Yokota S
Department of Anatomy, Yamanashi Medical School, Japan.
Eur J Cell Biol. 1990 Oct;53(1):112-21.
After administration of a hypolipidemic drug, MLM-160, to male rats, liver peroxisomes were studied by biochemical, cytochemical, and immunocytochemical methods. The activities of D-amino acid oxidase, glycolate oxidase, and urate oxidase increased 2 to 3-fold by the treatment. The increase of the oxidases was confirmed by immunoblotting analysis. By light microscopy, immunoreaction for catalase was present in the cytoplasmic granules of hepatocytes. The stained granules formed some clusters and overlapped each other after MLM-160 treatment. However, immunostaining for D-amino acid oxidase and urate oxidase was present in discrete fine granules which did not overlap each other. By electron microscopy, many peroxisomes showed ring-like extensions and cavitation of the matrix, often giving the appearance of a peroxisome-within-a-peroxisome. In many cases, these unusual peroxisomes seemed to be interconnected with each other. Within the peroxisomes, the catalase was localized in the matrix. Urate oxidase was associated with the crystalloid cores. D-amino acid oxidase was localized focally in a small part of the matrix where the catalase was mostly negative. In conclusion, the administration of MLM-160 to male rats induces some peroxisomal oxidases, accompanying the appearance of unusual peroxisomes. The precise localization of peroxisomal enzymes suggested that there are subcompartments within the liver peroxisomes as shown in rat kidney peroxisomes.
给雄性大鼠施用降血脂药物MLM - 160后,通过生化、细胞化学和免疫细胞化学方法研究了肝脏过氧化物酶体。经该处理后,D - 氨基酸氧化酶、乙醇酸氧化酶和尿酸氧化酶的活性增加了2至3倍。通过免疫印迹分析证实了这些氧化酶的增加。光学显微镜下,过氧化氢酶的免疫反应出现在肝细胞的细胞质颗粒中。MLM - 160处理后,染色的颗粒形成了一些簇并且相互重叠。然而,D - 氨基酸氧化酶和尿酸氧化酶的免疫染色存在于不相互重叠的离散细颗粒中。电子显微镜下,许多过氧化物酶体显示出基质的环状延伸和空泡化,常常呈现出一个过氧化物酶体包在另一个过氧化物酶体中的外观。在许多情况下,这些异常的过氧化物酶体似乎相互连接。在过氧化物酶体内,过氧化氢酶定位于基质中。尿酸氧化酶与晶体核心相关。D - 氨基酸氧化酶局部定位于基质的一小部分,此处过氧化氢酶大多呈阴性。总之,给雄性大鼠施用MLM - 160会诱导一些过氧化物酶体氧化酶,并伴随着异常过氧化物酶体的出现。过氧化物酶体酶的精确定位表明,肝脏过氧化物酶体内存在亚区室,正如在大鼠肾过氧化物酶体中所显示的那样。