Stacchiotti A, Borsani E, Rodella L, Rezzani R, Bianchi R, Lavazza A
Division of Human Anatomy, Department of Biomedical Sciences and Biotechnology, University of Brescia, Brescia, Italy.
Ultrastruct Pathol. 2003 Jul-Aug;27(4):253-9. doi: 10.1080/01913120309921.
Mercuric chloride (HgCl(2)) produces an acute renal failure in experimental animal models. Since the mechanism of tubular injury has not completely been clarified, this morpho-quantitative study was undertaken to better understand the effects of 2 sublethal doses (T1=1 mg/kg and T3.5=3.5 mg/kg) of HgCl(2) in rat proximal tubules. Morphometrical analysis was performed to quantify both cytoplasmic and nuclear changes found in treated in respect to saline-injected proximal tubules. In the controls, single-cell damage was occasional and nucleolar changes were absent. HgCl(2) induced progressively severe proximal tubule atrophy. In the T1 group, necrosis was limited to pars recta cells and nucleolar segregation was often partial. In the T3.5 group, atrophy was extensive in both convoluted and straight tracts, the nucleolus was completely segregated and coiled body-like inclusions were detached from it. Ultrastructural analysis confirmed dose-dependent changes within straight proximal tubules, i.e., necrosis, apoptosis, nucleolar segregation, swollen mitochondria, vacuolization, and disrupted brush border. In conclusion, in the rat kidney HgCl(2) induced dose-dependent alterations not only in the cytoplasm but also in the nucleus of proximal tubule cells. These findings will be useful for better understanding of the pathogenesis of mercury nephrotoxicity and its genotoxic effect.
氯化汞(HgCl₂)在实验动物模型中可导致急性肾衰竭。由于肾小管损伤的机制尚未完全阐明,因此进行了这项形态定量研究,以更好地了解两种亚致死剂量(T1 = 1 mg/kg和T3.5 = 3.5 mg/kg)的HgCl₂对大鼠近端肾小管的影响。进行形态计量分析以量化在接受治疗的近端肾小管中相对于注射生理盐水的近端肾小管所发现的细胞质和细胞核变化。在对照组中,单细胞损伤偶有发生,且不存在核仁变化。HgCl₂诱导近端肾小管逐渐严重萎缩。在T1组中,坏死仅限于直部细胞,核仁分离通常是部分性的。在T3.5组中,曲部和直部均出现广泛萎缩,核仁完全分离,且有卷曲体样包涵体从核仁上脱离。超微结构分析证实了直部近端肾小管内存在剂量依赖性变化,即坏死、凋亡、核仁分离、线粒体肿胀、空泡化和刷状缘破坏。总之,在大鼠肾脏中,HgCl₂不仅在近端肾小管细胞的细胞质中,而且在细胞核中均诱导了剂量依赖性改变。这些发现将有助于更好地理解汞肾毒性的发病机制及其遗传毒性作用。