Mabuchi M
Jpn J Exp Med. 1979 Dec;49(6):365-72.
The effect of protein deficiency on the hepatotoxicity and carcinogenicity of sterigmatocystin was studied in rats. Sterigmatocystin, 500 ppm/day, fed in a regular diet induced marked toxic effects and there was a high incidence of hepatocellular carcinoma and hyperplastic nodules. The same dosage fed in a protein-deficient diet produced toxic signs followed by a high incidence of death within 27 weeks. Surviving animals showed dysplastic liver cell changes but no tumors were noted. The incidence of hepatocellular carcinoma was 87% in rats receiving 15 ppm of the substance per day for 200 days in a protein-deficient diet. Sequential histologic and histochemical studies revealed that hyperplastic and preneoplastic liver lesions appeared at 28--32 weeks after inseption of the sterigmatocystin-supplemented diet. No cirrhotic changes and only transient fibrosis were noted. The morphogenesis of the sterigmatocystin-induced lesions was compared with that of aflatoxin B1-induced lesions.
在大鼠中研究了蛋白质缺乏对杂色曲霉素肝毒性和致癌性的影响。以500 ppm/天的剂量将杂色曲霉素添加到常规饮食中喂养,可诱导明显的毒性作用,肝细胞癌和增生性结节的发生率很高。在蛋白质缺乏的饮食中给予相同剂量,则会产生毒性迹象,并在27周内出现高死亡率。存活的动物表现出发育异常的肝细胞变化,但未发现肿瘤。在蛋白质缺乏的饮食中,每天接受15 ppm该物质达200天的大鼠中,肝细胞癌的发生率为87%。连续的组织学和组织化学研究表明,在添加杂色曲霉素的饮食开始后28 - 32周出现增生性和癌前肝病变。未观察到肝硬化变化,仅发现短暂的纤维化。将杂色曲霉素诱导的病变的形态发生与黄曲霉毒素B1诱导的病变进行了比较。