Abstract

The effect of prazosin, an α 1-selective adrenoceptor antagonist, on the hydrogen peroxide (H 2O 2)-induced mechanical and metabolic derangements was studied in the isolated rat heart, which was perfused aerobically by the Langendorffs technique at a constant flow rate and driven electrically. H 2O 2 (600 μM) produced both mechanical dysfunction ( e.g., increase in the left ventricular end-diastolic pressure) and metabolic damage ( e.g., decrease in the level of adenosine triphosphate) associated with lipid peroxidation ( e.g., increase in the level of malondialdehyde). The H 2O 2-induced mechanical and metabolic derangements were attenuated by 2.5, 5, or 10 μM prazosin, and the increase in the level of malondialdehyde was attenuated by 5 or 10 μM prazosin. Nevertheless, prazosin had practically no effects on the mechanical function and energy metabolism of the H 2O 2-untreated normal heart at 2.5 or 5 μM, although it reduced the mechanical function at 10 μM. Prazosin was shown to have a hydroxyl radical scavenging effect. These results suggest that prazosin attenuates the H 2O 2-induced mechanical and metabolic derangements probably because of attenuation of the H 2O 2-induced lipid peroxidation in the heart.

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