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Serotonin Receptor Heterogeneity and the Role of Potassium Channels in Neuronal Excitability

  • J. S. Kelly
  • P. Larkman
  • N. J. Penington
  • D. G. Rainnie
  • H. McAllister-Williams
  • J. Hodgkiss
Part of the Advances in Experimental Medicine and Biology book series (AEMB, volume 287)

Summary

Intracellular recordings in vitro from a variety of central neuronal types have shown both inhibition and excitation to be modulatory consequences of serotonin (5-HT) receptor activation. These responses can be seen in isolation or in some cases (e.g. hippocampal pyramidal cells) as a complex biphasic combination of hyperpolarisation followed by depolarisation, suggesting overall control of neuronal excitability may be dependent on the interaction between activation of more than one postsynaptic receptor and/or mechanism. Our studies have confirmed the 5-HT evoked depolarisation of rat facial motorneurones (FM’s) and the hyperpolarisation seen in presumed serotonergic neurones of the dorsal raphe nucleus (DRN) to be the result of opposite effects on K+ ion permeability. Suppression of a resting K+ conductance leads to depolarisation while activation leads to hyperpolarisation. The same mechanisms appear to be responsible for the 5-HT evoked responses in hippocampal pyramidal cells but in addition there is also a suppression of a Ca++ dependent K+ conductance responsible for the long spike after hyperpolarisation (AHP) . Data from the hippocampus and DRN indicate the 5-HT induced hyperpolarisation to be sensitive to Pertussis Toxin (PTX) and irreversibly mimicked by GTPγS, a non-hydrolysable analogue of GTP, suggesting the involvement of a G protein in K+ channel activation. The mechanism of K+ channel closure is less clear as it is unaffected by PTX or activation of adenylate cyclase, however there is indirect evidence that the phosphoinositide pathway may be involved from the cloned 5-HT1c receptor which also closes a K+ channel in cell lines. The results show that hyperpolarisation evoked by 5-HT in the hippocampus and DRN to be mimicked and blocked by 5-HT1A agonists and antagonists. However, the depolarisations in the hippocampus and FM’s are mediated by site-dependent receptors with profiles which do not fit into the current 5-HT receptor subtype classification.

Keywords

Reversal Potential Dorsal Raphe Nucleus Potassium Conductance Hippocampal Pyramidal Cell Lateral Septal Nucleus 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Plenum Press, New York 1991

Authors and Affiliations

  • J. S. Kelly
    • 1
  • P. Larkman
    • 1
  • N. J. Penington
    • 1
  • D. G. Rainnie
    • 1
  • H. McAllister-Williams
    • 1
  • J. Hodgkiss
    • 1
  1. 1.Department of PharmacologyEdinburgh UniversityEdinburghUK

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