Bäckman L, Sundelin B, Bohman S O
Karolinska Institutet, Department of Pathology, Huddinge Hospital, Sweden.
APMIS Suppl. 1988;4:27-36.
Although acute cyclosporine nephrotoxicity has been extensively studied both in humans and in experimental animals, little has been written about experimentally-induced chronic renal changes after cyclosporine treatment. Groups of rats were therefore given cyclosporin A (CyA), 10 mg/kg pelleted food, for 21, 32 and 66 weeks. This corresponds to a daily CyA dose of 5-6 mg/kg body weight which is comparable to both the minimal immunosuppressive dose in rats and the doses given to patients. Kidney tissue was investigated using light microscopic morphometry and electron microscopy. After 32 wk, mild renal lesions in the form of focal glomerulosclerosis and nephron atrophy were present in the CyA-treated animals but nearly absent in the controls (p less than 0.05). At 66 wk, the changes were extensive in the CyA-treated animals. Similar but much less pronounced changes known as "chronic nephropathy of the rat" were found in the untreated rats. The proportion of glomeruli with segmental lesions was 33% in the CyA-treated animals and 7.5% in the controls (p = 0.014). No significant vascular lesions were found in either group. Electron microscopy confirmed the light microscopic observations but no ultrastructural changes specific for CyA treatment were identified. In conclusion, as with humans, chronic irreversible renal lesions can be induced in the rat by administering moderate doses of CyA over a long period.
尽管急性环孢素肾毒性已在人类和实验动物中得到广泛研究,但关于环孢素治疗后实验诱导的慢性肾脏变化的报道却很少。因此,将大鼠分组,给予含10 mg/kg环孢素A(CyA)的颗粒饲料,持续21周、32周和66周。这相当于每日CyA剂量为5 - 6 mg/kg体重,这与大鼠的最小免疫抑制剂量以及给予患者的剂量相当。使用光学显微镜形态计量学和电子显微镜对肾脏组织进行研究。32周后,接受CyA治疗的动物出现了以局灶性肾小球硬化和肾单位萎缩形式存在的轻度肾脏病变,但对照组几乎没有(p < 0.05)。在66周时,接受CyA治疗的动物的变化广泛。在未治疗的大鼠中发现了类似但不太明显的变化,称为“大鼠慢性肾病”。接受CyA治疗的动物中出现节段性病变的肾小球比例为33%,而对照组为7.5%(p = 0.014)。两组均未发现明显的血管病变。电子显微镜证实了光学显微镜观察结果,但未发现环孢素治疗特有的超微结构变化。总之,与人类一样,长期给予大鼠中等剂量的环孢素可诱导慢性不可逆性肾脏病变。