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可卡因毒性:大鼠中可卡因诱导致死率的基因差异

Cocaine toxicity: genetic differences in cocaine-induced lethality in rats.

作者信息

George F R

机构信息

Department of Pharmacology and Toxicology, School of Pharmacy University of Maryland, Baltimore 21201.

出版信息

Pharmacol Biochem Behav. 1991 Apr;38(4):893-5. doi: 10.1016/0091-3057(91)90259-5.

Abstract

Cocaine produces stimulation, depression, convulsions and death, and binds at several receptor sites. Thus cocaine may produce toxicity through similar or distinct pathways from those associated with stimulation. Genetic differences in stimulant response to cocaine have recently been reported for four inbred rat strains, ACI, F344, LEW and NBR. In the present study, significant genetic differences were found in cocaine-induced lethality, with a two-fold difference in LD50 values seen between the most sensitive (NBR) and least sensitive (LEW) strains. Sensitivity to lethality was not correlated with sensitivity to stimulation, but was highly correlated with baseline activity. This lack of strong association between stimulant and lethal effects of cocaine may be important in clinical manifestations of the cocaine sudden death syndrome.

摘要

可卡因会产生兴奋、抑制、惊厥和死亡作用,并作用于多个受体位点。因此,可卡因可能通过与兴奋作用相关的相似或不同途径产生毒性。最近有报道称,ACI、F344、LEW和NBR这四种近交系大鼠品系对可卡因的兴奋反应存在基因差异。在本研究中,发现可卡因诱导的致死率存在显著的基因差异,最敏感(NBR)和最不敏感(LEW)品系之间的半数致死剂量(LD50)值相差两倍。对致死性的敏感性与对兴奋的敏感性无关,但与基础活动高度相关。可卡因兴奋作用和致死作用之间缺乏紧密关联,这可能在可卡因猝死综合征的临床表现中具有重要意义。

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