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首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Acute toxicity of some synthetic cyanogens in rats: Time-dependent cyanide generation and cytochrome oxidase inhibition in soft tissues after sub-lethal oral intoxication
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Acute toxicity of some synthetic cyanogens in rats: Time-dependent cyanide generation and cytochrome oxidase inhibition in soft tissues after sub-lethal oral intoxication

机译:某些合成氰在大鼠中的急性毒性:亚致死性口腔中毒后软组织中时间依赖性氰化物的产生和细胞色素氧化酶的抑制

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摘要

Cyanogens include complex nitrile-containing compounds that can generate free cyanide of toxicological significance. Acute toxicity, time-dependent cyanide generation and cytochrome oxidase (CYTOX) inhibition in soft tissues, and urinary thiocyanate levels were measured after acute cyanogen intoxication in rats. Order of cyanogens in terms of LD50 was: malononitrile (MCN)propionitrile (PCN)≈sodium nitroprusside (SNP)acrylonitrile (ACN)succinonitrile (SCN)acetonitrile (ATCN) for oral, and SNPMCNACNPCNSCNATCN for intraperitoneal and subcutaneous routes. MCN was most toxic by oral (LD50=66.4mg/kg) and SNP by intraperitoneal (LD50=16.7mg/kg) and subcutaneous (LD50=11.9mg/kg) routes. Minimum survival time (25min) was recorded after 4.0 LD50 ATCN. Order of cyanogens (0.75 LD50; oral) on the basis of maximum blood cyanide and time of peak cyanide generation were: ATCNSNPSCNPCNMCNACN, and MCN (30min)SNP (1h)PCN≈ACN (8h)SCN (24h)ATCN (72h), respectively. In most cases, time profile of cyanide generation correlated with corresponding CYTOX inhibition and urinary thiocyanate levels. With the understanding of time-dependent toxicity of different cyanogens, suitable therapeutic windows can be designed for their management.
机译:氰化物包括复杂的含腈化合物,这些化合物会生成具有毒理学意义的游离氰化物。在急性氰化物中毒后,对大鼠软组织中的急性毒性,时间依赖性氰化物生成和细胞色素氧化酶(CYTOX)抑制以及尿中的硫氰酸盐水平进行了测量。从LD50的角度看,氰化物的顺序为:丙二腈(MCN)>丙腈(PCN)≈硝普钠(SNP)>丙烯腈(ACN)>琥珀腈(SCN)>乙腈(ATCN)口服,以及SNP> MCN> ACN> PCN > SCN> ATCN用于腹膜内和皮下途径。口服(LD50 = 66.4mg / kg)的MCN毒性最高,腹膜内(LD50 = 16.7mg / kg)和皮下(LD50 = 11.9mg / kg)的MNP毒性最高。在4.0 LD50 ATCN后记录最小生存时间(25分钟)。基于最大血液氰化物和氰化物峰值生成时间的氰化物顺序(0.75 LD50;口服)为:ATCN> SNP> SCN> PCN> MCN> ACN,并且MCN(30min)

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