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赛拉嗪调节大鼠脑内甘氨酸和天冬氨酸的释放。

Xylazine Regulates the Release of Glycine and Aspartic Acid in Rat Brain.

作者信息

Zhang Yi-Ming, Yu Dong-Xu, Yin Bai-Shuang, Li Xin-Ran, Li Li-Na, Li Ya-Nan, Wang Yu-Xin, Chen Yu, Liu Wen-Han, Gao Li

机构信息

College of Veterinary Medicine, Northeast Agricultural University, Harbin 150000, China.

出版信息

J Vet Res. 2018 Mar 30;62(1):121-128. doi: 10.1515/jvetres-2018-0017. eCollection 2018 Mar.

Abstract

INTRODUCTION

Xylazine, a type of α-adrenoceptors, is a commonly used drug in veterinary medicine. Xylazine-induced changes in the content of amino acid neurotransmitters - glycine (Gly) and aspartic acid (Asp), in different brain regions and neurons were studied.

MATERIAL AND METHODS

Wistar rats were administered 50 mg/kg or 70 mg/kg of xylazine by intraperitoneal injection. In addition, experiments were conducted, in which neurons were treated with 15 μg/mL, 25 μg/mL, 35μg/mL, and 45 μg/mL of xylazine. Test methods were based on the enzyme-linked immunosorbent assays (ELISA).

RESULTS

During anaesthesia, Asp levels in each brain area were significantly lower compared to the control group. Except for the cerebrum, levels of Gly in other brain areas were significantly increased during the anaesthesia period. , xylazine-related neuron secretion of Gly increased significantly compared to the control group at 60 min and 90 min. Moreover, xylazine caused a significant decrease in the levels of Asp secreted by neurons at 20 min, but gradually returned to the level of the control group.

CONCLUSION

The data showed that during anaesthesia the overall levels of Asp decreased and overall levels of Gly increased. In addition, the inhibitory effect of xylazine on Asp and the promotion of Gly were dose-dependent. Our data showed that different effects of xylazine on excitatory and inhibitory neurotransmitters provided a theoretical basis for the mechanism of xylazine activity in clinical anaesthesia.

摘要

引言

赛拉嗪是一种α-肾上腺素能受体类药物,是兽医学中常用的药物。研究了赛拉嗪诱导不同脑区和神经元中氨基酸神经递质——甘氨酸(Gly)和天冬氨酸(Asp)含量的变化。

材料与方法

通过腹腔注射给Wistar大鼠施用50mg/kg或70mg/kg的赛拉嗪。此外,还进行了实验,用15μg/mL、25μg/mL、35μg/mL和45μg/mL的赛拉嗪处理神经元。检测方法基于酶联免疫吸附测定(ELISA)。

结果

麻醉期间,与对照组相比,各脑区的Asp水平显著降低。除大脑外,麻醉期间其他脑区的Gly水平显著升高。与对照组相比,赛拉嗪相关的神经元Gly分泌在60分钟和90分钟时显著增加。此外,赛拉嗪在20分钟时导致神经元分泌的Asp水平显著降低,但逐渐恢复到对照组水平。

结论

数据表明,麻醉期间Asp的总体水平降低,Gly的总体水平升高。此外,赛拉嗪对Asp的抑制作用和对Gly的促进作用呈剂量依赖性。我们的数据表明,赛拉嗪对兴奋性和抑制性神经递质的不同作用为其在临床麻醉中的作用机制提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ee8/5957471/b97525b3dcd3/jvetres-62-121-g001.jpg

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