In vivo morphologic changes in the rat osteoclast induced by gallium nitrate: the result of toxicity or other effects?

H E Gruber, H J Norton, F R Singer
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引用次数: 3

Abstract

Gallium nitrate, an approved antitumor drug, has found clinical application in the treatment of cancer-related hypercalcemia and of Paget's disease; the exact mechanism of its action, however, remains unknown. The present study utilized rats in a 7-day exposure to gallium at doses similar to those used clinically. Quantitative histomorphometry and ultrastructural examination of osteoclast fine structure were carried out on specimens from animals with documented hypocalcemia. Gallium exposure produced striking changes in the osteoclast. The number of nuclei/osteoclast increased, and the ruffled borders of the osteoclasts were markedly decreased along the length of the Howship's lacunar cavity. The absence of a decrease in osteoclast number and the types of changes seen in ultrastructure suggest that the mechanism of action of gallium seen here may differ from that of calcitonin, a nontoxic, reversible antiresorbing agent. Results underscore the difficulty in assessing the toxicity of agents such as gallium on the osteoclast, a mature differentiated cell which does not divide and which does not produce a characteristic extracellular matrix component.

硝酸镓诱导大鼠破骨细胞的体内形态变化:是毒性还是其他作用的结果?
硝酸镓是一种获批的抗肿瘤药物,已被临床应用于治疗癌症相关的高钙血症和佩吉特病;然而,其作用的确切机制尚不清楚。本研究利用大鼠进行为期7天的镓暴露,剂量与临床使用的剂量相似。对记录的低钙动物标本进行了破骨细胞精细结构的定量组织形态学和超微结构检查。镓暴露使破骨细胞发生显著变化。细胞核/破骨细胞数量增加,破骨细胞皱边沿Howship腔隙长度明显减少。在超微结构中观察到的破骨细胞数量和变化类型没有减少,这表明镓的作用机制可能与降钙素不同,降钙素是一种无毒、可逆的抗吸收剂。研究结果强调了评估诸如镓等药物对破骨细胞毒性的难度。破骨细胞是一种成熟的分化细胞,不会分裂,也不会产生典型的细胞外基质成分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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