Venomous fish


Venomous fish produce strong mixtures of toxins harmful to humans which they deliver by means of a bite, sting, or stab. This results in an envenomation. As a contrast, poisonous fish also produce a strong toxin, but they do not bite, sting, or stab to deliver the toxin. Instead they are poisonous to eat because the human digestive system does not destroy the toxin they contain in their body. Venomous fish don't necessarily cause poisoning if they are eaten, since the digestive system often destroys the venom.
There are at least 1200 species of venomous fish. This number accounts for two-thirds of the venomous vertebrate population. There are more venomous fish than venomous snakes and indeed more than the combined total of all other venomous vertebrates. Venomous fish are found in almost all habitats around the world, but mostly in tropical waters. They injure over 50,000 people every year.
They carry their venom in venom glands and use various delivery systems, such as spines or sharp fins, barbs, spikes and fangs. The most common venom delivery system is via dorsal spines. Venomous fish tend to be either very visible, using flamboyant colors to warn enemies, or skillfully camouflaged and maybe buried in the sand. Apart from the defense or hunting value, venom helps bottom dwelling fish by killing the bacteria that try to invade their skin. Few of these venoms have been studied. They are a yet-to-be tapped resource for bioprospecting to find drugs with medical uses.

Examples

Venomous fish are very often involved in human injury, usually by accident, but few studies have been done to investigate the constituents of fish venom. Even fewer studies have been done to create antivenom.
The only commercially available antivenom is for the Indo-Pacific stonefish, Synanceja trachynis Stonefish Antivenom.

Biological and pharmacological importance of fish venoms

It has been found that the mucous and sting venom of Potamotrygon cf. henlei, a species of stingray that is found in Brazil, is toxic to mice that have nociceptive, edematogenic, and proteolysis activities. Two peptides were isolated from the stingray venom, orpotrin, which causes vasoconstriction, and porflan, which causes inflammation. Knowing how these peptides are structured could lead to the development of a neutralization technique that could effectively act as an antivenom.
Of all the piscine venoms studied, they all produce profound cardiovascular alterations, both in vivo and in vitro. These changes stimulate the release of nitric oxide from the endothelial cells, smooth muscle contractions, and other effects of the atria. Piscine venoms also produce neuromuscular activity effects- depolarization of nerve and muscle cells. In addition, piscine venoms have strong cytolytic activity. In experimental models and in Western immunoblotting analysis, all tested piscine venoms showed structural similarity, which could lead to the advent of an overarching antivenom or other novel uses.