Key result
Oxfenicine reduced fatty acid oxidation and improved mechanical function in ischemic swine hearts, increasing left ventricular systolic pressure by 36% compared with placebo.
Why the study?
Does oxfenicine improve mechanical function and reduce fatty acid metabolism in regionally ischemic swine hearts?
Does oxfenicine improve mechanical function and reduce fatty acid metabolism in regionally ischemic swine hearts?
Answers are grounded in this paper and cite their sources.
Reducing fatty acid metabolism with oxfenicine improves mechanical function in regionally ischemic swine hearts.
Fatty acids in excess impair mechanical function and electrical stability in ischemic hearts. The purpose of the present studies was to test whether oxfenicine, an agent capable of reducing fatty acid metabolism, can prevent these consequences and in so doing improve hemodynamic performance. Two groups of working swine hearts (n = 15), extracorporeally perfused with whole blood, were compared over 90 min of controlled coronary perfusion. An emulsion of triacylglycerols (Intralipid) with heparin were administered systemically to augment serum fatty acids threefold (0.30 to 0.92 mumol/ml). Labeled [U14C]palmitate was administered selectively into the left anterior descending coronary circulation to follow fatty acid oxidation. Coronary flow in this bed was decreased by 50% over the final 30 min of perfusion. Saline (n = 7) or oxfenicine (17-33 mg/kg, n = 8) was administered to placebo or treated animals at 30 min perfusion. 14CO2 production from labeled palmitate was decreased by 55% (P less than 0.025) at normal flows in oxfenicine-treated hearts and was reduced further during ischemia. Tissue levels of acyl carnitine were significantly reduced and acetyl CoA levels significantly increased in oxfenicine-treated hearts both in aerobic and ischemic myocardium. These changes were associated with an improvement in mechanical function. Left ventricular systolic and developed pressures and maximum left ventricular dP/dt were increased by 36 delta %, P less than 0.01; 46 delta %, P less than 0.025; and 41 delta %, P less than 0.025, respectively, at end ischemia as compared with placebo hearts.(ABSTRACT TRUNCATED AT 250 WORDS)
No takes yet. Share an insight, caveat, or question.
Liedtke et al. (1984) studied Regionally ischemic hearts (n=15). Oxfenicine vs. Saline was evaluated on Left ventricular systolic pressure at end ischemia (36 delta % increase, p=<0.01). Oxfenicine reduced fatty acid oxidation and improved mechanical function in ischemic swine hearts, increasing left ventricular systolic pressure by 36% compared with placebo.
Synapse has enriched 10 related papers. Consider them for comparative context: