ACTIONS OF METHOXYLATED AMPHETAMINE HALLUCINOGENS ON SEROTONERGIC NEURONS OF THE BRAIN

Authors
Citation
Nj. Penington, ACTIONS OF METHOXYLATED AMPHETAMINE HALLUCINOGENS ON SEROTONERGIC NEURONS OF THE BRAIN, Progress in neuro-psychopharmacology & biological psychiatry, 20(6), 1996, pp. 951-965
Citations number
37
Categorie Soggetti
Neurosciences,"Clinical Neurology","Pharmacology & Pharmacy",Psychiatry
ISSN journal
02785846
Volume
20
Issue
6
Year of publication
1996
Pages
951 - 965
Database
ISI
SICI code
0278-5846(1996)20:6<951:AOMAHO>2.0.ZU;2-5
Abstract
1. Previous studies of phenethylamine hallucinogenic drugs have report ed that intravenous injection of DOI or similar compounds produce an i nhibition of the firing rate of serotonergic dorsal raphe neurons of t he rat; potentially lowering levels of 5-HT throughout the brain. 2. D irect application by iontophoresis demonstrated only weak non-specific effects, but injection into the nucleus produced slowing of cell firi ng possibly due to the reduction of on-going synaptic excitation. 3. T he literature concerning phenethlyamine hallucinogens is discussed in the context of new results obtained from acutely isolated raphe neuron s. The effect of DOI (10 mu M) was tested on isolated DR neurons that responded to 5-HT with the activation of an inwardly rectifying K+ cur rent but it was without effect. Under conditions that isolated inward Ca2+ current in raphe neurons that was inhibited by 5-HT, DOI was simi larly without effect, neither blocking nor mimicking the action of 5-H T. Brief applications of glutamate produced an inward current similar to those produced by synaptic excitation in a slice preparation, but D OI failed to influence the size or duration of these responses. 4. The se results suggest that DOI does not directly influence the cell bodie s of DR neurons. 5. Further studies using raphe slices subject to syna ptic influences will be required to reveal any indirectly mediated mec hanism that may underlie the effects of DOI on DR neurons. Alternative indirect mechanisms of DR neuronal inhibition by i.v. DOI and DOM are suggested.