The fauna of Saudi Arabia comprises a large number of venomous species
of snakes, fish, scorpions, insects, coelenterates and molluscs. The
venoms of these animals show a remarkable diversity of actions on huma
n tissues. Neurotoxins (for example, from the Arabian cobra Naja haje
arabica) interrupt transmission at peripheral neuromuscular junctions
or (for example scorpion neurotoxins) stimulate voltage sensitive syna
ptic sodium and potassium channels with release of acetylcholine and c
atecholamines. The venoms of Red Sea carnivorous marine snails (genus
Conus) contain ''conotoxins'' which have effects on voltage sensitive
calcium and sodium channels, acetylcholine receptors, the vasopressin
receptor and N-methyl-D-aspartate receptors. Of particular interest ar
e sarafotoxins from the venom of the burrowing asp (Atractaspis engadd
ensis, Atractaspididae), which cause coronary artery vasoconstriction
and atrioventricular block. They are homologous with human endogenous
endothelins. Human Victims of bites by this species may die very rapid
ly after developing anaphylactic/autonomic symptoms, shock and atriove
ntricular conduction abnormalities. Improved ovine Fab fragment antive
noms are being developed for treatment of envenoming by Saudi Arabian
snakes and scorpions. These Fab antivenoms have the pharmacological ad
vantage of more rapid tissue distribution, a larger apparent volume of
distribution and less risk of Fc or aggregate-induced complement acti
vation than conventional F (ab')(2) antivenoms.