TY - JOUR
T1 - Cresylbenzodioxaphosphorin oxide pretreatment alters soman-induced toxicity and inhibition of tissue cholinesterase activity of the rat
AU - Jimmerson, Vernon R.
AU - Tsung-Ming, Shih
AU - Maxwell, Donald M.
AU - Mailman, Richard
PY - 1989/7
Y1 - 1989/7
N2 - The toxicity of soman was investigated in the rat with and without pretreatment with Cresylbenzodioxa-phosphorin oxide (CBDP). Without pretreatment, the 24-h LD50 for soman was 118.2 μg/kg s.c., and soman inhibited Carboxylesterase (CaE) activity in plasma (ED50 of 55 μg/kg) and cholinesterase (ChE) activity in brain regions (ED50 values of 65-105 μg/kg) in a dose-related manner. With pretreatment, the 24-h LD50 for soman was reduced by approximately 6-fold and 8-fold (by 1.0 mg/kg and 16.0 mg/kg of CBDP, respectively), and the ED50 values for soman-induced inhibition of ChE activity in brain regions were reduced by approximately 10-fold (by 1.0 mg/kg of CBDP). The dose-dependent severity of soman intoxication varied widely in rats treated with soman alone but not in CBDP-pretreated rats, and the ED50 for the occurrence of signs of soman intoxication was reduced approximately 7-fold following CBDP (1.0 mg/kg) pretreatment. These data support the hypothesis that CBDP pretreatment effectively blocks tissue CaE sites which serve to detoxify soman, thus potentiating both the soman-induced inhibition of ChE in the CNS and the lethality of soman.
AB - The toxicity of soman was investigated in the rat with and without pretreatment with Cresylbenzodioxa-phosphorin oxide (CBDP). Without pretreatment, the 24-h LD50 for soman was 118.2 μg/kg s.c., and soman inhibited Carboxylesterase (CaE) activity in plasma (ED50 of 55 μg/kg) and cholinesterase (ChE) activity in brain regions (ED50 values of 65-105 μg/kg) in a dose-related manner. With pretreatment, the 24-h LD50 for soman was reduced by approximately 6-fold and 8-fold (by 1.0 mg/kg and 16.0 mg/kg of CBDP, respectively), and the ED50 values for soman-induced inhibition of ChE activity in brain regions were reduced by approximately 10-fold (by 1.0 mg/kg of CBDP). The dose-dependent severity of soman intoxication varied widely in rats treated with soman alone but not in CBDP-pretreated rats, and the ED50 for the occurrence of signs of soman intoxication was reduced approximately 7-fold following CBDP (1.0 mg/kg) pretreatment. These data support the hypothesis that CBDP pretreatment effectively blocks tissue CaE sites which serve to detoxify soman, thus potentiating both the soman-induced inhibition of ChE in the CNS and the lethality of soman.
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U2 - 10.1016/0378-4274(89)90190-2
DO - 10.1016/0378-4274(89)90190-2
M3 - Article
C2 - 2749782
AN - SCOPUS:0024384490
SN - 0378-4274
VL - 48
SP - 93
EP - 103
JO - Toxicology Letters
JF - Toxicology Letters
IS - 1
ER -