Literature DB >> 2449308

Effects of histrionicotoxin derivatives on ion channels and acetylcholine receptor-channel complexes in bullfrog sympathetic ganglia.

T Ogura1, A Warashina.   

Abstract

1. Four synthetic histrionicotoxin derivatives (H8-, H12-, C4H10- and C5H10-HTX) were applied to bullfrog (Rana catesbeiana) sympathetic ganglia and their effects were compared electrophysiologically. 2. The derivatives (60-100 microM) blocked both acetylcholine receptor-channel complex (ACh RC complex) and Na+ channel to cause a transmission failure. They also blocked K+ and Ca2+ channels. 3. Although all 4 derivatives exhibited similar effects, their potencies on respective ionic channels differed from one another. 4. Two types of (presumably subsynaptic and extrasynaptic) ACh RC complexes in ganglion cells were distinguished based on their differential sensitivities to HTX derivatives.

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Year:  1987        PMID: 2449308     DOI: 10.1016/0742-8413(87)90117-4

Source DB:  PubMed          Journal:  Comp Biochem Physiol C        ISSN: 0742-8413


  2 in total

1.  Nicotinic receptor-elicited sodium flux in rat pheochromocytoma PC12 cells: effects of agonists, antagonists, and noncompetitive blockers.

Authors:  J W Daly; Y Nishizawa; M W Edwards; J A Waters; R S Aronstam
Journal:  Neurochem Res       Date:  1991-04       Impact factor: 3.996

2.  Decahydroquinoline alkaloids: noncompetitive blockers for nicotinic acetylcholine receptor-channels in pheochromocytoma cells and Torpedo electroplax.

Authors:  J W Daly; Y Nishizawa; W L Padgett; T Tokuyama; P J McCloskey; L Waykole; A G Schultz; R S Aronstam
Journal:  Neurochem Res       Date:  1991-11       Impact factor: 3.996

  2 in total

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