Attenuation of burn-induced changes in hemodynamics and glucose metabolism by the PAF antagonist SRI 63-675

Charles Lang, Cornel Dobrescu

    Research output: Contribution to journalArticlepeer-review

    18 Scopus citations

    Abstract

    The importance of platelet-activating factor (PAF) in producing hypotension, hemoconcentration and alterations in carbohydrate metabolism following thermal injury was investigated in chronically catheterized rats. Animals were fasted overnight, anesthetized with pentobarbital, and then injected with saline or the PAF antagonist SRI 63-675 prior to a 25% body surface area scald injury. Burned animals showed a sustained 20-30 fall in mean arterial pressure that was attenuated by the PAF antagonist. Burn also produced a prolonged increased in hematocrit. Animals pretreated with SRI 63-675 showed a similar degree of polycythemia after 1 h, but thereafter hematocrit fell and was not different from sham-burned animals. Burn increased the plasma glucose (45-52%) and lactate (5-6 fold) concentrations, and tended to produce an early increase and a later decrease in the rate of glucose appearance (Ra). These metabolic changes were associated with elevated plasma levels of glucagon and catecholamines. The PAF antagonist prevented the hyperglycemia, reduced the hyperlactacidemia, and prevented the late fall of glucose Ra. Treated animals still showed increased levels of glucagon, while catecholamine concentrations were reduced by 50%. Short-term survival (4 h) was markedly improved (86 vs. 43%). These results suggest that PAF produced following thermal injury is responsible, at least in part, for the early hemodynamic changes and hemoconcentration. However, the role of PAF as a mediator of burn-induced glucose dyshomeostasis appears secondary to its hemodynamic effects.

    Original languageEnglish (US)
    Pages (from-to)207-214
    Number of pages8
    JournalEuropean Journal of Pharmacology
    Volume156
    Issue number2
    DOIs
    StatePublished - Nov 1 1988

    All Science Journal Classification (ASJC) codes

    • Pharmacology

    Fingerprint

    Dive into the research topics of 'Attenuation of burn-induced changes in hemodynamics and glucose metabolism by the PAF antagonist SRI 63-675'. Together they form a unique fingerprint.

    Cite this