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Department of Molecular Biosciences, University of Kansas, Lawrence, Kansas 66045
We reported previously that the thromboxane A2 (TxA2) mimetic U-46619 stimulates cardiac vagal afferent nerves, eliciting a reflex decrease in heart rate (HR) and arterial blood pressure (ABP). The present experiments were designed to test the hypothesis that TxA2 evokes these changes via the release of serotonin [5-hydroxytryptamine (5-HT)] and activation of the 5-HT3 receptor. Injections of the 5-HT3 antagonist tropisetron (1 mg of 3-tropanyl-indole-3-carboxylate or ICS-205-930) attenuated the decreases in HR and ABP induced by left atrial injections of U-46619 (20 µg). Tropisetron administration also eliminated the U-46619-induced increase in impulse frequency in a majority of cardiac, vagal afferent units tested. Measurement of serum 5-HT levels revealed an elevation in serum 5-HT levels after U-46619 injection in those rabbits that displayed a significant HR change following injection of U-46619. These results indicate that although other factors may also contribute to these reflex responses, the release of 5-HT and stimulation of the 5-HT3 receptor plays a significant role in coronary reflexes induced by TxA2.
U-46619; tropisetron; pheylbiguanide; vagal afferent units; anesthetized rabbit
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