Literature DB >> 4390195

A pharmacological study of the toxin in a Cnidarian, Chironex fleckeri Southcott.

S E Freeman, R J Turner.   

Abstract

1. A study has been made of the pharmacological actions of toxic preparations obtained from the box jellyfish Chironex fleckeri Southcott. Two toxin preparations were used. One was a tentacle extract which was partially purified by Sephadex gel filtration; the second was obtained by a process analogous to snake milking, and is probably similar in composition to the material injected into victims.2. All preparations were extremely toxic; death in animals, following minimally lethal doses, occurred in minutes. Respiratory arrest of central origin appeared to be the terminal event in all species tested. This was accompanied by marked signs of cardiotoxicity. The heart was slowed, irregular, and showed varying degrees of conduction delay. Terminally it showed atrioventricular block.3. Blood pressure changes were biphasic. An initial rise in carotid pressure was followed by a profound fall; a second rise to an above normal level frequently followed this. These blood pressure oscillations were damped down by prior treatment with hexamethonium but the hypertensive response remained.4. Blood samples taken before terminal apnoea showed a variable degree of haemolysis and a raised K(+) level.5. Experiments with isolated organ preparations suggested that the toxin had a non-specific lytic effect on cells, but did not contain pharmacologically active substances of small molecular weight such as 5-hydroxytryptamine.6. It is suggested that the toxin(s) act by altering membrane permeability; the signs at death may reflect the sensitivity of the target organs to such a change.

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Year:  1969        PMID: 4390195      PMCID: PMC1703363          DOI: 10.1111/j.1476-5381.1969.tb08292.x

Source DB:  PubMed          Journal:  Br J Pharmacol        ISSN: 0007-1188            Impact factor:   8.739


  6 in total

1.  Effect of catecholamines and their chloroanalogs on the in vitro release of histamine from cells of rat peritoneal fluid.

Authors:  A M ROTHSCHILD
Journal:  Biochem Pharmacol       Date:  1962-10       Impact factor: 5.858

2.  A method for the quantitative estimation of drugs on the isolated intact trachea.

Authors:  D JAMIESON
Journal:  Br J Pharmacol Chemother       Date:  1962-10

3.  Release of pharmacologically active substances from the rat skin in vivo following thermal injury.

Authors:  M ROCHA E SILVA; S R ROSENTHAL
Journal:  J Pharmacol Exp Ther       Date:  1961-04       Impact factor: 4.030

4.  Pharmacologic action of Physalia toxin.

Authors:  C E Lane
Journal:  Fed Proc       Date:  1967 Jul-Aug

5.  Studies on the cardiotoxicity of streptolysin O.

Authors:  B N Halpern; S Rahman
Journal:  Br J Pharmacol Chemother       Date:  1968-03

6.  The basic proteins of cobra venom. II. Mechanism of action of cobramine B on thyroid tissue.

Authors:  J Wolff; H Salabè; M Ambrose; P R Larsen
Journal:  J Biol Chem       Date:  1968-03-25       Impact factor: 5.157

  6 in total
  6 in total

1.  Degranulation of rat mast cells in vitro by the fungal cytolysins phallolysin, rubescenslysin and fascicularelysin.

Authors:  R Seeger; E Bunsen
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1980       Impact factor: 3.000

2.  A myotoxin secreted by some piscivorous Conus species.

Authors:  S E Freeman; R J Turner
Journal:  Br J Pharmacol       Date:  1972-10       Impact factor: 8.739

3.  Cardiovascular effects of toxins isolated from the cnidarian Chironex fleckeri Southcott.

Authors:  S E Freeman; R J Turner
Journal:  Br J Pharmacol       Date:  1971-01       Impact factor: 8.739

4.  The partial purification and bioassay of a toxin present in extracts of the sea anemone, Tealia felina (L.).

Authors:  S I Aldeen; R C Elliott; M Sheardown
Journal:  Br J Pharmacol       Date:  1981-02       Impact factor: 8.739

Review 5.  The pathology of Chironex fleckeri venom and known biological mechanisms.

Authors:  Melissa Piontek; Jamie E Seymour; Yide Wong; Tyler Gilstrom; Jeremy Potriquet; Ernest Jennings; Alan Nimmo; John J Miles
Journal:  Toxicon X       Date:  2020-02-24

6.  Cubozoan venom-induced cardiovascular collapse is caused by hyperkalemia and prevented by zinc gluconate in mice.

Authors:  Angel A Yanagihara; Ralph V Shohet
Journal:  PLoS One       Date:  2012-12-12       Impact factor: 3.240

  6 in total

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