el Nahas A M, Le Carpentier J E, Bassett A H
Department of Renal Medicine, Northern General Hospital, Sheffield, UK.
Nephrol Dial Transplant. 1990;5(2):123-9. doi: 10.1093/ndt/5.2.123.
Recent experimental evidence suggests that insulin-like growth factor-I (IGF-I) may be involved in compensatory renal growth (CRG). This study was designed to determine the relative contribution of IGF-I and growth hormone (GH) to the CRG that takes place in rats following uninephrectomy (UNx). We also studied the respective role of GH and IGF-I in the stimulation of CRG induced by a high protein diet (HPD). CRG was studied 7 days after UNx in Wistar rats and in a new mutant strain of dwarf rats, selectively deficient in GH. Prior to UNx, rats of both strains were pre-fed (14 days) either a medium-protein diet (MPD, casein 18%) or a HPD (54%). On MPD, CRG was comparable in Wistar (17.6 +/- 3.1%, M +/- SD) and dwarf (14.4 +/- 4.8%) rats. The HPD enhanced CRG in the Wistars (27 +/- 3.9%, P less than 0.005) but not in the dwarfs (14.9 +/- 2%). CRG in both experimental groups involved renal hypertrophy and hyperplasia. Control (baseline) serum, liver and kidney IGF-I were significantly less in dwarf rats. However, following UNx, on a MPD, kidney IGF-I increased significantly in both Wistar and dwarf rats: Wistar, pre-UNx, 310 +/- 46 ng/g tissue; post-UNx, 405 +/- 54 ng/g, P less than 0.005; dwarfs, pre-UNx, 205 +/- 35 ng/g; post-UNx 426 +/- 90 ng/g, P less than 0.001. On a HPD a further significant increase in renal IGF-I was only observed in Wistar rats (505 +/- 46 ng/g). No change in serum or liver IGF-I was observed after UNx in either strain.(ABSTRACT TRUNCATED AT 250 WORDS)
近期实验证据表明,胰岛素样生长因子-I(IGF-I)可能参与代偿性肾生长(CRG)。本研究旨在确定IGF-I和生长激素(GH)对大鼠单侧肾切除(UNx)后发生的CRG的相对贡献。我们还研究了GH和IGF-I在高蛋白饮食(HPD)诱导的CRG刺激中的各自作用。在Wistar大鼠和一种新的选择性缺乏GH的侏儒大鼠突变品系中,于UNx后7天研究CRG。在UNx之前,两个品系的大鼠均预先喂食(14天)中等蛋白饮食(MPD,酪蛋白18%)或HPD(54%)。在MPD上,Wistar大鼠(17.6±3.1%,均值±标准差)和侏儒大鼠(14.4±4.8%)的CRG相当。HPD增强了Wistar大鼠的CRG(27±3.9%,P<0.005),但未增强侏儒大鼠的CRG(14.9±2%)。两个实验组的CRG均涉及肾肥大和增生。对照(基线)血清、肝脏和肾脏中的IGF-I在侏儒大鼠中显著较低。然而,在UNx后,在MPD上,Wistar大鼠和侏儒大鼠的肾脏IGF-I均显著增加:Wistar大鼠,UNx前,310±46 ng/g组织;UNx后,405±54 ng/g,P<0.005;侏儒大鼠,UNx前,205±35 ng/g;UNx后426±90 ng/g,P<0.001。在HPD上,仅在Wistar大鼠中观察到肾脏IGF-I进一步显著增加(505±46 ng/g)。在任一品系中,UNx后血清或肝脏IGF-I均未观察到变化。(摘要截断于250字)