Dr. Christophe MALLET

Journal articles

2023

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Baptiste Jouffre, Alexandre Acramel, Mathilde Belnou, Maria Francesca Santolla, Marianna Talia, et al.. Identification of a human estrogen receptor α tetrapeptidic fragment with dual antiproliferative and anti-nociceptive action. Scientific Reports, 2023, 13 (1), pp.1326. ⟨10.1038/s41598-023-28062-9⟩. ⟨hal-04087799⟩

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Baptiste Jouffre, Alexandre Acramel, Yves Jacquot, Laurence Daulhac, Christophe Mallet. GPER involvement in inflammatory pain. Steroids, 2023, 200, pp.109311. ⟨10.1016/j.steroids.2023.109311⟩. ⟨hal-04337675⟩

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Christophe Mallet, Jules Desmeules, Rassa Pegahi, Alain Eschalier. An Updated Review on the Metabolite (AM404)-Mediated Central Mechanism of Action of Paracetamol (Acetaminophen): Experimental Evidence and Potential Clinical Impact. Journal of Pain Research, 2023, 16, pp.1081 – 1094. ⟨10.2147/jpr.s393809⟩. ⟨hal-04337681⟩

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Elodie Picard, Nicolas Kerckhove, Amaury François, Ludivine Boudieu, Elisabeth Billard, et al.. Role of T CD4+ cells, macrophages, C-low threshold mechanoreceptors and spinal Cav3.2 channels in inflammation and related pain-like symptoms in murine inflammatory models. British Journal of Pharmacology, 2023, 180 (4), pp.385-400. ⟨10.1111/bph.15956⟩. ⟨hal-03790651⟩

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2022

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Sophie L Fayad, Guillaume Ourties, Benjamin Le Gac, Baptiste Jouffre, Sylvain Lamoine, et al.. Centrally expressed Cav3.2 T-type calcium channel is critical for the initiation and maintenance of neuropathic pain. eLife, 2022, 11, pp.e79018. ⟨10.7554/elife.79018⟩. ⟨hal-03942925⟩

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Vassili Prudhomme, Mélissa Cucca, Lionel Nauton, Elsa Andrieu, Mathilde Fereyrolles, et al.. Design, synthesis and biological evaluation of conformationnally-restricted analogues of E7010 as inhibitors of tubulin assembly (ITA) and vascular disrupting agents (VDA). European Journal of Medicinal Chemistry, 2022, 244, pp.114809. ⟨10.1016/j.ejmech.2022.114809⟩. ⟨hal-03959739⟩

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2021

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Johan Å.Nilsson, Christophe Mallet, Kiseko Shionoya, Anders Blomgren, Anders Sundin, et al.. Paracetamol analogues conjugated by FAAH induce TRPV1-mediated antinociception without causing acute liver toxicity. European Journal of Medicinal Chemistry, 2021, 213, pp.113042. ⟨10.1016/j.ejmech.2020.113042⟩. ⟨hal-04256629⟩

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Christine Courteix, Alain Eschalier, Christophe Mallet. L’évaluation de la douleur chez l’animal de laboratoire. Douleur et Analgésie, 2021, 34 (2), pp.114-122. ⟨10.3166/dea-2021-0145⟩. ⟨hal-03418812⟩

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Christophe Mallet, Ludivine Boudieu, Sylvain Lamoine, Catherine Coudert, Yves Jacquot, et al.. The Antitumor Peptide ERα17p Exerts Anti-Hyperalgesic and Anti-Inflammatory Actions Through GPER in Mice. Frontiers in Endocrinology, 2021, 12, ⟨10.3389/fendo.2021.578250⟩. ⟨hal-04256623⟩

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2020

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David André Barrière, Fawzi Boumezbeur, Romain Dalman, Roberto Cadeddu, Damien Richard Richard, et al.. Paracetamol is a centrally acting analgesic using mechanisms located in the periaqueductal grey. British Journal of Pharmacology, 2020, 177 (8), pp.1773-1792. ⟨10.1111/bph.14934⟩. ⟨hal-02380187⟩

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2019

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Zoltan Dekan, Setareh Sianati, Arsalan Yousuf, Katy Sutcliffe, Alexander Gillis, et al.. A tetrapeptide class of biased analgesics from an Australian fungus targets the µ-opioid receptor. Proceedings of the National Academy of Sciences of the United States of America, 2019, 116 (44), pp.22353-22358. ⟨10.1073/pnas.1908662116⟩. ⟨hal-04257287⟩

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Nicolas Kerckhove, Ludivine Boudieu, Guillaume Ourties, Justine Bourdier, Laurence Daulhac, et al.. Ethosuximide improves chronic pain-induced anxiety- and depression-like behaviors. European Neuropsychopharmacology, 2019, 29, pp.1419 – 1432. ⟨10.1016/j.euroneuro.2019.10.012⟩. ⟨hal-03488870⟩

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Rosamaria Lappano, Christophe Mallet, Bruno Rizzuti, Fedora Grande, Giulia Raffaella Galli, et al.. The Peptide ERα17p Is a GPER Inverse Agonist that Exerts Antiproliferative Effects in Breast Cancer Cells. Cells, 2019, Molecular and Cellular Mechanisms of Cancers: Breast Cancer, 8 (6), pp.590. ⟨10.3390/cells8060590⟩. ⟨hal-02273130⟩

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Elodie Picard, Frédéric Antonio Carvalho, Francina Agosti, Emmanuel Bourinet, Denis Ardid, et al.. Inhibition of Cav3.2 calcium channels: A new target for colonic hypersensitivity associated with low‐grade inflammation. British Journal of Pharmacology, 2019, 176 (7), pp.950-963. ⟨10.1111/bph.14608⟩. ⟨hal-04317223⟩

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2018

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Romain Jouve, Vincent Thery, Sylvie Ducki, Julie Helfenbein, Christophe Thiery, et al.. Optimization of the synthesis of a key intermediate for the preparation of glucocorticoids. Steroids, 2018, 137, pp.14 – 21. ⟨10.1016/j.steroids.2018.06.007⟩. ⟨hal-01875170⟩

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2016

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Nicolas Kerckhove, Christophe Mallet, Bruno Pereira, Chouki Chenaf, Christian Duale, et al.. Assessment of the effectiveness and safety of Ethosuximide in the Treatment of non-Diabetic Peripheral Neuropathic Pain: EDONOT—protocol of a randomised, parallel, controlled, double-blinded and multicentre clinical trial. BMJ Open, 2016, 6 (12), pp.e013530. ⟨10.1136/bmjopen-2016-013530⟩. ⟨hal-04337204⟩

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Christophe Mallet, Claude Dubray, Christian Dualé. FAAH inhibitors in the limelight, but regrettably. International Journal of Clinical Pharmacology and Therapeutics, 2016, 54 (07), pp.498 – 501. ⟨10.5414/cp202687⟩. ⟨hal-04337687⟩

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J. Scanzi, A. Accarie, E. Muller, Bruno Pereira, Y. Aissouni, et al.. Colonic overexpression of the T‐type calcium channel Cav 3.2 in a mouse model of visceral hypersensitivity and in irritable bowel syndrome patients. Neurogastroenterology & Motility, 2016, 28 (11), pp.1632-1640. ⟨10.1111/nmo.12860⟩. ⟨hal-04317301⟩

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2015

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Romain Dalmann, Laurence Daulhac, Myriam Antri, Alain Eschalier, Christophe Mallet. Supra-spinal FAAH is required for the analgesic action of paracetamol in an inflammatory context. Neuropharmacology, 2015, 91, pp.63-70. ⟨10.1016/j.neuropharm.2014.11.006⟩. ⟨hal-04326283⟩

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2014

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Nicolas Kerckhove, Christophe Mallet, Amaury François, Mathieu Boudes, Jean Chemin, et al.. Cav3.2 calcium channels: the key protagonist of the supraspinal effect of paracetamol. Pain, 2014, 155 (4), pp.764-772. ⟨10.1016/j.pain.2014.01.015⟩. ⟨hal-02356344⟩

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Christophe Mallet, Chouki Chenaf. Prise en charge médicamenteuse de la douleur. Cerveau & psycho. L’essentiel, 2014, 17. ⟨hal-04273988⟩

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2013

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David A Barrière, Christophe Mallet, Anders Blomgren, Charlotte Simonsen, Laurence Daulhac, et al.. Fatty Acid Amide Hydrolase-Dependent Generation of Antinociceptive Drug Metabolites Acting on TRPV1 in the Brain. PLoS ONE, 2013, 8 (8), pp.e70690. ⟨10.1371/journal.pone.0070690⟩. ⟨hal-04337223⟩

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Peter M Zygmunt, Anna Ermund, Pouya Movahed, David A Andersson, Charlotte Simonsen, et al.. Monoacylglycerols Activate TRPV1 – A Link between Phospholipase C and TRPV1. PLoS ONE, 2013, 8 (12), pp.e81618. ⟨10.1371/journal.pone.0081618⟩. ⟨hal-04337227⟩

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2012

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Christophe Mallet, Alain Eschalier. Mise au point sur les mécanismes de l’action antalgique du paracétamol. Urgence Pratique, 2012, 115, pp.29-31. ⟨hal-04273935⟩

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Christophe Mallet, David Barrière, Alain Eschalier. Le paracétamol : un ancêtre plein d’avenir. Therapies, 2012, 67 (4), pp.277-281. ⟨10.2515/therapie/2012039⟩. ⟨hal-04337690⟩

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2011

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Elena Bagley, Jennifer Hacker, Vladimir Chefer, Christophe Mallet, Gavan Mcnally, et al.. Drug-induced GABA transporter currents enhance GABA release to induce opioid withdrawal behaviors. Nature Neuroscience, 2011, 14 (12), pp.1548-1554. ⟨10.1038/nn.2940⟩. ⟨hal-04337230⟩

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2010

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David André Barrière, Christophe Mallet, Alain Eschalier. Le paracétamol, de nouvelles cibles pour un vieux médicament. La Lettre de l’Institut UPSA de la Douleur, 2010, 33. ⟨hal-04273458⟩

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Christophe Mallet, David Barrière, Anna Ermund, Bo Jönsson, Alain Eschalier, et al.. TRPV1 in Brain Is Involved in Acetaminophen-Induced Antinociception. PLoS ONE, 2010, 5 (9), pp.e12748. ⟨10.1371/journal.pone.0012748⟩. ⟨hal-04326308⟩

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2009

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Macdonald Christie, Christophe Mallet. Endocannabinoids Can Open the Pain Gate. Science Signaling, 2009, 2 (88), ⟨10.1126/scisignal.288pe57⟩. ⟨hal-04337579⟩

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2008

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Christophe Mallet, Laurence Daulhac, Jérôme Bonnefont, Catherine Ledent, Monique Etienne, et al.. Endocannabinoid and serotonergic systems are needed for acetaminophen-induced analgesia. Pain, 2008, 139 (1), pp.190-200. ⟨10.1016/j.pain.2008.03.030⟩. ⟨hal-04326295⟩

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2007

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Jérôme Bonnefont, Laurence Daulhac, Monique Etienne, Eric Chapuy, Christophe Mallet, et al.. Acetaminophen recruits spinal p42/p44 mAPKs and GH/IGF-1 receptors to produce analgesia via the serotonergic system. Molecular Pharmacology, 2007, 71 (2), pp.407-415. ⟨10.1124/mol.106.025775⟩. ⟨hal-02659399⟩

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2006

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Laurence Daulhac, Christophe Mallet, Christine Courteix, Monique Etienne, Eliane Duroux, et al.. Diabetes-Induced Mechanical Hyperalgesia Involves Spinal Mitogen-Activated Protein Kinase Activation in Neurons and Microglia via N -Methyl-D-aspartate-Dependent Mechanisms. Molecular Pharmacology, 2006, 70 (4), pp.1246-1254. ⟨10.1124/mol.106.025478⟩. ⟨hal-04326273⟩

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Conference papers

2021

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Christophe Mallet, David André Barrière, Fouad Boumezbeur, Romain Dalmann, Roberto Cadeddu, et al.. Paracetamol is a centrally acting analgesic using mechanisms located in the periaqueductal grey. Annual Meeting of French Society of Pharmacology and Therapeutics, Jun 2021, Online, France. ⟨hal-03745618⟩

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Book sections

2018

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Nicolas Authier, Bénédicte Eschalier, Chouki Chenaf, Marie Zenut, Christophe Mallet, et al.. Traitements de la douleur, Approche pharmacologique. Traité de Médecine (5ème édition), TDM, pp.S10-P01-C11, 2018, 9782901094012. ⟨hal-04273871⟩

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2015

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Christophe Mallet, Alain Eschalier. Pharmacology and Mechanism of Action of Acetaminophen. Pharmacology of Pain, IASP press, 2015, 0931092787. ⟨hal-04337640⟩

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Poster communications

2019

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Guillaume Ourties, Laurence Daulhac, Alain Eschalier, Christophe Mallet. Involvment of Cav3.2 calcium channels in oesteoarthritis pain. EFIC pain school, Jun 2019, cracovie, Poland. ⟨hal-02363984⟩

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Preprints, Working Papers, …

2022

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Sophie L Fayad, Guillaume Ourties, Benjamin Le Gac, Baptiste Jouffre, Sylvain Lamoine, et al.. Centrally expressed Cav3.2 T-type calcium channel is critical for the initiation and maintenance of neuropathic pain. 2022. ⟨hal-03746638⟩

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