Kifer E T, Matysiak W J, Romanowska-Sarlej J E, Piróg Z M
Gegenbaurs Morphol Jahrb. 1985;131(4):525-35.
Examinations of the rat kidney metabolism were carried out by histological (staining with haematoxylin and eosin), histochemical (response to lactate and succinic dehydrogenases activities), and electrophoretic methods (separation of isoenzymes of lactate dehydrogenase) after treating animals with the sulphonamide Biseptol 480, for 7 (consecutive) d by stomach tube. Biseptol given to the animals exceeded 10 times human therapeutical dose. It was found out that Biseptol 480, applied to the animals with healthy urinary system, does not pathologically disturb the examined stages of the metabolic processes in the rat's kidney.
在用磺胺类药物必思添480经胃管连续给药7天处理动物后,通过组织学方法(苏木精和伊红染色)、组织化学方法(对乳酸脱氢酶和琥珀酸脱氢酶活性的反应)以及电泳方法(乳酸脱氢酶同工酶的分离)对大鼠肾脏代谢进行了检测。给予动物的必思添剂量超过人类治疗剂量的10倍。结果发现,将必思添480应用于泌尿系统健康的动物时,不会对大鼠肾脏代谢过程的检测阶段造成病理性干扰。