Kronka M C, Watanabe I, Lopes M G O, Silva M C P
Department of Anatomy, Institute of Biomedical Sciences, University of São Paulo, São Paulo, Brazil.
Gerontology. 2006;52(4):199-203. doi: 10.1159/000093651.
Data associating palatine mucosa, microvascular architecture, aging and diabetes mellitus are few, so the aim of the present study was to examine these conditions structurally and ultrastructurally.
We used 18 female rabbits, aged about 2 years at the beginning of the experiment, distributed into 2 groups: aging diabetic and aging animals, prepared by three different methodologies: light microscopy, scanning electron microscopy and transmission electron microscopy. The samples were stained with hematoxylin-eosin for light microscopy, and for scanning electron microscopy, we used Mercox Cl-2B vascular corrosion casts. For transmission electron microscopy, the specimens were fixed and embedded in Epon 812 resin.
Under light microscopy, we noted small amounts of underdeveloped connective papillae and significant flattened areas through the epithelium-connective tissue interface in the aging diabetic group. Larger blood vessels were deeply located in the palatine mucosa, branching off in the direction of the epithelium-connective tissue interface. Capillaries followed the interface contour. In both groups, vascular corrosion casts revealed capillaries sprouting out in disorganized rows but parallel between themselves. 'Hair-pin' capillary loops and convoluted capillary loops were noted.
The aging diabetic group showed rarefying microvasculature areas with complex tortuous capillary loops. Transmission electron microscopy results showed that the aging diabetic group presented small cytoplasmatic projections directed to the vessel lumen and micropinocytic vesicle, i.e. caveolas. Epithelium-connective tissue interface, connective papillae, microangioarchitecture, and information about endothelial cells alterations were observed in the aging diabetic and aging animals.
关于腭黏膜、微血管结构、衰老与糖尿病之间关系的数据较少,因此本研究旨在从结构和超微结构方面对这些情况进行研究。
我们选用了18只雌性兔子,实验开始时年龄约为2岁,分为两组:衰老糖尿病组和衰老组动物,采用三种不同方法制备样本:光学显微镜、扫描电子显微镜和透射电子显微镜。样本用苏木精-伊红染色用于光学显微镜观察,对于扫描电子显微镜,我们使用Mercox Cl-2B血管铸型。对于透射电子显微镜,标本固定后嵌入Epon 812树脂。
在光学显微镜下,我们注意到衰老糖尿病组中结缔乳头发育不良且数量较少,上皮-结缔组织界面存在明显的扁平区域。较大的血管位于腭黏膜深处,朝着上皮-结缔组织界面方向分支。毛细血管沿界面轮廓分布。在两组中,血管铸型显示毛细血管呈无序排列但相互平行地长出。观察到“发夹”状毛细血管袢和盘绕状毛细血管袢。
衰老糖尿病组显示微血管稀疏区域伴有复杂曲折的毛细血管袢。透射电子显微镜结果显示,衰老糖尿病组出现指向血管腔的小细胞质突起和微吞饮小泡,即小窝。在衰老糖尿病组和衰老组动物中观察到上皮-结缔组织界面、结缔乳头、微血管结构以及内皮细胞改变的相关信息。