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Journal ArticleDOI

Effects of equinatoxin on the guinea-pig atrium

TLDR
The results suggest that the cardiac inhibitory effect of equinatoxin is mainly due to release of adenyl compounds, while the cardiac stimulant effect of the toxin may result from the liberation of arachidonic acid and subsequent formation of prostaglandins in the guinea-pig atrium.
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This article is published in Toxicon.The article was published on 1987-01-01. It has received 34 citations till now. The article focuses on the topics: Cardiac stimulant & Tachyphylaxis.

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Citations
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Journal ArticleDOI

Cytolytic peptide and protein toxins from sea anemones (Anthozoa: Actiniaria).

TL;DR: The crystal structure of equinatoxin II has been determined at 1.9A resolution, and biological, structure-function, and pharmacological characteristics of these cytolysins are reviewed.
Journal ArticleDOI

Pore formation by the sea anemone cytolysin equinatoxin II in red blood cells and model lipid membranes.

TL;DR: It was inferred that EqT-II increases membrane permeability by forming oligomeric channels comprising several copies of the cytolysin monomer, indicating the formation of cation-selective channels.
Journal ArticleDOI

Mechanism of action of equinatoxin II, a cytolysin from the sea anemone Actinia equina L. belonging to the family of actinoporins

TL;DR: Actinia equina equinatoxin II (EqT-II) is a representative of a family of pore-forming, basic, polypeptide toxins from sea anemones, now called actinoporins, which is active against a variety of mammalian cells including leukocytes, platelets and cardiomiocytes.
Journal ArticleDOI

Polypeptide cytolytic toxins from sea anemones (Actiniaria)

TL;DR: Putative biological roles of toxins, based on their channel-forming activity, in the capture and killing of prey, digestion, repelling of predators and intraspecific spatial competition are suggested.
Journal ArticleDOI

Primary and secondary structure of a pore-forming toxin from the sea anemone, Actinia equina L., and its association with lipid vesicles

TL;DR: It is proposed that at least part of the alpha-helix content increase of equinatoxin II is due to the insertion of its N-terminus into the lipid bilayer, which shares structural homology with membrane active peptides like melittin and viral fusion peptides.
References
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Journal ArticleDOI

The importance of phospholipase-A2 in prostaglandin biosynthesis

TL;DR: Phospholipase is the key enzyme which mobilises free fatty acids for prostaglandin biosynthesis during these types of cell injury, indicating that substrate availability is not the only requirement for stimulation of prostaglanders biosynthesis.
Journal ArticleDOI

Firefly luminescence in the study of energy transfer mechanisms. I. Substrate and enzyme determination.

TL;DR: Preliminary examination of certain biological processes with the Farrand photofluorometer suggests its wide applicability for routine surveys of phosphorylative energetic mechanisms.
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The initial action of thrombin on platelets. Conversion of phosphatidylinositol to phosphatidic acid preceding the production of arachidonic acid.

TL;DR: The data indicate the existence of a quinacrine-insensitive phospholipase C which can initially convert a given amount of PI to PA and which is closely associated to the thrombin receptor.
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8-Phenyltheophylline: A potent P1-purinoceptor antagonist

TL;DR: It is concluded that 8-phenyltheophylline is a more potent P1-purinoceptor antagonist than theophylla in antagonizing the inhibitory effects of adenosine in guinea-pig driven left atrium, rabbit basilar artery and electrically stimulated guinea -pig ileum preparations.
Journal ArticleDOI

The effects of mepacrine and p-bromophenacyl bromide on arachidonic acid release in human platelets☆

TL;DR: Two inhibitors of thrombin-stimulated arachidonic acid release from platelets, p-bromophenacyl bromide and mepacrine, were examined for their ability to inhibit the phosphatidylinositol-specific phospholipase C-diglyceride lipase pathway.
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