Am. J. Respir. Crit. Care Med., Volume 158, Number 6, December 1998, 1990-1998

Reversal of Hypocalcemia and Decreased Afterload in Sepsis
Effect on Myocardial Systolic and Diastolic Function

ATTILA KOVACS, MICHAEL R. COURTOIS, BENICO BARZILAI, IRENE E. KARL, PHILIP A. LUDBROOK, and RICHARD S. HOTCHKISS

Divisions of Cardiovascular Disease and Metabolism, Department of Medicine, and the Department of Anesthesiology, Research Unit, Washington University School of Medicine, St. Louis, Missouri

Sepsis is a major cause of death in intensive care units. Clinically, sepsis induces a number of physiologic and metabolic abnormalities, including decreased myocardial contractility and decreased plasma ionized calcium. There is debate about the proper therapy of hypocalcemia in sepsis because calcium administration may worsen cell function by causing intracellular Ca²⁺ overload. We investigated the effect of Ca²⁺ administration on myocardial systolic and diastolic function in an extensively utilized rat model of sepsis, i.e., the cecal ligation and puncture model (CLP). Approximately 24 h after CLP or sham surgery, rats were anesthetized and myocardial function assessed in vivo by a left ventricular Millar catheter and simultaneous two-dimensional guided M-mode echocardiography. Septic rats had a 28% decrease in peak left ventricular developed pressure, a 30% decrease in +dP/ dt, and a 23% decrease in dP/dt (p < 0.05). Plasma ionized Ca²⁺ was decreased in septic compared with that in sham rats: 4.9 ± 0.9 and 5.6 ± 0.01 mg/dl, respectively (p < 0.05). CaCl₂ improved both systolic and diastolic function and there was no evidence of adverse effects of Ca²⁺ even at supraphysiologic levels. Surprisingly, correction of decreased afterload in septic rats, using the pure -agonist phenylephrine, caused normalization of all indices of cardiac contractility, indicating that the presumed decrease in cardiac function was due entirely to an effect of the decreased afterload to "unload" the left ventricle. We conclude that Ca²⁺ administration is not detrimental to cardiac function in the rat CLP model. Although the rat CLP model is widely utilized and reproduces many of the clinical hallmarks of sepsis, it does not cause intrinsic myocardial depression and, therefore, it may not be an appropriate model to investigate the clinical cardiac dysfunction that occurs in patients with sepsis.

This article has been cited by other articles:

				R. N. Dickerson, L. M. Morgan, M. A. Croce, G. Minard, and R. O. Brown Treatment of Moderate to Severe Acute Hypocalcemia in Critically Ill Trauma Patients JPEN J Parenter Enteral Nutr, May 1, 2007; 31(3): 228 - 233. [Abstract] [Full Text] [PDF]

				A. D. Niederbichler, L. M. Hoesel, M. V. Westfall, H. Gao, K. R. Ipaktchi, L. Sun, F. S. Zetoune, G. L. Su, S. Arbabi, J. V. Sarma, et al. An essential role for complement C5a in the pathogenesis of septic cardiac dysfunction J. Exp. Med., January 23, 2006; 203(1): 53 - 61. [Abstract] [Full Text] [PDF]

				H. B. Suliman, K. E. Welty-Wolf, M. Carraway, L. Tatro, and C. A. Piantadosi Lipopolysaccharide induces oxidative cardiac mitochondrial damage and biogenesis Cardiovasc Res, November 1, 2004; 64(2): 279 - 288. [Abstract] [Full Text] [PDF]