Phillips L S, Bajaj V R, Fusco A C, Matheson C K
Diabetes. 1983 Dec;32(12):1117-25. doi: 10.2337/diab.32.12.1117.
Diabetics may have normal somatomedins by radioimmunoassay yet decreased somatomedin activity by bioassay. The discrepancy appears due to circulating inhibitory factors; inhibitors in whole diabetic serum antagonize the action of both somatomedins and insulin via noncompetitive interactions. Since little is known about the nature of the inhibitory activity, serum from streptozotocin-diabetic rats was fractionated, and inhibitory activity measured as the ability of fractions to blunt stimulation of SO4 uptake by hypophysectomized rat costal cartilage exposed in vitro to somatomedins in normal rat serum. After establishing that inhibitory activity was stable to pH and lyophilization, diabetic rat serum was gel filtered at pH 7 (somatomedins bound to carrier proteins) and 2.4 (somatomedins dissociated, mol wt approximately 8000). Using Sephadex and Sephacryl columns at neutral pH, inhibitors were detected at mol wt approximately 250,000, approximately 24,000, and approximately 940. Predominant activity was at approximately 24,000 and approximately 940. In contrast, Sephadex columns at acid pH revealed inhibitors only at mol wt approximately 21,000. Diabetic rat serum was also subjected to ion-exchange chromatography on CM-Sepharose. A single band of activity at pH 5-7 was found on elution with increasing pH, suggesting an isoelectric point(s) lower than that of the somatomedins. However, three areas of activity were seen on elution with increasing ionic strength at pH 5-at 0.02 M and 0.14-1.4 M and at 2.0 M pH 5.0-5.5. These studies indicate that reduced anabolism in diabetes may be due in part to three species of circulating somatomedin inhibitors, largely of mol wt approximately 21-24,000 and approximately 940, and also of mol wt approximately 250,000.(ABSTRACT TRUNCATED AT 250 WORDS)
糖尿病患者通过放射免疫测定法检测时生长调节素可能正常,但通过生物测定法检测时其活性却降低。这种差异似乎是由于循环抑制因子所致;糖尿病患者全血清中的抑制剂通过非竞争性相互作用拮抗生长调节素和胰岛素的作用。由于对抑制活性的性质了解甚少,因此对链脲佐菌素诱导糖尿病大鼠的血清进行了分级分离,并将抑制活性测定为各分级分离物抑制垂体切除大鼠肋软骨在体外暴露于正常大鼠血清中的生长调节素时对硫酸摄取刺激的能力。在确定抑制活性对pH和冻干稳定后,将糖尿病大鼠血清在pH 7(生长调节素与载体蛋白结合)和2.4(生长调节素解离,分子量约8000)下进行凝胶过滤。在中性pH下使用葡聚糖凝胶和琼脂糖凝胶柱,在分子量约250,000、约24,000和约940处检测到抑制剂。主要活性在约24,000和约940处。相比之下,在酸性pH下的葡聚糖凝胶柱仅在分子量约21,000处显示出抑制剂。糖尿病大鼠血清还在CM-琼脂糖凝胶上进行离子交换色谱分析。在pH 5 - 7下,随着pH升高洗脱时发现单一活性带,表明其等电点低于生长调节素。然而,在pH 5下随着离子强度增加洗脱时,在0.02 M和0.14 - 1.4 M以及2.0 M、pH 5.0 - 5.5处观察到三个活性区域。这些研究表明,糖尿病中合成代谢降低可能部分归因于三种循环生长调节素抑制剂,其分子量主要约为21 - 24,000和约940,也有分子量约250,000的。(摘要截断于250字)