Regulation of Rostral Nucleus of the Solitary Tract Responses to Afferent Input by A-type K+ Current

• Published in: Neuroscience 2022-07, Vol.495, p.115-125
• Main Authors: Chen, Z., Terman, D.H., Travers, S.P., Travers, J.B.
• Format: Article
• Language: English
• Subjects: Animals; dynamic clamp; Electric Stimulation; GABAergic Neurons; gamma-Aminobutyric Acid - pharmacology; inhibition; Mice; patch clamp; Patch-Clamp Techniques; Solitary Nucleus; taste; Taste - physiology
• ISSN: 0306-4522; 1873-7544; 1873-7544
• DOI: 10.1016/j.neuroscience.2022.05.036

•IA K+ currents suppress the response of rNST neurons to afferent stimulation.•GABAergic inhibition also suppresses afferent-induced responses.•GABAergic inhibition and IA appear to operate independently. Responses in the rostral (gustatory) nucleus of the solitary tract (rNST) are modified by synaptic interactions within the nucleus and the constitutive membrane properties of the neurons themselves. The potassium current IA is one potential source of modulation. In the caudal NST, projection neurons with IA show lower fidelity to afferent stimulation compared to cells without. We explored the role of an A-type K+ current (IA) in modulating the response to afferent stimulation and GABA-mediated inhibition in the rNST using whole cell patch clamp recording in transgenic mice that expressed channelrhodopsin (ChR2 H134R) in GABAergic neurons. The presence of IA was determined in current clamp and the response to electrical stimulation of afferent fibers in the solitary tract was assessed before and after treatment with the specific Kv4 channel blocker AmmTX3. Blocking IA significantly increased the response to afferent stimulation by 53%. Using dynamic clamp to create a synthetic IA conductance, we demonstrated a significant 14% decrease in responsiveness to afferent stimulation in cells lacking IA. Because IA reduced excitability and is hyperpolarization-sensitive, we examined whether IA contributed to the inhibition resulting from optogenetic release of GABA. Although blocking IA decreased the percent suppression induced by GABA, this effect was attributable to the increased responsiveness resulting from AmmTX3, not to a change in the absolute magnitude of suppression. We conclude that rNST responses to afferent input are regulated independently by IA and GABA.