Modulation of 5‐hydroxytryptamine‐induced head‐twitch response by drugs acting at GABA and related receptors

Abstract

The effects of drugs acting at the γ‐aminobutyric acid (GABA) receptors and other chloride ionophore‐related sites have been studied for their ability to modulate the head‐twitch induced by 1–5‐hydroxytryptophan (5‐HTP) in the mouse. The GABAa receptor agonists, muscimol, imidazoleacetic acid and 3‐aminopropanesulphonic acid, produced a dose‐related potentiation, while bicuculline inhibited the head‐twitch. The GABAb receptor agonist, baclofen, produced dose‐related inhibition. Diazepam potentiated the head‐twitch while the ‘inverse’ benzodiazepine receptor agonist ethyl‐β‐carboline‐3‐carboxylate inhibited the head‐twitch. The antagonist Ro15‐1788 also produced inhibition. Ro05‐4864, a ligand for the benzodiazepine ‘acceptor’ site, potentiated the head‐twitch. Pentobarbitone and pentylenetetrazol potentiated the 5‐HTP‐induced head‐twitch at low doses, changing to inhibition as the dose was increased. Picrotoxin in subconvulsant doses, produced only potentiation. More than one site may be involved in the action of these substances. GABA, amino‐oxyacetic acid and 1–2‐4‐diaminobutyric acid inhibited the head‐twitch, while the GABA‐depletor, 3‐mercaptopropionic acid potentiated it. Of all the agents tested, only muscimol produced head‐twitching when given alone. It was concluded that both GABAa and GABAb receptors modulate the head‐twitch response to 5‐HTP. 1985 British Pharmacological Society