Hua K M, Hodgkinson S C, Bass J J
AgResearch, Ruakura Agricultural Centre, Hamilton, New Zealand.
J Endocrinol. 1995 Dec;147(3):507-16. doi: 10.1677/joe.0.1470507.
Plasma levels of IGFs-I and -II were measured in 4-month-old ewe lambs (n = 20) and 2-year-old ewes (n = 16), which were well fed (n = 18) or fasted (n = 18) for 3 days. Half of each nutrition group was given daily (0900 h) injections of bovine GH (bGH, 0.1 mg/kg body weight per day) for 3 days. Blood samples were collected immediately before the GH injection every morning. Plasma IGFs were extracted by acid gel permeation chromatography using a Waters Protein Pak 125 column, fitted to a Pharmacia fast protein liquid chromatography system, then freeze-dried, reconstituted (at pH 7.4) and estimated by RIA. At the end of the experiment, IGF-I levels in plasma were increased (P < 0.01) by exogenous bGH in both fed ewes and lambs but not in the fasted animals; plasma IGF-I levels were depressed by fasting (P < 0.01) at all ages. IGF-I levels were also found to be significantly higher (P < 0.01) in ewes than lambs. In contrast, plasma IGF-II concentrations were depressed (P = 0.02) by administration of bGH in all groups and elevated in the ewes (P < 0.05) by fasting. However, the lambs showed no significant changes in IGF-II with fasting. The IGF-II levels were significantly higher (P < 0.001) in lambs than ewes. Results from the present study demonstrate that GH administration stimulated an increase in plasma IGF-I and induced a decrease in plasma IGF-II. On the other hand, fasting depressed plasma IGF-I and elevated plasma IGF-II in the sheep. A significant GH/nutrition interaction for IGF-I (P < 0.01), but not for IGF-II, and a significant nutrition/age interaction for IGF-II (P < 0.01), but not for IGF-I, in the present study suggest that GH has a greater stimulating effect on plasma levels of IGF-I in the fed rather than fasted sheep and that nutrition has a greater influence on plasma levels of IGF-II in the older rather than younger animals, indicating that plasma IGFs-I and -II are differentially regulated by nutrition, GH and developmental stage in postnatal sheep.
在4月龄母羊羔(n = 20)和2岁母羊(n = 16)中测量胰岛素样生长因子-I(IGF-I)和胰岛素样生长因子-II(IGF-II)的血浆水平,这些羊被分为营养良好组(n = 18)或禁食组(n = 18),禁食3天。每个营养组的一半羊每天(09:00)注射牛生长激素(bGH,0.1 mg/kg体重/天),持续3天。每天早晨在注射生长激素之前立即采集血样。血浆中的IGF通过酸性凝胶渗透色谱法提取,使用与Pharmacia快速蛋白质液相色谱系统相连的Waters Protein Pak 125柱,然后冷冻干燥、复溶(pH 7.4)并通过放射免疫分析进行测定。实验结束时,外源性bGH使营养良好的母羊和羊羔血浆中的IGF-I水平升高(P < 0.01),但禁食动物中未升高;禁食使所有年龄段的血浆IGF-I水平降低(P < 0.01)。还发现母羊的IGF-I水平显著高于羊羔(P < 0.01)。相反,所有组中bGH的给药使血浆IGF-II浓度降低(P = 0.02),禁食使母羊的血浆IGF-II浓度升高(P < 0.05)。然而,禁食对羊羔的IGF-II没有显著影响。羊羔的IGF-II水平显著高于母羊(P < 0.001)。本研究结果表明,生长激素给药刺激血浆IGF-I增加并导致血浆IGF-II降低。另一方面,禁食使绵羊的血浆IGF-I降低,血浆IGF-II升高。本研究中IGF-I存在显著的生长激素/营养相互作用(P < 0.01),而IGF-II不存在,IGF-II存在显著的营养/年龄相互作用(P < 0.01),而IGF-I不存在,这表明生长激素对营养良好而非禁食绵羊的血浆IGF-I水平具有更大的刺激作用,营养对年龄较大而非较小的动物的血浆IGF-II水平影响更大,表明出生后绵羊的血浆IGF-I和IGF-II受到营养、生长激素和发育阶段的不同调节。