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女性血清胰岛素样生长因子结合蛋白的年龄相关变化。

Age-related changes in serum insulin-like growth factor-binding proteins in women.

作者信息

Donahue L R, Hunter S J, Sherblom A P, Rosen C

机构信息

Department of Nutrition, University of Maine, Orono 04473.

出版信息

J Clin Endocrinol Metab. 1990 Sep;71(3):575-9. doi: 10.1210/jcem-71-3-575.

DOI:10.1210/jcem-71-3-575
PMID:1697597
Abstract

Plasma insulin-like growth factor-I (IGF-I) concentrations are reported to decline with advancing age. Five IGF-binding proteins (IGF-BPs) have recently been characterized in human serum, although their biological role beyond circulatory transport of IGF-I is unknown. We studied plasma IGF-I (by RIA) and serum IGF-BPs (by Western ligand blotting) in healthy elderly (n = 21) and healthy young (n = 22) women to determine if aging alters IGF-I and its high affinity BPs. Plasma IGF-I was significantly lower in the elderly than in the young group (0.78 +/- 0.08 vs. 1.22 +/- 0.11 U/ml; P less than 0.005). The number and size of IGF-BPs did not differ between age groups, but the IGF-BP binding ratios (binding of one BP fraction/binding of all fractions) for the BP-53 acid-stable complex (41.5K and 38.5K BPs), the 30K IGF-BP, and the 24K IGF-BP were all lower in the elderly than in the young group (P less than 0.01 for each fraction, elderly vs. young). In contrast, the 34K IGF-BP binding ratio was significantly greater in the elderly than in the young (0.30 +/- 0.03 vs. 0.12 +/- 0.01; P less than 0.001) and correlated closely with advancing age (r = 0.64; P less than 0.01). The changes in IGF-BPs found in the elderly are quite similar to alterations in serum IGF-BPs previously reported in GH deficiency. Since several IGF-BPs in vitro have been shown to modulate the mitogenic activity of IGF-I, the serum IGF-BP changes noted above may be important for the growth and maintenance of connective tissue, muscle, and bone during the aging process.

摘要

据报道,血浆胰岛素样生长因子-I(IGF-I)浓度会随着年龄的增长而下降。最近在人血清中鉴定出了五种IGF结合蛋白(IGF-BP),尽管它们在IGF-I循环运输之外的生物学作用尚不清楚。我们研究了健康老年女性(n = 21)和健康年轻女性(n = 22)的血浆IGF-I(通过放射免疫分析)和血清IGF-BP(通过Western配体印迹法),以确定衰老是否会改变IGF-I及其高亲和力结合蛋白。老年组的血浆IGF-I显著低于年轻组(0.78±0.08对1.22±0.11 U/ml;P<0.005)。各年龄组之间IGF-BP的数量和大小没有差异,但老年组中BP-53酸稳定复合物(41.5K和38.5K BP)、30K IGF-BP和24K IGF-BP的IGF-BP结合率(一个BP组分的结合/所有组分的结合)均低于年轻组(每组P<0.01,老年组与年轻组相比)。相反,34K IGF-BP结合率在老年组中显著高于年轻组(0.30±0.03对0.12±0.01;P<0.001),并且与年龄增长密切相关(r = 0.64;P<0.01)。在老年人中发现的IGF-BP变化与先前报道的生长激素缺乏症患者血清IGF-BP的变化非常相似。由于体外研究表明几种IGF-BP可调节IGF-I的促有丝分裂活性,上述血清IGF-BP的变化可能对衰老过程中结缔组织、肌肉和骨骼的生长和维持很重要。

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