Cotterill A M, Holly J M, Wass J A
Department of Endocrinology, St Bartholomew's Hospital, London, UK.
Clin Endocrinol (Oxf). 1993 Sep;39(3):357-62. doi: 10.1111/j.1365-2265.1993.tb02377.x.
Insulin-like growth factor binding protein (IGFBP)-1 levels increase overnight, being inversely related to changes in insulin. With prolonged fasting IGFBP-1 levels increase further. In animal studies high IGFBP-1 levels increase plasma glucose levels possibly by regulating the insulin-like actions of 'bio-available' plasma IGF. Following prolonged fasting, there is an increase in insulin requirement. A proportion of this reversible insulin resistance may be due to inhibitory effects of high IGFBP-1 levels on IGF action. This study examined the regulation of IGFBP-1 in the presence of reversible insulin resistance.
Nine normal adult volunteers, seven female and two male (mean age 27.6 +/- SD 2.6 years, range 21.7-46.0 years) of normal body mass index were studied.
Subjects fasted from 2200 h day 0 to 0900 h day 3 (59 hours), the fast being completed with a 75-g glucose meal. At least one week later, an 11-hour overnight fast was performed, followed by a repeat glucose meal. Blood samples were taken at regular intervals from 0900 h day 1 and for 5 hours during both glucose meal studies via an indwelling cannula.
Serum levels of IGFBP-1, insulin, GH, glucose, IGF-I and cortisol were measured at varying intervals during the fast and both glucose meal studies.
Following the initial 11-hour overnight fast IGFBP-1 levels rose from (mean +/- SEM) 32 +/- 5 micrograms/l to reach a maximum of 144 +/- 24 micrograms/l after 32 hours of fasting. IGFBP-1 levels then fluctuated, falling in the morning (93 +/- 8 micrograms/l) and then rising overnight (126 +/- 9 micrograms/l), but not regaining the initial peak levels. The increase of IGFBP-1 from overnight fasting levels was associated with a fall in plasma insulin from 5.7 +/- 0.7 to 2.2 +/- 0.2 mU/l. In comparison, 30 minutes after termination of the fast with the glucose meal, IGFBP-1 levels fell from 120 +/- 11 to 24 +/- 2 micrograms/l within 4 hours. After an overnight fast IGFBP-1 levels fell from 35 +/- 5 to 13 +/- 2 micrograms/l within 3 hours. There was glucose intolerance and increased insulin levels following the glucose meal preceded by the 59-hour fast when compared with the overnight fast. The fall of IGFBP-1 levels after the glucose meal was best expressed, taking into account subject variation, by the following regression equations: Glucose meal preceded by 11-hour fast: log [IGFBP-1] = 1.64-0.255 log [1 h previous insulin] (R2 0.51); Glucose meal preceded by 59-hour fast: log [IGFBP-1] = 1.41-0.265 log [1 h previous insulin] + 0.557 log [current glucose] (R2 0.82).
In man, insulin appears to regulate circulating IGFBP-1 levels in all circumstances, this regulation being unaffected by the resistance to insulin action induced by prolonged fasting. The high IGFBP-1 levels were statistically related to the higher glucose levels and may have directly contributed to the increased insulin requirement observed after prolonged fasting.
胰岛素样生长因子结合蛋白(IGFBP)-1水平在夜间升高,与胰岛素变化呈负相关。长时间禁食后IGFBP-1水平进一步升高。在动物研究中,高IGFBP-1水平可能通过调节“生物可利用”血浆IGF的胰岛素样作用来升高血糖水平。长时间禁食后,胰岛素需求量增加。这种可逆性胰岛素抵抗的一部分可能归因于高IGFBP-1水平对IGF作用的抑制效应。本研究在存在可逆性胰岛素抵抗的情况下检测了IGFBP-1的调节情况。
研究了9名正常体重指数的正常成年志愿者,7名女性和2名男性(平均年龄27.6±标准差2.6岁,范围21.7 - 46.0岁)。
受试者从第0天22:00禁食至第3天09:00(59小时),禁食结束时给予75克葡萄糖餐。至少一周后,进行11小时的夜间禁食,随后重复葡萄糖餐试验。在第1天09:00开始定期采集血样,并在两次葡萄糖餐试验期间通过留置套管连续采集5小时血样。
在禁食期间以及两次葡萄糖餐试验期间的不同时间点测量血清IGFBP-1、胰岛素、生长激素(GH)、葡萄糖、IGF-I和皮质醇水平。
经过最初11小时的夜间禁食后,IGFBP-1水平从(均值±标准误)32±5微克/升上升,禁食32小时后达到最高值144±24微克/升。随后IGFBP-1水平波动,早晨下降(93±8微克/升),然后夜间再次上升(126±9微克/升),但未恢复到最初的峰值水平。IGFBP-1从夜间禁食水平的升高与血浆胰岛素从5.7±0.7降至2.2±0.2毫单位/升相关。相比之下,在葡萄糖餐结束禁食后30分钟内,IGFBP-1水平在4小时内从120±11降至24±2微克/升。经过夜间禁食后,IGFBP-1水平在3小时内从35±5降至13±2微克/升。与夜间禁食相比,59小时禁食后给予葡萄糖餐时出现葡萄糖不耐受且胰岛素水平升高。考虑个体差异后,葡萄糖餐后IGFBP-1水平的下降情况通过以下回归方程能得到最佳表达:11小时禁食后给予葡萄糖餐:log[IGFBP-1]=1.64 - 0.255log[前1小时胰岛素](R² 0.51);59小时禁食后给予葡萄糖餐:log[IGFBP-1]=1.41 - 0.265log[前1小时胰岛素]+0.557log[当前葡萄糖](R² 0.82)。
在人类中,胰岛素似乎在所有情况下均调节循环IGFBP-1水平,这种调节不受长时间禁食诱导的胰岛素作用抵抗的影响。高IGFBP-1水平与较高的血糖水平在统计学上相关,并且可能直接导致了长时间禁食后观察到的胰岛素需求量增加。