and mice [19, 32, 33]. Furthermore, adenoviral gene transfer of ETC-642 has been shown to decrease atherosclerosis in apoE-/- mice [21].

Conclusions

Using a cholesterol-fed rabbit model of chronic vascular inflammation we have demonstrated that mimetic peptide ETC-642 inhibits endothelial expression of adhesion molecules, markers of the earliest stages of atherosclerosis. These studies provide additional support for the therapeutic efficacy of mimetic peptides in the treatment of inflammation and cardiovascular disease.

Methods

Isolation of rabbit HDL and apolipoprotein A-I

Rabbit HDL were isolated from rabbit plasma (100 ml) by sequential ultracentrifugation in the 1.063 < d < 1.21 g/ml density range [34] and dialyzed against endotoxin-free phosphate buffered saline (PBS). Human HDL were isolated from pooled samples of autologously donated human plasma (Gribbles Pathology, South Australia) by sequential ultracentrifugation in the same density range. The human HDL were delipidated and apoA-I isolated by anion chromatography [34].

Preparation of rHDL containing apoA-I and PLPC

Discoidal rHDL containing apoA-I complexed to 1-palmitoyl-2-linoleoyl phosphatidylcholine (PLPC) (Avanti Polar Lipids, Alabaster, AL, USA) (initial PLPC/apoA-I molar ratio 100:1). were prepared using the cholate dialysis method [35]. The resulting rHDL were dialysed extensively against endotoxin-free PBS (pH 7.4) before use.

Preparation of ETC-642

The ETC-642 was provided as a lyophilized solid by Esperion Therapeutics, Pfizer (Groton, MI, USA). The complex consists of ESP-2418, an amphipathic peptide containing 22 L-amino acid residues: P-V-L-D-L-F-R-E-L-L-N-E-L-L-E-A-L-K-Q-K-L-K with a molecular weight of 2623 daltons that is complexed to sphingomyelin and 1,2-dipalmitoyl-sn- glycero-3-phosphocholine (DPPC) (peptide/sphingomyelin/DPPC molar ratio 1/3.75/3.75. The lyophilized solid was rehydrated with 50 ml of a sterile bicarbonate saline solution (Esperion Therapeutics, Pfizer, Groton, CT, USA) and gently swirled to mix. Three cycles of warming at 50°C and cooling to room temperature were performed to ensure complete reconstitution. The final protein concentration of ETC-642 was 10 mg/ml and the peptide was stored at 4°C until use.

Animal Experiments

The Sydney South West Area Health Service Animal Welfare Committee approved all animal procedures. Thirty male NZW rabbits weighing approximately 3 kg were obtained from the Institute of Medical and Veterinary Sciences (Adelaide, South Australia). Following a seven-day acclimatisation period, baseline plasma cholesterol and HDL levels were determined prior to placing the animals on a diet of normal chow supplemented with 0.2% (w/w) cholesterol for 6 weeks. Five weeks after commencement of the diet, the rabbits were randomised into three treatment groups (n = 10/group). A blood sample (3 mL) was collected from each animal at this time point. Plasma cholesterol levels were then determined to confirm that there were no significant differences between treatment groups. The animals then received two intravenous infusions of saline (control group), rHDL (8 mg/kg apoA-I) or ETC-642 (30 mg/kg peptide) on the third and fifth days of the final (sixth) week of dietary intervention and were sacrificed at the end of the sixth week of high cholesterol feeding. The animals were euthanased with an intravenous overdose of sodium pentobarbital (100 mg/kg). Plasma was collected via cardiac puncture. The thoracic aortae were then removed, flushed with chilled PBS before placement in cold 4% (v/v) paraformaldehyde overnight. The aortae were then transferred to 70% (v/v) ethanol and stored at 4°C, then paraffin embedded for histological analysis.

Immunohistochemistry

Sections (5 mm) of the paraffin-embedded vessels were cut, dewaxed, and rehydrated. Mouse anti-rabbit VCAM-1 and ICAM-1 antibodies (gifts from Dr M Cybulsky, University of Toronto) were used to assess endothelial expression of adhesion molecules in the thoracic aorta. For the assessment of macrophages, thoracic aortic sections were stained for RAM11 (1:100; Dako). Thoracic aortic sections (10 sections/rabbit) were analysed using ImagePro Plus 4.5 (Media Cybernetics, Silver Spring, MD) as described [3, 19]. Image analysis results are expressed as image units.

Plasma Analyses and HDL composition

Total cholesterol concentrations were determined on rabbit plasma and isolated rabbit HDL enzymatically using commercially available kits (Roche Diagnostics). HDL cholesterol concentrations were determined on rabbit plasma by enzymatic assay following precipitation of apolipoprotein B containing lipoproteins with polyethylene glycol [36]. Phospholipid, unesterified cholesterol, cholesterol ester and triglyceride concentrations were assessed in rabbit HDL also using commercially available kits (Wako Pure Chemicals).

Endothelial cell culture

Human coronary artery endothelial cells (HCAECs) were grown in MesoEndo cell culture medium (Cell Applications Inc., CA, USA) and seeded at 1 × 106 cells/well in 12-well plates. Cells were then treated for 24 h with PBS, rHDL (1 mg/ml final apoA-I concentration) or isolated rabbit HDL (1 mg/ml final protein concentration). Following this cells were washed 1× with PBS and then stimulated with tumor necrosis factor-α (TNF-α) (1 ng/ml). After 5 h the cells were harvested and stored at -80°C until required.

Real-time PCR

Total RNA was extracted using the Trizol method, quantitated and normalised to 100 ng/uL using SYBR Green II assay (Invitrogen). RNA was then reverse transcribed in triplicate to cDNA using iSCRIPT (BioRad). Real-time PCR was performed in triplicate using iQSYBR Green Supermix (BioRad) and an iCycler iQ Real-time thermocycler (BioRad). The threshold cycle was calculated using iCycler iQ Real-time PCR detection system software version 3.0A (BioRad). Relative changes in mRNA expression between treatments were determined using the cT method. Results were normalised using GAPDH.

Statistical Analyses

All results are expressed as mean ± SEM. Statistical comparisons were made by two-tailed Student's t-tests and one way ANOVA with Bonferroni's test post hoc using GraphPad Prism Version 4.0 (San Diego, CA). A value of p < 0.05 was considered statistically significant.

Abbreviations

(apoA-I):

Apolipoprotein A-I

(apoE):

Apolipoprotein E, (DPPC): 1,2-dipalmitoyl-sn-glycero-3-phosphocholine, (GAPDH): Glyceraldehyde 3-phosphate dehydrogenase, (HDL): High-density lipoproteins, (HCAECs): Human coronary artery endothelial cells, (ICAM-1): Intracellular cell adhesion molecule-1, (mRNA): Messenger ribonucleic acid, NZW rabbits: New Zealand White rabbits, (NF-κB): Nuclear factor kappa-light-chain-enhancer of activated B cells, (p65): p65 subunit of NF-κB, (PLPC): 1-palmitoyl-2-linoleoyl phosphatidylcholine, (PBS): Phosphate buffered saline, (rHDL): Reconstituted HDL, (TNF-α): Tumour necrosis factor-α

(VCAM-1):

Vascular cell adhesion molecule-1.

References

  1. Libby P: Inflammation in atherosclerosis. Nature. 2002, 420: 868-874. 10.1038/nature01323

    Article  CAS  PubMed  Google Scholar 

  2. Barter PJ, Nicholls S, Rye KA, Anantharamaiah GM, Navab M, Fogelman AM: Antiinflammatory properties of HDL. Circ Res. 2004, 95: 764-772. 10.1161/01.RES.0000146094.59640.13

    Article  CAS  PubMed  Google Scholar 

  3. Nicholls SJ, Dusting GJ, Cutri B, Bao S, Drummond GR, Rye KA, Barter PJ: Reconstituted high-density lipoproteins inhibit the acute pro-oxidant and proinflammatory vascular changes induced by a periarterial collar in normocholesterolemic rabbits. Circulation. 2005, 111: 1543-1550. 10.1161/01.CIR.0000159351.95399.50

    Article  CAS  PubMed  Google Scholar 

  4. Clay MA, Pyle DH, Rye KA, Vadas MA, Gamble JR, Barter PJ: Time sequence of the inhibition of endothelial adhesion molecule expression by reconstituted high density lipoproteins. Atherosclerosis. 2001, 157: 23-29. 10.1016/S0021-9150(00)00659-6

    Article  CAS  PubMed  Google Scholar 

  5. Cockerill GW, Rye KA, Gamble JR, Vadas MA, Barter PJ: High-density lipoproteins inhibit cytokine-induced expression of endothelial cell adhesion molecules. Arterioscler Thromb Vasc Biol. 1995, 15: 1987-1994. 10.1161/01.ATV.15.11.1987

    Article  CAS  PubMed  Google Scholar 

  6. Bursill CA, Castro ML, Beattie DT, Nakhla S, van der Vorst E, Heather AK, Barter PJ, Rye KA: High-density lipoproteins suppress chemokines and chemokine receptors in vitro and in vivo. Arterioscler Thromb Vasc Biol. 30: 1773-1778.

  7. Dimayuga P, Zhu J, Oguchi S, Chyu KY, Xu XO, Yano J, Shah PK, Nilsson J, Cercek B: Reconstituted HDL containing human apolipoprotein A-1 reduces VCAM-1 expression and neointima formation following periadventitial cuff-induced carotid injury in apoE null mice. Biochem Biophys Res Commun. 1999, 264: 465-468. 10.1006/bbrc.1999.1278

    Article  CAS  PubMed  Google Scholar 

  8. Puranik R, Bao S, Nobecourt E, Nicholls SJ, Dusting GJ, Barter PJ, Celermajer DS, Rye KA: Low dose apolipoprotein A-I rescues carotid arteries from inflammation in vivo. Atherosclerosis. 2008, 196: 240-247. 10.1016/j.atherosclerosis.2007.05.008

    Article  CAS  PubMed  Google Scholar 

  9. Ou Z, Ou J, Ackerman AW, Oldham KT, Pritchard KA: L-4F, an apolipoprotein A-1 mimetic, restores nitric oxide and superoxide anion balance in low-density lipoprotein-treated endothelial cells. Circulation. 2003, 107: 1520-1524. 10.1161/01.CIR.0000061949.17174.B6

    Article  CAS  PubMed  Google Scholar 

  10. Garber DW, Datta G, Chaddha M, Palgunachari MN, Hama SY, Navab M, Fogelman AM, Segrest JP, Anantharamaiah GM: A new synthetic class A amphipathic peptide analogue protects mice from diet-induced atherosclerosis. J Lipid Res. 2001, 42: 545-552.

    CAS  PubMed  Google Scholar 

  11. Navab M, Anantharamaiah GM, Hama S, Garber DW, Chaddha M, Hough G, Lallone R, Fogelman AM: Oral administration of an Apo A-I mimetic Peptide synthesized from D-amino acids dramatically reduces atherosclerosis in mice independent of plasma cholesterol. Circulation. 2002, 105: 290-292. 10.1161/hc0302.103711

    Article  CAS  PubMed  Google Scholar 

  12. Ou J, Wang J, Xu H, Ou Z, Sorci-Thomas MG, Jones DW, Signorino P, Densmore JC, Kaul S, Oldham KT, Pritchard KA: Effects of D-4F on vasodilation and vessel wall thickness in hypercholesterolemic LDL receptor-null and LDL receptor/apolipoprotein A-I double-knockout mice on Western diet. Circ Res. 2005, 97: 1190-1197. 10.1161/01.RES.0000190634.60042.cb

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  13. Tabet F, Remaley AT, Segaliny AI, Millet J, Yan L, Nakhla S, Barter PJ, Rye KA, Lambert G: The 5A apolipoprotein A-I mimetic peptide displays antiinflammatory and antioxidant properties in vivo and in vitro. Arterioscler Thromb Vasc Biol. 30: 246-252.

  14. Blackburn DJ, Venkatachalapathi YV, Pillion DJ, Koopman WJ, Segrest JP, Anantharamaiah GM: Apolipoprotein A-I decreases neutrophil degranulation and superoxide production. J Lipid Res. 1991, 32: 1911-1918.

    CAS  PubMed  Google Scholar 

  15. Anantharamaiah VY, Brouillette CG, Segrest JP: Use of synthetic peptide analogues to localize lecithin:cholesterol acyltransferase activating domain in apolipoprotein A-I. Arteriosclerosis. 1990, 10: 95-105. 10.1161/01.ATV.10.1.95

    Article  CAS  PubMed  Google Scholar 

  16. Di Bartolo BA, Nicholls SJ, Bao S, Rye KA, Heather AK, Barter PJ, Bursill C: The apolipoprotein A-I mimetic peptide ETC-642 exhibits anti-inflammatory properties that are comparable to high density lipoproteins. Atherosclerosis.

  17. Finking G, Hanke H: Nikolaj Nikolajewitsch Anitschkow (1885-1964) established the cholesterol-fed rabbit as a model for atherosclerosis research. Atherosclerosis. 1997, 135: 1-7. 10.1016/S0021-9150(97)00161-5

    Article  CAS  PubMed  Google Scholar 

  18. Li H, Cybulsky MI, Gimbrone MA, Libby P: An atherogenic diet rapidly induces VCAM-1, a cytokine-regulatable mononuclear leukocyte adhesion molecule, in rabbit aortic endothelium. Arterioscler Thromb. 1993, 13: 197-204. 10.1161/01.ATV.13.2.197

    Article  PubMed  Google Scholar 

  19. Nicholls SJ, Cutri B, Worthley SG, Kee P, Rye KA, Bao S, Barter PJ: Impact of short-term administration of high-density lipoproteins and atorvastatin on atherosclerosis in rabbits. Arterioscler Thromb Vasc Biol. 2005, 25: 2416-2421. 10.1161/01.ATV.0000184760.95957.d6

    Article  CAS  PubMed  Google Scholar 

  20. Busseuil D, Shi Y, Mecteau M, Brand G, Kernaleguen AE, Thorin E, Latour JG, Rheaume E, Tardif JC: Regression of aortic valve stenosis by ApoA-I mimetic peptide infusions in rabbits. Br J Pharmacol. 2008, 154: 765-773.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  21. Bodary SY, Westrick RJ, Lalwani ND, Drake SL, Dasseux JLH: Gene Transfer of an ApoA-I mimetic peptide reduces atherosclerosis in mice. J Am Coll Cardiol. 2004, 43 (Suppl 2): A465-A466.

    Article  Google Scholar 

  22. Rothblat GH, Phillips MC: High-density lipoprotein heterogeneity and function in reverse cholesterol transport. Curr Opin Lipidol. 21: 229-238.

  23. Besler C, Heinrich K, Riwanto M, Luscher TF, Landmesser U: High-density lipoprotein-mediated anti-atherosclerotic and endothelial-protective effects: a potential novel therapeutic target in cardiovascular disease. Curr Pharm Des. 16: 1480-1493.

  24. Navab M, Anantharamaiah GM, Reddy ST, Hama S, Hough G, Grijalva VR, Yu N, Ansell BJ, Datta G, Garber DW, Fogelman AM: Apolipoprotein A-I mimetic peptides. Arterioscler Thromb Vasc Biol. 2005, 25: 1325-1331. 10.1161/01.ATV.0000165694.39518.95

    Article  CAS  PubMed  Google Scholar 

  25. Khan MLN, Drake SL, Crockatt JG, Dasseux JLH: Single-dose intravenous infusion of ETC-642, a 22-Mer ApoA-I analogue and phospholipids complex, elevates HDL-C in atherosclerosis patients. Circulation. 2003, 108 (Suppl IV): 563-564.

    Google Scholar 

  26. Patel S, Di Bartolo BA, Nakhla S, Heather AK, Mitchell TW, Jessup W, Celermajer DS, Barter PJ, Rye KA: Anti-inflammatory effects of apolipoprotein A-I in the rabbit. Atherosclerosis. 212: 392-397.

  27. Gordon SM, Deng J, Lu LJ, Davidson WS: Proteomic characterization of human plasma high density lipoprotein fractionated by gel filtration chromatography. J Proteome Res. 9: 5239-5249.

  28. Davidson WS, Silva RA, Chantepie S, Lagor WR, Chapman MJ, Kontush A: Proteomic analysis of defined HDL subpopulations reveals particle-specific protein clusters: relevance to antioxidative function. Arterioscler Thromb Vasc Biol. 2009, 29: 870-876. 10.1161/ATVBAHA.109.186031

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  29. Hadad N, Tuval L, Elgazar-Carmom V, Levy R: Endothelial ICAM-1 protein induction is regulated by cytosolic phospholipase A2alpha via both NF-kappaB and CREB transcription factors. J Immunol. 186: 1816-1827.

  30. Ju J, Naura AS, Errami Y, Zerfaoui M, Kim H, Kim JG, Abd Elmageed ZY, Abdel-Mageed AB, Giardina C, Beg AA, Smulson ME, Boulares AH: Phosphorylation of p50 NF-kappaB at a single serine residue by DNA-dependent protein kinase is critical for VCAM-1 expression upon TNF treatment. J Biol Chem. 285: 41152-41160.

  31. McGrath KC, Li XH, Puranik R, Liong EC, Tan JT, Dy VM, DiBartolo BA, Barter PJ, Rye KA, Heather AK: Role of 3beta-hydroxysteroid-delta 24 reductase in mediating antiinflammatory effects of high-density lipoproteins in endothelial cells. Arterioscler Thromb Vasc Biol. 2009, 29: 877-882. 10.1161/ATVBAHA.109.184663

    Article  CAS  PubMed  Google Scholar 

  32. Choudhury RP, Rong JX, Trogan E, Elmalem VI, Dansky HM, Breslow JL, Witztum JL, Fallon JT, Fisher EA: High-density lipoproteins retard the progression of atherosclerosis and favorably remodel lesions without suppressing indices of inflammation or oxidation. Arterioscler Thromb Vasc Biol. 2004, 24: 1904-1909. 10.1161/01.ATV.0000142808.34602.25

    Article  CAS  PubMed  Google Scholar 

  33. Rong JX, Li J, Reis ED, Choudhury RP, Dansky HM, Elmalem VI, Fallon JT, Breslow JL, Fisher EA: Elevating high-density lipoprotein cholesterol in apolipoprotein E-deficient mice remodels advanced atherosclerotic lesions by decreasing macrophage and increasing smooth muscle cell content. Circulation. 2001, 104: 2447-2452. 10.1161/hc4501.098952

    Article  CAS  PubMed  Google Scholar 

  34. Rye KA, Garrety KH, Barter PJ: Preparation and characterization of spheroidal, reconstituted high-density lipoproteins with apolipoprotein A-I only or with apolipoprotein A-I and A-II. Biochim Biophys Acta. 1993, 1167: 316-325.

    Article  CAS  PubMed  Google Scholar 

  35. Matz CE, Jonas A: Micellar complexes of human apolipoprotein A-I with phosphatidylcholines and cholesterol prepared from cholate-lipid dispersions. J Biol Chem. 1982, 257: 4535-4540.

    CAS  PubMed  Google Scholar 

  36. Allen JK, Hensley WJ, Nicholls AV, Whitfield JB: An enzymic and centrifugal method for estimating high-density lipoprotein cholesterol. Clin Chem. 1979, 25: 325-327.

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

This study was supported by a Heart Research Institute PhD scholarship (Dr Di Bartolo) and a Heart Foundation Career Development Fellowship (Dr Bursill) (CR07S3331).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Christina A Bursill.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

BAD-Performed in vivo and in vitro studies as well as the histology. Also assisted in the preparation of the manuscript. LZV-Performed quantitative PCR experiments. JTMT-Assisted in in vitro studies and quantitative PCR experiments. SB-Performed analysis of histological sections. KAR-Conceived the project and experimental design and assisted in the preparation of the manuscript. PJB-Conceived the project and assisted in the preparation of the manuscript. CAB-Assisted with the experiments and prepared the manuscript. All authors have read and approved the manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Rights and permissions

Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Di Bartolo, B.A., Vanags, L.Z., Tan, J.T. et al. The apolipoprotein A-I mimetic peptide, ETC-642, reduces chronic vascular inflammation in the rabbit. Lipids Health Dis 10, 224 (2011). https://doi.org/10.1186/1476-511X-10-224

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/1476-511X-10-224

Keywords