Effects of lysergic acid diethylamide on autonomic post-ganglionic transmission
1. Six sites of autonomic post-ganglionic transmission were examined for susceptibility to LSD. Inhibition of transmission by LSD was confined to the three sympathetic junctions. 2. Inhibition of sympathetic transmission was maximal with short trains of pulses and declined considerably as train leng...
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Veröffentlicht in: | The Journal of physiology 1975-04, Vol.246 (3), p.571-593 |
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Zusammenfassung: | 1. Six sites of autonomic post-ganglionic transmission were examined for susceptibility to LSD. Inhibition of transmission
by LSD was confined to the three sympathetic junctions. 2. Inhibition of sympathetic transmission was maximal with short trains
of pulses and declined considerably as train length was increased. 3. Evidence for a presynaptic mode of action was obtained.
This was the predominant effect of LSD in the rat anococcygeus and dog retractor penis because alpha-adrenoceptor-blocking
properties were feeble or absent; but in dog splenic strips LSD produced marked post-synaptic alpha-blockade. 4. The presynaptic
inhibitory effect of LSD was unrelated to its 5-hydroxytryptamine-blocking property because it was not shared by methysergide.
Neither was it mediated by prostaglandin release because it was unaltered by indomethacin, which suppresses prostaglandin
synthesis. 5. In the rat anococcygeus and dog retractor penis larger doses of LSD induced slow contractions and, as a result
of the concurrent block of motor transmission, revealed relaxation responses on transmural stimulation, caused by the excitation
of sacral inhibitory fibres present in these muscles. 6. The LSD contractions were due to stimulation of post-synaptic alpha-adrenoceptors
because they were abolished by phentolamine or yohimbine but were present as usual in preparations taken from reserpinized
animals. 7. LSD blocked presynaptic alpha-adrenoceptors in the cholinergic motor fibres to the longitudinal muscle of the
guinea-pig ileum. |
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ISSN: | 0022-3751 1469-7793 |
DOI: | 10.1113/jphysiol.1975.sp010905 |