Skip to main content
British Journal of Pharmacology logoLink to British Journal of Pharmacology
. 1998 Nov;125(6):1361–1367. doi: 10.1038/sj.bjp.0702206

A microdialysis study of the in vivo release of 5-HT in the median raphe nucleus of the rat

Albert Adell 1,*, Francesc Artigas 1
PMCID: PMC1565710  PMID: 9863668

Abstract

  1. The present study has examined several characteristics of the release of 5-HT in the median raphe nucleus in terms of its dependence of nerve impulse, provenance of a vesicular storage fraction as well as the regulatory role played by 5-HT1A receptors.

  2. Tetrodotoxin (1 μM) and reserpine (5 mg kg−1, i.p.) virtually suppressed the output of 5-HT.

  3. The administration of EEDQ (10 mg kg−1, i.p.) did not alter the basal release of 5-HT but abolished the reduction of 5-HT release induced by 8-OH-DPAT (0.1 mg kg−1, s.c.).

  4. The perfusion of 1–100 μM of 8-OH-DPAT or the novel 5-HT1A agonist BAY×3702 decreased the efflux of 5-HT, whereas the perfusion of the 5-HT1A antagonist WAY-100635 failed to alter 5-HT release.

  5. The decrease in dialysate 5-HT induced by 100 μM 8-OH-DPAT was reversed by the concurrent perfusion of 100 μM WAY-100635. Also, the perfusion of 100 μM WAY-100635 for 2 h inhibited partly the reduction of 5-HT release evoked by the systemic administration of 8-OH-DPAT (0.1 mg kg−1).

  6. These results indicate that extracellular 5-HT in the median raphe nucleus is stored in vesicles and released in an impulse-dependent manner. Also, the basal release of 5-HT in the median raphe nucleus does not appear to be under the tonic control of somatodendritic 5-HT1A receptors by endogenous 5-HT. Instead, this feedback mechanism seems to be triggered when an excess of the transmitter or a 5-HT1A agonist is present in the extracellular space of the median raphe nucleus.

Keywords: 5-HT, 5-HT1A receptors, reserpine, TTX, EEDQ, 8-OH-DPAT, BAY×3702, WAY-100635, median raphe nucleus, microdialysis

Full Text

The Full Text of this article is available as a PDF (305.8 KB).


Articles from British Journal of Pharmacology are provided here courtesy of The British Pharmacological Society

RESOURCES