Cechowska-Pasko M, Pałka J
Department of Biochemistry, Medical Academy of Białystok, Poland.
Mol Cell Biochem. 2000 Feb;205(1-2):45-52. doi: 10.1023/a:1007076809488.
During fasting or aging of animals there is a decreased content of skin glycosaminoglycans (GAGs). It has been found that the skin of adult rats contains about 60% of GAGs found in the skin of young animals. Fasting of both groups of animals (young and adult) resulted in decrease of GAG content. However, GAG content in the skin of fasted young rats decreased by 30% and in fasted adult rats by 15% only, compared to fed animals, respectively. The mechanism for the phenomena is not known. We considered insulin-like growth factor-I (IGF-I) as a potential candidate involved in regulation of GAG biosynthesis in both experimental models of animals. Adult rat sera were found to contain about 75% of IGF-I recovered from young rat sera. Fasting of both groups of animals resulted in dramatic decrease in serum IGF-I levels to about 50% of initial values. Since IGF-I activity and IGF-I serum half-life depends on the level of specific IGF-binding proteins (IGFBPs) we determined (i) relationship between main groups of IGFBPs, namely high molecular weight binding proteins (HMWBPs) and low molecular weight binding proteins (LMWBPs) and (ii) the amounts of IGF-I bound to respective proteins in the sera of all experimental animals. Control young rat serum was found to contain about 90% of HMWBPs and about 10% of LMWBPs as determined by ligand binding assay. In contrast, control adult rat serum contained about 60% of HMWBPs and about 40% of LMWBPs. Fasting of both groups of animals resulted in significant increase in serum levels of LMWBPs. Control young rat serum was found to contain about 8% IGF-I bound to LMWBPs while serum of control adult rats contained 18% IGF-I bound to these proteins. In sera of fasted young animals however, about 75% of the bound IGF-I was recovered from LMWBPs (about 60% of total serum IGF-I) while in sera of fasted adult animals only about 56% of the bound IGF-I was recovered from LMWBPs (about 50% of total serum IGF-I). Evidence was provided that during fasting of both groups of animals there is a significant decrease in serum BP-3 and dramatic increase in serum BP-1 concentrations, compared to respective controls. However, the concentration of BP-1 in serum of fasted young rats was increased by about 60 fold while in serum of fasted adult rats only by about 10 fold, compared to respective control animals. Negative correlation between skin GAG content and LMWBPs derived IGF-I during fasting of young (r = -0.943, p < 0.001) and adult ( r = -0.571, p < 0.01) rats was found. The data presented suggest that the effects of aging and fasting on decreased skin GAG content may be due to induction of LMWBPs that are known to (i) inhibit IGF-I dependent function and (ii) increase clearance of IGF-I from circulation. However, the effects of fasting are distinct in respect to young and adult rats suggesting that mechanisms involved in regulation of IGF-I bioactivity during aging are more complex that during fasting.
在动物禁食或衰老过程中,皮肤糖胺聚糖(GAGs)含量会降低。已发现成年大鼠皮肤中的GAGs含量约为幼龄动物皮肤中GAGs含量的60%。两组动物(幼龄和成年)禁食均导致GAG含量下降。然而,与喂食的动物相比,禁食幼龄大鼠皮肤中的GAG含量仅下降了30%,而禁食成年大鼠皮肤中的GAG含量仅下降了15%。该现象的机制尚不清楚。我们认为胰岛素样生长因子-I(IGF-I)是参与这两种动物实验模型中GAG生物合成调节的潜在候选因素。发现成年大鼠血清中的IGF-I含量约为从幼龄大鼠血清中回收的IGF-I含量的75%。两组动物禁食均导致血清IGF-I水平急剧下降至初始值的约50%。由于IGF-I活性和IGF-I血清半衰期取决于特定IGF结合蛋白(IGFBPs)的水平,我们测定了(i)主要IGFBP组,即高分子量结合蛋白(HMWBPs)和低分子量结合蛋白(LMWBPs)之间的关系,以及(ii)所有实验动物血清中与相应蛋白结合的IGF-I量。通过配体结合测定发现,对照幼龄大鼠血清中约含90%的HMWBPs和约10%的LMWBPs。相比之下,对照成年大鼠血清中约含60%的HMWBPs和约40%的LMWBPs。两组动物禁食均导致血清LMWBPs水平显著升高。发现对照幼龄大鼠血清中约8%的IGF-I与LMWBPs结合,而对照成年大鼠血清中18%的IGF-I与这些蛋白结合。然而,在禁食幼龄动物的血清中,约75%的结合IGF-I是从LMWBPs中回收的(约占血清总IGF-I的60%),而在禁食成年动物的血清中,只有约56%的结合IGF-I是从LMWBPs中回收的(约占血清总IGF-I的50%)。有证据表明,与各自的对照组相比,两组动物禁食期间血清BP-3显著降低,血清BP-1浓度急剧升高。然而,与各自的对照动物相比,禁食幼龄大鼠血清中BP-1的浓度增加了约60倍,而禁食成年大鼠血清中仅增加了约10倍。发现幼龄(r = -0.943,p < 0.001)和成年(r = -0.571,p < 0.01)大鼠禁食期间皮肤GAG含量与LMWBPs衍生的IGF-I之间呈负相关。所呈现的数据表明,衰老和禁食对皮肤GAG含量降低的影响可能是由于LMWBPs的诱导,已知LMWBPs(i)抑制IGF-I依赖性功能,(ii)增加IGF-I从循环中的清除。然而,禁食对幼龄和成年大鼠的影响是不同的,这表明衰老过程中调节IGF-I生物活性的机制比禁食过程中更复杂。