Literature DB >> 1613827

Tumor necrosis factor and cardiac function.

J E DeMeules1, F A Pigula, M Mueller, S J Raymond, R L Gamelli.   

Abstract

The direct effect of tumor necrosis factor (TNF), a product of activated macrophages, on myocardial performance was determined using an isolated papillary muscle technique and a modified Langendorff preparation. Papillary muscle was obtained from male adult rats 4-5 hours after they received either 100 ng/kg TNF (group A), or 100 micrograms/kg TNF (group B) or saline (control). Group B animals exhibited significantly greater peak tension development and velocity of contraction compared with controls (p less than 0.05). In group A animals these variables were not significantly different from those of the controls (p greater than 0.05). Electrophysiologic measurements revealed a significant decrease in resting membrane potential in both group A and group B animals compared with the controls (p less than 0.05). Whole hearts perfused with serum from animals treated with TNF 18-22 hours earlier exhibited significant impairment of contractility, decreased rate of systolic pressure development, and decreased rate of relaxation compared with the controls (p less than 0.05). Coronary flow and myocardial water content were similar for both groups of perfused hearts. These data suggest that tumor necrosis factor stimulates an early beneficial effect on myocardial function, which 18-22 hours later is associated with impairment of myocardial performance. This effect appears to be serum transferable.

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Year:  1992        PMID: 1613827     DOI: 10.1097/00005373-199206000-00003

Source DB:  PubMed          Journal:  J Trauma        ISSN: 0022-5282


  9 in total

Review 1.  Myocardial microvascular permeability, interstitial oedema, and compromised cardiac function.

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2.  Shedding kinetics of soluble tumor necrosis factor (TNF) receptors after systemic TNF leaking during isolated limb perfusion. Relevance to the pathophysiology of septic shock.

Authors:  D Aderka; P Sorkine; S Abu-Abid; D Lev; A Setton; A P Cope; D Wallach; J Klausner
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3.  Subchronic exposure of cardiomyocytes to low concentrations of tumor necrosis factor alpha attenuates the positive inotropic response not only to catecholamines but also to cardiac glycosides and high calcium concentrations.

Authors:  P Boekstegers; I Kainz; W Giehrl; W Peter; K Werdan
Journal:  Mol Cell Biochem       Date:  1996-03-23       Impact factor: 3.396

4.  Haemodynamic effects of endothelin receptor antagonist, tezosentan, in tumour necrosis factor-alpha treated anaesthetized rats.

Authors:  Reza Tabrizchi; Carol Ann Ford
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2003-01-18       Impact factor: 3.000

Review 5.  Elucidating molecular mechanisms of septic cardiomyopathy--the cardiomyocyte model.

Authors:  K Werdan; U Müller-Werdan
Journal:  Mol Cell Biochem       Date:  1996 Oct-Nov       Impact factor: 3.842

6.  The role of tumor necrosis factor and nitric oxide in the acute cardiovascular response to endotoxin.

Authors:  T J Fahey; T Yoshioka; G T Shires; G A Fantini
Journal:  Ann Surg       Date:  1996-01       Impact factor: 12.969

7.  Origin and health impacts of emissions of toxic by-products and fine particles from combustion and thermal treatment of hazardous wastes and materials.

Authors:  Stephania A Cormier; Slawo Lomnicki; Wayne Backes; Barry Dellinger
Journal:  Environ Health Perspect       Date:  2006-06       Impact factor: 9.031

Review 8.  Potential role of ultrafine particles in associations between airborne particle mass and cardiovascular health.

Authors:  Ralph J Delfino; Constantinos Sioutas; Shaista Malik
Journal:  Environ Health Perspect       Date:  2005-08       Impact factor: 9.031

Review 9.  Clinical review: Myocardial depression in sepsis and septic shock.

Authors:  Olivier Court; Aseem Kumar; Joseph E Parrillo; Anand Kumar
Journal:  Crit Care       Date:  2002-09-12       Impact factor: 9.097

  9 in total

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