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钠氢交换体1在病理性心肌肥厚大鼠心肌组织及血浆中的表达

Expression of Sodium-Hydrogen Exchanger 1 in Cardiac Tissue and Plasma of Rats with Cardiac Hypertrophy
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摘要 目的:研究异丙肾上腺素诱导的病理性心肌肥厚大鼠心肌组织及血浆中钠氢交换体1(sodium-hydrogen exchanger 1,NHE-1)的表达,探讨NHE1在心肌肥厚发生和发展中的作用。方法:30只雄性SD大鼠随机并平均分为2组:病理性心肌肥厚组和对照组,每组15只,病理性心肌肥厚组(以下简称ISO组)予以ISO(异丙肾上腺素)连续每日以20、10和5mg/kg的剂量递减皮下注射,再以3mg/kg的剂量维持皮下注射7d,对照组予相同剂量生理盐水皮下注射。给药结束后进行心脏超声检测左室舒张末径(LVEDD)、左室收缩末径(LVESD)、室间隔厚度(IVST)、短轴缩短率(FS)、左室射血分数(LVEF)。分别测定各组大鼠体重(BW)、心室重量(VW)、左心室重量(LVW),计算心室重量指数VWI(VW/BW)、左心室重量指数LVW(ILVW/BW)。取血检测血浆中NHE-1的浓度,并取心肌组织观察病理形态学特征,用免疫组化法检测心肌组织中NHE-1的表达量。结果:与对照组相比,ISO组大鼠LVEF、IVST显著增加(P<0.05),LVESD明显降低(P<0.05),VWI、LVWI明显增加(P<0.01),血浆NHE-1浓度明显升高(P<0.01),心肌组织NHE-1表达增多(P<0.01)。结论:NHE-1可能在病理性心肌肥厚的发生和发展过程中起着重要作用。 Objective: To investigate the effects of Sodium-Hydrogen Exchanger 1 (NHE-1)on the initiation and development of cardiovascular diseases and to investigate the role of NHE-1 in cardiac hypertrophy. Methods: A total of thirty male Sprague-Ddwley (SD) rabbits were randomly and equally divided into 2 groups: Rat myocardial hypertrophy models were established by subcutaneous injection of isoproterenol, while the control group received an equivalent volume of 0.9% saline alone. Left ventricular end diastolic diameter (LVEDD), left ventricular end systolic diameter (LVESD), interventricular septum (IVST), fractional shortening (FS), and left ventricular ejection fraction (LVEF) were assessed by echocardiogram. The body weight (BW), ventricular weight (VW), left ventricular weight (LVW), ventricular weight index (VWI) and left ventricular weight index (LVWI) were determinated.The pathomorphological features of the myocardium were observed by electronmicroscope. Plasma levels of NHE-1 in the myocardial muscle were measured. Results: There was no significance difference between the model group and control group in LVEF, IVST, VWI and LVW/(P〈0. 05). The LVESD decreased (P〈0.05) compared with that in control group. The myocardial and plasma levels of NHE-1 in the model group were obviously higher than those of the control group (P〈0.01). Conclusion: NHE-1 may play an important role in the progress of cardiac hypertrophy.
出处 《现代生物医学进展》 CAS 2011年第11期2037-2040,共4页 Progress in Modern Biomedicine
基金 湖南省自然科学基金(07JJ3083)
关键词 心肌肥厚 异丙肾上腺素 钠氢交换体1 NHE-1 Cardiac hypertrophy Isoproterenol Sodium-Hydrogen Exchanger 1 NHE-!
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参考文献10

  • 1Bruckner BA, Razeghi P, Stetson S, et al. Degree of cardiac fibrosis and hypertrophy at time of implanutation predicts myocardial im- provement during left ventricular assist device support [J]. J Heart Lung Transplant, 2004, 23 (1) :36 - 42.
  • 2Fujisawa G, Okada K, Muto S, et al. Na+ / H+ exchange isoform 1 is involved in minemlocorticoid / salt-induced cardiac injury [J]. Hy- pertension, 2003,41 (3):493 -498.
  • 3Cingolani HE, Rebolledo OR, Portiansky EL, et al. Regression of hypertensive myocardial fibrosis by Na~ / H+ exchange inhibition [J]. Hypertension, 2003,41(2):373-377.
  • 4Ennis IL, Escudero EM, Console GM, et al. Regression of isopro- terenol-induced cardiac hypertrophy by Na~/H~ exchanger inhibition [J]. Hypertension, 2003,41 (6): 1324-1329.
  • 5Engelhardt S, Hein L, Keller U, et al .Inhibition ofNa+ / H+ exchange prevents hypertrophy,fibrosis,and heart failure in beta( 1)-- adrenergic receptor transgenic mice [J]. Circ Res, 2002,90(7): 814-819.
  • 6宋俊燕,李沙,宁阳根.钠氢交换体1在慢性心衰大鼠心肌组织及血浆中的表达[J].现代生物医学进展,2010,10(20):3816-3819. 被引量:1
  • 7Karmazyn M, Gan XT, Humphreys RA, et al. The myocardial Na+-H+ exchange:structure,regulation and its role in heart disease [J]. Circ Res, 1999,85(9):777-786.
  • 8Hayasaki KY, Kitano Y, Lwasaki T, et al. Na+ influx via Na+ / H+ exchange activates protein kinase C isozymes delta and epsilon in cul- tured neonatal rat cardiac myocytes [J]. J Mol Cell Cardiol, 1999, 31 (8):1559-1572.
  • 9石家冲,魏玲.钠氢交换体1与心血管疾病关系研究进展[J].医学综述,2008,14(24):3710-3712. 被引量:6
  • 10金振晓,辛梅,陈涛,周京军.NHE1在心肌肥大,心肌纤维化和心衰中的作用[J].国际病理科学与临床杂志,2005,25(6):536-538. 被引量:6

二级参考文献52

  • 1吴伟康,杨辉,赵明奇.阿霉素性心力衰竭模型的氧化应激和凋亡机制[J].中国病理生理杂志,2004,20(8):1437-1439. 被引量:22
  • 2Hisamitsu T, Yamada K, Nakamura TY, et al. Functional importance of charged residues within the putative intracellular loops in pH regulation by Na^+/H^+ exchanger NHE1 [ J ]. FEBS J, 2007, 274(16) :4326-4335.
  • 3Orlowski J, Grinstein S. Diversity of the mammalian sodium/proton exchanger SLC9 gene family [ J ]. Pflugers Arch, 2004,447 ( 5 ) : 549-565.
  • 4Nakamura N,Tanaka S, Teko Y. Four Na^+/H^+ exchanger isoforms are distributed to Golgi and post-Golgi compartments and are involved in organdie pH regulation [ J ]. J Biol Chem,2005,280 (2) : 1561-1572.
  • 5Johnstone ED, Speake PF, Sibley CP. Epidermal growth factor and sphingosine-l-phosphate stimulate Na^+/H^+ exchanger activity in the human placental syncytiotrophoblast [ J ]. Am J Physiol Regul Integr Comp Physiol,2007,293 (6) : R2290-2294.
  • 6Slepkov ER, Rainey JK, Sykes BD, et al. Structural and functional analysis of the Na^+/H^+ exchanger [ J]. Biochem J, 2007,401 (3) :623-633.
  • 7Snabaitis AK, Hearse DJ, Avkiran M. Regulation of sarcolemmal Na ( + )/H( + ) exchange by hydrogen peroxide in adult rat ventricular myocytes[ J]. Cardiovasc Res ,2002,53 (2) :470-480.
  • 8Nakamura TY, Iwata Y, Arai Y, et al. Activation of Na^+/H^+ changer 1 is sufficient to generate Ca^2+ signals that induce cardiac hypertrophy and heart failure [ J ]. Circ Res,2005,103 (8) :891-899.
  • 9Bianchini L, WoodsideM, SardetC, et al. Okadaic acid, a phosphatase inhibitor,induces activation and phosphorylation of the Na^+/H^+ antiport [ J ]. Biol Chem,2001,266 (23) : 15406-15413.
  • 10Yokoyama H, Yasutake M, Avkiran M. Alpha 1-adrenergic stimulation of sarcolemmal Na^+/H^+ exchanger activity in rat ventrieular myocytes:evidenee for selective mediation by the alpha 1A-adrenoceptor subtype[J].Circ Res,1998,82(10) :1078-1085.

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