Central Role for the Cardiotonic Steroid Marinobufagenin in the Pathogenesis of Experimental Uremic Cardiomyopathy

Patients with chronic renal failure develop a “uremic” cardiomyopathy characterized by diastolic dysfunction, cardiac hypertrophy, and systemic oxidant stress. Patients with chronic renal failure are also known to have increases in the circulating concentrations of the cardiotonic steroid marinobufagenin (MBG). On this background, we hypothesized that elevations in circulating MBG may be involved in the cardiomyopathy. First, we observed that administration of MBG (10 &mgr;g/kg per day) for 4 weeks caused comparable increases in plasma MBG as partial nephrectomy at 4 weeks. MBG infusion caused increases in conscious blood pressure, cardiac weight, and the time constant for left ventricular relaxation similar to partial nephrectomy. Decreases in the expression of the cardiac sarcoplasmic reticulum ATPase, cardiac fibrosis, and systemic oxidant stress were observed with both MBG infusion and partial nephrectomy. Next, rats were actively immunized against a MBG-BSA conjugate or BSA control, and partial nephrectomy was subsequently performed. Immunization against MBG attenuated the cardiac hypertrophy, impairment of diastolic function, cardiac fibrosis, and systemic oxidant stress seen with partial nephrectomy without a significant effect on conscious blood pressure. These data suggest that the increased concentrations of MBG are important in the cardiac disease and oxidant stress state seen with renal failure.

[1]  J. Himmelfarb,et al.  Plasma aminothiol oxidation in chronic hemodialysis patients. , 2002, Kidney international.

[2]  R. Foley,et al.  Left ventricular hypertrophy in the renal patient. , 2001, Journal of the American Society of Nephrology : JASN.

[3]  Chi Han,et al.  Effect of green tea extract on cardiac hypertrophy following 5/6 nephrectomy in the rat. , 2003, Kidney international.

[4]  H. Masaki,et al.  A novel endogenous digitalis, telocinobufagin, exhibits elevated plasma levels in patients with terminal renal failure. , 2005, Clinical biochemistry.

[5]  B. Pitt Effectiveness of spironolactone added to an angiotensin-converting enzyme inhibitor and a loop diuretic for severe chronic congestive heart failure (the Randomized Aldactone Evaluation Study [RALES]). , 1996, The American journal of cardiology.

[6]  L. Bouter,et al.  Mild renal insufficiency is associated with increased cardiovascular mortality: The Hoorn Study. , 2002, Kidney international.

[7]  N. Bricker On the pathogenesis of the uremic state--an exposition of the trade-off hypothesis. , 1972, Nihon Jinzo Gakkai shi.

[8]  A. Askari,et al.  Involvement of Src and epidermal growth factor receptor in the signal-transducing function of Na+/K+-ATPase. , 2000, The Journal of biological chemistry.

[9]  W. Border,et al.  Transforming growth factor beta in tissue fibrosis. , 1994, The New England journal of medicine.

[10]  J. Willey,et al.  Effect of chronic renal failure on cardiac contractile function, calcium cycling, and gene expression of proteins important for calcium homeostasis in the rat. , 2003, Journal of the American Society of Nephrology : JASN.

[11]  P. Douglas,et al.  Serial echocardiographic assessment of left ventricular geometry and function after large myocardial infarction in the rat. , 1994, Circulation.

[12]  H. D. de Wardener Franz Volhard Lecture 1996. Sodium transport inhibitors and hypertension. , 1996, Journal of hypertension. Supplement : official journal of the International Society of Hypertension.

[13]  E. Lakatta,et al.  Brain ouabain stimulates peripheral marinobufagenin via angiotensin II signalling in NaCl-loaded Dahl-S rats , 2005, Journal of hypertension.

[14]  Jiang Tian,et al.  Ouabain interaction with cardiac Na+/K+-ATPase initiates signal cascades independent of changes in intracellular Na+ and Ca2+ concentrations. , 2000, The Journal of biological chemistry.

[15]  E. Zvartau,et al.  Involvement of endogenous digitalis-like factors in voluntary selection of alcohol by rats. , 1999, Life sciences.

[16]  B. Kahn,et al.  Multiple Signal Transduction Pathways Link Na+/K+-ATPase to Growth-related Genes in Cardiac Myocytes , 1998, The Journal of Biological Chemistry.

[17]  O. Fedorova,et al.  Plasma marinobufagenin-like and ouabain-like immunoreactivity in adrenocorticotropin-treated rats. , 1998, American journal of hypertension.

[18]  Sfj Langer Differential laws of left ventricular isovolumic pressure fall. , 2002, Physiological research.

[19]  R. Foley,et al.  Congestive heart failure in renal transplant recipients: risk factors, outcomes, and relationship with ischemic heart disease. , 2002, Journal of the American Society of Nephrology : JASN.

[20]  Bertram L Kasiske,et al.  Kidney disease as a risk factor for development of cardiovascular disease: a statement from the American Heart Association Councils on Kidney in Cardiovascular Disease, High Blood Pressure Research, Clinical Cardiology, and Epidemiology and Prevention. , 2003, Circulation.

[21]  R. Buñag,et al.  Tail‐Cuff Blood Pressure Measurement without External Preheating in Awake Rats , 1982, Hypertension.

[22]  H. E. Wardener Franz Volhard Lecture 1996. Sodium transport inhibitors and hypertension. , 1996 .

[23]  C. van Hardeveld,et al.  An assay for sarcoplasmic reticulum Ca2(+)-ATPase activity in muscle homogenates. , 1990, Analytical biochemistry.

[24]  E. Lakatta,et al.  Endogenous Ligand of &agr;1 Sodium Pump, Marinobufagenin, Is a Novel Mediator of Sodium Chloride–Dependent Hypertension , 2002, Circulation.

[25]  P. Parfrey Is renal insufficiency an atherogenic state? Reflections on prevalence, incidence, and risk. , 2001, American journal of kidney diseases : the official journal of the National Kidney Foundation.

[26]  J. Himmelfarb,et al.  Plasma protein thiol oxidation and carbonyl formation in chronic renal failure. , 2000, Kidney international.

[27]  A. Pinaev,et al.  Effects of two endogenous Na+,K(+)-ATPase inhibitors, marinobufagenin and ouabain, on isolated rat aorta. , 1995, European journal of pharmacology.

[28]  J. Himmelfarb,et al.  Albumin is the major plasma protein target of oxidant stress in uremia. , 2001, Kidney international.

[29]  H. Li,et al.  Ouabain-induced hypertrophy in cultured cardiac myocytes is accompanied by changes in expression of several late response genes. , 1997, Journal of molecular and cellular cardiology.

[30]  G. Bianchi,et al.  Organ Hypertrophic Signaling within Caveolae Membrane Subdomains Triggered by Ouabain and Antagonized by PST 2238* , 2004, Journal of Biological Chemistry.

[31]  P. Parfrey,et al.  Risk factors for the development of left ventricular hypertrophy in a prospectively followed cohort of dialysis patients. , 1994, Journal of the American Society of Nephrology : JASN.

[32]  N S Bricker,et al.  The control of sodium excretion with normal and reduced nephron populations. The pre-eminence of third factor. , 1967, The American journal of medicine.

[33]  J. Shapiro,et al.  Intracellular Reactive Oxygen Species Mediate the Linkage of Na+/K+-ATPase to Hypertrophy and Its Marker Genes in Cardiac Myocytes* , 1999, The Journal of Biological Chemistry.

[34]  M. Young,et al.  Mineralocorticoid receptors and pathophysiological roles for aldosterone in the cardiovascular system. , 2002, Journal of hypertension.

[35]  R. Foley,et al.  Risk factors for cardiac morbidity and mortality in dialysis patients. , 1994, Current opinion in nephrology and hypertension.

[36]  T. Hostetter,et al.  Role of aldosterone in the remnant kidney model in the rat. , 1996, The Journal of clinical investigation.

[37]  A. Garg,et al.  Moderate renal insufficiency and the risk of cardiovascular mortality: results from the NHANES I. , 2002, Kidney international.

[38]  J. Shapiro,et al.  Ouabain-induced endocytosis of the plasmalemmal Na/K-ATPase in LLC-PK1 cells requires caveolin-1. , 2005, Kidney international.

[39]  W. Border,et al.  Transforming Growth Factor β in Tissue Fibrosis , 1994 .

[40]  J. Shapiro,et al.  Salt loading induces redistribution of the plasmalemmal Na/K-ATPase in proximal tubule cells. , 2005, Kidney international.

[41]  Bertram L Kasiske,et al.  Kidney disease as a risk factor for development of cardiovascular disease: a statement from the American Heart Association Councils on Kidney in Cardiovascular Disease, High Blood Pressure Research, Clinical Cardiology, and Epidemiology and Prevention. , 2003, Hypertension.

[42]  Zijian Xie,et al.  Role of caveolae in signal-transducing function of cardiac Na+/K+-ATPase. , 2003, American journal of physiology. Cell physiology.

[43]  B. Brenner,et al.  Hyperfiltration in remnant nephrons: a potentially adverse response to renal ablation. , 1981, The American journal of physiology.

[44]  O. Fedorova,et al.  Endogenous marinobufagenin-like factor in acute plasma volume expansion. , 1998, Clinical and experimental hypertension.