Paik W K, Lew B, Farooqui J, Kim S
Biochem Med. 1984 Jun;31(3):352-61. doi: 10.1016/0006-2944(84)90091-7.
Arginase activity in the liver, brain, and testis of rats was examined during the different phases of life span. When expressed as specific activity (micromoles of L-arginine hydrolyzed per minute per gram of whole homogenate protein), the enzyme activity in the brain and testis decreased markedly during the early stage of life and stayed low during the remainder of the life span. On the other hand, the arginase in the liver showed a great dependency on the developmental phase of the animal, showing two distinct peaks: one during the early phase (20 days after birth) and the other at a later time (3 months of age). This pattern of change in the hepatic arginase activity closely coincided with the pattern of the rate of urea synthesis determined with liver slices and expressed in terms of micromoles of urea formed per hour per gram of tissue slice. In contrast to the above observations, however, curves obtained by plotting the total liver arginase or urea synthetic activity vs the developmental stage of rats showed no measurable discontinuity. Further studies revealed that the observed pattern of specific activity of hepatic arginase was, in part, due to the change in the relative concentration of arginase protein in the liver.
在大鼠寿命的不同阶段,对其肝脏、大脑和睾丸中的精氨酸酶活性进行了检测。当以比活性(每克全匀浆蛋白每分钟水解的L-精氨酸微摩尔数)表示时,大脑和睾丸中的酶活性在生命早期显著下降,并在寿命的其余时间保持在较低水平。另一方面,肝脏中的精氨酸酶对动物的发育阶段有很大依赖性,呈现出两个明显的峰值:一个在早期阶段(出生后20天),另一个在后期(3个月大时)。肝脏精氨酸酶活性的这种变化模式与用肝切片测定的尿素合成速率模式密切吻合,尿素合成速率以每克组织切片每小时形成的尿素微摩尔数表示。然而,与上述观察结果相反,通过绘制大鼠肝脏总精氨酸酶或尿素合成活性与发育阶段的关系曲线,未发现可测量的间断点。进一步研究表明,观察到的肝脏精氨酸酶比活性模式部分归因于肝脏中精氨酸酶蛋白相对浓度的变化。