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首页> 外文期刊>Neurochemical research >Ethanol and Acetaldehyde After Intraperitoneal Administration to Aldh2-Knockout Mice-Reflection in Blood and Brain Levels
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Ethanol and Acetaldehyde After Intraperitoneal Administration to Aldh2-Knockout Mice-Reflection in Blood and Brain Levels

机译:乙醇和乙醛腹膜内给药后对Aldh2基因敲除小鼠的血和脑水平影响

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摘要

This paper reports, for the first time, on the analysis of ethanol (EtOH) and acetaldehyde (AcH) concentrations in the blood and brains of Aldh2-knockout (Aldh2-KO) and C57B6/6J (WT) mice. Animals were administrated EtOH (1.0, 2.0 or 4.0 g/kg) or 4-methylpyrazole (4-MP, 82 mg/kg) plus AcH (50, 100 or 200 mg/kg) intraperitoneally. During the blood tests, samples from the orbital sinus of the eye were collected. During the brain tests, dialysates were collected every 5 min (equal to a 15 A mu l sample) from the striatum using in vivo brain microdialysis. Samples were collected at 5, 10, 15, 20, 25, 30 and 60 min intervals post-EtOH and -AcH injection, and then analyzed by head-space GC. In the EtOH groups, high AcH levels were found in the blood and brains of Aldh2-KO mice, while only small traces of AcH were seen in the blood and brains of WT mice. No significant differences in EtOH levels were observed between the WT and the Aldh2-KO mice for either the EtOH dose. EtOH concentrations in the brain were comparable to the EtOH concentrations in the blood, but the AcH concentrations in the brain were four to five times lower compared to the AcH concentrations in the blood. In the AcH groups, high AcH levels were found in both WT and Aldh2-KO mice. Levels reached a sharp peak at 5 min and then quickly declined for 60 min. Brain AcH concentrations were almost equal to the concentrations found in the blood, where the AcH concentrations were approximately two times higher in the Aldh2-KO mice than in the WT mice, both in the blood and the brain. Our results suggest that systemic EtOH and AcH administration can cause a greater increase in AcH accumulation in the blood and brains of Aldh2-KO mice, where EtOH concentrations in the Aldh2-KO mice were comparable to the EtOH concentrations in the WT mice. Furthermore, detection of EtOH and AcH in the blood and brain was found to be dose-dependent in both genotypes.
机译:本文首次报道了Aldh2-敲除(Aldh2-KO)和C57B6 / 6J(WT)小鼠血液和大脑中乙醇(EtOH)和乙醛(AcH)浓度的分析。腹膜内给予动物EtOH(1.0、2.0或4.0 g / kg)或4-甲基吡唑(4-MP,82 mg / kg)加AcH(50、100或200 mg / kg)。在验血期间,从眼睛的眶窦收集了样品。在脑部测试期间,每隔5分钟使用体内脑部微透析从纹状体收集一次透析液(相当于15 A微升样品)。在注射EtOH和-AcH之后的5、10、15、20、25、30和60分钟的间隔收集样品,然后通过顶空GC进行分析。在EtOH组中,在Aldh2-KO小鼠的血液和脑中发现高水平的AcH,而在WT小鼠的血液和脑中仅发现少量的AcH。对于EtOH剂量,在WT和Aldh2-KO小鼠之间未观察到EtOH水平的显着差异。大脑中的EtOH浓度与血液中的EtOH浓度相当,但是与血液中的AcH浓度相比,大脑中的AcH浓度低四到五倍。在AcH组中,WT和Aldh2-KO小鼠均发现高AcH水平。浓度在5分钟达到一个尖峰,然后迅速下降60分钟。大脑中的AcH浓度几乎等于血液中的浓度,在血液和大脑中,Aldh2-KO小鼠中的AcH浓度约为WT小鼠中的两倍。我们的研究结果表明,全身施用EtOH和AcH可以引起Aldh2-KO小鼠血液和大脑中AcH积累的更大增加,其中Aldh2-KO小鼠中的EtOH浓度与WT小鼠中的EtOH浓度相当。此外,发现两种基因型中血液和脑中EtOH和AcH的检测均呈剂量依赖性。

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