Abstract

Uptake of circulating macromolecules by the arterial wall may be a critical step in atherogenesis. Here we investigate the age-related changes in patterns of uptake that occur in the rabbit. In immature aortas, uptake was elevated in a triangle downstream of branch ostia, a region prone to disease in immature rabbits and children. By 16-22 months, uptake was high lateral to ostia, as is lesion prevalence in mature rabbits and young adults. In older rabbits there was a more upstream pattern, similar to the disease distribution in older people. These variations were predominantly caused by the branches themselves, rather than reflecting larger patterns within which the branches happened to be situated (as may occur with patterns of haemodynamic wall shear stress). The narrow streaks of high uptake reported in some previous studies were shown to be post mortem artefacts. Finally, heparin (which interferes with the NO pathway) had no effect on the difference in uptake between regions upstream and downstream of branches in immature rabbits but reversed the difference in older rabbits, as does inhibiting NO synthesis directly. Nevertheless, examination of uptake all around the branch showed that changes occurred at both ages and that they were quite subtle, potentially explaining why inhibiting NO has only minor effects on lesion patterns in mature rabbits and contradicting the earlier conclusion that mechanotransduction pathways change with age. We suggest that recently-established changes in the patterns of haemodynamic forces themselves are more likely to account for the age-dependence of uptake patterns.

Highlights

  • Atherosclerosis is characterized by focal accumulations of lipids, fibrous proteins and cells within the arterial wall

  • Patterns of albumin uptake around intercostal branch ostia changed with age Fig. 1a-c show patterns of mass transfer coefficients around intercostal branch ostia in male rabbits aged 9 weeks, 6 months and 16–22 months

  • Uptake of plasma macromolecules by the arterial wall is less widely studied than other critical factors in atherogenesis and that may in part reflect a lack of convenient techniques

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Summary

Introduction

Atherosclerosis is characterized by focal accumulations of lipids, fibrous proteins and cells within the arterial wall. The lipid originates predominantly from circulating lipoproteins and its preferential deposition at well-defined sites may reflect variation in lipoprotein uptake by the wall. Evidence for a spatial correlation between such transport and the development of atherosclerosis derives from studies of arterial branch points. Wall uptake of plasma macromolecules and the prevalence of lesions are both greater downstream than upstream of branch ostia in the immature rabbit aorta; they are both greater upstream than downstream of ostia in the mature rabbit aorta [1]. Note that because there is a change in the pattern of both properties, the spatial correlation is only revealed when comparisons are made at the same age.

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