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乙醛和乙醇对小鼠的低温效应。

Acetaldehyde and the hypothermic effects of ethanol in mice.

机构信息

Centre de Neurosciences Cognitives et Comportementales, Université de Liège, Liège, Belgium.

出版信息

Alcohol Clin Exp Res. 2009 Nov;33(11):2005-14. doi: 10.1111/j.1530-0277.2009.01039.x. Epub 2009 Aug 31.

Abstract

BACKGROUND

Acetaldehyde, the first metabolite of ethanol, has been suggested to be involved in many behavioral effects of ethanol. However, few studies have investigated the hypothermic effects of acetaldehyde or the contribution of acetaldehyde to ethanol-induced hypothermia. The aim of the present study is to better understand the hypothermic effects of acetaldehyde and the possible contribution of acetaldehyde in ethanol-induced hypothermia, especially under conditions leading to acetaldehyde accumulation.

METHODS

Female Swiss mice were injected intraperitoneally with ethanol and acetaldehyde and their rectal temperatures were measured with a digital thermometer at various time points after the injections. Experiment 1 compared the hypothermic effects of various acetaldehyde doses (0 to 300 mg/kg) with a reference dose of ethanol (3 g/kg). Experiment 2 tested the effects of a pretreatment with the aldehyde dehydrogenase (ALDH) inhibitor cyanamide (25 mg/kg) on ethanol- and acetaldehyde-induced hypothermia. In experiments 3 and 4, mice received a combined pretreatment with cyanamide and the alcohol dehydrogenase (ADH) inhibitor 4-Methylpyrazole (10 mg/kg) before the injection of ethanol or acetaldehyde.

RESULTS

Acetaldehyde at doses between 100 and 300 mg/kg induced significant hypothermic effects, but of shorter duration than ethanol-induced hypothermia. The inhibition of ALDH enzymes by cyanamide induced a strong potentiation of both ethanol- and acetaldehyde-induced hypothermia. The pretreatment with 4-MP prevented the potentiation of ethanol-induced hypothermia by cyanamide, but slightly increased the potentiation of acetaldehyde-induced hypothermia by cyanamide.

CONCLUSIONS

The results of the present study clearly show that acetaldehyde has hypothermic properties in mice at least at relatively high concentrations. Furthermore, the accumulation of acetaldehyde following ALDH inhibition strongly enhanced the hypothermic effects of ethanol. These latter results confirm the hypothermic properties of acetaldehyde and show that acetate, the next step in ethanol metabolism, is not involved in these hypothermic effects. Finally, the experiment with 4-MP indicates that the potentiating effects of cyanamide are mediated by the peripheral accumulation of acetaldehyde, which then reaches the brain to induce a severe hypothermia.

摘要

背景

乙醛是乙醇的第一代谢产物,据推测其参与了乙醇的许多行为效应。然而,很少有研究调查乙醛的解热作用或乙醛对乙醇引起的解热作用的贡献。本研究旨在更好地了解乙醛的解热作用,以及乙醛在乙醇引起的解热作用中的可能作用,特别是在导致乙醛积累的情况下。

方法

雌性瑞士小鼠经腹腔注射乙醇和乙醛,并在注射后不同时间点用数字温度计测量直肠温度。实验 1 比较了不同剂量的乙醛(0 至 300mg/kg)与参考剂量乙醇(3g/kg)的解热作用。实验 2 测试了醛脱氢酶(ALDH)抑制剂氰酰胺(25mg/kg)预处理对乙醇和乙醛引起的解热作用的影响。在实验 3 和 4 中,小鼠在注射乙醇或乙醛前接受氰酰胺和乙醇脱氢酶(ADH)抑制剂 4-甲基吡唑(10mg/kg)联合预处理。

结果

100 至 300mg/kg 剂量的乙醛引起明显的解热作用,但持续时间短于乙醇引起的解热作用。ALDH 酶的抑制氰酰胺强烈增强了乙醇和乙醛引起的解热作用。4-MP 的预处理可预防氰酰胺增强乙醇引起的解热作用,但轻微增加了氰酰胺增强乙醛引起的解热作用。

结论

本研究的结果清楚地表明,乙醛在小鼠中至少在相对较高的浓度下具有解热作用。此外,ALDH 抑制后乙醛的积累强烈增强了乙醇的解热作用。这些结果证实了乙醛的解热作用,并表明乙醇代谢的下一步产物乙酸酯不参与这些解热作用。最后,用 4-MP 的实验表明,氰酰胺的增强作用是由外周乙醛的积累介导的,然后乙醛到达大脑引起严重的解热作用。

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