Sivan Eyal, Boden Guenther
Division of Endocrinology/Diabetes/Metabolism, Temple University Hospital, 3401 North Broad Street, Philadelphia, PA 19140, USA.
Curr Diab Rep. 2003 Aug;3(4):319-22. doi: 10.1007/s11892-003-0024-y.
Acute elevation of plasma free fatty acid (FFA) levels causes insulin resistance to rise dose dependently in pregnant and nonpregnant women. Plasma FFA levels are commonly elevated during late pregnancy, partly due to rising blood levels of lipolytic placental hormones, and are a likely cause for much of the increase in insulin resistance occurring at that time in all pregnant women. Plasma FFA levels are similar or higher and the insulin resistance is comparable or more severe in women with gestational diabetes mellitus (GDM) than in nondiabetic pregnant women. In contrast to healthy pregnant women, insulin secretion in women with GDM is defective and, therefore, is unable to rise adequately to compensate for the insulin resistance; the result is hyperglycemia. The mechanism by which elevated plasma FFA levels cause insulin resistance in skeletal muscle includes intramyocellular accumulation of diacylglycerol, which activates protein kinase C (the b II and d isoforms). This results in reduction of tyrosine phosphorylation of the insulin receptor substrate-1 and inhibits activation of phosphoinositol-3 kinase, an enzyme that is essential for normal insulin-stimulated glucose uptake.
血浆游离脂肪酸(FFA)水平的急性升高会使孕妇和非孕妇的胰岛素抵抗呈剂量依赖性上升。在妊娠晚期,血浆FFA水平通常会升高,部分原因是脂解胎盘激素的血液水平升高,这可能是所有孕妇在该时期胰岛素抵抗增加的主要原因。与非糖尿病孕妇相比,妊娠期糖尿病(GDM)女性的血浆FFA水平相似或更高,胰岛素抵抗相当或更严重。与健康孕妇不同,GDM女性的胰岛素分泌存在缺陷,因此无法充分升高以补偿胰岛素抵抗;结果就是高血糖。血浆FFA水平升高导致骨骼肌胰岛素抵抗的机制包括二酰甘油在肌细胞内积累,从而激活蛋白激酶C(βII和δ亚型)。这会导致胰岛素受体底物-1的酪氨酸磷酸化减少,并抑制磷酸肌醇-3激酶的激活,而该酶对于正常胰岛素刺激的葡萄糖摄取至关重要。