Evces S, Lindahl R
Cancer Res. 1986 Jul;46(7):3587-92.
Chronic exposure to ethionine (0.05%) combined with dietary choline deficiency was used to study changes in aldehyde dehydrogenase (ALDH) activity during hepatocarcinogenesis in male Sprague-Dawley rats. Over a period of 43 weeks, animals were sacrificed at intervals and the ALDH phenotype of normal liver and any lesions was characterized by histochemical analysis, total activity assays, and gel electrophoresis, using propionaldehyde and nicotinamide adenine dinucleotide (NAD+) to detect normal liver ALDH activity and benzaldehyde and nicotinamide adenine dinucleotide phosphate (NADP+) for tumor-associated ALDH. In animals receiving ethionine plus choline deficiency, significant changes in ALDH were observed histochemically by 9 weeks, when there was a distinct shift in activity from its normal centrilobular pattern to a periportal distribution. The first NAD+- and NADP+-dependent ALDH-positive enzyme-altered foci were also seen at 9 weeks. There was no correlation between the ALDH and gamma-glutamyl transpeptidase phenotypes of an individual focus. Areas of cholangiofibrosis, cystic degeneration, and bile duct proliferation were distinctly ALDH negative. No significant changes in benzaldehyde and NADP+ ALDH activity were detectable by total activity assays or gel electrophoresis prior to the appearance of overt neoplasms at 26 weeks. No significant changes in ALDH activity occurred in animals receiving either ethionine or choline deficient diet alone. By histochemistry, total activity assays and gel electrophoresis, only 7 of the 28 (25%) of the hepatic neoplasms examined expressed the tumor-associated ALDH phenotype. An additional five neoplasms had barely detectable levels of benzaldehyde and NADP+ ALDH activity. These results are in striking contrast to changes in ALDH activity occurring during hepatocarcinogenesis induced by other protocols we have tested previously in which from 50 to 96% of all neoplasms were ALDH positive.
采用慢性暴露于乙硫氨酸(0.05%)并结合饮食中胆碱缺乏的方法,研究雄性斯普拉格-道利大鼠肝癌发生过程中醛脱氢酶(ALDH)活性的变化。在43周的时间里,定期处死动物,通过组织化学分析、总活性测定和凝胶电泳,以丙醛和烟酰胺腺嘌呤二核苷酸(NAD +)检测正常肝脏ALDH活性,以苯甲醛和烟酰胺腺嘌呤二核苷酸磷酸(NADP +)检测肿瘤相关ALDH,从而对正常肝脏和任何病变的ALDH表型进行表征。在接受乙硫氨酸加胆碱缺乏的动物中,到9周时,通过组织化学观察到ALDH有显著变化,此时其活性从正常的小叶中央模式明显转变为门静脉周围分布。在9周时还首次观察到第一个依赖NAD +和NADP +的ALDH阳性酶改变灶。单个病灶的ALDH和γ-谷氨酰转肽酶表型之间没有相关性。胆管纤维化、囊性变性和胆管增生区域明显为ALDH阴性。在26周出现明显肿瘤之前,通过总活性测定或凝胶电泳未检测到苯甲醛和NADP + ALDH活性有显著变化。单独接受乙硫氨酸或胆碱缺乏饮食的动物中,ALDH活性没有显著变化。通过组织化学、总活性测定和凝胶电泳,在所检查的28个肝肿瘤中,只有7个(25%)表达肿瘤相关ALDH表型。另外5个肿瘤的苯甲醛和NADP + ALDH活性水平几乎检测不到。这些结果与我们之前测试的其他方案诱导肝癌发生过程中ALDH活性的变化形成了鲜明对比,在其他方案中,所有肿瘤中有50%至96%为ALDH阳性。