Goltermann N, Majumdar A P
Horm Res. 1979;11(3):142-50. doi: 10.1159/000179049.
Protein synthesis in gastric mucosa was studied by measuring the incorporation of labeled amino acids into protein by isolated gastric mucosal ribosomes in a cell-free system. In 48-hour fasted rats, administration of the synthetic analogues pentagastrin, tetragastrin and gastrin-17 or naturally occurring molecular forms of human gastrin (G-14, G-34) markedly enhanced (23-123%) the capacity of the gastric mucosal ribosomes to synthesize endogenous mRNA-directed protein in a cell-free system. In the presence of exogenous mRNA (poly-U), the gastric mucosal ribosomes from the saline-treated controls showed a higher poly(U)-directed protein synthesis, compared to each fo the gastrin-treated groups. The protein/polyphenylalanine ratio which represents a ratio of polysomes to monosomes was found increased in ribosomes from the gastrin-treated groups.
通过在无细胞系统中测量分离的胃黏膜核糖体将标记氨基酸掺入蛋白质的情况,对胃黏膜中的蛋白质合成进行了研究。在禁食48小时的大鼠中,给予合成类似物五肽胃泌素、四肽胃泌素和胃泌素-17或天然存在的人胃泌素分子形式(G-14、G-34),显著增强了(23%-123%)胃黏膜核糖体在无细胞系统中合成内源性mRNA指导的蛋白质的能力。在外源mRNA(聚尿苷酸)存在的情况下,与每个胃泌素处理组相比,盐水处理对照组的胃黏膜核糖体显示出更高的聚尿苷酸指导的蛋白质合成。在胃泌素处理组的核糖体中,发现代表多核糖体与单核糖体比例的蛋白质/聚苯丙氨酸比率增加。