Yamazaki K, Nakashima H, Eyden B P, Sakai T, Omae K, Sakurai H
Department of Pathology, School of Medicine, Keio University, Tokyo, Japan.
J Submicrosc Cytol Pathol. 1992 Apr;24(2):257-68.
Tetraethyl orthosilicate (Si(OC2H5)4, or TEOS) is a silicon-containing compound which has widespread industrial applications and which has been documented as biohazardous. The histopathological features and mechanism of TEOS toxicity in the kidney of ICR mice were investigated in a light and electron microscopy study, which included energy dispersive X-ray microanalysis. TEOS was given to mice as intraperitoneal injection of approximately 1,670 mg/kg body weight in experiments based on a 24 h time-scale. Tissues were examined after sampling either immediately on death if this occurred within 24 h or, in the case of surviving animals, after sacrifice at 24 h. Renal injury was considered to be the most probable cause of death, on the basis of the following main findings: 1) acute tubular necrosis (glomerular lesions were absent); 2) a dense deposit of silicon over the microvilli of dead tubular epithelial cells; 3) an abundant aggregation of hydroxyapatite crystals containing calcium in the cytoplasm and mitochondria of the dead tubular epithelial cells; and 4) abundant myelinosomes and some hydroxyapatite crystals in the cytoplasm of viable proximal convoluted tubule epithelial cells. It was speculated that silicon compounds may bind to the plasma membranes of the proximal convoluted tubule epithelial cell microvilli and damage or interfere with membrane calcium channels. The resulting calcium ion imbalance may play a role in the subsequent progression of acute tubular necrosis by TEOS.
正硅酸四乙酯(Si(OC₂H₅)₄,或TEOS)是一种含硅化合物,具有广泛的工业应用,且已被记录为具有生物危害性。在一项包括能量色散X射线微分析的光镜和电镜研究中,对ICR小鼠肾脏中TEOS毒性的组织病理学特征及机制进行了研究。在基于24小时时间尺度的实验中,以腹腔注射约1670毫克/千克体重的剂量给小鼠注射TEOS。如果动物在24小时内死亡,则在死亡后立即取样检查组织;对于存活的动物,则在24小时后处死取样。基于以下主要发现,认为肾损伤最有可能是死亡原因:1)急性肾小管坏死(无肾小球病变);2)死亡肾小管上皮细胞微绒毛上有致密的硅沉积物;3)死亡肾小管上皮细胞的细胞质和线粒体中有大量含钙的羟基磷灰石晶体聚集;4)存活的近端曲管上皮细胞的细胞质中有大量髓鞘小体和一些羟基磷灰石晶体。据推测,硅化合物可能与近端曲管上皮细胞微绒毛的质膜结合,损害或干扰膜钙通道。由此产生的钙离子失衡可能在TEOS导致的急性肾小管坏死的后续进展中起作用。