Tracy R E
Department of Pathology, Louisiana State University Medical School, New Orleans 70112, USA.
Virchows Arch. 1995;427(2):131-8. doi: 10.1007/BF00196517.
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.
与主动脉和冠状动脉相比,衰老的基底动脉存在一些差异和相似之处。随着非坏死性内膜厚度随时间增加,冠状动脉和主动脉中平滑肌细胞数量在25 - 30岁左右达到稳定状态,但基底动脉中的平滑肌细胞数量持续增加,甚至到90岁仍在增加。单位组织中的细胞数量(细胞密度)随年龄下降,且在所有三个动脉段中下降模式在数量上相似。到目前为止检查的所有动脉表现相似,即动脉粥样坏死出现在内膜平滑肌细胞密度足够低的标本中。这些结果将低内膜细胞密度确定为识别易发生动脉粥样坏死的动脉的一个标准。一种可能的解释是,纤维化增厚和衰老内膜中的细胞减少,通过用不断扩展的基质材料使平滑肌细胞分散开来,可能是导致动脉粥样坏死侵入的调节因素。