Moore S A, Bohlen H G, Miller B G, Evan A P
Blood Vessels. 1985;22(6):265-77. doi: 10.1159/000158613.
Microvascular pathology is one of the major problems associated with prolonged diabetes mellitus. The purpose of the present study was to determine if anatomical cellular pathology of the cerebral cortical microvessels could be detected very early after the onset of a streptozotocin-induced model of diabetes. Male rats at age 14-16 weeks were hyperglycemic (greater than 250 mg/dl) for 4 weeks prior to scanning and transmission electron microscopic analysis of the external and internal cell and vessel wall morphology of the arterioles. Scanning electron microscopic studies indicated that many processes of vascular smooth muscle cells changed their normal spindle shape to a branched or stellate configuration. The internal cellular changes included swollen mitochondria and cisternae of the endoplasmic reticulum and reduced cytoplasmic staining. Necrosis of arteriolar endothelial cells was evident in virtually every vessel section studied. These data indicate that vascular smooth muscle and endothelial cellular degeneration of cerebral cortical arterioles begins in the very early stages of the streptozotocin model of diabetes.
微血管病变是长期糖尿病相关的主要问题之一。本研究的目的是确定在链脲佐菌素诱导的糖尿病模型发病后很早阶段,是否能检测到大脑皮质微血管的解剖学细胞病理学变化。14 - 16周龄的雄性大鼠在进行扫描以及对小动脉的外部和内部细胞及血管壁形态进行透射电子显微镜分析之前,已高血糖(大于250mg/dl)4周。扫描电子显微镜研究表明,许多血管平滑肌细胞的突起将其正常的纺锤形变为分支状或星状结构。内部细胞变化包括线粒体肿胀、内质网池以及细胞质染色减少。在几乎每个研究的血管切片中,小动脉内皮细胞坏死都很明显。这些数据表明,大脑皮质小动脉的血管平滑肌和内皮细胞变性在链脲佐菌素糖尿病模型的很早阶段就开始了。