Huffman Jacob, Hoffmann Christina, Taylor George T
Jacob Huffman, Christina Hoffmann, George T Taylor, Behavioral Neuroscience Program, Department of Psychological Sciences, University of Missouri, St. Louis, MO 63121, United States.
World J Diabetes. 2017 Feb 15;8(2):45-55. doi: 10.4239/wjd.v8.i2.45.
Brain integrity and cognitive aptitude are often impaired in patients with diabetes mellitus, presumably a result of the metabolic complications inherent to the disease. However, an increasing body of evidence has demonstrated the central role of insulin-like growth factor 1 (IGF1) and its relation to sex hormones in many neuroprotective processes. Both male and female patients with diabetes display abnormal IGF1 and sex-hormone levels but the comparison of these fluctuations is seldom a topic of interest. It is interesting to note that both IGF1 and sex hormones have the ability to regulate phosphoinositide 3-kinase-Akt and mitogen-activated protein kinases-extracellular signal-related kinase signaling cascades in animal and cell culture models of neuroprotection. Additionally, there is considerable evidence demonstrating the neuroprotective coupling of IGF1 and estrogen. Androgens have also been implicated in many neuroprotective processes that operate on similar signaling cascades as the estrogen-IGF1 relation. Yet, androgens have not been directly linked to the brain IGF1 system and neuroprotection. Despite the sex-specific variations in brain integrity and hormone levels observed in diabetic patients, the IGF1-sex hormone relation in neuroprotection has yet to be fully substantiated in experimental models of diabetes. Taken together, there is a clear need for the comprehensive analysis of sex differences on brain integrity of diabetic patients and the relationship between IGF1 and sex hormones that may influence brain-health outcomes. As such, this review will briefly outline the basic relation of diabetes and IGF1 and its role in neuroprotection. We will also consider the findings on sex hormones and diabetes as a basis for separately analyzing males and females to identify possible hormone-induced brain abnormalities. Finally, we will introduce the neuroprotective interplay of IGF1 and estrogen and how androgen-derived neuroprotection operates through similar signaling cascades. Future research on both neuroprotection and diabetes should include androgens into the interplay of IGF1 and sex hormones.
糖尿病患者的脑完整性和认知能力通常会受损,这可能是该疾病固有代谢并发症的结果。然而,越来越多的证据表明胰岛素样生长因子1(IGF1)在许多神经保护过程中发挥核心作用,且与性激素有关。糖尿病男性和女性患者的IGF1和性激素水平均显示异常,但这些波动的比较很少成为研究热点。值得注意的是,在神经保护的动物和细胞培养模型中,IGF1和性激素都有能力调节磷酸肌醇3激酶-蛋白激酶B以及丝裂原活化蛋白激酶-细胞外信号调节激酶信号级联反应。此外,有大量证据表明IGF1和雌激素具有神经保护耦合作用。雄激素也参与了许多与雌激素-IGF1关系类似信号级联反应的神经保护过程。然而,雄激素尚未与脑IGF1系统和神经保护直接联系起来。尽管在糖尿病患者中观察到脑完整性和激素水平存在性别差异,但在糖尿病实验模型中,IGF1-性激素在神经保护中的关系尚未得到充分证实。综上所述,显然需要对糖尿病患者脑完整性的性别差异以及可能影响脑健康结果的IGF1与性激素之间的关系进行综合分析。因此,本综述将简要概述糖尿病与IGF1的基本关系及其在神经保护中的作用。我们还将把关于性激素和糖尿病的研究结果作为分别分析男性和女性的基础,以确定可能由激素引起的脑异常。最后,我们将介绍IGF1和雌激素的神经保护相互作用,以及雄激素衍生的神经保护如何通过类似的信号级联反应发挥作用。未来关于神经保护和糖尿病的研究应将雄激素纳入IGF1和性激素的相互作用研究中。