Organism |
Test Type |
Route |
Reported Dose (Normalized Dose) |
Effect |
Source |
mouse |
LD50 |
intraperitoneal |
160ug/kg (0.16mg/kg) |
|
Toxicology Letters. Vol. 71, Pg. 97, 1994. |
rat |
LDLo |
intravenous |
1mg/kg (1mg/kg) |
SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE
BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY)
LUNGS, THORAX, OR RESPIRATION: RESPIRATORY STIMULATION |
Agents and Actions, A Swiss Journal of Pharmacology. Vol. 8, Pg. 113, 1978. |
The venom of Tityus serrulatus is the most potent of the toxins from the species (Clemente, Rossoni et al. 1999). Tityustoxin-1, TsTX-I is the most toxic protein among the neurotoxins in this venom, with an intravenous and intracisternal LD50 (mouse) of 76 k 9 and 1.1 + 0.3 /lg/kg, respectively. The identification of TsTX-I as a potent component of T. serrulatus venom characterized it as the major and main neurotoxin from this venom (Correa, Sampaio et al. 1997). Poisoning effects in man evoked by T. serrulatus venom are sialorrhea, lacrimation and rhinorrhea. (Clemente, Rossoni et al. 1999) and acute pancreatitis (Correa, Sampaio et al. 1997). Catecholamines by the adrenal glands and postganglionic nerve terminals and Ach by ganglions and postganglionic nerve terminals are released when the poison strikes. Also other neurotransmitters are released by the whole venom and isolated toxins (Correa, Sampaio et al. 1997). In rats, the Tityustoxin caused dramatic effects on the circulatory and respiratory systems, consisting of hypotension, tachypnea, hyperpnea, ataxic and gasping breathing. Following these initial effects, 5 or 10 pg of TsTX induced hypertension and hyperpnea. The largest dose produced apnea and death about 70 min later (Lima and Freire-Maia 1977).