[1] Baigent C, Keech A, Kearney PM, et al. Efficacy and safety of cholesterol-lowering treatment:prospective meta-analysis of data from 90056 participants in 14 randomized trials of statins[J]. Lancet, 2005, 366(9493):1267-1278. [2] 赵佳慧, 程庆砾, 叶平. 阿托伐他汀治疗对肾脏衰老的影响[J]. 中国应用生理学杂志, 2011, 27(1):98-101. [3] 韩磊, 叶平, 李鸣皋. PPARα信号通路在阿托伐他汀抑制衰老心肌MMP-9表达中的作用[J]. 中国应用生理学杂志, 2013, 29(5):469-472. [4] Ridker PM, Genest J, Boekholdt SM, et al. HDL cholesterol and residual risk of first cardiovascular events after treatment with potent statin therapy:an analysis from the JUPITER trial[J]. Lancet, 2010, 376(9738):333-339. [5] Grip O, Janciauskiene S, Lindgren S. Pravastatin down-regulates inflammatory mediators in human monocytes in vitro[J]. Eur J Harmacol, 2000, 410(1):83-92. [6] Grip O, Janciauskiene S, Lindgren S. Atorvastatin activates PPAR-γand attenuates the inflammatory response in human monocytes[J]. Inflamm Res, 2002, 51(2):58-62. [7] Olzinski AR, Turner GH, Bernard RE, et al. Pharmacological inhibition of C-C chemokine receptor 2 decreases macrophage infiltration in the aortic root of the human C-C chemokine receptor 2/apolipoprotein E-/-mouse:magnetic resonance imaging assessment[J]. Arterioscler Thromb Vasc Biol, 2010, 30(2):253-259. [8] Tacke F, Randolph GJ. Migratory fate and differentiation of blood monocyte subsets[J]. Immunobiol, 2006, 211(6-8):609-618. [9] Izikson L, Klein RS, Charo IF, et al. Resistance to experimental autoimmune encephalomyelitis in mice lacking the CC chemokine receptor (CCR)2[J]. J Exp Med, 2000, 192(7):1075-1080. [10] Brodmerkel CM, Huber R, Covington M, et al. Discovery and pharmacological characterization of a novel rodentactive CCR2 antagonist, INCB3344[J]. J Immunol, 2005, 175(8):5370-5378. [11] Han KH, Ryu J, Hong KH, et al. HMG-CoA reductase inhibition reduces monocyte CC chemokine receptor 2 expression and monocyte chemoattractant protein-1-mediated monocyte recruitment in vivo[J]. Circulation, 2005, 111(11):1439-1447. [12] Yuichi M, Daisuke O, Jun W, et al. Activation of peroxisome proliferator-activated receptord inhibits streptozotocin-induced diabetic nephropathy through anti-inflammatory mechanisms in mice[J]. Diabetes, 2011, 60(3):960-968. [13] Fan Y, Wang Y, Tang Z, et al. Suppression of pro-inflammatory adhesion molecules by PPAR-delta in human vascular endothelial cells[J]. Arterioscler Thromb Vasc Biol, 2008, 28(2):315-321. [14] Barish GD, Atkins AR, Downes M, et al. PPARdelta regulates multiple proinflammatory pathways to suppress atherosclerosis[J]. Proc Natl Acad Sci USA, 2008, 105(11):4271-4276. [15] Schnegg CI, Kooshki M, Hsu FC, et al. PPARδ prevents radiation-induced proinflammatory responses in microglia via transrepression of NF-κB and inhibition of the PKCα/MEK1/2/ERK1/2/AP-1 pathway[J]. Free Radical Biol Med, 2012, 52(9):1734-1743. [16] Liu G, Li X, Li Y, et al. PPARε agonist GW501516 inhibits pdgf-stimulated pulmonary arterial smooth muscle cell function related to pathological vascular remodeling[J]. Biomed Res Int, 2013, 2013:903947. [17] Lazar A, Bojic, Amy C, et al. Peroxisome proliferator-activated receptorδagonist GW1516 attenuates diet-induced aortic inflammation, insulin resistance, and atherosclerosis in low-density lipoprotein receptor knockout mice[J]. Arterioscler Thromb Vasc Biol, 2014, 34(1):52-60. [18] Inoue I, Itoh F, Aoyagi S, et al. Fibrate and statin synergistically increase the transcriptional activities of PPARa/RXRa and decrease the transactivation of NF-kB[J]. Biochem Biophys Res Commun, 2002, 290(1):131-139. |