科研之友
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摘要
Adenosine and dopamine (DA) act as neurotransmitters or neuromodulators at the carotid body (CB) chemosensory synapse, but their mechanisms of action are not fully understood. Using a functional co-culture model of rat CB chemoreceptor (type I) cell clusters and juxtaposed afferent petrosal neurons (PNs), we tested the hypothesis that adenosine and DA act postsynaptically to modulate a hyperpolarization-activated, cyclic nucleotide-gated (HCN) cation current (I-h). In whole-cell recordings from hypoxia-responsive PNs, cAMP mimetics enhanced I-h whereas the HCN blocker ZD7288 (2 mu m) reversibly inhibited I-h. Adenosine caused a potentiation of I-h (EC50 similar to 35 nm) that was sensitive to the A2a blocker SCH58261 (5 nm), and an similar to 16mV depolarizing shift in V-1/2 for voltage dependence of I-h activation. By contrast, DA (10 mu m) caused an inhibition of I-h that was sensitive to the D2 blocker sulpiride (1-10 mu m), and an similar to 11mV hyperpolarizing shift in V-1/2. Sulpiride potentiated I-h in neurons adjacent to, but not distant from, type I cell clusters. DA also decreased PN action potential frequency whereas adenosine had the opposite effect. During simultaneous paired recordings, SCH58261 inhibited both the presynaptic hypoxia-induced receptor potential in type I cells and the postsynaptic PN response. By contrast, SCH58261 inhibited only the postsynaptic PN response induced by isohydric hypercapnia. Confocal immunofluorescence confirmed the localization of HCN4 subunits in tyrosine hydroxylase-positive chemoafferent neurons in tissue sections of rat petrosal ganglia. These data suggest that adenosine and DA, acting through A2a and D2 receptors respectively, regulate PN excitability via their opposing actions on I-h.
- 出版日期2018-8-1
