Hay R, Tammi K, Ryffel B, Mihatsch M J
Clin Nephrol. 1986;25 Suppl 1:S23-6.
We examined whether ultrastructural changes in renal mitochondria associated with Cyclosporine A treatment might reflect underlying alterations in mitochondrial molecular structure. A nonrejected renal transplant removed from a patient treated with Cyclosporine A showed a decreased level of beta subunit antigen of mitochondrial F1-ATPase compared to controls. This decrease was more marked in the medulla than in the cortex (56% vs. 70% of pooled controls). Spontaneously hypertensive rats treated with a high dose of Cyclosporine A showed a similar decrease of beta-subunit antigen in the renal medulla and decreased levels of two subunit antigens of cytochrome c oxidase, but had increased medullary levels of the alpha subunit antigen of the F1-ATPase. Such changes were not detected in a normotensive strain of rats. Our data indicate that Cyclosporine A administration is associated with structural alterations in renal mitochondria at the molecular level, predominantly in the medulla, and that additional renal damage due to ischemia or hypertension may predispose to this cyclosporine effect.
我们研究了与环孢素A治疗相关的肾线粒体超微结构变化是否可能反映线粒体分子结构的潜在改变。与对照组相比,取自接受环孢素A治疗患者的未被排斥的肾移植组织显示线粒体F1 - ATP酶β亚基抗原水平降低。这种降低在髓质比皮质更明显(分别为合并对照组的56%和70%)。用高剂量环孢素A治疗的自发性高血压大鼠肾髓质中β亚基抗原也有类似降低,细胞色素c氧化酶的两个亚基抗原水平降低,但F1 - ATP酶α亚基抗原的髓质水平升高。在正常血压大鼠品系中未检测到此类变化。我们的数据表明,给予环孢素A与肾线粒体分子水平的结构改变相关,主要发生在髓质,并且由于缺血或高血压导致的额外肾损伤可能易引发这种环孢素效应。