Sorenson R L, Brelje T C
Department of Cell Biology and Neuroanatomy, University of Minnesota Medical School, Minneapolis 55455, USA.
Horm Metab Res. 1997 Jun;29(6):301-7. doi: 10.1055/s-2007-979040.
Pregnancy is a unique event in the life span of islet beta-cells. Under the influence of pregnancy islet beta-cells undergo major long term up-regulatory structural and functional changes in response to the increased demand for insulin. Adaptive changes that occur in islets during normal pregnancy include: 1) increased glucose-stimulated insulin secretion with a lowered threshold for glucose-stimulated insulin secretion, 2) increased insulin synthesis, 3) increased beta-cell proliferation and islet volume, 4) increased gap-junctional coupling among beta-cells, 5) increased glucose metabolism, and 6) increased c-AMP metabolism. Of the islet changes that occur during pregnancy the increase in beta-cell division and enhanced glucose sensitivity of insulin secretion are most notable. The increase in beta-cell division leads to an increase in islet mass that contributes to the ability of islets to respond to the increased need for insulin. However, the increased glucose sensitivity of beta-cells is likely to be more important. The lowering of the threshold for glucose stimulated insulin secretion is the primary mechanism by which beta-cells can release significantly more insulin under normal blood glucose concentrations. Although the hormonal changes which occur during pregnancy are complex, it appears that lactogenic influences (either placental lactogen and/or prolactin) are sufficient to induce all of the up-regulatory changes that occur in islets during pregnancy. We have demonstrated that rat placental lactogens I and II are the hormones responsible for up-regulating islets during rodent pregnancy. Although most studies have been done using rodent islets, available evidence strongly suggests that human placental lactogen and/or human prolactin are the responsible lactogens for up-regulating islets during human pregnancy. A model for how lactogens up-regulate islets during pregnancy is proposed.
怀孕是胰岛β细胞生命周期中的一个独特事件。在怀孕的影响下,胰岛β细胞会经历重大的长期上调性结构和功能变化,以应对胰岛素需求的增加。正常怀孕期间胰岛发生的适应性变化包括:1)葡萄糖刺激的胰岛素分泌增加,葡萄糖刺激胰岛素分泌的阈值降低;2)胰岛素合成增加;3)β细胞增殖和胰岛体积增加;4)β细胞之间的缝隙连接耦联增加;5)葡萄糖代谢增加;6)环磷酸腺苷(c-AMP)代谢增加。在怀孕期间发生的胰岛变化中,β细胞分裂增加和胰岛素分泌的葡萄糖敏感性增强最为显著。β细胞分裂增加导致胰岛质量增加,这有助于胰岛应对胰岛素需求的增加。然而,β细胞葡萄糖敏感性的增加可能更为重要。葡萄糖刺激胰岛素分泌阈值的降低是β细胞在正常血糖浓度下能够释放更多胰岛素的主要机制。尽管怀孕期间发生的激素变化很复杂,但似乎催乳素的影响(胎盘催乳素和/或催乳素)足以诱导怀孕期间胰岛发生的所有上调性变化。我们已经证明,大鼠胎盘催乳素I和II是啮齿动物怀孕期间上调胰岛的激素。尽管大多数研究是使用啮齿动物的胰岛进行的,但现有证据强烈表明,人胎盘催乳素和/或人催乳素是人类怀孕期间上调胰岛的催乳素。本文提出了一个关于催乳素在怀孕期间如何上调胰岛的模型。