Role of Autoinhibitory Feedback in Cardiac Sympathetic Transmission

Abstract

The relationship between two indices of transmitter release measured simultaneously and the frequency of 4 field pulses (0.125–2 Hz) were obtained from superfused guinea pig right atria after labelling with ³H-noradrenaline. The relationships between ³H-efflux or rate responses and frequency were hyperbolic. Autoinhibitory feedback did not play a role since phentolamine (1 μM) did not alter the ³H-efflux or rate responses to 4 field pulses that gave 50–60% of the maximum rate response. In the presence of neuronal uptake block (desipramine (0.1 μM) phentolamine enhanced ³H-efflux and rate responses to 4 field pulses at all frequencies. In the absence of desipramine prolonged trains of field pulses (8–12 pulses) at low frequency (0.25 Hz) were not sufficient to activate autoinhibitory feedback. At 2 Hz phentolamine enhanced both responses at 12 field pulses. We conclude that in the right atrium autoinhibitory feedback plays little role in the modulation of transmitter release at levels of stimulation that cause 50–60% of maximum tissue response. The presence of neuronal uptake inhibition or high stimulus strengths are necessary to evoke autoinhibitory feedback.

Key Words:

• autoinhibitory feedback
• α₂-adrenoceptors
• phentolamine
• neuronal uptake
• right atrium