TY - JOUR T1 - Effects of <em>Delphinium</em> Alkaloids on Neuromuscular Transmission JF - Journal of Pharmacology and Experimental Therapeutics JO - J Pharmacol Exp Ther SP - 538 LP - 546 VL - 291 IS - 2 AU - Peter Dobelis AU - James E. Madl AU - James A. Pfister AU - Gary D. Manners AU - John P. Walrond Y1 - 1999/11/01 UR - http://jpet.aspetjournals.org/content/291/2/538.abstract N2 - The Delphinium alkaloids methyllycaconitine (MLA), nudicauline, 14-deacetylnudicauline (14-DN), barbinine, and deltaline were investigated for their effects on neuromuscular transmission in lizards. The substituent at C14 provides the only structural difference among the alkaloids MLA, nudicauline, 14-DN, and barbinine. Deltaline lacks the N-(methylsuccinyl)anthranilic acid at C18 common to the other four alkaloids. Each alkaloid reversibly reduced extracellularly recorded compound muscle action potential (CMAP) amplitudes in a concentration-dependent manner. The IC50values for CMAP blockade were between 0.32 and 13.2 μM for theN-(methylsuccinimido)anthranoyllycacotonine-type alkaloids and varied with the C14 moiety; the IC50 value for deltaline was 156 μM. The slopes of the concentration-response curves for CMAP blockade were similar for each alkaloid except barbinine, whose shallower curve suggested alternative or additional mechanisms of action. Each alkaloid reversibly reduced intracellularly recorded spontaneous, miniature end-plate potential (MEPP) amplitudes. Alkaloid concentrations producing similar reductions in MEPP amplitude were 0.05 μM for 14-DN, 0.10 μM for MLA, 0.50 μM for barbinine, and 20 μM for deltaline. Only barbinine altered the time constant for MEPP decay, further suggesting additional or alternative effects for this alkaloid. MLA and 14-DN blocked muscle contractions induced by exogenously added acetylcholine. All five alkaloids are likely nicotinic receptor antagonists that reduce synaptic efficacy and block neuromuscular transmission. The substituent at C14 determines the potency and possibly the mechanism of nicotinic acetylcholine receptor blockade for MLA, nudicauline, 14-DN, and barbinine at neuromuscular synapses. The lower potency of deltaline indicates that theN-(methylsuccinyl)anthranilic acid at C18 affects alkaloid interactions with nicotinic acetylcholine receptors at neuromuscular junctions. The American Society for Pharmacology and Experimental Therapeutics ER -