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本文引用的文献

1
The vascular contribution to insulin resistance: promise, proof, and pitfalls.血管对胰岛素抵抗的影响:前景、证据与陷阱。
Diabetes. 2012 Dec;61(12):3063-5. doi: 10.2337/db12-0948.
2
Central nervous system control of metabolism.中枢神经系统对代谢的控制。
Nature. 2012 Nov 15;491(7424):357-63. doi: 10.1038/nature11705.
3
Drug transport across the blood-brain barrier.药物穿越血脑屏障的转运。
J Cereb Blood Flow Metab. 2012 Nov;32(11):1959-72. doi: 10.1038/jcbfm.2012.126. Epub 2012 Aug 29.
4
Insulin-induced endothelial cell cortical actin filament remodeling: a requirement for trans-endothelial insulin transport.胰岛素诱导的内皮细胞皮质肌动蛋白丝重塑:跨内皮胰岛素转运的必要条件。
Mol Endocrinol. 2012 Aug;26(8):1327-38. doi: 10.1210/me.2012-1003. Epub 2012 Jun 25.
5
FoxOs integrate pleiotropic actions of insulin in vascular endothelium to protect mice from atherosclerosis.FoxOs 整合胰岛素在血管内皮中的多效作用,以保护小鼠免受动脉粥样硬化的侵害。
Cell Metab. 2012 Mar 7;15(3):372-81. doi: 10.1016/j.cmet.2012.01.018.
6
Banting lecture 2011: hyperinsulinemia: cause or consequence?班廷讲座 2011:高胰岛素血症:原因还是结果?
Diabetes. 2012 Jan;61(1):4-13. doi: 10.2337/db11-1483.
7
Insulin entry into muscle involves a saturable process in the vascular endothelium.胰岛素进入肌肉涉及血管内皮的一个饱和过程。
Diabetologia. 2012 Feb;55(2):450-6. doi: 10.1007/s00125-011-2343-x. Epub 2011 Oct 15.
8
A new method to study changes in microvascular blood volume in muscle and adipose tissue: real-time imaging in humans and rat.一种研究肌肉和脂肪组织中微血管血液体积变化的新方法:人体和大鼠的实时成像。
Am J Physiol Heart Circ Physiol. 2011 Aug;301(2):H450-8. doi: 10.1152/ajpheart.01174.2010. Epub 2011 May 27.
9
Insulin regulates its own delivery to skeletal muscle by feed-forward actions on the vasculature.胰岛素通过对血管的前馈作用来调节自身向骨骼肌的输送。
Am J Physiol Endocrinol Metab. 2011 Aug;301(2):E252-63. doi: 10.1152/ajpendo.00186.2011. Epub 2011 May 24.
10
Impaired insulin signaling in endothelial cells reduces insulin-induced glucose uptake by skeletal muscle.内皮细胞胰岛素信号转导受损会降低骨骼肌对胰岛素诱导的葡萄糖摄取。
Cell Metab. 2011 Mar 2;13(3):294-307. doi: 10.1016/j.cmet.2011.01.018.

内皮细胞:胰岛素抵抗发展中的“早期应答者”。

The endothelial cell: an "early responder" in the development of insulin resistance.

机构信息

Division of Endocrinology and Metabolism, Department of Medicine, University of Virginia School of Medicine, Charlottesville, VA, USA.

出版信息

Rev Endocr Metab Disord. 2013 Mar;14(1):21-7. doi: 10.1007/s11154-012-9232-6.

DOI:10.1007/s11154-012-9232-6
PMID:23306779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3594570/
Abstract

Vascular endothelium is an important insulin target and plays a pivotal role in the development of metabolic insulin resistance provoked by the Western lifestyle. It acts as a "first-responder" to environmental stimuli such as nutrients, cytokines, chemokines and physical activity and regulates insulin delivery to muscle and adipose tissue and thereby affecting insulin-mediated glucose disposal by these tissues. In addition, it also regulates the delivery of insulin and other appetite regulating signals from peripheral tissues to the central nervous system thus influencing the activity of nuclei that regulate hepatic glucose production, adipose tissue lipolysis and lipogenesis, as well as food consumption. Resistance to insulin's vascular actions therefore broadly impacts tissue function and contribute to metabolic dysregulation. Moreover, vascular insulin resistance negatively impacts vascular health by affecting blood pressure regulation, vessel wall inflammation and atherogenesis thereby contributing to the burden of vascular disease seen with diabetes and metabolic syndrome. In the current review, we examined the evidence that supports the general concept of vascular endothelium as a target of insulin action and discussed the biochemical and physiological consequences of vascular insulin resistance.

摘要

血管内皮细胞是胰岛素的一个重要靶标,在由西方生活方式引起的代谢性胰岛素抵抗的发展中起着关键作用。它作为一种“第一 responder”,对环境刺激(如营养物质、细胞因子、趋化因子和体育活动)做出反应,调节胰岛素向肌肉和脂肪组织的输送,从而影响这些组织对胰岛素介导的葡萄糖摄取。此外,它还调节胰岛素和其他来自外周组织的食欲调节信号向中枢神经系统的传递,从而影响调节肝脏葡萄糖生成、脂肪组织脂肪分解和脂肪生成的核的活性,以及食物的摄入。因此,胰岛素对血管作用的抵抗广泛影响组织功能,并导致代谢失调。此外,血管胰岛素抵抗通过影响血压调节、血管壁炎症和动脉粥样硬化形成来损害血管健康,从而导致糖尿病和代谢综合征患者的血管疾病负担增加。在本综述中,我们检查了支持血管内皮细胞作为胰岛素作用靶标的一般概念的证据,并讨论了血管胰岛素抵抗的生化和生理后果。