The intravenous anesthetics barbiturates inhibit hypoxia-inducible factor 1 activation

被引:22
作者
Wakamatsu, Takuhiko [1 ]
Tanaka, Tomoharu [1 ]
Oda, Seiko [1 ]
Nishi, Kenichiro [2 ]
Harada, Hiroshi [3 ]
Daijo, Hiroki [1 ]
Takabuchi, Satoshi [1 ]
Kai, Shinichi [1 ]
Fukuda, Kazuhiko [1 ]
Hirota, Kiichi [1 ]
机构
[1] Kyoto Univ, Kyoto Univ Hosp, Dept Anesthesia, Kyoto 6068507, Japan
[2] Kansai Med Univ, Dept Anesthesiol, Moriguchi, Osaka 570, Japan
[3] Kyoto Univ Hosp, Dept Radiat Oncol & Image Appl Therapy, Kyoto 606, Japan
基金
日本学术振兴会;
关键词
Anesthetic; Barbiturate; Hypoxia; Hypoxia-inducible factor 1 (HIF-1); Neuron; Translation; Macrophage; FACTOR-KAPPA-B; TRANSCRIPTIONAL ACTIVITY; ERYTHROPOIETIN PROTECT; DEPENDENT MANNER; OXYGEN-TENSION; UP-REGULATION; HIF-1; CELLS; DEGENERATION; HIF-1-ALPHA;
D O I
10.1016/j.ejphar.2009.06.060
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hypoxia-inducible factor 1 (HIF-1) is a master transcription factor of hypoxia-induced gene expression. Anesthetics and perioperative drugs have been reported to affect HIF-1 activity. However, the effect of barbiturates on HIF-1 activity has not been reported. In this study, we investigated the effect of thiopental and thiamylal on HIF-1 activity using the neuronal SH-SY5Y cells, the non-neuronal HEK293 cells, and the macrophage-differentiated THP-1 cells. Cells were exposed to 20% or 1% O-2 conditions with or without thiopental or thiamylal treatment The cell lysate were subjected to Western blot analysis using anti-HIF-1 alpha and -HIF-1 beta antibodies. HIF-1-dependent gene expression was investigated by semi-quantitative real-time RT-PCR and luciferase assay. Hydroxylation of HIF-1 alpha protein was evaluated by in vitro pulldown assay using recombinant protein. Both thiopental and thiamylal reversibly suppressed hypoxia-induced HIF-1 activation in the neuronal and the non-neuronal cells in a dose-dependent manner. Moreover, the barbiturates inhibited lipopolysaccharide-induced HIF-1 alpha expression in THP-1 cells. The HIF-1-downstream gene expression was also inhibited by the barbiturates. HIF alpha-hydroxylases activity and HIF-1 alpha stability were not affected but the HIF-1 alpha protein neosynthesis was inhibited by the barbiturates. Our experimental results indicate that barbiturates inhibit induced HIF-1 activation and downstream genes expression. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:17 / 22
页数:6
相关论文
共 35 条
[31]   Hydroxylation of HIF-1: Oxygen sensing at the molecular level [J].
Semenza, GL .
PHYSIOLOGY, 2004, 19 :176-182
[32]   The intravenous anesthetic propofol inhibits hypoxia-inducible factor 1 activity in an oxygen tension-dependent manner [J].
Takabuchi, S ;
Hirota, K ;
Nishi, K ;
Oda, S ;
Oda, T ;
Shingu, K ;
Takabayashi, A ;
Adachi, T ;
Semenza, GL ;
Fukuda, K .
FEBS LETTERS, 2004, 577 (03) :434-438
[33]   The inhibitory effect of sodium nitroprusside on HIF-1 activation is not dependent on nitric oxide-solube guanylyl cyclase pathway [J].
Takabuchi, S ;
Hirota, K ;
Nishi, K ;
Oda, S ;
Oda, T ;
Shingu, K ;
Takabayashi, A ;
Adachi, T ;
Semenza, GL ;
Fukuda, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 324 (01) :417-423
[34]   HYPOXIA-INDUCIBLE FACTOR-1 IS A BASIC-HELIX-LOOP-HELIX-PAS HETERODIMER REGULATED BY CELLULAR O-2 TENSION [J].
WANG, GL ;
JIANG, BH ;
RUE, EA ;
SEMENZA, GL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) :5510-5514
[35]   N-(6-chloro-pyridin-3-yl)-3,4-difluoro-benzamide (ICA-27243):: A novel, selective KCNQ2/Q3 potassium channel activator [J].
Wickenden, A. D. ;
Krajewski, J. L. ;
London, B. ;
Wagoner, P. K. ;
Wilson, W. A. ;
Clark, S. ;
Roeloffs, R. ;
McNaughton-Smith, G. ;
Rigdon, G. C. .
MOLECULAR PHARMACOLOGY, 2008, 73 (03) :977-986