Excitatory action of 5-HT on deglutitive substrates in the rat solitary complex.

The excitatory effect of serotonin (5-HT) on the pharyngeal stage of swallowing was investigated in urethane anaesthetised rats with respect to the involvement of neural substrates located in the central and intermediolateral regions of the nucleus tractus solitarii (NTS). Micropneumophoretic ejection of 5-HT 5-50 pmol either produced deglutitory responses or selectively facilitated the S-glutamate-evoked pharyngeal responses when applied in 1-10 pmol prepulses. The excitatory/facilitatory effect of 5-HT was enhanced by intravenous threshold doses of the 5-HT-mimetic, quipazine (0.3-1 mumol/kg) and reversibly blocked by the 5-HT2-receptor antagonists, methysergide, metergoline and ketanserin. 5-HT doses exceeding 10-60 pmol gave rise to a non-selective reversible inhibition of glutamate- and acetylcholine (ACh)-evoked pharyngeal or oesophageal responses which was not prevented or reversed by 5-HT2-receptor antagonists, but was readily overcome by increasing the amount of glutamate or ACh ejected. Non-selective deglutitive inhibition after high doses of 5-HT could, therefore, result from neuronal desensitization secondary to excessive stimulation or activation of a different type of 5-HT receptor. These results corroborate an excitatory role of 5-HT in both reflex and automatic swallowing and demonstrate that the NTS is a major site of serotoninergic facilitation of swallowing.