Kling M A, Fox J G, Johnston S M, Tolkoff-Rubin N E, Rubin R H, Colvin R B
Lab Invest. 1984 May;50(5):526-35.
Because lithium salts are widely used for long-term therapy of affective disorders and have been recently implicated as a cause of tubulointerstitial renal disease, we have undertaken experiments designed to establish the site of the early and late pathologic lesions and to determine their correlation with the lithium-induced concentrating defect. Male Wistar rats given a semisynthetic diet that contained lithium carbonate, 90 mEq/kg dry weight, developed serum lithium levels in the human therapeutic range; pair-fed controls received sodium carbonate. Within 3 weeks, treated rats developed marked polyuria, with elevation of free water clearance and vasopressin-resistant diabetes insipidus. Early morphologic changes were confined to the cortical collecting tubules and, possibly, contiguous portions of distal tubules. The tubules were dilated and irregularly lined with cells that had bulging or thinned basophilic cytoplasm, enlarged nuclei, sometimes basal vacuolization, and a few mitoses. These changes were evident at 3 weeks and progressed through the end of the observation period at 18 weeks. The proliferative component of the lesion was demonstrated by the finding of a significant and specific increase in 3H-thymidine uptake by nuclei of collecting/distal tubules of lithium-treated rats. The lesion, but not the increased thymidine uptake, extended into the medullary collecting ducts at 9 and 18 weeks. Although occasional intratubular mononuclear cells were seen at 9 and 18 weeks, no interstitial inflammation or fibrosis was seen. These tubular epithelial lesions were not seen in the kidneys of Brattleboro rats or glucose-treated Wistar rats despite comparable polyuria. We suggest that this early, persistent, and reproducible lesion, characterized by reactive and proliferating tubular cells in the cortical collecting tubules, predisposes the kidney to injury from otherwise mild or insignificant insults and may explain the sporadic occurrence of serious tubulointerstitial disease in patients on long-term lithium therapy.
由于锂盐被广泛用于情感障碍的长期治疗,且最近被认为是肾小管间质性肾病的一个病因,我们进行了一些实验,旨在确定早期和晚期病理损害的部位,并确定它们与锂诱导的浓缩功能缺陷之间的关系。给雄性Wistar大鼠喂食含碳酸锂(90 mEq/kg干重)的半合成饮食,其血清锂水平达到人类治疗范围;配对喂养的对照组给予碳酸钠。在3周内,接受治疗的大鼠出现明显的多尿,自由水清除率升高以及抗血管加压素性尿崩症。早期形态学变化局限于皮质集合管,可能还有远端小管的相邻部分。这些小管扩张,内衬细胞不规则,这些细胞的嗜碱性细胞质膨出或变薄,细胞核增大,有时出现基底空泡化,并有一些有丝分裂。这些变化在3周时就很明显,并在观察期结束时的18周内持续进展。通过发现锂处理大鼠的集合管/远端小管细胞核对3H-胸腺嘧啶核苷的摄取显著且特异性增加,证实了病变的增殖成分。在9周和18周时,病变(但不是胸腺嘧啶核苷摄取增加)扩展到髓质集合管。尽管在9周和18周时偶尔可见管腔内单核细胞,但未发现间质炎症或纤维化。尽管有类似的多尿情况,但在布拉德福德大鼠或葡萄糖处理的Wistar大鼠的肾脏中未见到这些肾小管上皮病变。我们认为,这种早期、持续且可重复的病变,其特征是皮质集合管中的肾小管细胞反应性增生,使肾脏易受原本轻微或不显著的损伤影响,这可能解释了长期接受锂治疗的患者中偶尔发生严重肾小管间质性疾病的原因。