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ABCA1和PPARγ与糖尿病动脉粥样硬化关系的研究 被引量:2

Study on the Relationship between ABCA1 and PPARγ in Diabetic Atherosclerosis
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摘要 目的:研究ATP结合盒转运体A1(ABCA1)在多种糖尿病特有因素刺激下在巨噬细胞中的表达,以及PPARγ激动剂干预后其表达的变化,探讨ABCA1及PPARγ在糖尿病大血管并发症发展中的作用机制。从而为研究糖尿病大血管并发症的发生机制及防治提供一定的理论依据。方法:以巨噬细胞为研究对象,体外模拟糖尿病状态,分别以高葡萄糖、高胰岛素和糖基化终末产物刺激巨噬细胞,检测细胞中ABCA1表达的变化;以PPARγ激动剂预处理巨噬细胞后,再以上述因素刺激细胞,分别检测巨噬细胞中ABCA1的表达并比较。结果:高葡萄糖、高胰岛素和糖基化终末产物(AGE)可作为独立因素,导致细胞中ABCA1表达减少(P<0.05)。PPARγ激动剂预处理后,ABCA1表达量增加(P<0.05)。结论:糖尿病状态下,一些糖尿病特有的刺激因素如:高葡萄糖、高胰岛素和糖基化终末产物等作为独立因素使ABCA1表达减少,可能是糖尿病患者动脉粥样硬化发生率较非糖尿病人群增高的原因。PPARγ激动剂干预后,糖尿病状态下ABCA1的表达增加,这提示我们应用PPARγ激动剂可能延缓糖尿病患者动脉硬化进展。 Objective: To investigate the effects of various diabetic stimulating factors on the expression of ATP-binding cassette A1 (ABCA1) in macrophages. The effect of PPARγ/ receptor agonist on expression of ABCA1 in macrophages.In order to inquire the mechanisn of ABCA1 and PPARγ on diabetic atherosclerosis. Methods: Macrophages was incubated with high glucose, high insulin and advanced glycosylation end products (AGE); simultaneously, the cells pre-treated with PPARγ receptor agonist was incubated with above factors, the expression of ABCA1 was detected and compared. Results: Three factors inhibited the expression of ABCA1 independently (P〈0.05); PPARγ/receptor agonist increased the expression of ABCAI induced by three factors istinctly (P〈0.05). Conclusions: The expression of ABCA1 can be inhibited by these stimulating factors on diabetic state. The reason may be that more people on diabetes have atherosclerosis than normal.PPAR-y receptor agonist promotes the expression of ABCA1 in macrophages in diabetes, and can delay the process o f diabetic atherosclerosis.
出处 《现代生物医学进展》 CAS 2013年第3期452-455,共4页 Progress in Modern Biomedicine
关键词 ABCA1 PPARΓ 糖尿病 动脉粥样硬化 ABCA1 PPARγ/ Diabetes Atherosclerosis
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参考文献20

  • 1Bosevski M. Peripheral arterial disease and diabetes[J]. Prilozi,2012,3 3(1):65-78.
  • 2Pande RL.Approach to lipid therapy in the patient with atherosclerotic vascular disease[J]. Curr Treat Options Cardiovasc Med,2012,14(2):l 77-183.
  • 3Oram, JF. HDL apolipoprteins and ABCAI partners in the removal of excess cellular cholesterol [J]. Arterioscler Thromb Vasc Biol,2003, 23(5):720-727.
  • 4Srivastava N. ATP binding cassette transporter Al-key roles in cellular lipid transport and atherosclerosis[J]. Mol Cell Biochem,2002,237(1- 2):155-164.
  • 5Kellner-Weibel G, Luke S J, Rothblat GH. Cytotoxic cellular choleste- rol is selectively removed by apoA-I via ABCA1 [J]. Atherosclerosis,2 003,171 (2):235-243.
  • 6Tontonoz P, Nagy L, Alvarez JG, et al. PPAR gamma promotes mono- cyte/macrophage differentiation and uptake of oxidized LDL[J]. Cell, 1998,93(2) :241-252.
  • 7Wolffenbuttel BH, Sels JP, Huijberts MS. Rosiglitazone[J]. Expert Op- in Pharmacother,2001,2(3):467-478.
  • 8Lee JC, Young PR. Role of CSB/p38/RK stress response kinase in LPS and cytokine signaling mechanisms[J]. J Leukoc Biol, 1996,59(2): 152 -157.
  • 9欧阳新平,周寿红,田绍文,李兴,何平平,尹蔚兰,周钰娟,唐朝克.槟榔碱对泡沫细胞胆固醇流出和ABCA1表达的影响[J].中国动脉硬化杂志,2012,20(4):289-294. 被引量:12
  • 10刘芃,李公信,刘映峰,吕俊豪,缪绯,徐琳,赵欢.辛伐他汀对人脐静脉内皮细胞ABCA1表达的影响[J].广东医学,2010,31(4):416-418. 被引量:1

二级参考文献21

  • 1李华波,全智华.ABCA1与PPARs在胆固醇流出中的作用及相关性[J].医学综述,2005,11(11):974-976. 被引量:5
  • 2Belinda A Cutri,Neil J Hime,Stephen J Nicholls.High-density lipoproteins:an emerging target in the prevention of cardiovascular disease[J].Cell Research,2006,16(10):799-808. 被引量:6
  • 3FORMAN B M, RUAN B, CHEN J, et al. The orphan nuclear receptor LXRalpha is positively and negatively regulated by distinct products of mevalonate metabolism [ J ]. Proc Natl Acad Sci U S A, 1997, 94(20) : 10588-10593.
  • 4GUTIERREZ G, MENDOZA C, ZAPATA E, et al. Dehydroepiandrosterone inhibits the TNF - alpha - induced inflammatory response in human umbilical vein endothelial cells[ J]. Atherosclerosis, 2007, 190(1) : 90-99.
  • 5O'CONNELL B J, DENIS M, GENEST J. Cellular physiology of cholesterol efflux in vascular endothelial cells [ J]. Circulation, 2004, 110(18) : 2881 -2888.
  • 6ANDO H, TSURUOKA S, YAMAMOTO H, et al. Effects of pravastatin on the expression of ATP - binding cassette transporter AI[J]. J Pharmacol Exp Ther, 2004, 311(1) : 420-425.
  • 7ZANOTTI I, FAVARI E, SPOSITO A C, et al. Pitavastatin increases ABCA1 - mediated lipid efflux from Fu5AH rat hepatoma cells [ J ]. Biochem Biophys Res Commun, 2004, 321 (3) : 670 -- 674.
  • 8WONG J, QUINN C M, BROWN A J. Statins inhibit synthesis of an oxysterol ligand for the liver x receptor in human maerophages with consequences for cholesterol flux [ J ]. Artetioscler Thromb Vasc Biol, 2004, 24( 12): 2365-2371.
  • 9ZANOTTI I, POTI F, FAVARI E, et al. Pitavastatin effect on ATP binding cassette A1 - mediated lipid efllux from macrophages: evidence for liver X receptor (LXR) - dependent and LXR - independent mechanisms of activation by cAMP[ J]. J Pharmacol Exp Ther, 2006, 317(1): 395-401.
  • 10Guo H,Li R,Zucker S,et al.EMMPRIN (CD147),an inducer of matrix metalloproteinase synthesis,also binds interstitial collagenase to the tumor cell surface[J].Cancer Res,2000;60(4):888-91.

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  • 1Fagan TC, Sowers J. Type 2 diabetes mellitus: greater cardiovascular risks and greater benefits of therapy[J]. Arch Intern Med, 1999, 159 (10): 1033-1034.
  • 2Haffer SM. DysJipidemia management in adults with diabetes[J]. Diabetes Care, 1998,21(1): 160-178.
  • 3Chang YC, Sheu WH, Chien YS, et al. Hyperglycemia accelerates ATP-binding cassette transporter Al degradation via an ERK?dependent pathway in macrophages[J]. J Bioi Chern, 2013, 114(6): 13 64-1374.
  • 4Murao K, Yu X, Imachi H, et al. Hyperglycemia suppresses hepatic scavenger receptor class B type I expression[J]. Am J Physiol Endocrinol Metab, 2008, 294(1): 78-87.
  • 5DeRisi J, Penland L, Brown PO, et al. Use of a cDNA microarray to analyse gene expression patterns in human cancer[J]. Nature Genetics, 1996,14(4): 457-460.
  • 6Wang Z, Gerstein M, Snyder M. RNA-Seq: a revolution-ary tool or transcriptomics[J]. Nat Rev Genet, 2009,10(1): 57-63.
  • 7Fakhari FD, Dittmer DP. Charting latency transcripts in Kaposi's sarcoma-associated herpesvirus by whole-genomereal-time quantitati?ve PCR[J]. J Virol, 2002, 76(12): 6213-6223.
  • 8Jensen KK, Previs SF, Zhu L, et al. Demonstration of diet-induced decoupling of fatty acid and cholesterol synthesis by combining gene expression array and 2H20 quantification[J]. Am J Physiol Endocri?nol Metab, 2012, 302(2): 209-217.
  • 9Vance DE, Vance JE, Laura Liscum, et al. Biochemisntry of Lipids, lipoproteins and Memhranes[M]. Ireland: Elsevier, 2008: 399-422.
  • 10De Vogel-van den Bosch HM, de Wit NJ, Hooiveld GJ, et al. A cholesterol-free, high-fat diet suppresses gene expression of cholesterol transporters in murine small intestine[J]. Am J Physiol Gastrointest Liver Physiol, 2008,. 294(5): 1171-1180.

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