[1]王永 乐岭.GLP-1对血管重构中血管平滑肌细胞的影响[J].国际内分泌代谢杂志,2018,38(01):23-25,39.[doi:10.3760/cma.j.issn.1673-4157.2018.01.006]
 Wang Yong,Yue Ling.Effects of GLP-1 on vascular smooth muscle cells in vascular remodeling[J].International Journal of Endocrinology and Metabolism,2018,38(01):23-25,39.[doi:10.3760/cma.j.issn.1673-4157.2018.01.006]
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GLP-1对血管重构中血管平滑肌细胞的影响()
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《国际内分泌代谢杂志》[ISSN:1673-4157/CN:12-1383/R]

卷:
38
期数:
2018年01期
页码:
23-25,39
栏目:
综述
出版日期:
2018-01-20

文章信息/Info

Title:
Effects of GLP-1 on vascular smooth muscle cells in vascular remodeling
作者:
王永 乐岭
Author(s):
Wang Yong Yue Ling
Department of Endocrinology, Wuhan General Hospital of Chinese People's Liberation Army,Wuhan 430070,China
关键词:
胰高血糖素样肽-1 血管重构 血管平滑肌细胞
Keywords:
Glucagon-like peptide-1 Vascular remodeling Vascular smooth muscle cells
DOI:
10.3760/cma.j.issn.1673-4157.2018.01.006
摘要:
血管重构中血管平滑肌细胞(VSMC)的表型转换和过度增殖是导致其发生和发展的重要环节。大量研究发现,胰高血糖素样肽(GLP)-1可通过调控血糖、抑制内膜增生、调控线粒体动力学等方式参与调节VSMC 的功能,改善动脉粥样硬化,防治血管再狭窄,其在血管重构中发挥的调节作用受到广泛关注。
Abstract:
Phenotypic transformation and hyperproliferation of vascular smooth muscle cells(VSMC)in vascular remodeling are important links leading to its occurrence and development. A large number of studies have found that glucagon-like peptide-1(GLP-1)was involved in the regulation of VSMC function, and its role in vascular remodeling such as improving atherosclerosis and preventing vascular restenosis was widely concerned.

参考文献/References:


[1] Horowitz M,Flint A,Jones KL,et al.Effect of the once-daily human GLP-1 analogue liraglutide on appetite, energy intake, energy expenditure and gastric emptying in type 2 diabetes[J].Diabetes Res Clin Pract,2012,97(2):258-266.DOI:10.1016/j.diabres.2012.02.016.
[2] Dalle S,Burcelin R,Gourdy P.Specific actions of GLP-1 receptor agonists and DPP4 inhibitors for the treatment of pancreatic β-cell impairments in type 2 diabetes[J].Cell Signal,2013,25(2):570-579.DOI:10.1016/j.cellsig.2012.11.009.
[3] Chaabane C,Otsuka F,Virmani R,et al. Biological responses in stented arteries[J].Cardiovasc Res,2013,99(2):353-363.DOI:10.1093/cvr/cvt115.
[4] Muto A,Fitzgerald TN,Pimiento JM,et al.Smooth muscle cell signal transduction: implications of vascular biology for vascular surgeons[J].J Vasc Surg,2007,45 Suppl A:A15-A24.DOI:10.1016/j.jvs.2007.02.061.
[5] Grudzinska MK,Bojakowski K,Soin J,et al. RCMV increases intimal hyperplasia by inducing inflammation, MCP-1 expression and recruitment of adventitial cells to intima[J].Herpesviridae,2010,1(1):7.DOI:10.1186/2042-4280-1-7.
[6] Eriksson L,Saxelin R,Röhl S,et al.Glucagon-like peptide-1 receptor activation does not affect re-endothelialization but reduces intimal hyperplasia via direct effects on smooth muscle cells in a nondiabetic model of arterial injury[J].J Vasc Res,2015,52(1):41-52.DOI:10.1159/000381097.
[7] Goto H,Nomiyama T,Mita T,et al.Exendin-4, a glucagon-like peptide-1 receptor agonist, reduces intimal thickening after vascular injury[J].Biochem Biophys Res Commun,2011,405(1):79-84.DOI:10.1016/j.bbrc.2010.12.131.
[8] Hirata Y,Kurobe H,Nishio C,et al.Exendin-4, a glucagon-like peptide-1 receptor agonist, attenuates neointimal hyperplasia after vascular injury[J].Eur J Pharmacol,2013,699(1-3):106-111.DOI:10.1016/j.ejphar.2012.11.057.
[9] Erdogdu Ö,Eriksson L,Nyström T,et al.Exendin-4 restores glucolipotoxicity-induced gene expression in human coronary artery endothelial cells[J].Biochem Biophys Res Commun,2012,419(4):790-795.DOI:10.1016/j.bbrc.2012.02.106.
[10] Arakawa M,Mita T,Azuma K,et al.Inhibition of monocyte adhesion to endothelial cells and attenuation of atherosclerotic lesion by a glucagon-like peptide-1 receptor agonist, exendin-4[J].Diabetes,2010,59(4):1030-1037.DOI:10.2337/db09-1694.
[11] 吴杰萍, 郭志新,齐伟,等. 艾塞那肽通过下调p22phox、NOX4和TGF-β1减轻1型糖尿病大鼠主动脉的氧化应激损伤[J]. 中国动脉硬化杂志, 2013, 21(8):711-715.
[12] Mehta PK, Griendling KK. Angiotensin Ⅱ cell signaling: physiological and pathological effects in the cardiovascular system[J]. Am J Physiol Cell Physiol, 2007, 292(1):C82-C97. DOI:10.1152/ajpcell.00287.2006.
[13] Nagayama K,Kyotani Y,Zhao J,et al.Exendin-4 prevents vascular smooth muscle cell proliferation and migration by angiotensin Ⅱ via the inhibition of ERK1/2 and JNK signaling pathways[J].PLoS One,2015,10(9):e0137960.DOI:10.1371/journal.pone.0137960.
[14] Muñoz FJ,Jiménez M,Melón J,et al. Phenotypic changes in vascular smooth muscle cells during aging: insulin effect on migration[J].Gerontology,1998,44(3):149-152.
[15] Zhao L,Li AQ,Zhou TF,et al.Exendin-4 alleviates angiotensin Ⅱ-induced senescence in vascular smooth muscle cells by inhibiting Rac1 activation via a cAMP/PKA-dependent pathway[J].Am J Physiol Cell Physiol,2014,307(12):C1130-C1141. DOI:10.1152/ajpcell.00151.2014.
[16] Zhou T,Zhang M,Zhao L,et al.Activation of Nrf2 contributes to the protective effect of Exendin-4 against angiotensin Ⅱ-inducedvascular smooth muscle cell senescence[J].Am J Physiol Cell Physiol,2016,311(4):C572-C582.DOI:10.1152/ajpcell.00093.2016.
[17] Bakowski D,Nelson C,Parekh AB. Endoplasmic reticulum-mitochondria coupling: local Ca2+ signalling with functional consequences[J].Pflugers Arch,2012,464(1):27-32.DOI:10.1007/s00424-012-1095-x.
[18] Wang PT,Garcin PO,Fu M,et al. Distinct mechanisms controlling rough and smooth endoplasmic reticulum contacts with mitochondria[J].J Cell Sci,2015,128(15):2759-2765.DOI:10.1242/jcs.171132.
[19] Lim JH,Lee HJ,Ho Jung M,et al.Coupling mitochondrial dysfunction to endoplasmic reticulum stress response: a molecular mechanism leading to hepatic insulin resistance[J].Cell Signal,2009,21(1):169-177.DOI:10.1016/j.cellsig.2008.10.004.
[20] Ahn SY,Choi YS,Koo HJ,et al. Mitochondrial dysfunction enhances the migration of vascular smooth muscles cells via suppression of Akt phosphorylation[J].Biochim Biophys Acta,2010,1800(3):275-281.DOI:10.1016/j.bbagen.2009.09.005.
[21] Morales PE,Torres G,Sotomayor-Flores C,et al.GLP-1 promotes mitochondrial metabolism in vascular smooth muscle cells by enhancing endoplasmic reticulum-mitochondria coupling[J].Biochem Biophys Res Commun,2014,446(1):410-416. DOI:10.1016/j.bbrc.2014.03.004.
[22] Wang L,Yu T,Lee H,et al.Decreasing mitochondrial fission diminishes vascular smooth muscle cell migration and ameliorates intimal hyperplasia[J].Cardiovasc Res,2015,106(2):272-283.DOI:10.1093/cvr/cvv005.
[23] Torres G,Morales PE,García-Miguel M,et al. Glucagon-like peptide-1 inhibits vascular smooth muscle cell dedifferentiation through mitochondrial dynamics regulation[J].Biochem Pharmacol,2016,104:52-61.DOI:10.1016/j.bcp.2016.01.013.

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备注/Memo

备注/Memo:
基金项目:湖北省卫生计生委科研项目(WJ2015Z040)
通信作者:乐岭,Email:yueling1@medmail.com.cn
更新日期/Last Update: 2018-01-30