我们的网站为什么显示成这样?

可能因为您的浏览器不支持样式,您可以更新您的浏览器到最新版本,以获取对此功能的支持,访问下面的网站,获取关于浏览器的信息:

|本期目录/Table of Contents|

代谢抑制处理后大鼠心室肌细胞反向Na+/Ca2+交换体转运功能的变化(PDF)

《心脏杂志》[ISSN:1009-7236/CN:61-1268/R]

期数:
2005年第5期
页码:
413-415,423
栏目:
基础研究
出版日期:
2005-10-05

文章信息/Info

Title:
Changes of the reverse mode of Na+/Ca2+ exchanger in isolated rat ventricular myocytes subjected to metabilic inhibition
作者:
王波2 李树壮1 韦耿泽1 金振晓1 胡玉珍1 周京军1 张海锋1 何 炜4
第四军医大学:1.基础部生理学教研室,3.西京医院心脏外科,4.药学系化学教研室,陕西 西安 710032;2.陕西师范大学生命科学学院,陕西 西安 710062
Author(s):
WANG Bo2 LI Shuzhuang1 WEI Gengze1 JIN Zhenxiao3 HU Yuzhen1ZHOU Jingjun1 ZHANG Haifeng1 HE Wei4
Fourth Military Medical University: 1. Department of Physiology, 3. Department of Cardiology, Xijing Hospital, 4. Department of Chemistry,Shaanxi Xi’an 710032; 2. College of Life Sciences, Shaanxi Normal University, Shaanxi Xi’an 710062
关键词:
钠/钙交换体心肌细胞Ca2+测定代谢抑制
Keywords:
Na+/Ca2+ exchange ventricular myocytes calcium metabolic inhibition
分类号:
Q463
DOI:
-
文献标识码:
A
摘要:
目的 利用荧光标记法观察代谢抑制处理后,大鼠心肌细胞反向Na+/Ca2+交换体(NCX)转运功能的变化。方法 酶解法分离制备钙耐受心肌细胞用Fura2/AM负载,采用双激发荧光光电倍增系统(IonOptix Photometry System)检测钙信号。结果 细胞置于无Na+液后,可见[Ca2+]i逐渐升高,L型Ca2+通道阻断剂nifedipine在浓度为1 μmol/L时,不影响此现象;而NCX的抑制剂Ni2+,在浓度为1 mmol/L时,则完全阻断[Ca2+]i的升高。采用20 mmol/L乳酸加10 mmol/L脱氧葡萄糖作为代谢抑制物处理心肌细胞不同时间,正常Tyrode液灌流10 min,之后检测无Na+液引发[Ca2+]i升高效应的变化,发现5 min处理与对照组无显著性差异,10和30 min处理后此效应逐渐减弱。结论 首次发现,代谢抑制处理后心肌NCX的反向转运功能被抑制,阐明其调节机制,将为心肌缺血/再灌注损伤的治疗提供新思路。
Abstract:
AIM To study the reverse mode of Na+/Ca2+ exchanger (NCX) in isolated adult rat ventricular myocytes subjected to metabolic inhibition. METHODS Single left ventricular myocytes were enzymatically isolated and loaded with Fura2/AM. Intracellular calcium concentration ([Ca2+]i) was measured by IonOptix Photometry System. RESULTS ① [Ca2+]i was increased after ventricular myocytes exposed to Na+free solution (NMDG solution), and returned to baseline following washout. Nifedipine (1 μmol/L), the selective inhibitor of Ltype calcium channel, did not affect NMDG solutioninduced increases in [Ca2+]i, while Ni2+ (1 mmol/L), the selective inhibitor of NCX, almost completely blocked the effect. ②In myocyte subjected to 20 mmol/L lactate and 10 mmol/L Deoxyglucose treatment for 5, 10 and 30 min respectively, followed by 10 min normal Tyrode solution perfusion, NMDG solutioninduced increases of [Ca2+]i was timedependently inhibited. CONCLUSION The findings provide evidence that after metabolic inhibition treatment the reverse mode of NCX in ventricular myocytes is attenuated.

参考文献/References

[1] 杨学东,赵连友,李雪,等. 精氨酸加压素诱导大鼠心脏成纤维细胞胶原合成的作用[J].心脏杂志,2000,12(3):169-171.

[2] 曾朝荣,陈维永,刘璟瑜. 高血压与左心室肥厚[J].中国心血管杂志,2002 ,7(1):54-56.

[3] Van Zwieten PA. The influence of antihypertensive drug treatment on the prevention and regression of left ventricular hypertrophy[J]. Cardiovasc Res, 2000,45(1):82-91.

[4 ]Onodera T,Okazaki F,Miyazaki H,et al. Perindopril reverses myocyte remodeling in the hypertensive heart[J]. Hypertens Res,2002,25(1):85-90.

[5] 王荣,张运,蔡恒,等. 比索洛尔逆转高血压左室心肌肥厚和纤维化的超声评价研究[J].中国医学影像技术,2003, 19(12):1643-1645.

[6] Simon T, MaryKrause M, FunckBrentano C,et al. Bisoprolol doseresponse relationship in patients with congestive heart failure: a subgroup analysis in the cardiac insufficiency bisoprolol study(CIBIS II) [J]. Eur Heart J, 2003,24(6):552-559.

[7] Gullestad L, Manhenke C, Aarsland T,et al. Effect of metoprolol CR/XL on exercise tolerance in chronic heart failure-a substudy to the MERITHF trial[J]. Eur J Heart Fail, 2001,3(4):463-468.

[8] Hjalmarson A,Goldstein S,Fagerberg B, et al. Effects of controlledrelease metoprolol on total mortality,hospitalizations,and wellbeing in patients with heart failure. The Metoprolol CR/XL Randomized Intervention Trial in congestive heart failure(MERITHF) [J]. JAMA, 2000, 283(10):1295-1302.

[9] Packer M,Coats AJ,Fowler MB,et al. Effect of carvedilol on survival in severe chronic heart failure[J]. N Engl J Med,2001,344(22):1651-1658.

[10]BetaBlocker Evaluation of Survival Trial Investigators. A trial of the betablocker bucindolol in patients with advanced chronic heart fallure[J]. N Engl J Med, 2001, 344(22): 1659-1667.

备注/Memo

备注/Memo:
收稿日期:2005-01-19.基金项目:国家自然科学基金(No.30400177)
更新日期/Last Update: 2010-01-05