Yoshida Y, Sue W, Okano M, Oyama T, Yamane T, Mitsumata M
Department of Pathology, Yamanashi Medical College, Japan.
Ann N Y Acad Sci. 1990;598:256-73. doi: 10.1111/j.1749-6632.1990.tb42298.x.
In order to clarify mechanisms determining different degrees of vulnerability of atherogenesis between the apical and the proximal lateral walls at branchings, both regions of the inferior mesenteric artery in human autopsy cases were investigated electron microscopically. The lateral wall and the apex have been accepted by many researchers as the most preferential and the most resistant sites, respectively, for the disease. In regard to blood flow, the apex is exposed to laminar high shear stress, but the outer lateral wall to turbulent low shear stress. In newborns, intimal thickness in the apex was greater than that in the lateral wall, due mainly to the proliferation of SMC. After the 3rd decade, collagen fibers drastically increased in the apical intima, and SMC embedded between the collagen fibers, modulating their phenotypes from synthetic to contractile. In the lateral intima, SMC remained as the synthetic type. Synthetic SMC are considered capable of proliferation in the arterial wall. The lateral intima was generally abundant in proteoglycans and lacked collagen (including subendothelial basement membranes) as well as elastic fibers, particularly in the upper part of the intima. Such a structural difference may cause favorable conditions for atherosclerosis. Results of in vitro studies revealed that collagen gel suppressed proliferation of SMC and changed their phenotype from synthetic to contractile. Therefore, laminar high shear stress gives the arterial wall resistancy to atherogenesis through this phenotypic change. Rabbits showed preferential regions in certain areas of the flow divider for lipid deposition which were different from those of human beings. These regions were covered by ellipsoidal endothelial cells, which should be exposed to relatively low mean shear stress. Ellipsoidal endothelial cells had already been observed in intact rabbits. Therefore, we can conclude that atherogenic processes could be initiated by relatively low mean shear stress in either humans or rabbits.
为了阐明决定分支处肠系膜下动脉顶端和近端侧壁动脉粥样硬化不同程度易损性的机制,对人体尸检病例中该动脉的这两个区域进行了电子显微镜研究。许多研究人员已将侧壁和顶端分别视为该疾病最易发生和最不易发生的部位。就血流而言,顶端承受层流高剪切应力,而外侧壁承受紊流低剪切应力。在新生儿中,顶端的内膜厚度大于侧壁,主要是由于平滑肌细胞(SMC)增殖。30岁以后,顶端内膜中的胶原纤维急剧增加,SMC嵌入胶原纤维之间,其表型从合成型转变为收缩型。在外侧内膜中,SMC仍为合成型。合成型SMC被认为能够在动脉壁中增殖。外侧内膜通常富含蛋白聚糖,缺乏胶原(包括内皮下基底膜)以及弹性纤维,尤其是在内膜上部。这种结构差异可能为动脉粥样硬化创造有利条件。体外研究结果表明,胶原凝胶可抑制SMC增殖并使其表型从合成型转变为收缩型。因此,层流高剪切应力通过这种表型变化赋予动脉壁抗动脉粥样硬化能力。兔子在分流器的某些区域显示出脂质沉积的优先区域,这些区域与人类不同。这些区域被椭圆形内皮细胞覆盖,这些细胞应承受相对较低的平均剪切应力。在完整的兔子中已经观察到椭圆形内皮细胞。因此,我们可以得出结论,无论是在人类还是兔子中,动脉粥样硬化过程都可能由相对较低的平均剪切应力引发。