Zobrazeno 1 - 10
of 200
pro vyhledávání: '"Alain Beaudet"'
Autor:
Alain Beaudet
Publikováno v:
McGill Journal of Medicine, Vol 6, Iss 1 (2020)
N/A
Externí odkaz:
https://doaj.org/article/da3715d90ab34b6181d8ffff8aa3d266
Autor:
Francis Collins, Alain Beaudet, Ruxandra Draghia-Akli, Peter Gruss, John Savill, André Syrota, Alice Dautry, Mats Ulfendahl, Mark Walport, James Onken, Roger I Glass
Publikováno v:
The Lancet Global Health, Vol 1, Iss 2, Pp e64-e65 (2013)
Externí odkaz:
https://doaj.org/article/059878b3a0b349fab141c18265581365
Autor:
M.J. Esdaile, H. Pan, Françoise Mennicken, Catherine M. Cahill, Lakshmi A. Devi, Alain Beaudet, Louis Gendron, Thomas Stroh, Jean-Pierre Vincent, Dajan O'Donnell
Publikováno v:
Gendron, L; Esdaile, MJ; Mennicken, F; Pan, H; O’Donnell, D; Vincent, J-P; et al.(2007). Morphine priming in rats with chronic inflammation reveals a dichotomy between antihyperalgesic and antinociceptive properties of deltorphin. Neuroscience, 144(1), 263-274. doi: 10.1016/j.neuroscience.2006.08.077. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/5rb9n3mk
We previously showed that prolonged morphine treatment and chronic inflammation both enhanced delta opioid receptor (deltaOR) cell surface density in lumbar spinal cord neurons. Here, we sought to determine whether administration of morphine to rats
Autor:
Françoise Mennicken, Anna Lisa Lucido, Louis Gendron, Jean-Pierre Vincent, Alain Beaudet, Dajan O'Donnell, Thomas Stroh
Publikováno v:
The Journal of Neuroscience. 26:953-962
The present study demonstrates that perikaryalδ-opioid receptors (δORs) in rat dorsal root ganglion (DRG) neurons bind and internalize opioid ligands circulating in the CSF. Using confocal and electron microscopy, we found that prolonged morphine t
Autor:
Jean Martinez, Michael J. Esdaile, Alain Beaudet, Amélie Perron, Philippe Sarret, Thomas Stroh
Publikováno v:
The Journal of Neuroscience. 25:8188-8196
Intrathecal administration of the neuropeptide neurotensin (NT) was shown previously to exert antinociceptive effects in a variety of acute spinal pain paradigms including hotplate, tail-flick, and writhing tests. In the present study, we sought to d
Publikováno v:
médecine/sciences. 21:741-746
L’apéline a été découverte en 1998 comme étant le ligand naturel du récepteur orphelin humain, le récepteur APJ. Elle est issue d’un précurseur de 77 acides aminés, la proapéline, qui comporte à son extrémité carboxyterminale une sé
Publikováno v:
Journal of Molecular Neuroscience. 25:207-214
In recent years, we demonstrated that prolonged (48-h) treatment of rats or mice with selective m-opioid receptor ((mu)OR) agonists induced a translocation of delta-opioid receptors ((delta)ORs) from intracellular compartments to neuronal plasma memb
Autor:
Nicole Gallo-Payet, Louis Gendron, Alain Beaudet, Marcel D. Payet, Philippe Sarret, Amélie Perron
Publikováno v:
Molecular Pharmacology. 66:1421-1430
The role and signaling properties of the low-affinity neurotensin receptor (NTS2) are still controversial. In particular, it is unclear whether neurotensin acts as an agonist, inverse agonist, or antagonist at this site. In view of the growing eviden
Publikováno v:
Morinville, A; Cahill, CM; Kieffer, B; Collier, B; & Beaudet, A. (2004). Mu-opioid receptor knockout prevents changes in delta-opioid receptor trafficking induced by chronic inflammatory pain. Pain, 109(3), 266-273. doi: 10.1016/j.pain.2004.01.011. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/47p2m3mm
Previous studies from our laboratory have demonstrated that both chronic inflammatory pain, induced by intraplantar injection of complete Freund's adjuvant (CFA), and prolonged (48 h) stimulation of mu-opioid receptors (muOR) by systemic administrati
Autor:
Patricia Forgez, Alain Beaudet, William Rostène, Catherine Llorens Cortes, Mireille Toy-Miou-Leong
Publikováno v:
Journal of Biological Chemistry. 279:12636-12646
Most G protein-coupled receptors are internalized after interaction with their respective ligand, a process that subsequently contributes to cell desensitization, receptor endocytosis, trafficking, and finally cell resensitization. Although cellular