Abstract
The effects of pindolol, a beta-adrenoceptor blocker/putative 5-hydroxytryptamine (5-HT)(1A/1B) antagonist, on both the single-unit activity of serotonergic neurons in the dorsal raphe nucleus (DRN) and extracellular 5-HT levels in the caudate nucleus, were examined in freely moving cats. Administration of (±)-pindolol (1 and 10 mg/kg, s.c.) decreased neuronal activity and increased 5-HT levels in a dose- and time-dependent manner. The subsequent administration of WAY-100635 {(N-[2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]-N-(2-pyridinyl)cyclohexanecarboxamide} (0.2 mg/kg, s.c.), a selective 5-HT(1A) receptor antagonist, blocked pindolol-induced neuronal suppression and potentiated 5-HT output. These results indicate that pindolol may be acting at the level of the nerve terminal to increase 5-HT. Copyright (C) 1999 Elsevier Science B.V.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 187-191 |
| Number of pages | 5 |
| Journal | European Journal of Pharmacology |
| Volume | 377 |
| Issue number | 2-3 |
| DOIs | |
| State | Published - Jul 21 1999 |
All Science Journal Classification (ASJC) codes
- Pharmacology
Keywords
- 5-HT (5-hydroxytryptamine), extracellular
- 5-HT(1A) autoreceptor
- Microdialysis
- Pindolol
- Serotonergic neuronal activity
- Serotonin
- WAY-100635
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