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尿毒症患者血清诱导正常脂肪组织产生胰岛素抵抗。

Induction of insulin resistance in normal adipose tissue by uremic human serum.

作者信息

McCaleb M L, Mevorach R, Freeman R B, Izzo M S, Lockwood D H

出版信息

Kidney Int. 1984 Feb;25(2):416-21. doi: 10.1038/ki.1984.33.

DOI:10.1038/ki.1984.33
PMID:6374254
Abstract

An incubation of uremic human serum with normal rat adipose tissue will make the subsequently isolated adipocytes less responsive to insulin. To examine the extent of insulin resistance, we obtained sera from nondiabetic, uremic patients, who had not undergone dialysis therapy. The sera were then dialyzed (3500 molecular-weight cutoff) for 18 hr against a defined culture medium to eliminate possible in vitro effects of altered levels of end-product metabolites, electrolytes, and metabolic substrates. After an incubation of epididymal fat tissue from normal rats, for 3 hr with the dialyzed sera (50% vol/vol), cells were isolated and washed. The insulin stimulation of 14C-glucose (0.2 mM) incorporation to 14CO2 and total lipids was significantly reduced in the adipocytes pretreated with sera from 19 of the 29 uremic patients. Although elevated in the uremic patients, the sera levels of insulin, and parathyroid and growth hormones were not correlated to insulin resistant activity. Furthermore, incubation of adipose tissue for 3 hr with insulin, glucagon, or PTH did not produce resistance. The uremic sera reduced glucose utilization equally at 0.2 and 50 mM glucose, suggesting that the insulin resistance was induced additionally at a site distal to the glucose transport system. However, the concentration of insulin (22 microunits/ml) required for half-maximal stimulation of glucose metabolism was not altered by pretreatment with uremic serum. Also, neither the isoproterenol-stimulated lipolysis nor the inhibition of this cellular event was influenced by pretreatment with uremic sera.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

尿毒症患者的血清与正常大鼠脂肪组织共同孵育,会使随后分离出的脂肪细胞对胰岛素的反应性降低。为了检测胰岛素抵抗的程度,我们采集了未接受透析治疗的非糖尿病尿毒症患者的血清。然后将血清用截留分子量为3500的透析袋在特定培养基中透析18小时,以消除终产物代谢物、电解质和代谢底物水平改变可能产生的体外影响。用透析后的血清(50%体积/体积)与正常大鼠的附睾脂肪组织孵育3小时后,分离并洗涤细胞。在29例尿毒症患者中,有19例患者的血清预处理过的脂肪细胞中,14C-葡萄糖(0.2 mM)掺入14CO2和总脂质的胰岛素刺激作用显著降低。尽管尿毒症患者的胰岛素、甲状旁腺激素和生长激素水平升高,但这些血清水平与胰岛素抵抗活性无关。此外,脂肪组织与胰岛素、胰高血糖素或甲状旁腺激素孵育3小时并未产生抵抗。尿毒症血清在0.2 mM和50 mM葡萄糖浓度下均同等程度地降低葡萄糖利用,这表明胰岛素抵抗是在葡萄糖转运系统远端的一个位点额外诱导产生的。然而,用尿毒症血清预处理并未改变葡萄糖代谢半最大刺激所需的胰岛素浓度(22微单位/毫升)。同样,异丙肾上腺素刺激的脂肪分解以及对这一细胞事件的抑制均未受到尿毒症血清预处理的影响。(摘要截短至250字)

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1
Induction of insulin resistance in normal adipose tissue by uremic human serum.尿毒症患者血清诱导正常脂肪组织产生胰岛素抵抗。
Kidney Int. 1984 Feb;25(2):416-21. doi: 10.1038/ki.1984.33.
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Characterization and partial purification of a factor from uremic human serum that induces insulin resistance.对一种来自尿毒症患者血清、可诱导胰岛素抵抗的因子的特性鉴定及部分纯化。
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Postbinding defects of insulin action in human adipocytes from uremic patients.尿毒症患者人体脂肪细胞中胰岛素作用的结合后缺陷。
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Insulin resistance in uremia: in vitro model in the rat liver using human serum to study mechanisms.尿毒症中的胰岛素抵抗:利用人血清在大鼠肝脏建立体外模型以研究机制
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