Differential mechanisms involved in the effect of nicotinic agonists DMPP and lobeline to release [3H]5-HT from rat hippocampal slices

Neuropharmacology. 1996;35(12):1769-77. doi: 10.1016/s0028-3908(96)00115-3.

Abstract

In the present study we investigated the effect of different nicotinic agonists (dimethylphenyl-piperazinium-iodide (DMPP), (-)nicotine, cytisine, (-)-lobeline, and (-)epibatidine) and antagonists (mecamylamine and dihydro-beta-erythroidine) on the release of [3H]5-HT from hippocampal slices. The nicotinic agonists DMPP and lobeline and electrical field stimulation, released [3H]5-HT from the hippocampus; other nicotinic agonists, such as (-)-nicotine, cytisine, and (-)-epibatidine had no effect. Unlike lobeline-induced release of [3H]5-HT, the effect of DMPP (10 and 40 microM) was antagonized by mecamylamine (20 and 10 microM). The effect of DMPP was [Ca2+]o-independent. In experiments carried out at 7 degrees C, i.e. the membrane carrier proteins are inhibited and the release by lobeline was abolished while the DMPP-induced release of 5-HT was rather potentiated. It is proposed that the effect of DMPP and lobeline, to enhance the release of [3H]5-HT from the hippocampus, was mediated by two different mechanisms. While DMPP-induced 5-HT release can be linked to a non-classical nAChR activation ([Ca2+]o-independence), the effect of lobeline was likely mediated by uptake carriers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids / pharmacology
  • Animals
  • Azocines
  • Bridged Bicyclo Compounds, Heterocyclic / pharmacology
  • Calcium / metabolism
  • Dimethylphenylpiperazinium Iodide / pharmacology*
  • Electric Stimulation
  • Hippocampus / drug effects
  • Hippocampus / physiology*
  • In Vitro Techniques
  • Kinetics
  • Lobeline / pharmacology*
  • Male
  • Mecamylamine / pharmacology
  • Nicotine / pharmacology
  • Nicotinic Agonists / pharmacology*
  • Pyridines / pharmacology
  • Quinolizines
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Nicotinic / physiology
  • Serotonin / metabolism*
  • Tritium
  • Tubocurarine / pharmacology

Substances

  • Alkaloids
  • Azocines
  • Bridged Bicyclo Compounds, Heterocyclic
  • Nicotinic Agonists
  • Pyridines
  • Quinolizines
  • Receptors, Nicotinic
  • Tritium
  • Serotonin
  • cytisine
  • Dimethylphenylpiperazinium Iodide
  • Mecamylamine
  • Nicotine
  • Lobeline
  • epibatidine
  • Calcium
  • Tubocurarine