Chang L O
Pediatr Res. 1977 Jan;11(1 Pt 1):6-8.
Enzymatic and immunologic methods were used in the studies of the development of mitochondrial pyruvate carboxylase (PC) in the perinatal rat liver. Rabbit antibodies to purified rat liver mitochondrial PC and to rat liver mitochondria were made. The monospecific activity of the anti-PC serum was demonstrated. Results of the study of developmental PC formation showed a simple quantitative change in PC activity and PC protein. A minute amount of PC (0.10-0.45 mumol/g liver/min; 2-10 mug/g liver) in fetal liver mitochondria increased to 1.9 +/- 0.12 mumol/g/min; 60 +/- 4 mug/g at 4-5 hr after birth, peaked (7.11 +/- 0.50 mumol/g/min; 175 +/- 12 mug/g) on the fifth day, and then declined to the normal level (4.68 +/- 0.42 mumol/g/min; 130 mug/g) found in adult liver during the third week. Results of the studies concerning the effects of premature and postmature delivery on the developmental pattern of PC during the first 8 hr after birth suggest that the postnatal increase of this enzyme is not triggered by the process of birth itself. Speculation The increase of mitochondrial PC activity and PC protein in the neonatal liver will lead to a greater availability of glucogenic carbon in the cytosol and will make a significant contribution to the overall enhancement of neonatal gluconeogenesis.
酶学和免疫学方法被用于围产期大鼠肝脏中线粒体丙酮酸羧化酶(PC)发育的研究。制备了针对纯化的大鼠肝脏线粒体PC和大鼠肝脏线粒体的兔抗体。证实了抗PC血清的单特异性活性。发育中PC形成的研究结果显示PC活性和PC蛋白存在简单的定量变化。胎儿肝脏线粒体中微量的PC(0.10 - 0.45微摩尔/克肝脏/分钟;2 - 10微克/克肝脏)在出生后4 - 5小时增加到1.9±0.12微摩尔/克/分钟;60±4微克/克,在第五天达到峰值(7.11±0.50微摩尔/克/分钟;175±12微克/克),然后在第三周下降到成年肝脏中的正常水平(4.68±0.42微摩尔/克/分钟;130微克/克)。关于早产和过期产对出生后前8小时PC发育模式影响的研究结果表明,该酶的产后增加不是由出生过程本身触发的。推测新生儿肝脏中线粒体PC活性和PC蛋白的增加将导致细胞质中糖异生碳的可用性增加,并将对新生儿糖异生的整体增强做出重大贡献。