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牛磺酸在短暂性全脑缺血后神经元保护中的作用。

The role of taurine in neuronal protection following transient global forebrain ischemia.

作者信息

Khan S H, Banigesh A, Baziani A, Todd K G, Miyashita H, Eweida M, Shuaib A

机构信息

Saskatchewan Stroke Research Centre, University of Saskatchewan, Saskatoon, Canada.

出版信息

Neurochem Res. 2000 Feb;25(2):217-23. doi: 10.1023/a:1007519419342.

Abstract

Osmoregulation and post ischemic glutamate surge suppression (PIGSS) are important mechanisms in the neuroprotective properties of taurine. We studied the role of taurine in PIGSS following transient global forebrain ischemia (TGFI). A group of gerbils received a high dose of continuous intracerebral taurine during the peri-ischemic period. Beta-alanine was given similarly to a negative control group. The control group consisted of animals undergoing only TGFI. On the fourth day following commencement of drug administration, TGFI was induced. Concurrently, half the animals from each group receiving an agent had intracerebral microdialysis. All animals underwent histological assessment at day 7. The microdialysis and histological data was analyzed. Our results showed that taurine treatment did not cause PIGSS. The histological difference between the three groups was statistically insignificant. We conclude that intracerebral taurine in the dosage administered during peri-ischemic period, does not result in PIGSS or histologically evident neuroprotection.

摘要

渗透调节和缺血后谷氨酸激增抑制(PIGSS)是牛磺酸神经保护特性的重要机制。我们研究了牛磺酸在短暂性全脑缺血(TGFI)后PIGSS中的作用。一组沙鼠在缺血周围期接受高剂量的持续脑内牛磺酸注射。β-丙氨酸以类似方式给予阴性对照组。对照组由仅接受TGFI的动物组成。在给药开始后的第四天,诱导TGFI。同时,每组接受药物的动物中有一半进行脑内微透析。所有动物在第7天进行组织学评估。对微透析和组织学数据进行分析。我们的结果表明,牛磺酸治疗并未引起PIGSS。三组之间的组织学差异无统计学意义。我们得出结论,在缺血周围期给予的剂量下,脑内牛磺酸不会导致PIGSS或组织学上明显的神经保护作用。

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