Watanabe M
Acta Pathol Jpn. 1978 Nov;28(6):867-89. doi: 10.1111/j.1440-1827.1978.tb01277.x.
Lysosomal involvement in renal tubular lesions was studied mainly by electronmicroscopy after single and repeated administrations of cephacetrile, cephalothin, cephaloridine, gentamicin or leupeptin and combine administrations of cephalothin and gentamicin or gentamicin and leupeptin in female Wistar rats. Large cytosomes of high density were increased due probably to either reabsorption and secretion of drugs or their metabolites. These cytosomes displaying acid phosphatase activity were demonstrated histochemically and were identified as heterolysosomes. In rats treated with cephaloridine, gentamicin or leupeptin, disruption of lysosomal membrane was noted and regional cytoplasmic destruction was seen in the vicinity of the disrupted heterolysosomes. Necrotic epithelial cells and renal insufficiency were observed in these animals. On the other hand, neither destruction of lysosomes nor cell lesion was found in rats treated with cephacetrile or cephalothin. It was speculated that lysosomal destruction might be the cause of the cell lesions found in cephaloridine, gentamicin or leupeptin treated rats.
在雌性Wistar大鼠单次及重复给予头孢乙腈、头孢噻吩、头孢噻啶、庆大霉素或亮抑酶肽,以及联合给予头孢噻吩与庆大霉素或庆大霉素与亮抑酶肽后,主要通过电子显微镜研究了溶酶体在肾小管病变中的作用。高密度的大胞质体增多,这可能是由于药物或其代谢产物的重吸收和分泌所致。通过组织化学方法证实了这些显示酸性磷酸酶活性的胞质体,并将其鉴定为异溶酶体。在用头孢噻啶、庆大霉素或亮抑酶肽治疗的大鼠中,观察到溶酶体膜破裂,且在破裂的异溶酶体附近可见局部细胞质破坏。在这些动物中观察到坏死的上皮细胞和肾功能不全。另一方面,在用头孢乙腈或头孢噻吩治疗的大鼠中,未发现溶酶体破坏或细胞损伤。据推测,溶酶体破坏可能是在用头孢噻啶、庆大霉素或亮抑酶肽治疗的大鼠中发现的细胞损伤的原因。