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The role of propofol hydroxyl group in 5-lipoxygenase recognition.
Yuki, Koichi; Bu, Weiming; Eckenhoff, Roderic G; Yokomizo, Takehiko; Okuno, Toshiaki.
Afiliación
  • Yuki K; Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital, Boston, MA, 02115, USA; Department of Anaesthesia, Harvard Medical School, Boston, MA, 02115, USA. Electronic address: koichi.yuki@childrens.harvard.edu.
  • Bu W; Department of Anesthesiology and Critical Care, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, 19104, USA.
  • Eckenhoff RG; Department of Anesthesiology and Critical Care, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, 19104, USA.
  • Yokomizo T; Department of Biochemistry, Juntendo University Faculty of Medicine, Bunkyo-Ku, Tokyo, 113-8421, Japan.
  • Okuno T; Department of Biochemistry, Juntendo University Faculty of Medicine, Bunkyo-Ku, Tokyo, 113-8421, Japan. Electronic address: tokuno@juntendo.ac.jp.
Biochem Biophys Res Commun ; 525(4): 909-914, 2020 05 14.
Article en En | MEDLINE | ID: mdl-32171526
Propofol is a clinically important intravenous anesthetic. We previously reported that it directly inhibited 5-lipoxygenase (5-LOX), a key enzyme for leukotriene biosynthesis. Because the hydroxyl group in propofol (propofol 1-hydroxyl) is critical for its anesthetic effect, we examined if its presence would be inevitable for 5-lipoxygenase recognition. Fropofol is developed by substituting the hydroxy group in propofol with fluorine. We found that propofol 1-hydroxyl was important for 5-lipoxygenase recognition, but it was not absolutely necessary. Azi-fropofol bound to 5-LOX at one of the two propofol binding sites of 5-LOX (pocket around Phe-187), suggesting that propofol 1-hydroxyl is important for 5-LOX inhibition at the other propofol binding site (pocket around Val-431). Interestingly, 5-hydroperoxyeicosatetraenoic acid (5-HpETE) production was significantly increased by stimulation with calcium ionophore A23187 in HEK293 cells expressing 5-LOX, suggesting that the fropofol binding site is important for the conversion from 5-HpETE to leukotriene A4. We also indicated that propofol 1-hydroxyl might have contributed to interaction with wider targets among our body.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Araquidonato 5-Lipooxigenasa / Propofol Límite: Humans Idioma: En Revista: Biochem Biophys Res Commun Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Araquidonato 5-Lipooxigenasa / Propofol Límite: Humans Idioma: En Revista: Biochem Biophys Res Commun Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos