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高脂血症肾损害大鼠体内辅脂酶的变化

Changes of colipase in lipid-renal damage rats
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摘要 目的观察高脂血症大鼠血脂、尿蛋白、血肌酐,以及血清和肾皮质辅脂酶浓度及辛伐他汀治疗后的影响,探讨辅脂酶在高脂血症大鼠肾损害中可能的作用机制。方法将30只SD大鼠随机分为正常对照组、高脂血症模型组和辛伐他汀(10mg·kg-1d-1)治疗组,每组10只,12周后检测三组大鼠的血脂、血肌酐、24h尿蛋白水平以及血清和肾皮质辅脂酶浓度。结果高脂血症组尿蛋白明显高于正常对照组(P<0.01),肾组织辅脂酶水平低于正常对照组(P<0.05)。辛伐他汀治疗组总胆固醇(TC)、甘油三脂(TG)、低密度脂蛋白胆固醇(LDL-C)、24h尿蛋白定量显著低于高脂血症组(P<0.01),血清及肾组织colipase含量高于高脂血症组。结论辅脂酶可能参与了高脂血症肾损害的发生,辛伐他汀可能通过调节辅脂酶水平来保护高脂血症肾损害。 Objective To study the mechanism of Simvastatin in protecting lipid-renal damage rats by observing the serum levels of lipid,Cr,urine protein and colipase content in serum and renal cortex.Methods Thirty rats were randomly divided into 3 groups:control group,hyperlipidemic group(HL-untreated) and Simvastatin-treated group(HL-treated,10 mg·kg-1d-1).The levels of lipid,Cr,urine protein and colipase content in serum and renal cortex were measured.Results Hyperlipidemic rats had higher level of urine protein and lower level of colipase in serum and renal cortex compared with those of control subjects.Significant decrease of level of urine protein and serum lipid and increase of colipase in serum and renal cortex were found in Simvastatin-treated rats.Conclusion Colipase may be involved in lipid-renal damage.Simvastatin can protect renal damage by regulating the level of colipase.
出处 《热带医学杂志》 CAS 2011年第1期35-37,共3页 Journal of Tropical Medicine
基金 广州市医药卫生科技项目(2007-YB-149)
关键词 辛伐他汀 高脂血症 辅脂酶 Simvastatin hyperlipidemia renal colipase
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参考文献8

  • 1Moorhead JF, Chan MK, El-Nahas M, et al. Lipid nephrotoxicity in chronic progressive gtomerular and tubulo-interstitial disease [J]. Lancet, 1982,2(8311 ) : 1309-1311.
  • 2McNamee HP, Liley HG, lngber DE. Integrin-dependent control of irositol lipid synthesis in vascular endothelial cells and smooth muscle cells[J ]. Exp Cell Res, 1996,224( 1 ) : 116-122.
  • 3Fleming l, Mohamed A, Galle J, et al. Oxidize dlow density lipo protein increases upperoxide production by endothelial nitricoxide synthase by inhibiting PK Calpha [J]. Cardiovasc Res,2005,65 (4) : 897-906.
  • 4Weyrich P, Albet S, Lammers R,et al. Genetic variability of procolipase associates with altered insulin secretion in non-diabetic Caucasians [ J]. Exp Clin Endocrinol Diabetes, 2009,117 ( 2 ) : 83- 87.
  • 5吴峻,孙明,陈敏生,何兆初.辛伐他汀保护高脂血症肾损害大鼠机制探讨[J].中国现代医学杂志,2006,16(23):3568-3570. 被引量:5
  • 6Alves BN, Marshall K, Tamang DL, et al. Lipid-dependent cytotoxicity by the lipase PLRP2 and by PLRP2-positive cytotoxic Tlymphocytes (CTLs) [J].Cell Biochem Funct,2009,27(5): 296-308.
  • 7Song CY, Kim BC, Hong HK, et al. Oxidize LDL activates PAI-I transeription through autocrine activation of TGF-beta signaling in mesangial cells [ J]. Kidney Int, 2005,67 ( 5 ) : 1743-1752.
  • 8Kerfelec B, Allouche M, Colin D, et al. Computlional study of colipase interaction with lipid droplets and bile salt micelles [J]. Proteins, 2008.73 (4) : 828-838.

二级参考文献6

  • 1MOORHEAD JF,CHAN MK,NAHAS ME.Lipid nephrotoxicity in chronic progressive glomerular and tubulo-interstitial disease[J].Lancet,1982,1:139.
  • 2MCNAMEE HP,LILEY HG,INGBER DE.Integrin-dependent control of irositol lipid synthesis in vascular endothelial cells and smooth muscle cells[J].Exp Cell Res,1996,224(1):116-122.
  • 3FLEMING I,MOHAMED A,GALLE J,et al.Oxidize dlow density lipo protein increases upperoxide production by endothelial nitricoxide synthase by inhibiting PK Calpha[J].Cardiovasc Res,2005,65(4):897-906.
  • 4KARLIDAG T,ILHAN N,KAYGUSUA I,et al.Rloesoffree radicals,nitricoxide,and scavenging enzyme sinnasal polyp development[J].Ann Otol Rhinol Laryngol,2005,114(2):122-126.
  • 5SONG CY,KIM BC,HONG HK,et al.Oxidize LDL activates PAI-1 transcription through autocrine activation of TGF-beta signaling in mesangial cells[J].Kidney Int,2005,67 (5):1743-1752.
  • 6WILSON SH,CHADE AR,FELDSTEIN A,et al.Lipid-lowering-independent effects of simvastatin on the kidney in experimental hypercholesterolaemia[J].Nephrol Dial Transplant,2003,18(4):703-709.

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