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胰岛素样生长因子-I(IGF-I)系统对长期营养不良的反应及其在大鼠躯体和骨骼肌生长迟缓中的作用。

Response of the IGF-I system to prolonged undernutrition and its involvement in somatic and skeletal muscle growth retardation in rats.

作者信息

Gautsch T A, Kandl S M, Donovan S M, Layman D K

机构信息

Department of Food Science and Human Nutrition, University of Illinois, Urbana 61801, USA.

出版信息

Growth Dev Aging. 1998 Spring-Summer;62(1-2):13-25.

PMID:9666353
Abstract

We examined the response of the IGF-I system to prolonged undernutrition and its involvement in somatic and skeletal muscle growth retardation. Male rats were food-restricted to 50% of freely-fed controls (C) from birth to 120 days postpartum. Serum and tissues were collected at d 50 and d 120 postpartum. Somatic growth of food-restricted animals (R) was proportional to food intake while organ and tissue growth was disproportionate. Skeletal muscle DNA content and synthesis rates were depressed by undernutrition and DNA synthesis decreased with age. Food-restriction abated serum IGF-I concentrations, serum IGFBP-3 expression and hepatic IGF-I mRNA levels at d 50. Conversely, at d 120, hepatic IGF-I mRNA levels in R were similar to C despite decreased serum IGF-I concentrations and serum IGFBP-3 expression. Hepatic IGFBP-1 and -2 mRNA expression in R was increased at both d 50 and 120, and hepatic IGFBP-4 mRNA expression was elevated on d 120 compared to C. Gastrocnemius IGF-I mRNA levels in R were not different from C at either d 50 or 120. These results suggest that hepatic IGF-I sensitivity to undernutrition decreases with increasing age, and endocrine regulation of IGF-I following adaptation to chronic undernutrition occurs post-transcriptionally. Further, local production of IGF-I in skeletal muscle does not appear to be responsible for the marked decline in muscle DNA synthesis, for skeletal muscle IGF-I mRNA expression was not altered by undernutrition.

摘要

我们研究了胰岛素样生长因子-I(IGF-I)系统对长期营养不良的反应及其在躯体和骨骼肌生长迟缓中的作用。将雄性大鼠从出生到产后120天进行食物限制,使其摄入量为自由进食对照组(C组)的50%。在产后第50天和第120天采集血清和组织样本。食物限制组动物(R组)的躯体生长与食物摄入量成正比,而器官和组织生长不成比例。营养不良会降低骨骼肌DNA含量和合成速率,且DNA合成随年龄增长而下降。在第50天时,食物限制降低了血清IGF-I浓度、血清IGFBP-3表达和肝脏IGF-I mRNA水平。相反,在第120天时,尽管血清IGF-I浓度和血清IGFBP-3表达下降,但R组的肝脏IGF-I mRNA水平与C组相似。R组肝脏IGFBP-1和-2 mRNA表达在第50天和第120天都增加,与C组相比,R组肝脏IGFBP-4 mRNA表达在第120天时升高。在第50天和第120天时,R组腓肠肌IGF-I mRNA水平与C组无差异。这些结果表明,肝脏IGF-I对营养不良的敏感性随年龄增长而降低,在适应慢性营养不良后,IGF-I的内分泌调节发生在转录后水平。此外,骨骼肌中IGF-I的局部产生似乎不是肌肉DNA合成显著下降的原因,因为营养不良并未改变骨骼肌IGF-I mRNA表达。

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