Sd. Proctor et Jcl. Mamo, ARTERIAL FATTY LESIONS HAVE INCREASED UPTAKE OF CHYLOMICRON REMNANTS BUT NOT LOW-DENSITY LIPOPROTEINS, Coronary artery disease, 7(3), 1996, pp. 239-245
Background This study compares the accumulation of pre-formed chylomic
ron-remnants, chylomicrons and low-density lipoproteins (LDL) in rabbi
t thoracic aorta, To determine whether lipoproteins are delivered via
the vasa vasorum, the aortic uptake of lipoproteins was compared to th
at of the common carotid artery, The uptake of chylomicron remnants an
d LDL were compared in lesioned and non-lesioned aortic tissue from Wa
tanabe heritable hyperlipidaemic (WHHL) rabbits.Methods Chylomicrons,
chylomicron-remnants and LDL were radio-labelled with tyramine-cellobi
ose and injected into rabbits, Arterial uptake was determined after 2
h as the percentage of injected lipoproteins associated with arterial
tissue and also expressed as a fraction of mean arterial exposure. Res
ults Aortic accumulation of radio-labelled chylomicron-remnants was su
bstantially greater than for chylomicrons, and both were significantly
greater than LDL, The data suggests that chylomicrons must first be h
ydrolysed to smaller particles before uptake, In normal rabbits, there
was no difference in uptake of the lipoproteins between the aorta and
carotid vessels, suggesting that the vasa vasorum is not significantl
y involved in lipoprotein delivery, However, in WHHL rabbits there was
significantly greater aortic uptake of chylomicrons and LDL compared
to the carotid vessel and, in cholesterol-fed rabbits, significantly g
reater aortic uptake of chylomicrons, suggesting that in hypercholeste
rolaemia the lipoprotein retention properties of some arterial beds ch
ange, In arterial fatty lesions from WHHL and cholesterol-fed rabbits
there was an exclusive increase in chylomicron remnant uptake, whereas
LDL uptake was similar to non-lesioned tissue. Conclusions Chylomicro
n remnants and not their precursors might be primary atherogenic lipop
rotein because they penetrate arterial tissue efficiently and are sele
ctively retained in sites of lesion formation.