Takabuchi Satoshi, Hirota Kiichi, Nishi Kenichiro, Oda Seiko, Oda Tomoyuki, Shingu Koh, Takabayashi Arimichi, Adachi Takehiko, Semenza Gregg L, Fukuda Kazuhiko
Department of Anesthesia, The Tazuke Kofukai Medical Research Institute, Kitano Hospital, 2-4-20, Ohgimachi, Kita-ku, Osaka 530-8480, Japan.
FEBS Lett. 2004 Nov 19;577(3):434-8. doi: 10.1016/j.febslet.2004.10.042.
Hypoxia elicits a wide range of responses that occur at different organizational levels in the body. Hypoxia is not only a signal for energy conservation and metabolic change, but triggers expression of a select set of genes. The transcription factor hypoxia-inducible factor 1 (HIF-1) is now appreciated to be a master factor of the gene induction. Although knowledge on molecular mechanisms of HIF-1 activation in response to hypoxia is accumulating, the molecular mechanism of maintenance of HIF-1 activity under normoxic conditions remains to be elucidated. We demonstrate that the intravenous anesthetic propofol reversibly inhibits HIF-1 activity and the gene expression mediated by HIF-1 by blocking the synthesis of the HIF-1alpha subunit under 20% or 5% O2 conditions, but not under 1% O2 conditions.
缺氧会引发身体不同组织层面的多种反应。缺氧不仅是能量保存和代谢变化的信号,还会触发一组特定基因的表达。转录因子缺氧诱导因子1(HIF-1)如今被认为是基因诱导的主导因子。尽管关于缺氧时HIF-1激活的分子机制的知识不断积累,但常氧条件下HIF-1活性维持的分子机制仍有待阐明。我们证明,静脉麻醉药丙泊酚在20%或5%氧气条件下,通过阻断HIF-1α亚基的合成,可逆性地抑制HIF-1活性以及由HIF-1介导的基因表达,但在1%氧气条件下则不然。