Starklint H, Hansen H V, Kemp M, Leyssac P P, Kemp E, Dieperink H
Laboratory of Nephropathology, Odense University Hospital, Denmark.
APMIS. 1994 May;102(5):347-55.
Cyclosporin A (CyA) nephrotoxicity was examined in Spraque-Dawley rats given CyA (12.5 (n = 45) or 25 (n = 45) mg/kg/day perorally for 16 weeks. Control rats (n = 45) received CyA vehicle. All rats were given either isradipine (ISRA) 1 or 5 mg/kg/day orally, or isradipine vehicle. Fifteen rats died from interstitial pneumonia caused by Staphylococcus xylosus. A predefined morphological CyA nephrotoxicity scoring system, based on semiquantitative scores for basophilic tubules and for interstitial fibrosis, performed on hematoxylin-eosin-stained tissue, yielded mean scores for basophilic tubules of 0.2 (range 0-1) in controls, 1.4 (range 0-3) in rats given CyA 12.5 mg/kg/day (p < 0.001), and 1.7 (range 0-3) in CyA 25 mg/kg/day rats (p < 0.001 as compared to controls). Rats given CyA were grouped according to their score for interstitial fibrosis: 0.2 (range 0-1) in CyA 12.5 mg/kg/day and 1.7 (range 0-3) in CyA 25 mg/kg/day rats (p < 0.001). When scores for basophilic tubules and interstitial fibrosis were pooled, none of the control rats had a score above 1, while 47% of the low-dose and 95% of the high-dose rats scored above 1. Thus, this CyA nephrotoxicity scoring system provided an easy, efficacious, and reproducible identification of rats with morphological CyA nephrotoxicity, and may be of clinical interest in the assessment of CyA nephrotoxicity. Kidney tissue from rats not treated with isradipine was further investigated with periodic acid-Schiff (PAS) with and without diastase treatment, and with Sirius Red. The latter confirmed the increase in connective tissue following tubular atrophy in CyA-treated rats. PAS reaction disclosed diastase-resistant positivity in the glomerular arterioles (score in controls: mean 0.4, range 0-1, in CyA 12.5 mg/kg/day mean 2.2, range 1-3, p < 0.001 as compared to controls; in CyA 25 mg/kg/day mean 1.1, range 0-2, p < 0.005 as compared to controls, p < 0.05 as compared to CyA 12.5 mg/kg/day). Furthermore, the straight part of the distal tubules of rats given the highest CyA dose contained considerable amounts of glycogen. The significance of this finding is unknown. Renal functional studies confirmed previous results since CyA decreased inulin clearance (Cin) from 1.2 +/- 0.5 to 0.8 +/- 0.3 ml/min/g kidney weight (kW) (p < 0.05), and lithium clearance (CLi) was reduced from 263 +/- 113 to 119 +/- 61 microliters/min/gKW (p < 0.001). Isradipine had no significant effect.
在给予环孢素A(CyA)的Spraque-Dawley大鼠中检测了环孢素A肾毒性。这些大鼠口服给予CyA(12.5mg/kg/天,n = 45;或25mg/kg/天,n = 45),持续16周。对照大鼠(n = 45)给予CyA溶媒。所有大鼠口服给予伊拉地平(ISRA)1mg/kg/天或5mg/kg/天,或伊拉地平溶媒。15只大鼠死于木糖葡萄球菌引起的间质性肺炎。基于苏木精-伊红染色组织中嗜碱性小管和间质纤维化的半定量评分,对预先定义的形态学CyA肾毒性评分系统进行分析,对照大鼠嗜碱性小管的平均评分为0.2(范围0 - 1),给予12.5mg/kg/天CyA的大鼠为1.4(范围0 - 3)(p < 0.001),给予25mg/kg/天CyA的大鼠为1.7(范围0 - 3)(与对照相比p < 0.001)。给予CyA的大鼠根据其间质纤维化评分进行分组:给予12.5mg/kg/天CyA的大鼠评分为0.2(范围0 - 1),给予25mg/kg/天CyA的大鼠评分为1.7(范围0 - 3)(p < 0.001)。当将嗜碱性小管和间质纤维化的评分合并时,对照大鼠中没有一只评分高于1,而低剂量组47%的大鼠和高剂量组95%的大鼠评分高于1。因此,这种CyA肾毒性评分系统为具有形态学CyA肾毒性的大鼠提供了一种简便、有效且可重复的识别方法,在评估CyA肾毒性方面可能具有临床意义。对未用伊拉地平治疗的大鼠的肾组织进行了过碘酸希夫(PAS)染色(有无淀粉酶处理)和天狼星红染色。后者证实了CyA处理大鼠肾小管萎缩后结缔组织增加。PAS反应显示肾小球小动脉中有淀粉酶抗性阳性(对照评分:平均0.4,范围0 - 1;给予12.5mg/kg/天CyA的大鼠平均为2.2,范围1 - 3,与对照相比p < 0.001;给予25mg/kg/天CyA的大鼠平均为1.1,范围0 - 2,与对照相比p < 0.005,与给予12.5mg/kg/天CyA的大鼠相比p < 0.05)。此外,给予最高CyA剂量的大鼠远端小管直部含有大量糖原。这一发现的意义尚不清楚。肾功能研究证实了先前的结果,因为CyA使菊粉清除率(Cin)从1.2±0.5降至0.8±0.3ml/min/g肾重(kW)(p < 0.05),锂清除率(CLi)从263±113降至119±61微升/min/gKW(p < 0.001)。伊拉地平无显著影响。