Atherosclerosis and Lipoproteins |
From the Department of Internal Medicine (J.R.S., M.S., B.M., A.S.), Division of Cardiology, University of Marburg. Marburg; the Department of Medicine (K.W., M.M.H., H.S., H.W., W.M.), Division of Clinical Chemistry, University of Freiburg, Freiburg; and Childrens Hospital (H.S.), University of Marburg, Marburg, Germany.
Correspondence to Dr Winfried März, Department of Medicine, Division of Clinical Chemistry, Hugstetter Strasse 55, 79106 Freiburg, Germany. E-mail maerz{at}med1.ukl.uni-freiburg.de
| Abstract |
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Key Words: hypercholesterolemia reverse cholesterol transport tracer kinetics stable isotopes
| Introduction |
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Recently, we identified a homozygous FDB patient3 4 and studied the in vivo kinetics of apoB-100containing lipoproteins in this subject by using a stable isotope tracer technique.5 Our investigation revealed an increased removal of VLDL apoE, whereas the VLDL apoB-100 residence time was prolonged. The LDL apoB-100 production was reduced (7.4 versus 15 mg · kg-1 · d-1 in normals), and the residence time of LDL was increased (8.3 versus 2.3 days in normals).5 These findings are in agreement with data from heterozygous FDB subjects.6 They indicate that the metabolism of apoB-100containing lipoproteins is distinct in FDB compared with that in familial hypercholesterolemia (FH) due to LDL receptor deficiency.
In FH, HDL metabolism has also been found to be abnormal. Schaefer et al7 demonstrated decreased production and increased fractional catabolism of apoA-I in individuals with FH, suggesting a "cross-talk" between LDL and HDL metabolism. On the background of these observations, we decided to examine whether HDL metabolism might be altered in FDB as well. We therefore investigated the kinetics of HDL apoA-I in a homozygous FDB subject by using the stable-isotope tracer technique.
| Methods |
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-glutamyl transferase (36 U/L; upper limit of normal, 27
U/L). The patient did not take any lipid-lowering drugs in the 6 weeks
before and during the study. Six healthy, normolipidemic male subjects
served as controls. All but one (No. 6 was apoE 2/4) had an apoE 3/3
phenotype and normal body-weight.
Sequencing of ApoA-I
DNA of the homozygous FDB patient was extracted from white blood
cells by using blood polymerase chain reaction (PCR) DNA isolation
cartridges (Diagen GmbH). Oligonucleotide primers were
synthesized (BIG) to allow amplification of part of the promoter and of
individual exons of the apoA-I gene: apoA-I promoter 5': 5'-AGA GCT GAT
CCT TGA ACT CTT AAG-3' (77100); apoA-I promoter 3': 5'-GAC ACC TAC
CCG TCA GGA AGA GCA-3' (475499); apoA-I exon 2, 5': 5'-TCA CCT GGC
TGC AAT GAG T-3' (343362); apoA-I exon 2, 3': 5'-ACG GGG ATT TAG GGA
GAA AG-3' (530549); apoA-I exon 3, 5': 5'-CTG GCC TGA TCT GGG TCT
C-3' (644662); apoA-I exon 3, 3': 5'-CCA GTC TGG CTT CAA CAT CA-3'
(898908); apoA-I exon 4, 5': 5'-GGC TCA CCC CTG ATA GGC-3'
(13591376); and apoA-I exon 4, 3': 5'-GCA CGG AGT TGT TGA GAT CC-3'
(21792198). Typical PCR conditions were as follows: 50 ng of DNA,
50 mmol/L KCl, 10 mmol/L Tris-HCl (pH 8.3), 1.5 mmol/L
MgCl2, 0.2 mmol/L dNTPs, 1 µmol/L of
each primer, and 0.5 U Taq polymerase (Roche) in a 50-µL
reaction. Amplification was performed by using an initial denaturing
step at 95°C for 3 minutes and then 30 cycles at 95°C for 45
seconds, 60°C for 1 minute, and 72°C for 1 minute, followed by a
final elongation step at 72°C for 10 minutes. Purified PCR
products were directly sequenced with the dideoxy chain-termination
method (BigDye sequencing kit, Perkin-Elmer) on an ABI 377
sequencer.
Study Protocol
The in vivo turnover study followed a protocol that has recently
been described.7 The protocol had been approved by the
Internal Review Boards of the Philips University Marburg and of the
Albert Ludwigs University Freiburg. Informed, written consent was
obtained from each study subject. Three days before the study all
subjects received a standardized isocaloric diet. The stable-isotope
turnover study was performed under fasting conditions in all subjects,
starting at 8 AM. Two plastic indwelling catheters were
placed intravenously on contralateral arm veins: one was
used for the tracer infusion and the other was used for the frequent
blood sampling during the study.
[2H3]L-leucine
(L-leucine-methyl-D3 99,
Cambridge Isotope Laboratories) was administered as a priming bolus of
1.34 mg/kg, immediately followed by a constant infusion of 22 µg
· kg-1 · min-1
for up to 12 hours. Blood samples (9 mL) were drawn into tubes
containing EDTA at a final concentration of 1 g/L before the tracer
injection; after 10, 20, 30, 40, 60, 90, and 120 minutes; and then
hourly for up to 12 hours. The blood was kept on ice and the plasma was
immediately separated by centrifugation
(3000g, 20 minutes at 4°C). NaN3 and
aprotinin were added to the plasma at final concentrations of 0.5 g/L
and 200 000 KIU/L, respectively.
Lipoproteins and Apolipoproteins
VLDL (d<1.006 g/mL), LDL (d=1.019 to
1.063 g/mL), and HDL (d=1.063 to 1.21 g/mL) were isolated by
sequential preparative ultracentrifugation from 5 mL of
plasma (50.3 Ti rotor, L8-55M centrifuge; Beckman Instruments).
VLDL apoB-100 and HDL apoA-I were isolated by preparative gradient
(T=5% to 15%) SDSpolyacrylamide gel electrophoresis.
Cholesterol, triglycerides, and phospholipids
were measured by using enzymatic reagents provided by Wako Chemicals.
ApoA-I and A-II were quantified turbidimetrically with the use of
antibodies from Rolf Greiner.
Determination of Isotopic Enrichment
Samples were prepared for analysis by gas
chromatographymass spectrometry (GC-MS) as described
previously. Apolipoprotein bands were excised from the gels and
hydrolyzed in 6 mol/l HCl at 110°C for 24 hours under
N2. The protein hydrolysates were lyophilized in
a Speed-Vac evaporator (Savant Instruments). Free amino acids were
purified from plasma or protein hydrolysates by cation exchange
chromatography (AG-50W-X6, Bio-Rad Laboratories) and
then derivatized to n-heptafluorobutyrylisobutyl esters and
analyzed by GC-MS in the chemical ionization and selected ion
monitoring mode as reported recently.8 The ions
monitored were 363.1 m/z (mass-to-charge ratio)
for unlabeled L-leucine and 366.1
m/z for radiolabeled
[2H3]L-leucine
as parent ions (first MS) and 280.1 m/z for the
daughter ions of both types of leucine (second MS). Tracer enrichment
was calculated as the tracer-to-tracee ratio according to Cobelli et
al.9
A monoexponential function was fitted to the tracer-to-tracee curves of VLDL apoB-100 and HDL apoA-I with the use of SAAM 30 software as previously described. The function was defined as Et=Ep[1 -e-k(t-d)], where Et is the tracer-to-tracee ratio at time t of HDL apoA-I and Ep is the tracer-to-tracee ratio at plateau of the precursor pool of interest (VLDL apoB-100)10 ; d is the delay time and k is the fractional catabolic rate.
| Results and Discussion |
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Defective apoB-100 leads to significant changes in the in vivo kinetics of apoB-containing lipoproteins. We and others have shown that both the production rate of LDL apoB and its fractional catabolic rate are reduced compared with normal,2 5 6 but the metabolic situation in FDB is completely different from that in FH. In FH, delayed fractional catabolism of LDL apoB occurs together with an increased production of LDL apoB.11 12 13 Moreover, in homozygous FH, in an earlier report we found dramatic changes in HDL apoA-I kinetics, characterized by a decrease in apoA-I production and an increased fractional catabolic rate of apoA-I.7 In FH, coordinated regulation of apoB and apoA-I kinetics was thus suggested, and we were interested to search for a similar effect in FDB.
This is the first study to examine the metabolism of HDL apoA-I in FDB. The single homozygous individual presented in this study may not be completely representative of the entire disorder. However, owing to the potential influence of normal apoB-100 in heterozygous FDB, the study of a homozygous individual may provide more valid information about the metabolism in FDB than would study of several individuals heterozygous for the disease.
Despite normal apoA-I levels, we found an increased fractional catabolic rate of apoA-I in FDB and a marked increase in the total production rate of apoA-I. These changes may indicate that reverse cholesterol transport is upregulated in FDB. Increased production of apoA-I is found in subjects with the longevity syndrome.14 In addition, an increased fractional catabolic rate of apoA-I might be beneficial, since it is known that hypoalphalipoproteinemia due to increased fractional catabolism of apoA-I appears to be less atherogenic compared with the inborn abnormalities of apoA-I metabolism associated with decreased apoA-I production.15 The increased production of apoA-I may thus protect our FDB homozygote from atherosclerosis.
The metabolic basis for the increase in apoA-I production and fractional catabolism in FDB is currently unclear. Alterations of the apoA-I gene in our homozygous FDB patient and major alterations of the composition of HDL have been excluded as possible reasons for our findings. A speculative possibility is that the increase in the fractional catabolism of apoA-I in FDB is due to an increase in the catabolic rate of apoE-containing HDL. ApoE-containing HDLs are known to be catabolized by the LDL receptor,16 and LDL receptor activity appears increased in FDB due to the low influx of LDL cholesterol into the liver.4 5
Brown et al17 demonstrated an increase in apoA-I levels when they transferred human LDL receptors by using a recombinant adenovirus into LDL receptordeficient rabbits, a finding that, at first sight, appears inconsistent with an increased apoA-I fractional catabolic rate in FDB due to the upregulation of LDL receptors. However, in the study by Brown et al, the greatest increase of apoA-I was found in pre-ß-HDL, a fraction considered to contain mainly nascent HDL. This suggests that the increase in HDL was due to an increase in apoA-I production rather than decreased catabolism of apoA-I. Such interpretation of their data would then completely align with our findings in FDB, wherein we observed an increased apoA-I production together with an increased fractional catabolic rate. A mechanism linking the upregulation of LDL receptors and stimulation of apoA-I production is also not readily apparent at this time. The existence of such a mechanism, however, is well in agreement with studies by Mitchell et al,18 as well as with the studies of our group. In rats treated with drugs that upregulate the LDL receptor, Mitchell et al18 demonstrated an increase in apoA-I mRNA and a decrease in hepatic apoB mRNA. Consistently in subjects treated with the 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor pravastatin, we have found an increased production rate of apoA-I.19 Finally, we recently obtained evidence of increased production of apoA-I during administration of lifibrol to individuals with moderate hyperlipidemia.20 Lifibrol is a novel hypolipidemic compound that stimulates LDL receptors without substantially affecting cholesterol biosynthesis.21 22
In conclusion, the finding of a significantly increased HDL metabolism in FDB is in clear contrast to the situation in FH. In FH there is an increased fractional catabolic rate of apoA-I combined with a decrease in apoA-I production. With this combination, there are major metabolic differences between FDB and FH, with respect to not only the kinetics of apoB-containing lipoproteins but also in the kinetics of apoA-I. These differences might contribute to the rather benign clinical course of FDB compared with homozygous FH.
Received March 18, 1999; accepted March 31, 2000.
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21. Scharnagl H, Wieland H, März W. Lifibrol: first member of a new class of lipid lowering drugs? Expert Opin Investig Drugs. 1997;6:583591.
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