Zuzek_2017_Toxicol.Lett_281_95

Reference

Title : Natural polymeric 3-alkylpyridinium salt affects vertebrate skeletal muscle contractility by preferentially blocking neuromuscular transmission - Zuzek_2017_Toxicol.Lett_281_95
Author(s) : Zuzek MC , Grandic M , Benoit E , Frangez R
Ref : Toxicol Lett , 281 :95 , 2017
Abstract :

The effects of natural polymeric alkylpyridinium salt (nPoly-3-APS), a potent acetylcholinesterase inhibitor isolated from the marine sponge Reniera sarai, were studied on isolated mouse phrenic nerve-hemidiaphragm muscle preparations using electrophysiological approaches. nPoly-3-APS inhibited nerve-evoked isometric muscle twitch and tetanic contraction in a concentration-dependent manner (IC50=29.4muM and 18.5muM, respectively) and produced a 30-44% decrease of directly muscle-elicited twitch and tetanus amplitudes at 54.4muM. Additionally, nPoly-3-APS (9.1-27.2muM) markedly decreased the amplitude of miniature endplate potentials, while their frequency was only affected at the highest concentration used. Endplate potentials were also inhibited by nPoly-3-APS in a concentration-dependent manner (IC50=20.1muM), without significant change in the resting membrane potential of muscle fibers (up to 54.4muM). In conclusion, our results show, for the first time, that nPoly-3-APS preferentially blocks the neuromuscular transmission, in vitro, by a non-depolarizing mechanism. This strongly suggests that the in vivo toxicity of nPoly-3-APS mainly occurs through an antagonist action of the compound on nicotinic acetylcholine receptors of skeletal muscles.

PubMedSearch : Zuzek_2017_Toxicol.Lett_281_95
PubMedID: 28939337

Related information

Citations formats

Zuzek MC, Grandic M, Benoit E, Frangez R (2017)
Natural polymeric 3-alkylpyridinium salt affects vertebrate skeletal muscle contractility by preferentially blocking neuromuscular transmission
Toxicol Lett 281 :95

Zuzek MC, Grandic M, Benoit E, Frangez R (2017)
Toxicol Lett 281 :95