Tryfiates G P, Saus F L, Morris H P
J Natl Cancer Inst. 1975 Oct;55(4):839-41. doi: 10.1093/jnci/55.4.839.
Induction of tyrosine aminotransferase (TAT) (EC 2.6.1.5) by hydrocortisone was studied during cofactor (pyridoxal phosphate) depletion in hepatoma-bearing BUF strain female rats. Pairs of rats were matched for weight and age and one from each pair was fed ad libitum a diet lacking pyridoxine; the other (referred to as "pair-fed") was given the same diet supplemented with the vitamin, with the amount restricted to that consumed by the matched animal on the deficient diet. All animals were inoculated with Morris hepatoma no. 7777 cell after 21 days on the respective diets. TAT specific activity was determined weekly in host liver and hepatoma, in the presence and absence of cofactor, before and after the administration of hydrocortisone. Free and bound pyridoxal phosphate was estimated enzymatically. The average weight of hepatomas from pair-fed animals was 1.5-fold to twofold greater than that of hepatomas from animals on deficient diets. TAT activity of hepatomas was two times greater than that of host liver, and lack of dietary pyridoxine was without effect. Hormonal induction of enzymatic activity was maximal after the first week of tumor growth and subsequently reached minimal values. In pair-fed animals, tumor TAT was approximately 60% saturated with cofactor. In vitamin-deficient animals, only 6% of the tumor enzyme was saturated with the cofactor. The percent saturation of host liver TAT varied, with minimal values found in the vitamin-deficient animals. Hepatic and tumor pyridoxal phosphate content of pair-fed animals was unusually high (10 mug/g); in vitamin-deficient animals, only the coenzyme content of hepatomas was high (7.0 mug/g). The results showed that presence of the tumor altered the a) specific activity level of TAT and tissue content of cofactor, b) pattern of hormonal induction of the enzyme, and c) effects of the absence of dietary pyridoxine on TAT induction observed in animals without tumors.
在荷瘤BUF品系雌性大鼠的辅因子(磷酸吡哆醛)耗竭期间,研究了氢化可的松对酪氨酸转氨酶(TAT)(EC 2.6.1.5)的诱导作用。将大鼠按体重和年龄配对,每对中的一只随意喂食缺乏吡哆醇的饲料;另一只(称为“配对喂食”)给予添加了该维生素的相同饲料,其摄入量限制为与缺乏饲料的配对动物所消耗的量相同。在各自的饮食上喂养21天后,所有动物均接种了Morris 7777号肝癌细胞。在给予氢化可的松之前和之后,每周在宿主肝脏和肝癌中测定有无辅因子情况下的TAT比活性。通过酶法估算游离和结合的磷酸吡哆醛。配对喂食动物的肝癌平均重量比缺乏饮食动物的肝癌平均重量大1.5倍至2倍。肝癌的TAT活性比宿主肝脏的TAT活性高两倍,且饮食中缺乏吡哆醇没有影响。酶活性的激素诱导在肿瘤生长的第一周后达到最大值,随后降至最小值。在配对喂食的动物中,肿瘤TAT约60%被辅因子饱和。在维生素缺乏的动物中,只有6%的肿瘤酶被辅因子饱和。宿主肝脏TAT的饱和百分比各不相同,在维生素缺乏的动物中发现最小值。配对喂食动物的肝脏和肿瘤磷酸吡哆醛含量异常高(10微克/克);在维生素缺乏的动物中,只有肝癌的辅酶含量高(7.0微克/克)。结果表明,肿瘤的存在改变了:a)TAT的比活性水平和辅因子的组织含量;b)该酶的激素诱导模式;c)饮食中缺乏吡哆醇对无肿瘤动物中TAT诱导的影响。