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在雄性Wistar大鼠中,缺乏证据表明在乙醇存在的情况下,丙氧芬过量会增加致死率。

Lack of evidence of increased lethality due to propoxyphene overdose in the presence of ethanol in male Wistar rats.

作者信息

Bodd E, Olsen H, Gulliksen M, Mørland J

出版信息

Arch Toxicol. 1985 Jan;56(3):170-4. doi: 10.1007/BF00333422.

Abstract

The primary purpose of the present investigation was to evaluate if the presence of ethanol increased lethality induced by propoxyphene. A secondary aim was to study the effect of naloxone on propoxyphene lethality alone, and on the concomitant administration of propoxyphene and ethanol. Male Wistar rats (210-330 g) were used as test animals. Propoxyphene (175 mg/kg) and ethanol (2 g/kg) were administered by gastric intubation, naloxone (2 mg/kg) by subcutaneous injection. Four groups, each consisting of 19 rats, received either of the following drug treatments: Propoxyphene, ethanol + propoxyphene, naloxone + propoxyphene, and naloxone + ethanol + propoxyphene respectively. The drugs were given in the sequence mentioned at the beginning of the experiment. Naloxone was also given 45 and 90 min later. Mortality was reduced to 42% in the group that received ethanol and propoxyphene compared to 73% in the group that received propoxyphene only. Naloxone protected against lethality in both groups. Some animals died despite naloxone administration, possibly due to a nonopioid cardiotoxic effect of propoxyphene or its metabolite. An increase in the propoxyphene/norpropoxyphene (P/N) ratio due to an increase in the absolute concentrations of propoxyphene and a decrease in the absolute levels of norpropoxyphene in blood, brain, and heart tissues was observed in the ethanol + propoxyphene group, compared to the propoxyphene group. In the animals which died, the highest P/N ratio was observed in brain tissue and the lowest in heart muscle. Despite the pharmacokinetic data obtained in this investigation indicating impaired propoxyphene metabolism in the presence of ethanol, ethanol did not enhance propoxyphene-induced lethality.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究的主要目的是评估乙醇的存在是否会增加丙氧芬所致的致死率。次要目的是研究纳洛酮单独对丙氧芬致死率的影响,以及对丙氧芬与乙醇联合给药时致死率的影响。雄性Wistar大鼠(210 - 330克)用作实验动物。丙氧芬(175毫克/千克)和乙醇(2克/千克)通过胃内插管给药,纳洛酮(2毫克/千克)通过皮下注射给药。四组,每组由19只大鼠组成,分别接受以下药物治疗:丙氧芬、乙醇 + 丙氧芬、纳洛酮 + 丙氧芬、纳洛酮 + 乙醇 + 丙氧芬。药物按照实验开始时提到的顺序给予。纳洛酮也在45分钟和90分钟后给予。与仅接受丙氧芬的组中73%的死亡率相比,接受乙醇和丙氧芬的组中死亡率降至42%。纳洛酮在两组中均能预防致死率。尽管给予了纳洛酮,仍有一些动物死亡,可能是由于丙氧芬或其代谢产物的非阿片类心脏毒性作用。与丙氧芬组相比,乙醇 + 丙氧芬组在血液、脑和心脏组织中观察到丙氧芬/去甲丙氧芬(P/N)比值增加,这是由于丙氧芬的绝对浓度增加以及去甲丙氧芬的绝对水平降低所致。在死亡的动物中,脑组织中观察到最高的P/N比值,心肌中最低。尽管本研究获得的药代动力学数据表明在乙醇存在下丙氧芬代谢受损,但乙醇并未增强丙氧芬所致的致死率。(摘要截断于250字)

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