The Metal Chelators, Trientine and Citrate, Inhibit the Development of Cardiac Pathology in the Zucker Diabetic Rat

被引:29
作者
Baynes, John W. [2 ]
Murray, David B. [1 ,3 ]
机构
[1] Univ S Carolina, Dept Cell & Dev Biol & Anat, Columbia, SC 29208 USA
[2] Univ S Carolina, Dept Exercise Sci, Columbia, SC 29208 USA
[3] Univ Mississippi, Dept Pharmacol, University, MS 38677 USA
关键词
LEFT-VENTRICULAR HYPERTROPHY; ADVANCED GLYCATION ENDPRODUCTS; OXIDATIVE STRESS; CARDIOVASCULAR-DISEASE; AGE-BREAKERS; END-PRODUCTS; IN-VITRO; COMPLICATIONS; RECEPTOR; COPPER;
D O I
10.1155/2009/696378
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose. The objective of this study was to determine the efficacy of dietary supplementation with the metal chelators, trientine or citric acid, in preventing the development of cardiomyopathy in the Zucker diabetic rat. Hypothesis. We hypothesized that dietary chelators would attenuate metal-catalyzed oxidative stress and damage in tissues and protect against pathological changes in ventricular structure and function in type II diabetes. Methods. Animals (10 weeks old) included lean control (LC, fa/+), untreated Zucker diabetic fatty (ZDF, fa/fa), and ZDF rats treated with either trientine (triethylenetetramine) or citrate at 20 mg/d in drinking water, starting when rats were frankly diabetic. Cardiac functional assessment was determined using a Millar pressure/volume catheter placed in the left ventricle at 32 weeks of age. Results. End diastolic volume for the ZDF animals increased by 36% indicating LV dilatation (P < .05) and was accompanied by a 30% increase in the end diastolic pressure (P <= .05). Both trientine and citric acid prevented the increases in EDV and EDP (P < .05). Ejection fraction and myocardial relaxation were also significantly improved with chelator treatment. Conclusion. Dietary supplementation with trientine and citric acid significantly prevented structural and functional changes in the diabetic heart, supporting the merits of mild chelators for prevention of cardiovascular disease in diabetes. Copyright (c) 2009 J. W. Baynes and D. B. Murray.
引用
收藏
页数:6
相关论文
共 38 条
  • [1] Role of oxidative stress in diabetic complications - A new perspective on an old paradigm
    Baynes, JW
    Thorpe, SR
    [J]. DIABETES, 1999, 48 (01) : 1 - 9
  • [2] Glycoxidation and lipoxidation in atherogenesis
    Baynes, JW
    Thorpe, SR
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (12) : 1708 - 1716
  • [3] Understanding RAGE, the receptor for advanced glycation end products
    Bierhaus, A
    Humpert, PM
    Morcos, M
    Wendt, T
    Chavakis, T
    Arnold, B
    Stern, DM
    Nawroth, PP
    [J]. JOURNAL OF MOLECULAR MEDICINE-JMM, 2005, 83 (11): : 876 - 886
  • [4] Effects of an extracellular metal chelator on neurovascular function in diabetic rats
    Cameron, NE
    Cotter, MA
    [J]. DIABETOLOGIA, 2001, 44 (05) : 621 - 628
  • [5] Serum ferritin levels in poorly- and well-controlled diabetes mellitus
    Canturk, Z
    Çetinarslan, B
    Tarkun, I
    Canturk, NZ
    [J]. ENDOCRINE RESEARCH, 2003, 29 (03) : 299 - 306
  • [6] Concentric versus eccentric remodeling
    Carabello, BA
    [J]. JOURNAL OF CARDIAC FAILURE, 2002, 8 (06) : S258 - S263
  • [7] Effect of antioxidant treatment of streptozotocin-induced diabetic rats on endoneurial blood flow, motor nerve conduction velocity, and vascular reactivity of epineurial arterioles of the sciatic nerve
    Coppey, LJ
    Gellett, JS
    Davidson, EP
    Dunlap, JA
    Lund, DD
    Yorek, MA
    [J]. DIABETES, 2001, 50 (08) : 1927 - 1937
  • [8] The epidemiology of left ventricular hypertrophy in type 2 diabetes mellitus
    Dawson, A
    Morris, AD
    Struthers, AD
    [J]. DIABETOLOGIA, 2005, 48 (10) : 1971 - 1979
  • [9] Fridlyand LE, 2006, CURR DIABETES REV, V2, P241, DOI 10.2174/157339906776818541
  • [10] Galaris D, 2008, CRIT REV CL LAB SCI, V45, P1, DOI [10.1080/10408360701713104, 10.1080/10408360701713104 ]