Minami H, Miyamoto K, Fujii Y, Nakabou Y, Hagihira H
J Biochem. 1985 Jul;98(1):133-9. doi: 10.1093/oxfordjournals.jbchem.a135251.
Intestinal and hepatic ornithine decarboxylase (ODC) activities increased to a peak 4 h after administration of a diet containing casein or an amino acid mixture simulating that of casein to rats starved for 12 h. All amino acids except cysteine with a two or three carbon skeleton, including those with a D-configuration, and alpha-amino-isobutyric acid (AIB) strongly induced intestinal ODC when given in the diet or administered intragastrically. Amino acids with a four carbon skeleton were far less effective as inducers and other amino acids did not induce intestinal ODC at all. The amino acids that induced hepatic ODC showed no particular structural characteristics: glycine and cysteine were very effective, threonine, tryptophan, methionine, and phenylalanine were less effective, and serine, valine, isoleucine, and histidine were only slightly effective. Elevation of ODC activity after amino acid administration was not due to stabilization of the enzyme protein with the amino acids. Intestinal ODC was induced by intragastric but not intraperitoneal injection of glycine, although these treatments resulted in similar increases in the tissue concentration of glycine. On the contrary, hepatic ODC was induced by glycine regardless of the administration route. Intestinal ODC was also induced only in the segment of the intestine perfused with a solution of an amino acid with which the activity increased in the feeding experiment. These results suggest that the accumulation of an amino acid per se is not a trigger for induction of intestinal ODC and that an amino acid must act on the mucosal surface to induce the enzyme.
给饥饿12小时的大鼠喂食含酪蛋白的日粮或模拟酪蛋白的氨基酸混合物后,肠道和肝脏中的鸟氨酸脱羧酶(ODC)活性在4小时后升至峰值。除含两个或三个碳骨架的氨基酸(包括具有D构型的氨基酸)和α-氨基异丁酸(AIB)外,所有氨基酸,当添加到日粮中或经胃内给药时,均能强烈诱导肠道ODC。具有四个碳骨架的氨基酸作为诱导剂的效果要差得多,而其他氨基酸根本不会诱导肠道ODC。诱导肝脏ODC的氨基酸没有特定的结构特征:甘氨酸和半胱氨酸非常有效,苏氨酸、色氨酸、蛋氨酸和苯丙氨酸效果较差,丝氨酸、缬氨酸、异亮氨酸和组氨酸只有轻微效果。氨基酸给药后ODC活性的升高并非由于氨基酸对酶蛋白的稳定作用。胃内注射甘氨酸可诱导肠道ODC,但腹腔注射则不能,尽管这两种给药方式导致组织中甘氨酸浓度的升高幅度相似。相反,无论给药途径如何,甘氨酸均可诱导肝脏ODC。肠道ODC也仅在灌注了在喂养实验中可使其活性增加的氨基酸溶液的肠段中被诱导。这些结果表明,氨基酸本身的积累并非诱导肠道ODC的触发因素,氨基酸必须作用于粘膜表面才能诱导该酶。