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Serotonin pp 283–288Cite as

5-Hydroxytryptamine (5-HT) Receptor Subtypes in Invertebrates

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Abstract

The pharmacological profiles of the 5-hydroxytryptamine (5-HT) receptors on Helix central neurones, Helix heart muscle and Helix pharyngeal retractor muscle (PRM) have been investigated. 5-Carboxyamidotryptamine proved a potent agonist at all sites, producing responses which were very similar to those of 5-HT. In general tryptamine analogues were active while non-tryptamine compounds possessed little or no 5-HT-like activity. A range of 5-HT antagonists were also tested against the excitatory responses of Helix neurones to 5-HT and acetylcholine. Cinanserin, tryptamine and ketanserin were selective antagonists against 5-HT compared to acetylcholine while cyanopindolol, bopindolol and pindolol showed no selectivity to 5-HT. The 5-HT agonist, MK 212, selectively blocked 5-HT in preference to acetylcholine excitation and dopamine inhibition while RU 24969 and RU 28253 showed blocking selectivity towards dopamine compared with 5-HT. It is concluded that the 5-HT receptors studied here cannot easily be identified in terms of the vertebrate classification into 5-HT-1,2 and 3 subtypes based on agonist and antagonist profiles.

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References

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© 1990 Kluwer Academic Publishers

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Walker, R.J., Vehovszky, A. (1990). 5-Hydroxytryptamine (5-HT) Receptor Subtypes in Invertebrates. In: Paoletti, R., Vanhoutte, P.M., Brunello, N., Maggi, F.M. (eds) Serotonin. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-1912-9_36

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  • DOI: https://doi.org/10.1007/978-94-009-1912-9_36

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-7353-0

  • Online ISBN: 978-94-009-1912-9

  • eBook Packages: Springer Book Archive

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