Albumin resuscitation increases cardiomyocyte contractility and decreases nitric oxide synthase II expression in rat endotoxemia*
- 1 January 2003
- journal article
- research article
- Published by Wolters Kluwer Health in Critical Care Medicine
- Vol. 31 (1) , 187-194
- https://doi.org/10.1097/00003246-200301000-00029
Abstract
Hypotension and hypoperfusion during septic shock may contribute to tissue hypoxia and the intramyocardial inflammatory response that results in myocardial dysfunction. Therefore, we hypothesized that crystalloid or colloid resuscitation may alter myocardial dysfunction. Randomized, controlled, prospective animal study. University animal laboratory. Sprague-Dawley rats (250-300 g, n = 6/group). Rats received an intraperitoneal injection of 10 mg/kg lipopolysaccharide or control. One hour later, rats were randomized to intravenous resuscitation and received either 30 mL/kg normal saline, 10 mL/kg 10% pentastarch, 10 mL/kg 5% rat albumin, or no volume. We measured fractional shortening of cardiomyocytes isolated 5 hrs after lipopolysaccharide or control injection. In separate identical experiments, we measured myocardial interleukin-6, macrophage inhibitory protein-2, and nitric oxide synthase II protein and messenger RNA expression. Control fractional shortening of 24.1 +/- 2.2% was decreased by lipopolysaccharide to 18.8 +/- 1.2% (p <.001). Volume resuscitation after lipopolysaccharide significantly improved fractional shortening (p <.001). In particular, albumin resuscitation increased fractional shortening to 23.5 +/- 0.9%, which was more than either saline (fractional shortening 20.1 +/- 1.7%,p <.01) or pentastarch (fractional shortening 21.4 +/- 0.9%,p <.01). Myocardial macrophage inhibitory protein-2 protein and interleukin-6 and macrophage inhibitory protein-2 messenger RNA expression and neutrophil content were elevated following lipopolysaccharide (p <.05) but were not altered by volume resuscitation. Myocardial nitric oxide synthase II protein and messenger RNA expression increased following lipopolysaccharide (p <.01) and decreased with albumin resuscitation. We conclude that following lipopolysaccharide injection, volume resuscitation improves cardiomyocyte fractional shortening. Albumin resuscitation is particularly beneficial in preventing reduced cardiomyocyte contractility, and this benefit may be related to an albumin-induced reduction in nitric oxide synthase II protein and messenger RNA expression following endotoxin injection.Keywords
This publication has 36 references indexed in Scilit:
- MYOCARDIAL DYSFUNCTION IN SEPTIC SHOCKCritical Care Clinics, 2000
- Contraction-induced injury to single muscle fibers: velocity of stretch does not influence the force deficit.American Journal of Physiology-Cell Physiology, 1998
- l-2-Oxothiazolidine-4-Carboxylic Acid Prevents Endotoxin-induced Cardiac DysfunctionAmerican Journal of Respiratory and Critical Care Medicine, 1998
- Leukocytes and decreased left-ventricular contractility during endotoxemia in rabbits.American Journal of Respiratory and Critical Care Medicine, 1997
- Tumor necrosis factor alpha and interleukin 1beta are responsible for in vitro myocardial cell depression induced by human septic shock serum.The Journal of Experimental Medicine, 1996
- Anti-tumor necrosis factor-alpha prevents decreased ventricular contractility in endotoxemic pigs.American Journal of Respiratory and Critical Care Medicine, 1995
- The role of nitric oxide in cardiac depression induced by interleukin‐1β and tumour necrosis factor‐αBritish Journal of Pharmacology, 1995
- A circulating myocardial depressant substance in humans with septic shock. Septic shock patients with a reduced ejection fraction have a circulating factor that depresses in vitro myocardial cell performance.Journal of Clinical Investigation, 1985
- Profound but Reversible Myocardial Depression in Patients with Septic ShockAnnals of Internal Medicine, 1984
- Spectrum of cardiovascular function during gram-negative sepsisProgress in Cardiovascular Diseases, 1981