Samuels S E, Baracos V E
Department of Animal Science, University of Alberta, Edmonton, Canada.
J Nutr. 1995 Mar;125(3):520-30. doi: 10.1093/jn/125.3.520.
Infection in young growing animals is manifested by poor tissue protein accretion; during subsequent catch-up growth this is reversed. To account for these changes, protein synthesis and degradation were measured in vivo in skeletal muscle, skin, liver and small intestine in weanling rats during catch-up growth after Escherichia coli infection. Observations were made at d 4, 6, 8, 11 and 14, when infected rats had elevated nitrogen balance. Liver protein mass and turnover were not affected by treatment. Although protein mass of small intestine fell during infection, catch-up was achieved before d 4, suggesting a high priority for protein repletion in this tissue. On d 4, protein mass was lower (P < 0.05) in muscle (-19%) and skin (-23%) in infected vs. control rats. Thereafter growth rates of skeletal muscle and skin were higher (P < 0.001) in infected rats compared with controls. Catch-up growth was most pronounced early, but continued throughout the study. During catch-up growth, protein synthesis (mg/d) in muscle and skin was not different between control and infected animals. Protein synthesis was maintained in muscle because RNA mass was maintained. During catch-up growth in muscle and skin of infected rats, there was lower protein degradation (mg/d) than in controls (P < 0.05). We conclude that alterations in protein turnover during catch-up growth are tissue and time dependent and are different from those described in other hyperanabolic states.
幼龄生长动物感染的表现为组织蛋白积累不佳;在随后的追赶生长过程中,这种情况会逆转。为了解释这些变化,在大肠杆菌感染后的追赶生长期间,对断奶大鼠的骨骼肌、皮肤、肝脏和小肠进行了体内蛋白质合成和降解的测量。在第4、6、8、11和14天进行观察,此时感染大鼠的氮平衡升高。肝脏蛋白质含量和周转率不受治疗影响。尽管感染期间小肠蛋白质含量下降,但在第4天之前就实现了追赶,这表明该组织中蛋白质补充具有高度优先性。在第4天,感染大鼠的肌肉(-19%)和皮肤(-23%)中的蛋白质含量低于对照组(P<0.05)。此后,与对照组相比,感染大鼠的骨骼肌和皮肤生长速率更高(P<0.001)。追赶生长在早期最为明显,但在整个研究过程中持续存在。在追赶生长期间,对照组和感染动物的肌肉和皮肤中的蛋白质合成(mg/天)没有差异。肌肉中的蛋白质合成得以维持,因为RNA含量得以维持。在感染大鼠的肌肉和皮肤追赶生长期间,蛋白质降解(mg/天)低于对照组(P<0.05)。我们得出结论,追赶生长期间蛋白质周转的改变是组织和时间依赖性的,并且与其他合成代谢亢进状态中描述的不同。