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大鼠中的双硫仑-乙醇反应。1. 血液酒精、乙醛与肝脏乙醛脱氢酶的关系。

Disulfiram-ethanol reaction in the rat. 1. Blood alcohol, acetaldehyde, and liver aldehyde dehydrogenase relationships.

作者信息

Jensen J C, Faiman M D

出版信息

Alcohol Clin Exp Res. 1986 Jan-Feb;10(1):45-9. doi: 10.1111/j.1530-0277.1986.tb05612.x.

DOI:10.1111/j.1530-0277.1986.tb05612.x
PMID:3515991
Abstract

Studies were carried out to determine whether the disulfiram-ethanol reaction (DER) in the rat could be correlated with blood acetaldehyde, ethanol, and liver aldehyde dehydrogenase (ALDH) inhibition. Both hypothermia and hypotension were used as indices of the DER. Female Sprague-Dawley rats were given disulfiram (DSF) (100 mg/kg, i.p.) and low and high liver ALDH determined. No effect on high Km ALDH was found. Inhibition of low Km ALDH was dependent on DSF pretreatment time, with significant inhibition observed at 6, 8, and 12 hr following DSF. In rats receiving ethanol only, maximal blood ethanol was reached within 120 min. Blood acetaldehyde was almost undetectable. No change in rat core temperature was observed. In rats pretreated with DSF (100 mg/kg, i.p.) 8 hr before ethanol challenge (1 g/kg, i.p.), a marked increase in blood acetaldehyde was found and remained elevated throughout the temperature and blood pressure monitoring period. Blood ethanol reached a maximum within 90 min and then declined. Maximal hypothermia and hypotension occurred 120 min after ethanol. The administration of the dopamine receptor blocker pimozide (0.5 mg/kg, i.p.) 60 min before ethanol challenge, attenuated the hypothermia and hypotension. Pimozide was effective when given either 60 min before ethanol or 30 min after ethanol. The onset and duration of hypothermia and hypotension during the DER appears to follow the rise and fall of blood ethanol but not blood acetaldehyde.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

开展了多项研究以确定大鼠体内的双硫仑 - 乙醇反应(DER)是否与血液中的乙醛、乙醇以及肝脏醛脱氢酶(ALDH)抑制作用相关。体温过低和血压过低均被用作DER的指标。给雌性斯普拉格 - 道利大鼠注射双硫仑(DSF)(100毫克/千克,腹腔注射),并测定其肝脏中低活性和高活性的ALDH。未发现对高Km ALDH有影响。低Km ALDH的抑制作用取决于DSF的预处理时间,在DSF处理后6、8和12小时观察到显著抑制。仅接受乙醇的大鼠在120分钟内达到最大血液乙醇含量。血液中的乙醛几乎检测不到。未观察到大鼠核心体温变化。在乙醇激发(1克/千克,腹腔注射)前8小时用DSF(100毫克/千克,腹腔注射)预处理的大鼠中,发现血液乙醛显著增加,并在整个体温和血压监测期内持续升高。血液乙醇在90分钟内达到最大值,然后下降。乙醇注射后120分钟出现最大体温过低和血压过低。在乙醇激发前60分钟给予多巴胺受体阻滞剂匹莫齐特(0.5毫克/千克,腹腔注射),可减轻体温过低和血压过低。匹莫齐特在乙醇激发前60分钟或乙醇激发后30分钟给药均有效。DER期间体温过低和血压过低的发作和持续时间似乎跟随血液乙醇的升降,而非血液乙醛的变化。(摘要截短至250字)

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