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咪达唑仑可抑制中枢神经系统中缺氧诱导的促红细胞生成素上调。

Midazolam inhibits the hypoxia-induced up-regulation of erythropoietin in the central nervous system.

作者信息

Matsuyama Tomonori, Tanaka Tomoharu, Tatsumi Kenichiro, Daijo Hiroki, Kai Shinichi, Harada Hiroshi, Fukuda Kazuhiko

机构信息

Department of Anesthesia, Kyoto University Hospital, 54 Kawahara-Cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.

Department of Anesthesia, Kyoto University Hospital, 54 Kawahara-Cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.

出版信息

Eur J Pharmacol. 2015 Aug 15;761:189-98. doi: 10.1016/j.ejphar.2015.05.024. Epub 2015 May 19.

Abstract

Erythropoietin (EPO), a regulator of red blood cell production, is endogenously expressed in the central nervous system. It is mainly produced by astrocytes under hypoxic conditions and has proven to have neuroprotective and neurotrophic effects. In the present study, we investigated the effect of midazolam on EPO expression in primary cultured astrocytes and the mouse brain. Midazolam was administered to 6-week-old BALB/c male mice under hypoxic conditions and pregnant C57BL/6N mice under normoxic conditions. Primary cultured astrocytes were also treated with midazolam under hypoxic conditions. The expression of EPO mRNA in mice brains and cultured astrocytes was studied. In addition, the expression of hypoxia-inducible factor (HIF), known as the main regulator of EPO, was evaluated. Midazolam significantly reduced the hypoxia-induced up-regulation of EPO in BALB/c mice brains and primary cultured astrocytes and suppressed EPO expression in the fetal brain. Midazolam did not affect the total amount of HIF proteins but significantly inhibited the nuclear expression of HIF-1α and HIF-2α proteins. These results demonstrated the suppressive effects of midazolam on the hypoxia-induced up-regulation of EPO both in vivo and in vitro.

摘要

促红细胞生成素(EPO)是红细胞生成的调节剂,在中枢神经系统中内源性表达。它主要由缺氧条件下的星形胶质细胞产生,并已被证明具有神经保护和神经营养作用。在本研究中,我们研究了咪达唑仑对原代培养星形胶质细胞和小鼠脑中EPO表达的影响。在缺氧条件下给6周龄BALB/c雄性小鼠和在常氧条件下给怀孕的C57BL/6N小鼠注射咪达唑仑。原代培养的星形胶质细胞也在缺氧条件下用咪达唑仑处理。研究了小鼠脑和培养的星形胶质细胞中EPO mRNA的表达。此外,评估了作为EPO主要调节因子的缺氧诱导因子(HIF)的表达。咪达唑仑显著降低了BALB/c小鼠脑和原代培养星形胶质细胞中缺氧诱导的EPO上调,并抑制了胎脑中的EPO表达。咪达唑仑不影响HIF蛋白的总量,但显著抑制HIF-1α和HIF-2α蛋白的核表达。这些结果证明了咪达唑仑在体内和体外对缺氧诱导的EPO上调的抑制作用。

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