Okuno Toshiaki, Koutsogiannaki Sophia, Ohba Mai, Chamberlain Matthew, Bu Weiming, Lin Fu-Yan, Eckenhoff Roderic G, Yokomizo Takehiko, Yuki Koichi
Department of Biochemistry, Juntendo University School of Medicine, Tokyo Japan.
Division of Cardiac Anesthesia, Department of Anesthesiology, Perioperative and Pain Medicine, Boston Children's Hospital, Boston Massachusetts, USA.
FASEB J. 2017 Apr;31(4):1584-1594. doi: 10.1096/fj.201601095R. Epub 2017 Jan 9.
Propofol is an intravenous anesthetic that produces its anesthetic effect, largely the GABA receptor in the CNS, and also reduces the -formyl-methionyl-leucyl-phenylalanine (fMLP)-induced neutrophil respiratory burst. Because fMLP-stimulated neutrophils produce leukotriene (LT)B, we examined the effect of propofol on LTB production and Cecal ligation and puncture surgery was performed in mice, with or without exposure to propofol. Propofol attenuated the production of 5-lipoxygenase (5-LOX)-related arachidonic acid (AA) derivatives in the peritoneal fluid. Also, in the experiments on fMLP-stimulated neutrophils and 5-LOX-transfected human embryonic kidney cells, propofol attenuated the production of 5-LOX-related AA derivatives. Based on these results, we hypothesized that propofol would directly affect 5-LOX function. Using -azi-propofol (Azi), we photolabeled stable 5-LOX protein, which had been used to solve the X-ray crystallographic structure of 5-LOX, and examined the binding site(s) of propofol on 5-LOX. Two propofol binding pockets were identified near the active site of 5-LOX. Alanine scanning mutagenesis was performed for the residues of 5-LOX in the vicinity of propofol, and we evaluated the functional role of these pockets in LTB production. We demonstrated that these pockets were functionally important for 5-LOX activity. These two pockets can be used to explore a novel 5-LOX inhibitor in the future.-Okuno, T., Koutsogiannaki, S., Ohba, M., Chamberlain, M., Bu, W., Lin, F.-Y., Eckenhoff, R. G., Yokomizo T., Yuki, K. Intravenous anesthetic propofol binds to 5-lipoxygenase and attenuates leukotriene B production.
丙泊酚是一种静脉麻醉剂,其麻醉作用主要通过作用于中枢神经系统中的γ-氨基丁酸(GABA)受体产生,同时还能降低N-甲酰甲硫氨酰-亮氨酰-苯丙氨酸(fMLP)诱导的中性粒细胞呼吸爆发。由于fMLP刺激的中性粒细胞会产生白三烯(LT)B,我们研究了丙泊酚对LTB产生的影响。对小鼠进行盲肠结扎和穿刺手术,部分小鼠暴露于丙泊酚。丙泊酚可减弱腹膜液中5-脂氧合酶(5-LOX)相关花生四烯酸(AA)衍生物的产生。此外,在fMLP刺激的中性粒细胞和5-LOX转染的人胚肾细胞实验中,丙泊酚也减弱了5-LOX相关AA衍生物的产生。基于这些结果,我们推测丙泊酚会直接影响5-LOX的功能。我们使用叠氮丙泊酚(Azi)对已用于解析5-LOX X射线晶体结构的稳定5-LOX蛋白进行光标记,并研究丙泊酚在5-LOX上的结合位点。在5-LOX的活性位点附近鉴定出两个丙泊酚结合口袋。对丙泊酚附近的5-LOX残基进行丙氨酸扫描诱变,并评估这些口袋在LTB产生中的功能作用。我们证明这些口袋对5-LOX活性具有重要功能。这两个口袋未来可用于探索新型5-LOX抑制剂。-奥野,T.,库索吉安纳基斯,S.,大场,M.,张伯伦,M.,卜,W.,林,F.-Y.,埃肯霍夫,R.G.,横见,T.,由纪,K.静脉麻醉剂丙泊酚与5-脂氧合酶结合并减弱白三烯B的产生。