Narbonne J F, Daubeze M, Bonmort F
Ann Nutr Aliment. 1978;32(1):41-58.
The effect of a vitamin A deficient diet on liver proteosynthesis was studied with in vivo and in vitro methods. Weanling rats obtained from vitamin A rstricted female were fed "separate diet". Control animals received vitamin A in protein diet. Deficient rats were used at the weight plateau stage. The RNA, DNA and protein liver content was unaffected by vitamin A deficiency and the same result was found for free amino acid pool. The turn-over rate of protein and RNA of cellular fractions and total liver was studied. (14C) leucine and (3H) uridine was injected intraperitoneally. Animals were killed at 20-40 minutes and 2-4-6-8-10 days after injection. Synthesis rate of liver proteins was the same in both groups. Our results indicate no difference in the average rate of (14C) protein degradation between control and deficient animals. Vitamin A deficiency decrease the turn-over rate of total ribosomal and soluble RNA. Polyribosome and postribosomal supernatant from deficient rats liver were less active for protein synthesis in vitro than corresponding fractions from well nourished rats. The lesion was located in the post ribosomal supernatant fraction by "crossing over" experiments. Polyribosome desimentation analysis on sucrose gradients revealed no difference between the two groupe. The results indicate that vitamin A deficiency decrease cell proliferation without degeneracy. The limitative agent of proteosynthesis is situated at RNA level. However protein synthesis is unaffected in our experimental procedure.
采用体内和体外方法研究了缺乏维生素A的饮食对肝脏蛋白质合成的影响。从维生素A受限的雌性大鼠获得的断奶大鼠喂食“单独的饮食”。对照动物在蛋白质饮食中摄入维生素A。缺乏维生素A的大鼠在体重稳定阶段使用。肝脏中的RNA、DNA和蛋白质含量不受维生素A缺乏的影响,游离氨基酸池也得到相同结果。研究了细胞组分和整个肝脏中蛋白质和RNA的周转率。腹腔注射(14C)亮氨酸和(3H)尿苷。在注射后20 - 40分钟以及2 - 4 - 6 - 8 - 10天处死动物。两组肝脏蛋白质的合成速率相同。我们的结果表明,对照动物和缺乏维生素A的动物之间,(14C)蛋白质降解的平均速率没有差异。维生素A缺乏会降低总核糖体RNA和可溶性RNA的周转率。缺乏维生素A的大鼠肝脏中的多核糖体和核糖体后上清液在体外蛋白质合成方面比营养良好的大鼠的相应组分活性更低。通过“交叉”实验发现损伤位于核糖体后上清液组分。蔗糖梯度上的多核糖体沉降分析显示两组之间没有差异。结果表明,维生素A缺乏会减少细胞增殖但不会导致细胞退化。蛋白质合成的限制因素位于RNA水平。然而,在我们的实验过程中蛋白质合成不受影响。