Yamamoto N, Katakami C, Yamamoto M
Department of Ophthalmology, Mitsubishi Kobe Hospital, Hyogo, Japan.
Nippon Ganka Gakkai Zasshi. 1998 Aug;102(8):475-80.
In order to elucidate the mechanisms of diabetic corneal epitheliopathy, we investigated the proliferation of corneal epithelial cells of streptozotocin-induced diabetic rats in the 1st, 2nd, 3rd and 6th months after the onset of diabetes using 3H-thymidine autoradiography. After the 1st month in diabetic rats, histological examination revealed that corneal epithelial layer was thin, and proliferation of corneal epithelial cells was decreased compared with that of normal untreated rats. After the 2nd month, proliferation of corneal epithelial cells showed no difference from normal rats. After the 3rd month in diabetic rats, the attachment of the epithelial layer to the stroma was loose and proliferation of corneal epithelial cells was increased compared with that of normal untreated rats. After the 6th month, proliferation of corneal epithelial cells showed no difference between diabetic rats and normal rats. We suggest that increased turnover rate of corneal epithelial cells may account for increased proliferation of corneal epithelial cells in diabetic rats during the 3rd month.
为了阐明糖尿病角膜上皮病变的机制,我们采用3H-胸腺嘧啶核苷放射自显影术,对链脲佐菌素诱导的糖尿病大鼠在糖尿病发病后第1、2、3和6个月时角膜上皮细胞的增殖情况进行了研究。糖尿病大鼠在第1个月后,组织学检查显示角膜上皮层变薄,与未治疗的正常大鼠相比,角膜上皮细胞的增殖减少。第2个月后,角膜上皮细胞的增殖与正常大鼠无差异。糖尿病大鼠在第3个月后,上皮层与基质的附着疏松,与未治疗的正常大鼠相比,角膜上皮细胞的增殖增加。第6个月后,糖尿病大鼠和正常大鼠角膜上皮细胞的增殖无差异。我们认为,角膜上皮细胞更新率的增加可能是糖尿病大鼠在第3个月时角膜上皮细胞增殖增加的原因。