McAuliffe W G, Olesen O V
Nephron. 1983;34(2):114-24. doi: 10.1159/000182993.
Light and electron microscopy were used to study the effects of a lithium-supplemented diet on renal structure in the rat. At the end of a 7-week experimental period serum lithium levels were 1.14 +/- 0.20 mM. Lesions consisting of groups of dilated tubules were found in the immediate vicinity of the interlobular arteries in all experimental animals. These tubules were identified as the connecting tubule or the initial portion of the collecting tubule. The epithelium of these tubules was generally flattened but was punctuated by markedly swollen epithelial cells. PAS-positive deposits found in both types of cells were identified as glycogen. Electron microscopy revealed considerable lithium-induced damage in the swollen cells including increased numbers of mitochondria, many of which were swollen or otherwise damaged, dilated cisternae of endoplasmic reticulum and vacuolization of the apical cytoplasm. The flattened cells of these tubules were similar to the dark or intercalated cells of normal collecting tubules. Some detachment of epithelial cells from their basement membrane was evident in these tubules. Damage was less severe in distal convoluted tubules. Lithium-induced changes were not observed in glomeruli, proximal tubules or ascending thick limbs of Henle. In medullary collecting tubules damage was less severe than in cortical collecting tubules, but detachment of epithelial cells was a common finding. The interstitial tissue of the papilla exhibited histochemical and ultrastructural changes consistent with lithium blockade of the action of antidiuretic hormone. The ultrastructural damage to cortical tubules is similar to that found in patients receiving therapeutic lithium for long periods of time. The anatomic sites of lithium-induced pathology correspond to the location of lithium-induced pathophysiology.
运用光学显微镜和电子显微镜研究了补充锂的饮食对大鼠肾脏结构的影响。在为期7周的实验期末,血清锂水平为1.14±0.20毫摩尔。在所有实验动物的小叶间动脉紧邻区域发现了由扩张的肾小管群组成的病变。这些肾小管被确定为连接小管或集合小管的起始部分。这些肾小管的上皮细胞通常扁平,但有明显肿胀的上皮细胞间断出现。在这两种类型的细胞中发现的PAS阳性沉积物被鉴定为糖原。电子显微镜显示,肿胀细胞中有相当多的锂诱导损伤,包括线粒体数量增加,其中许多肿胀或有其他损伤,内质网池扩张以及顶端细胞质空泡化。这些肾小管的扁平细胞类似于正常集合小管的暗细胞或闰细胞。在这些肾小管中,一些上皮细胞与其基底膜分离明显可见。远端曲管的损伤较轻。在肾小球、近端小管或髓袢升支粗段未观察到锂诱导的变化。在髓质集合小管中,损伤比皮质集合小管轻,但上皮细胞分离是常见现象。乳头的间质组织表现出与锂对抗利尿激素作用的阻断相一致的组织化学和超微结构变化。皮质小管的超微结构损伤与长期接受锂治疗的患者中发现的损伤相似。锂诱导病理变化的解剖部位与锂诱导病理生理变化的位置相对应。