Published online before print June 6, 2005, doi: 10.1161/CIRCULATIONAHA.104.497107
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Circulation. 2005;111:3112-3118.)
© 2005 American Heart Association, Inc.
Vascular Medicine |
Apolipoprotein E Mimetic Peptide Dramatically Lowers Plasma Cholesterol and Restores Endothelial Function in Watanabe Heritable Hyperlipidemic Rabbits
From the Departments of Medicine, Biochemistry, and Molecular Genetics and the Atherosclerosis Research Unit, University of Alabama at Birmingham.
Correspondence to G.M. Anantharamaiah, PhD, 1808 7th Ave S, DH-668, UAB Medical Center, Birmingham, AL 35294. E-mail ananth{at}uab.edu
Received August 2, 2004; revision received December 3, 2004; accepted February 24, 2005.
 |
Abstract |
|---|
 Top Abstract IntroductionMethodsResultsDiscussionReferences |
|---|
Background— These studies were designed to determine whether the dual-domain peptide with a class A amphipathic helix linked to the receptor-binding domain of apolipoprotein (apo) E (Ac-hE-18A-NH2) possesses both antidyslipidemic and antiinflammatory properties.
Methods and Results— A single bolus (15 mg/kg IV) of Ac-hE-18A-NH2 that contains LRKLRKRLLR (141- to 150-residue region of apo E) covalently linked to apo A-I mimetic peptide 18A not only reduced plasma cholesterol levels (baseline, 562±29.0 mg/dL versus 287.7±22.0 mg/dL at 18 hours, P<0.001) in the Watanabe heritable hyperlipidemic rabbit model but also significantly improved arterial endothelial function. This improvement was associated with a reduction in 2 markers of oxidative stress. First, the plasma lipid hydroperoxide content was reduced significantly, an effect associated with a 5-fold increase in HDL paraoxonase activity. Second, the formation of superoxide anion, a scavenger of nitric oxide, was also significantly reduced in arteries of these animals.
Conclusions— Because dyslipidemia and endothelial dysfunction are common features of the atherosclerotic disease process, this unique dual-domain peptide has ideal composite properties that ameliorate key contributory factors to atherosclerosis.
Key Words: lipoproteins • endothelium • metabolism • nitric oxide • arteriosclerosis
|
Introduction |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
An ideal drug for the treatment of atherosclerosis not only would possess antiinflammatory properties that would restore endothelial function and prevent monocyte infiltration into the arterial wall but also would rapidly reduce plasma cholesterol. LDL is taken up by cell surface receptors, primarily through interaction of apolipoprotein (apo) B-100 with the cell surface LDL receptors (LDLRs), whereas other apo B–containing lipoproteins are taken up by interaction of apo E with receptors, such as LDLR and LDL receptorlike proteins. Apo E–containing atherogenic lipoproteins directly interact with heparan sulfate proteoglycans (HSPGs) in the space of Disse.1 Apo E supplementation by infusion into cholesterol-fed rabbits protects these animals from atherosclerosis.2 In addition to the class A lipid-associating domain at the C terminus, apo E possesses a receptor-binding domain.2,3 The arginine-rich domain of apo E (residues 141 to 150) has been shown to be important for the receptor-binding properties of apo E.3 Based on these observations, a dual-domain peptide has been designed that possesses the arginine-rich domain (LRKLRKRLLR, 141- to 150-residue region of apo E) from apo E, covalently linked to the well-characterized class A amphipathic helical peptide 18A.4 The resulting peptide (Ac-hE-18A-NH2) has been shown to promote the rapid uptake and clearance of atherogenic apo B–containing lipoproteins in vitro and in dyslipidemic mouse models.5–7 A peptide with the LRKLRKRLLR residues scrambled did not significantly enhance the uptake and degradation of apo B–containing lipoproteins.5 Administration of the peptide Ac-hE-18A-NH2 to LDLR-null mice did not reduce plasma cholesterol levels because the peptide was unable to associate with LDL.7 Thus, association of peptide Ac-hE-18A-NH2 to apo B–containing lipoproteins is a prerequisite for their clearance.7 Certain class A peptides have been shown to remove "seeding molecules" that are oxidized products of arachidonic and linoleic acids from the LDL surface.8,9 Because the peptide Ac-hE-18A-NH2 possesses a class A amphipathic helical domain that has been shown to possess several apo A-I–mimetic properties, we hypothesized that this peptide, in addition to dramatically reducing plasma cholesterol levels, would also possess antioxidative properties and exert a direct beneficial effect on endothelial function.
In this report, we show in the Watanabe heritable hyperlipidemic (WHHL) rabbit that a single administration of the peptide not only reduced plasma cholesterol levels but also restored endothelial function. The reduction of plasma cholesterol levels paralleled that of peptide clearance from plasma and was associated with a concomitant decrease in lipid hydroperoxides.
|
Methods |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
Peptide Synthesis
Peptides Ac-18A-NH2 (Ac-DWLKAFYDKVAEKLKEAF-NH2), Ac-LRKLRKRLLR-NH2, and Ac-hE18A-NH2 with the primary sequence Ac-LRKLRKRLLR-DWLKAFYDKVAEKLKEAF-NH2 were synthesized by the solid-phase method of peptide synthesis as described previously.5 The purity of synthetic peptides was established by analytical high-performance liquid chromatography and ion-spray mass spectrometry. The peptides Ac-18A-NH2 and Ac-hE-18A-NH2 were dialyzed against ammonium bicarbonate (100 µmol/L) and then distilled water and 0.01N HCl and were lyophilized before use. Lyophilized peptides were dissolved in sterile 0.15 mol/L NaCl, and the pH was adjusted to 7.0. Ac-LRKLRKRLLR-NH2 was dissolved in 0.15 mol/L NaCl, and the pH was adjusted to 7.0. The peptide solutions were sterilized by membrane filtration before administration.
Animals
Male homozygous WHHL rabbits were purchased at 6 months of age from Covance Research Products (Denver, Pa). Baseline cholesterol values and lipoprotein cholesterol profiles ensured the hypercholesterolemic phenotype (ie, total plasma cholesterol levels >500 mg/dL) of these animals. Rabbits were fed a standard laboratory chow and water ad libitum. For vessel reactivity studies, normolipidemic heterozygous WHHLs were used as controls. All procedures were reviewed and approved by the institutional Animal Use and Care Committee of the University of Alabama at Birmingham.
Injection Protocols
To study the effect of peptides on plasma cholesterol levels, animals were given a single dose of peptide (2.5 mg/kg, 7.5 mg/kg, or 15 mg/kg of Ac-hE-8A-NH2 or a mixture of 8.0 mg/kg Ac-LRKLRKRLLR-NH2) (an amount equivalent to a 7.5 mg/kg dose of the dual-domain peptide) and 10.5 mg/kg of Ac-18A-NH2 (molar equivalent of LRKLRKRLLR present in Ac-hE-18A-NH2) by intravenous injection of the marginal ear vein. Blood samples were collected at times noted in Results and in the figures. Stock solutions of peptide were prepared at a concentration of 
5 mg/mL. Control injections were vehicle only (same volume of sterile saline).
Electrophoretic Mobility Assay
Total lipoproteins were isolated from the plasma of WHHL rabbits by density-gradient centrifugation. Plasma density was adjusted to 1.21 g/mL with solid KBr and centrifuged for 48 hours at 100 000 rpm in a Beckman TL100.3 rotor and Beckman TL100 tabletop centrifuge. The top fraction (250 µL from the top of the tube) was separated and dialyzed to remove salt. Protein content of the sample was determined by the method of Lowry et al.10 Isolated lipoproteins (2 µg, based on protein content) from each sample were subjected to agarose gel electrophoresis according to the procedure of Asztalos et al11 on a 0.7% agarose gel. Tris-tricine buffer (25 mmol/L, pH 8.6) was used for both gel and electrode buffers. Samples were electrophoresed at constant voltage (100 V) for 2 hours or until the dye reached the top of the gel. The gel was then stained with Coomassie blue.
Separation of Lipoproteins by Column Chromatography
For plasma peptide-turnover studies, Ac-hE-18A-NH2 was labeled with 125I with the use of precoated IodoGen tubes (Pierce). Purified radiolabeled peptide was injected intravenously into WHHL rabbits, and plasma samples were collected at indicated time points as discussed in Results. The plasma samples (6-mL volume) were first adjusted to a density of 1.28 g/mL with solid KBr and layered under KBr solution (density, 1.21 g/mL). Each sample was then centrifuged at 50 000 rpm in a Beckman Ti 50.2 rotor for 48 hours to isolate the total plasma lipoproteins. The top 500 µL was collected; 300 µL of this sample was chromatographed on 2 Superose 6 columns in series that were equilibrated and eluted with phosphate-buffered saline (PBS). Protein in the eluent was detected by spectrophotometry at 280 nm. Fractions (0.5 mL) were collected and radioactive counts measured. Fractions in the HDL size range were used to determine paraoxonase (PON) activity. Column-chromatographic elution volumes of individual lipoprotein species were identified by elution volumes of known human lipoproteins isolated by sequential density ultracentrifugation.
Column Cholesterol Lipoprotein Profiles
Plasma cholesterol lipoprotein profiles were measured with the CLiP method.12 In brief, 5 to 10 µL of plasma was analyzed on a single Superose 6 (Pharmacia) column. Immediately after column chromatography, cholesterol reagent was introduced through a mixing tee, and the eluent-reagent mixture was passed into a postcolumn reaction coil. Cholesterol content of the eluent mixture was spectrophotometrically detected at 546 nm, and the data points were digitized. In some cases, fractions were collected to determine distribution of radioactive counts. Total cholesterol and triglyceride concentrations were determined enzymatically with commercially available reagents (Sigma Cholesterol 1000 and Thermo, respectively).
PON Assay
WHHL plasma samples were fractionated on Superose columns, and 2-µL fractions from the HDL region were added to 200 µL buffer (100 mmol/L Tris containing 2 mmol/L CaCl2, pH 8.0) containing paraoxon (1 mmol/L O,O-diethyl-O-p-nitrophenylphosphate), and the rate of release of 4-nitrophenol was determined spectrophotometrically. The assay was performed in a 96-well plate, and readings were taken every 2 minutes at 405 nm. The quantity of 4-nitrophenol formed was calculated from the molar extinction coefficient of 17 100 mol/L–1cm–1. One unit of PON activity was defined as 1 nmol of 4-nitrophenol formed per minute.
Determination of Plasma Lipid Hydroperoxide Content
Lipid hydroperoxides were measured with the FOX2 colorimetric assay to determine their content in the plasma of WHHL rabbits.13 In brief, 900 µL of the FOX reagent, containing 300 µmol/L FeSO4 7H2O, 120 µmol/L xylenol orange, 25 mmol/L H2SO4, and 4.4 mmol/L butylated hydroxytoluene in methanol, was added to 100 µL of the sample and incubated in the dark for 30 minutes. Absorbance was then measured at 560 nm. The test values were compared with a standard of cumene hydroperoxide to quantify the plasma hydroperoxide content.
In Vitro Assessment of Endothelial Function
Endothelium-dependent relaxation was monitored in isolated blood vessels of homozygous WHHL rabbits. Normolipidemic heterozygous WHHL rabbits were used as controls. Homozygous WHHL rabbits were randomized to receive either a single dose of Ac-hE-18A-NH2 (15 mg/kg, n=5) or an equivalent volume of saline (n=5) by intravenous injection. We used this dosage of peptide because we had previously found that it resulted in significant improvement in endothelial function in cholesterol-fed New Zealand White rabbits (authors’ unpublished observations). Heterozygous WHHL rabbits (n=6) received only saline. Rabbits were humanely killed 18 hours after treatment. Under ketamine/xylazine anesthesia, the thoracic aorta was excised and prepared for measurement of endothelium-dependent and -independent relaxation as described previously.14 Isometric tension was measured in indomethacin-treated, aortic ring segments bathed in a bicarbonate-buffered, Krebs-Henseleit solution and equilibrated with 95% O2–5% CO2. To assess endothelium-dependent relaxation, ring segments were submaximally constricted with phenylephrine (10–8 to 10–7 mol/L) followed by cumulative addition of acetylcholine (Ach, 10–9 to 3x10–6 mol/L). In related experiments, endothelium-independent relaxation was monitored by the addition of sodium nitroprusside (SNP, 10–9 to 3x10–6 mol/L). Effects of both agents on tension development were tested in 3 or 4 ring segments from each animal. Results were then averaged to yield a weighted mean for each animal.
Measurement of Vascular Superoxide Anion Production
The formation of O2·– was measured in the aortas of homozygous WHHL rabbits by coelenterazine-dependent chemiluminescence. The O2-dependent oxidation of coelenterazine results in the formation of a high-energy intermediate that emits light as it relaxes to the ground state. Aortas were excised from homozygous WHHL rabbits injected with either Ac-hE-18A-NH2 (n=6) or saline (n=7). The luminal surface of the artery was exposed, and tissue segments (16 mm2) were cut and placed in cell-culture wells containing PBS. Basal O2·– production was monitored with a luminometer (BMG Lab Technologies Inc). At the beginning of each experiment, coelenterazine was injected into each well to yield a final concentration of 10 µmol/L. O2-dependent chemiluminescence increased with time and stabilized after 3 to 5 minutes. Photon emission was measured during this plateau phase. The specificity of the chemiluminescence signal for O2·– production was verified in some experiments by addition of the superoxide dismutase mimetic tetrakis-(N-ethylpyridinium-2-yl) porphyrin (T2E, 100 U/mL). T2E used in these experiments was a generous gift of Incara, Inc. The assay was calibrated by monitoring the chemiluminescence signal of known amounts of O2·– generated by xanthine (50 µmol/L) and xanthine oxidase (0.1 to 0.5 mU/mL). Rates of O2·– production associated with these xanthine/xanthine oxidase incubation conditions were determined spectrophotometrically by measuring the O2-dependent reduction of ferricytochrome c. Chemiluminescence signals measured in isolated aortic tissues were then converted to rates of O2·– formation and normalized to tissue weight. Superoxide chemiluminescence was determined by subtraction of the signal that was not inhibited by T2E.
Statistics
Differences between treatment groups were determined with 2-tailed t tests. In some cases, differences were assessed by 1-way ANOVA with post hoc testing (Student-Newman-Keuls test). Differences were considered significant at P<0.05.
|
Results |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
A single intravenous injection of Ac-hE-18A-NH2 to WHHL rabbits produced a dose-dependent change in plasma cholesterol levels relative to the preinjection time point, reducing both VLDL and LDL contents (Figure 1A). At a dose of 2.5 mg/kg body weight, the mean cholesterol level at 18 hours compared with time 0 was 85.09±2.33% after injection (n=3); at 7.5 mg/kg, the level was 58.61±0.63% (n=2); and at 15 mg/kg, the level was 41.90±6.55% (n=3). The plasma cholesterol level reduction was accompanied by a change in agarose gel electrophoretic mobility of isolated LDL from the WHHL rabbits treated with peptide, demonstrating that the peptide associated with LDL and changed its surface charge and thus, its electrophoretic properties (Figure 1B). To determine whether the 2 domains could act independently of each other, a mixture of the 2 peptides (8.0 mg Ac-LRKLRKRLLR-NH2 and 10.5 mg Ac-18A-NH2) was administered to WHHL rabbits (n=3). These 2 peptides, being Ac- and amide-protected at the ends, do not covalently associate with each other. This resulted in a slight decrease in plasma cholesterol levels (81.83±3.3% of that of original value), a value similar to what was observed with the lowest dose (2.5 mg/kg) of Ac-hE-18A-NH2.
|
Plasma turnover of 125I–Ac-hE18A-NH2 and the kinetics of plasma cholesterol reduction were determined in 3 male WHHL rabbits injected intravenously with radiolabeled peptide (7.5 mg/kg). Blood samples were taken at the time points indicated in Figure 2A. Data through 12 hours after injection were fitted to biexponential equations as previously described15; use of the 24-hour time point caused the curve-fitting procedure to fail. The initial rapid phases of clearance for both peptide and cholesterol were similar, with the peptide having a t1/2 of 38.59 minutes and cholesterol having a t1/2 of 37.09 minutes. The second clearance phase for the peptide had a t1/2 of 17.03 hours, and cholesterol had a t1/2 of 48.91 hours. Furthermore, in a separate experiment, Ac-hE-18A-NH2 (7.5 mg/kg, n=8) or saline (n=3) was injected again intravenously into male WHHL rabbits (Figure 2B). The mean plasma triglyceride level was reduced by 45% for up to 8 hours after peptide injection but returned close to but significantly lower than preinjection levels by 24 hours (Figure 2B), reflecting the putative association of the peptide with VLDL, the major carrier of plasma triglycerides. Because single-domain peptides showed minimal effects on plasma cholesterol levels, plasma turnover experiments were not performed with these peptides.
|
) and plasma radioactivity (solid line, •). Data were fitted to biexponential equations as previously described (PKAnalyst). B, In separate experiments, male 6-month-old WHHL rabbits were injected with nonlabeled Ac-hE-18A-NH2 at dose of 7.5 mg/kg (solid line, 
, n=8) or saline (dashed line, •, n=3). Plasma triglyceride levels were determined at times shown. Owing to high baseline variation, data are expressed as mean±SEM percent change from baseline. *P<0.05, 
P<0.01, peptide vs saline, 2-tailed t test.Analyses of plasma at different time intervals showed that peptide Ac-hE-18A-NH2 radioactivity was distributed not only in VLDL and LDL but also in the HDL region (Figure 3), despite low levels of HDL cholesterol (Figure 1A). PON activity in the HDL region dramatically increased after injection of the peptide (Figure 4). A 5-fold increase in PON activity was observed at 90 minutes. The activity subsequently returned to baseline by 12 hours (data not shown). The increase in HDL-associated PON was accompanied by a decrease in total plasma lipid hydroperoxide levels, with the maximum reduction occurring over a similar time course as the maximum increase in PON (Figure 4). Administration of a mixture of single-domain peptides (8.0 mg/kg Ac-LRKLRKRLLR-NH2 and 10.5 mg Ac-18A-NH2) to the WHHL rabbits did not show changes in PON activity (320±20 U) at either time 0 or 90 minutes after injection. As expected, there was also no change in plasma lipid hydroperoxides (35±5 µmol/L) before and 90 minute after administration of the mixture of Ac-LRKLRKRLLR-NH2 and Ac-18A-NH2.
|
|
Endothelium-dependent and -independent relaxations were monitored in isolated aortic ring segments of homozygous WHHL rabbits 18 hours after treatment with either saline (n=5) or Ac-hE-18A-NH2 (n=5). As a control, we also monitored relaxation in ring segments of normolipidemic, saline-treated heterozygous WHHL rabbits (n=6). The plasma cholesterol level in homozygous WHHL rabbits was not different at baseline (saline, 532.6±12.9 mg/dL; Ac-hE-18A-NH2, 562.9±29.0 mg/dL) but was significantly reduced in peptide-treated rabbits 18 hours after injection (287.7±22.0 mg/dL, P<0.001). At the same time point, plasma cholesterol was unchanged in saline-treated WHHL rabbits (523.9±5.9 mg/dL). Ach-mediated relaxation was impaired in ring segments of homozygous WHHL rabbits (n, Figure 5A) compared with heterozygous WHHL controls (l, Figure 5A). Maximum Ach-induced relaxation in homozygous WHHL rabbits was 71±7% compared with 100±3% in normolipidemic heterozygous WHHL rabbits. Treatment with a single dose of Ac-hE-18A-NH2 (15 mg/kg) restored endothelium-dependent relaxation in ring segments of homozygotes (p, Figure 5A) essentially to the same level (95±6%) as that seen in normolipidemic heterozygous WHHL rabbits (Figure 5A). Thus, administration of the peptide improved Ach-induced relaxation by 24%. Endothelium-independent relaxation, assessed by SNP addition, was not impaired in any of these groups of rabbits (Figure 5B).
|
The formation of superoxide anion, O2·–, a known scavenger of nitric oxide (NO) in atherosclerotic blood vessels,16,17 was assessed in aortas of homozygous WHHL rabbits 18 hours after injection with saline (n=7) or Ac-hE-18A-NH2 (n=6, Figure 5C). The specificity of the chemiluminescent signal for O2·– was confirmed by addition of a superoxide dismutase mimetic, T2E, as noted in Methods (Figure 5C). Aortas of rabbits injected with the peptide had significantly reduced rates of O2·– production (68% decrease).
|
Discussion |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
The WHHL rabbit is commonly used as a model of atherosclerosis. These animals lack a functional LDLR and display elevated plasma concentrations of LDL and total cholesterol. WHHL rabbits closely approximate conditions associated with familial hypercholesterolemia in humans.18 Furthermore, arteries of WHHL rabbits display impaired endothelial function and develop vascular lesions (40% of the aortic surface at 6 months of age) similar to those found in human arteries.19
Although we found that peptide Ac-hE-18A-NH2 did not exert any effect on plasma cholesterol levels in LDLR-null mice,7 in the current study, we found that a single intravenous injection of Ac-hE-18A-NH2 to homozygous WHHL rabbits rapidly reduced total plasma cholesterol, with the maximum effect occurring at 6 hours. After 24 hours, plasma cholesterol levels were still significantly lower than at time 0 (Figure 2A). This response was characterized by a significant reduction in both VLDL and LDL content (Figure 1A). Administration of an equivalent dose of a mixture of single-domain peptides showed minimal changes in plasma cholesterol levels. Thus, Ac-hE-18A-NH2 is a peptide with unique properties not observed in the individual domains. Analysis of lipoproteins by agarose electrophoresis also showed that cationic Ac-hE-18A-NH2 associated with LDL and decreased its mobility owing to peptide association with LDL (Figure 1B). The accelerated clearance of VLDL and LDL in peptide Ac-hE-18A-NH2–treated WHHL rabbits probably occurs through LDLR family members, because LDLR expression in WHHL rabbits is defective. In previous studies, we have shown that the peptide enhanced the uptake and degradation of atherogenic apo B–containing lipoproteins via a pathway that requires binding to cell surface proteoglycans (HSPGs).6 The current studies clearly show a physical interaction between Ac-hE-18A-NH2 and LDL of WHHL rabbits (Figure 3). The results support our earlier observations that when the peptide is able to associate with apo B–containing lipoproteins, it induces a rapid reduction in plasma cholesterol levels via a high-capacity, low-affinity pathway involving HSPGs.1,5 Thus, the peptide Ac-hE-18A-NH2 is able to dramatically reduce plasma cholesterol and apo B-containing lipoprotein levels in WHHL rabbits.
In addition, the peptide Ac-hE-18A-NH2 also reduced plasma lipid hydroperoxide levels significantly when compared with those in control rabbits (Figure 4). This response was concomitant with an upregulation of PON activity, an HDL-associated enzyme that hydrolyzes oxidized phospholipids. Administration of a mixture of single-domain peptides (8.0 mg/kg Ac-LRKLRKRLLR-NH2 and 10.5 mg Ac-18A-NH2) to WHHL rabbits did not show significant changes in lipid hydroperoxides or PON activity. Previous studies have demonstrated that D-4F, an apo A-I mimetic peptide, stimulates an increase in plasma HDL concentration and PON activity.20 We have also shown earlier that whereas D-4F is highly effective in inhibiting LDL-induced monocyte chemotaxis, Ac-18A-NH2 is not.9 These and our earlier results with this peptide5–7 suggest that Ac-hE-18A-NH2 not only reduces plasma cholesterol in dyslipidemic animal models but also exerts antiinflammatory/antioxidant effects through its ability to scavenge "seeding molecules," whereas the 2 domains by themselves are not effective, suggesting that combining LRKLRKRLLR with the lipid-associating 18A produced a novel peptide with a highly effective dual function that combined dyslipidemic and antiinflammatory properties. Further studies are needed to understand the mechanism(s) by which the peptide exerts these effects.
The development of endothelial dysfunction is an early response to hypercholesterolemia and is now considered an independent clinical prognostic indicator in patients with or without established coronary artery disease.21 In this regard, it has been shown that the statin-mediated lowering of total plasma cholesterol and LDL is associated with improved endothelial function in humans at high risk for cardiovascular diseases.22 Laboratory studies indicate that NO bioactivity may be impaired by different mechanisms. First, NO may be modified in a hyperlipidemic environment through its interaction with elevated levels of O2·–, resulting in loss of NO function.16,17 Elevated plasma cholesterol may enhance O2·– formation by stimulating the expression of pro-oxidant enzymes such as NADPH oxidase and xanthine oxidase. Second, the hyperlipidemic environment may also diminish NO production itself by mediating the uncoupling of endothelial NO synthase (eNOS) from its substrate L-arginine.23 In support of these mechanisms, a recent report has shown that an apo A-I mimetic peptide both reduces LDL-mediated uncoupling of eNOS and reduces O2·– formation in cultured endothelial cells.23 Finally, lipid peroxyl radicals may also induce endothelial dysfunction by catalytically consuming NO.24
In the current study, we found that the Ach-induced relaxation of arterial segments of homozygous WHHL rabbits was significantly impaired compared with those from normolipidemic heterozygous controls. In contrast, relaxation induced by the endothelium-independent vasodilator SNP was not different between groups, suggesting that impaired vascular function was caused by changes at the level of the endothelium. We found that a single intravenous injection of Ac-hE-18A-NH2 significantly improved endothelial function (Figure 5A). This response was associated with a reduction in both vascular O2·– formation and plasma lipid hydroperoxide content. A dual mechanism of peptide action may explain the improvement in endothelial function in WHHL rabbits. First, cholesterol lowering coupled with increased PON activity will reduce lipid hydroperoxide content and thus, limit the direct scavenging of NO by peroxyl radicals. Second, decreased LDL should reduce O2·– formation by preventing the LDL-mediated uncoupling of eNOS.
Our results support the notion that the dual-domain synthetic peptide Ac-hE-18A-NH2 may have therapeutic potential for reducing common pathological features of atherosclerosis. Recent reports on apo A-IMilano:lipid complex infusion into mice,25 rabbits,26 and humans27 have stimulated new interest in HDL-based therapies. The end points in the apo A-IMilano studies were very different from those reported here and included regression of coronary lesions in humans, as measured by intravascular ultrasound, and a reduction of stent-induced hyperplasia in porcine coronary arteries. The apo A-IMilano preparations are complicated and costly; adding to this complexity is the production of a recombinant 28-kDa protein complexed to phospholipids. In this context, the present results indicate that a single administration of a 28-residue, amphipathic helical peptide that can be easily chemically synthesized in large quantities has effects on both plasma cholesterol reduction, similar to apo E, and antiinflammatory/antioxidant properties to improve endothelial relaxation, similar to apo A-I and HDL. Whether the Ac-hE-18A-NH2 peptide can inhibit lesion progression or even cause regression, like apo A-IMilano:lipid complexes, is the subject of current and future studies. Nonetheless, the Ac-hE-18A-NH2 dual-domain peptide has demonstrated that the beneficial properties of both apo A-I and apo E can be incorporated into a hybrid peptide. The implication then is that future designs may include even more targeted, beneficial properties into a single, perhaps even shorter, peptide. Thus, the ongoing investigation of minimized domain structure in apolipoproteins continues to be an ever-important asset to our understanding of the functions of apolipoproteins in atherogenesis and may yield new therapies in ameliorating cardiovascular diseases.
|
Acknowledgments |
|---|
This study was supported by National Institutes of Health grants HL65663, HL67930, and HL07703. The technical help of Matthew Kirksey and Dawn Horn is gratefully acknowledged.
Disclosure
G.M. Anantharamaiah is a principal in Bruin Pharma, LA, a start-up biotech company.
|
References |
|---|
|
TopAbstractIntroductionMethodsResultsDiscussionReferences |
|---|
- Mahley RW, Ji ZS. Remnant lipoprotein metabolism: key pathways involving cell-surface heparan sulfate proteoglycans and apolipoprotein E. J Lipid Res. 1999; 40: 1–6.
[Abstract/Free Full Text]
- Mahley RW, Weisgraber KH, Hussain MM, Greeman B, Fisher M, Vogel T, Gorecki M. Intravenous infusion of apolipoprotein E accelerates clearance of plasma lipoproteins in rabbits. J Clin Invest. 1989; 83: 2125–2130.[Medline]
[Order article via Infotrieve]
- Segrest JP, Garber DW, Brouillette CG, Harvey SC, Anantharamaiah GM. The amphipathic helix: the multifunctional, structural motif in plasma apolipoproteins. Adv Protein Chem. 1994; 45: 303–363.[Medline]
[Order article via Infotrieve]
- Anantharamaiah GM. Synthetic peptide analogs of apolipoproteins. Methods Enzymol. 1996; 128: 627–647.
- Datta G, Chaddha M, Garber DW, Chung BH, Tytler EM, Dashti N, Bradley WA, Gianturco SH, Anantharamaiah GM. The receptor binding domain of apolipoprotein E, linked to a model class A amphipathic helix, enhances internalization and degradation of LDL in fibroblasts. Biochemistry. 2000; 39: 213–220.[CrossRef][Medline]
[Order article via Infotrieve]
- Datta G, Garber DW, Chung BH, Chaddha M, Dashti N, Bradley WA, Gianturco SH, Anantharamaiah GM. Cationic domain 141–150 of apo E covalently linked to a class A amphipathic helix enhances atherogenic lipoprotein metabolism in vitro and in vivo. J Lipid Res. 2001; 42: 959–966.
[Abstract/Free Full Text]
- Garber DW, Handattu S, Aslan I, Datta G, Chaddha M, Anantharamaiah GM. Effect of an arginine-rich amphipathic helical peptide on plasma cholesterol in dyslipidemic mice. Atherosclerosis. 2003; 168: 229–237.[CrossRef][Medline]
[Order article via Infotrieve]
- Navab M, Hama SY, Anantharamaiah GM, Hassan K, Hough GP, Watson AD, Reddy ST, Sevanian A, Fonarow GC, Fogelman AM. Normal high density lipoproteins inhibits three steps in the formation of mildly oxidized low density lipoproteins steps 2 and 3. J Lipid Res. 2000; 41: 1494–1508.
- Datta G, Epand RM, Epand RF, Chaddha M, Kirksey MA, Garber DW, Lund-Katz S, Phillips MC, Hama S, Navab M, Fogelman AM, Palgunachari MN, Segrest JP, Anantharamaiah GM. Aromatic residue position on the nonpolar face of class A amphipathic helical peptides determines biological activity. J Biol Chem. 2004; 279: 26509–26517.
[Abstract/Free Full Text]
- Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951; 193: 265–275.
[Free Full Text]
- Asztalos BF, Sloop CH, Wong L, Roheim PS. Two-dimensional electrophoresis of plasma lipoproteins: recognition of new apo A-I-containing subpopulations. Biochim Biophys Acta. 1993; 1169: 291–300.[Medline]
[Order article via Infotrieve]
- Garber DW, Kulkarni KR, Anantharamaiah GM. A sensitive method for lipoprotein profile analysis of individual plasma samples. J Lipid Res. 2000; 41: 1020–1026.
[Abstract/Free Full Text]
- Wolff SP. Ferrous ion oxidation in presence of ferric ion indicator xylenol orange for measurement of hydroperoxides. Methods Enzymol. 1994; 233: 182–189.
- Zhang C, Reiter C, Eiserich JP, Boersma B, Parks DA, Beckman JS, Barnes S, Kirk M, Baldus S, Darley-Usmar VM, White CR. L-Arginine chlorination products inhibit endothelial nitric oxide production. J Biol Chem. 2001; 276: 27159–27165.
[Abstract/Free Full Text]
- Garber DW, Venkatachalapathi YV, Gupta KB, Ibdah J, Phillips MC, Hazelrig JB, Segrest JP, Anantharamaiah GM. Turnover of class A amphipathic peptide analogs of exchangeable apolipoproteins in rats. Arterioscler Thromb. 1992; 12: 886–894.
[Abstract/Free Full Text]
- White CR, Brock TA, Chang LY, Crapo J, Briscoe P, Ku D, Bradley WA, Gianturco SH, Gore J, Freeman BA, Tarpey MM. Superoxide and peroxynitrite in atherosclerosis. Proc Natl Acad Sci U S A. 1994; 91: 1044–1048.
[Abstract/Free Full Text]
- Ohara Y, Peterson TE, Harrison DG. Hypercholesterolemia increases endothelial superoxide anion production. J Clin Invest. 1993; 91: 2546–2551.[Medline]
[Order article via Infotrieve]
- Kita T, Brown MS, Watanabe Y, Goldstein JL. Deficiency of low density lipoprotein receptors in liver and adrenal gland of the WHHL rabbit, an animal model of familial hypercholesterolemia. Proc Natl Acad Sci U S A. 1981; 78: 2268–2272.
[Abstract/Free Full Text]
- Watanabe Y. Serial inbreeding of rabbits with hereditary hyperlipidemia (WHHL-rabbit). Atherosclerosis. 1980; 36: 261–268.[CrossRef][Medline]
[Order article via Infotrieve]
- Navab M, Anantharamaiah GM, Reddy ST, Hama S, Hough G, Grijalva VR, Wagner AC, Frank JS, Datta G, Garber D, Fogelman AM. Oral D-4F causes formation of pre-ß high density lipoprotein and improves high density lipoprotein–mediated cholesterol efflux and reverses cholesterol transport from macrophages in apolipoprotein E–null mice. Circulation. 2004; 109: 3215–3220.
[Abstract/Free Full Text]
- Halcox JP, Schenke WH, Zalos G, Mincemoyer R, Prasad A, Waclawiw MA, Nour KR, Quyyumi AA. Prognostic value of coronary vascular endothelial dysfunction. Circulation. 2002; 106: 653–658.
[Abstract/Free Full Text]
- Dupuis J, Tardif JC, Cernacek P, Théroux P. Cholesterol reduction rapidly improves endothelial function after acute coronary syndromes: the RECIFE (REduction of Cholesterol in Ischemia and Function of the Endothelium) trial. Circulation. 1999; 99: 3227–3233.
[Abstract/Free Full Text]
- Ou Z, Ou J, Ackerman AW, Oldham KT, Pritchard KA Jr. 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.
[Abstract/Free Full Text]
- O’Donnell VB, Taylor KB, Parthasarathy S, Kuhn H, Koesling D, Friebe A, Bloodsworth A, Darley-Usmar VM, Freeman BA. 15-Lipoxygenase catalytically consumes nitric oxide and impairs activation of guanylate cyclase J Biol Chem. 1999; 274: 20083–20091.
[Abstract/Free Full Text]
- Kaul S, Rukshin KS, Santos R, Azarbal B, Bisgaier CL, Johansson J, Tsang VT, Chyu KY, Cercek B, Mirocha J, Shah PK. Intramural delivery of recombinant apolipoprotein A-I Milano/phospholipid complex (ETC-216) inhibits in-stent stenosis in porcine coronary arteries. Circulation. 2003; 107: 2551–2554.
[Abstract/Free Full Text]
- Chiesa G, Monteggia E, Marchesi M, Lorenzon P, Lorusso V, Di Mario C, Karvouni E, Newton RS, Bisgaier CL, Franceschini G, Sirtori CR. Recombinant apolipoprotein A-IMilano infusion into rabbit carotid artery rapidly removes lipid from fatty streaks. Circ Res. 2002; 90: 974–980.
[Abstract/Free Full Text]
- Nissen SE, Tsunoda T, Tuzcu EM, Schoenhagen P, Cooper CJ, Yasin M, Eaton GM, Lauer MA, Sheldon WS, Grines CL, Halpren S, Crowe T, Blakenship JC, Kerensky R. Effect of recombinant ApoA-I Milano on coronary atherosclerosis in patients with acute coronary syndromes: a randomized controlled trial. JAMA. 2003; 290: 2292–2300.
[Abstract/Free Full Text]
Related Article:
-
Issue Highlights
Circulation 2005 111: 3015.[Full Text]
This article has been cited by other articles:
 |
|
 |
|
  A. Kontush and M. J. Chapman Functionally Defective High-Density Lipoprotein: A New Therapeutic Target at the Crossroads of Dyslipidemia, Inflammation, and Atherosclerosis Pharmacol. Rev., September 1, 2006; 58(3): 342 - 374. [Abstract] [Full Text] [PDF]
|
|
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||