Cargando…
Distinct Profiles of Desensitization of µ-Opioid Receptors Caused by Remifentanil or Fentanyl: In Vitro Assay with Cells and Three-Dimensional Structural Analyses
Remifentanil (REM) and fentanyl (FEN) are commonly used analgesics that act by activating a µ-opioid receptor (MOR). Although optimal concentrations of REM can be easily maintained during surgery, it is sometimes switched to FEN for optimal pain regulation. However, standards for this switching prot...
Autores principales: | Uezono, Eiko, Mizobuchi, Yusuke, Miyano, Kanako, Ohbuchi, Katsuya, Murata, Hiroaki, Komatsu, Akane, Manabe, Sei, Nonaka, Miki, Hirokawa, Takatsugu, Yamaguchi, Keisuke, Iseki, Masako, Uezono, Yasuhito, Hayashida, Masakazu, Kawagoe, Izumi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10179353/ https://www.ncbi.nlm.nih.gov/pubmed/37176075 http://dx.doi.org/10.3390/ijms24098369 |
Ejemplares similares
-
Ketamine Improves Desensitization of µ-Opioid Receptors Induced by Repeated Treatment with Fentanyl but Not with Morphine
por: Mizobuchi, Yusuke, et al.
Publicado: (2022) -
Novel Opioid Analgesics for the Development of Transdermal Opioid Patches That Possess Morphine-Like Pharmacological Profiles Rather Than Fentanyl: Possible Opioid Switching Alternatives Among Patch Formula
por: Komatsu, Akane, et al.
Publicado: (2022) -
Evaluation of the Intracellular Signaling Activities of κ-Opioid Receptor Agonists, Nalfurafine Analogs; Focusing on the Selectivity of G-Protein- and β-Arrestin-Mediated Pathways
por: Yamaguchi, Masahiro, et al.
Publicado: (2022) -
In Vitro Analyses of Spinach-Derived Opioid Peptides, Rubiscolins: Receptor Selectivity and Intracellular Activities through G Protein- and β-Arrestin-Mediated Pathways
por: Karasawa, Yusuke, et al.
Publicado: (2021) -
Therapeutic Potential of Orally Administered Rubiscolin-6
por: Karasawa, Yusuke, et al.
Publicado: (2023)