Literature DB >> 7582242

Declining density of intimal smooth muscle cells and age as preconditions for atheronecrosis in the basilar artery.

R E Tracy1.   

Abstract

The aging basilar artery has some differences and some similarities when compared with the aorta and coronary arteries. As the non-necrotic intimal thickness increases over time, the number of smooth muscle cells reaches a steady state around age 25-30 years in the coronaries and aorta, but continues to increase in the basilar artery, even to 90 years of age. The numbers of cells per unit of tissue (the cell density) declines with age, and the patterns of decline are quantitatively similar in all three arterial segments. All arteries so far examined behave alike in showing that atheronecrosis emerges in those specimens that have sufficiently low density of intimal smooth muscle cells. These results identify low intimal cell density as a criterion for recognizing arteries that are prone to atheronecrosis. One possible explanation is that depopulation of the fibrotically thickened and aged intima, by spreading apart the smooth muscle cells with expanding matrix materials, could be the conditioning factor that brings about the intrusion of atheronecrosis.

Mesh:

Year:  1995        PMID: 7582242     DOI: 10.1007/BF00196517

Source DB:  PubMed          Journal:  Virchows Arch        ISSN: 0945-6317            Impact factor:   4.064


  13 in total

1.  Focal intimal proliferation in the cerebral arteries.

Authors:  W E STEHBENS
Journal:  Am J Pathol       Date:  1960-03       Impact factor: 4.307

2.  Cerebrovascular disease. I. The large arteries of the circle of Willis.

Authors:  A B BAKER; A IANNONE
Journal:  Neurology       Date:  1959-05       Impact factor: 9.910

3.  The histogenesis of arteriosclerosis of the larger cerebral arteries, with an analysis of the importance of mechanical factors.

Authors:  H T BLUMENTHAL; F P HANDLER; J O BLACHE
Journal:  Am J Med       Date:  1954-09       Impact factor: 4.965

4.  Histological changes in cerebral arteries with increasing age.

Authors:  A C Klassen; J H Sung; E M Stadlan
Journal:  J Neuropathol Exp Neurol       Date:  1968-10       Impact factor: 3.685

5.  Spatial dispersion of stainable lipid in frozen sections of human aorta.

Authors:  R E Tracy; G E Kissling; M Gandia; C Reynolds
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1989

6.  Transitional features in human atherosclerosis. Intimal thickening, cholesterol clefts, and cell loss in human aortic fatty streaks.

Authors:  J R Guyton; K F Klemp
Journal:  Am J Pathol       Date:  1993-11       Impact factor: 4.307

7.  Comparisons of human populations for histologic features of atherosclerosis. A summary of questions and methods for geographic studies.

Authors:  R E Tracy; G E Kissling
Journal:  Arch Pathol Lab Med       Date:  1988-10       Impact factor: 5.534

8.  Age and fibroplasia as preconditions for atheronecrosis in human coronary arteries.

Authors:  R E Tracy; G E Kissling
Journal:  Arch Pathol Lab Med       Date:  1987-10       Impact factor: 5.534

9.  Development of the atherosclerotic core region. Chemical and ultrastructural analysis of microdissected atherosclerotic lesions from human aorta.

Authors:  J R Guyton; K F Klemp
Journal:  Arterioscler Thromb       Date:  1994-08

Review 10.  Composition and classification of human atherosclerotic lesions.

Authors:  H C Stary
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1992
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  1 in total

1.  Declining density of intimal smooth muscle cells as a precondition for atheronecrosis in the coronary artery.

Authors:  R E Tracy
Journal:  Virchows Arch       Date:  1997-02       Impact factor: 4.064

  1 in total

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