A. Mauborgne

发表

Microglial Janus kinase/signal transduction and activator of transcription 3 pathway activity directly impacts astrocyte and spinal neuron characteristics

Y. Boucher, D. Geny, J. Molet, 2016, Journal of neurochemistry.

Substance P levels in the synovium and synovial fluid from patients with rheumatoid arthritis and osteoarthritis.

C. Menkes, A. Mauborgne, M. Renoux, 1993, The Journal of rheumatology.

Spinal CCL2 pronociceptive action is no longer effective in CCR2 receptor antagonist‐treated rats

W. Rostène, P. Kitabgi, A. Mauborgne, 2008, Journal of neurochemistry.

CCL2 Released from Neuronal Synaptic Vesicles in the Spinal Cord Is a Major Mediator of Local Inflammation and Pain after Peripheral Nerve Injury

Juliette van Steenwinckel, P. Kitabgi, A. Mauborgne, 2011, The Journal of Neuroscience.

Altered opioid‐mediated control of the spinal release of dynorphin and met‐enkephalin in polyarthritic rats

M. Hamon, S. Ballet, A. Mauborgne, 2000, Synapse.

Biochemical mapping of cholecystokinin-, substance P-, [met]enkephalin-, [leu]enkephalin- and dynorphin a (1–8)-like immunoreactivities in the human cerebral cortex

Y. Agid, M. Hamon, F. Javoy‐Agid, 1988, Neuroscience.

Effects of Peripheral Axotomy on Cholecystokinin Neurotransmission in the Rat Spinal Cord

M. Hamon, A. Mauborgne, M. Pohl, 1999, Journal of neurochemistry.

Enkephalinergic and dynorphinergic neurons in the spinal cord and dorsal root ganglia of the polyarthritic rat — in vivo release and cDNA hybridization studies

M. Hamon, S. Ballet, A. Mauborgne, 1997, Brain Research.

Is substance P released from slices of the rat spinal cord inactivated by peptidase(s) distinct from both ‘enkephalinase’ and ‘angiotensin-converting enzyme’?

M. Hamon, A. Mauborgne, S. Bourgoin, 1991, Neuroscience Letters.

Neonatal capsaicin treatment abolishes the modulations by opioids of substance P release from rat spinal cord slices

M. Hamon, A. Mauborgne, M. Pohl, 1989, Neuroscience Letters.

Lentiviral-mediated Targeted NF-κB Blockade in Dorsal Spinal Cord Glia Attenuates Sciatic Nerve Injury-induced Neuropathic Pain in the Rat.

J. Mallet, M. Hamon, Alban Latremoliere, 2007, Molecular therapy : the journal of the American Society of Gene Therapy.

Lack of Change in Basal Ganglia Neuropeptide Content Following Subacute 1‐Methyl‐4‐Phenyl‐1,2,3,6‐Tetrahydropyridine Treatment of the Common Marmoset

Y. Agid, F. Javoy‐Agid, P. Jenner, 1986, Journal of neurochemistry.

Brain neuropeptides in progressive supranuclear palsy

Y. Agid, M. Hamon, F. Javoy‐Agid, 1987, Brain Research.

GABA, acting at both GABAA and GABAB receptors, inhibits the release of cholecystokinin-like material from the rat spinal cord in vitro

M. Hamon, A. Mauborgne, M. Pohl, 1992, Brain Research.

Differential inhibitory/stimulatory modulation of spinal CCK release by μ and δ opioid agonists, and selective blockade of μ-dependent inhibition by κ receptor stimulation

M. Hamon, A. Mauborgne, S. Bourgoin, 1991, Neuroscience Letters.

Regional Distribution of Calcitonin Gene‐Related Peptide‐, Substance P‐, Cholecystokinin‐, Met5‐Enkephalin‐, and Dynorphin A (1–8)‐Like Materials in the Spinal Cord and Dorsal Root Ganglia of Adult Rats: Effects of Dorsal Rhizotomy and Neonatal Capsaicin

A. Carayon, M. Hamon, A. Mauborgne, 1990, Journal of neurochemistry.

Hedgehog Pathway–Mediated Vascular Alterations Following Trigeminal Nerve Injury

Y. Boucher, A. Mauborgne, Luis Villanueva, 2017, Journal of dental research.

Differential Implication of Proinflammatory Cytokine Interleukin-6 in the Development of Cephalic versus Extracephalic Neuropathic Pain in Rats

M. Hamon, Alban Latremoliere, A. Mauborgne, 2008, The Journal of Neuroscience.

Increased calcitonin gene-related peptide- and cholecystokinin-like immunoreactivities in spinal motoneurones after dorsal rhizotomy

M. Hamon, J. Meunier, A. Mauborgne, 2005, Journal of Neural Transmission / General Section JNT.

The novel analgesic, cizolirtine, inhibits the spinal release of substance P and CGRP in rats

M. Hamon, S. Ballet, A. Mauborgne, 2001, Neuropharmacology.

Fentanyl-induced hyperalgesia and analgesic tolerance in male rats: common underlying mechanisms and prevention by a polyamine deficient diet

J. Simmers, A. Mauborgne, M. Pohl, 2021, Neuropsychopharmacology.

Polyarthritis-associated changes in the opioid control of spinal CGRP release in the rat

M. Hamon, S. Ballet, A. Mauborgne, 1998, Brain Research.

Differential effects of the novel analgesic, S 12813-4, on the spinal release of substance P- and calcitonin gene-related peptide-like materials in the rat

M. Hamon, A. Mauborgne, M. Pohl, 1994, Naunyn-Schmiedeberg’s Archives of Pharmacology.

The neuropeptide FF analogue, 1DME, enhances in vivo met-enkephalin release from the rat spinal cord

M. Hamon, S. Ballet, A. Mauborgne, 1999, Neuropharmacology.

Early alterations of Hedgehog signaling pathway in vascular endothelial cells after peripheral nerve injury elicit blood-nerve barrier disruption, nerve inflammation, and neuropathic pain development

P. Couraud, Y. Boucher, I. Romero, 2016, Pain.

Direct stimulatory effect of calcitonin on [3H]5-hydroxytryptamine release from the rat spinal cord.

M. Hamon, A. Mauborgne, M. Pohl, 1988, European journal of pharmacology.

In vivo tonic inhibition of spinal substance P (-like material) release by endogenous opioid(s) acting at δ receptors

M. Hamon, A. Mauborgne, F. Cesselin, 1991, Neuroscience.

Monoaminergic control of the release of calcitonin gene-related peptide- and substance P-like materials from rat spinal cord slices

M. Hamon, A. Mauborgne, M. Pohl, 1993, Neuropharmacology.

JAK/STAT3 pathway is activated in spinal cord microglia after peripheral nerve injury and contributes to neuropathic pain development in rat

A. Mauborgne, M. Pohl, C. Rivat, 2008, Journal of neurochemistry.

Antihyperalgesic effects of cizolirtine in diabetic rats: behavioral and biochemical studies

M. Hamon, A. Mauborgne, V. Kayser, 2004, Pain.

Mu and delta opioid receptors mediate opposite modulations by morphine of the spinal release of cholecystokinin-like material

M. Hamon, A. Mauborgne, S. Bourgoin, 1994, Brain Research.

Differential inhibitory/stimulatory modulation of spinal CCK release by mu and delta opioid agonists, and selective blockade of mu-dependent inhibition by kappa receptor stimulation.

M. Hamon, A. Mauborgne, S. Bourgoin, 1991, Neuroscience Letters.

Chronic stress induces transient spinal neuroinflammation, triggering sensory hypersensitivity and long-lasting anxiety-induced hyperalgesia

A. Mauborgne, M. Pohl, C. Rivat, 2010, PAIN.

In vitro effect of dopamine and L-dopa on prolactin and growth hormone release from human pituitary adenomas.

F. Peillon, A. Mauborgne, A. Brandi, 1979, The Journal of clinical endocrinology and metabolism.

Opioidergic control of the spinal release of neuropeptides. Possible significance for the analgesic effects of opioids

M. Hamon, A. Mauborgne, M. Pohl, 1994, Fundamental & clinical pharmacology.

Attenuation of pain-related behavior in a rat model of trigeminal neuropathic pain by viral-driven enkephalin overproduction in trigeminal ganglion neurons.

M. Hamon, Alban Latremoliere, A. Mauborgne, 2005, Molecular therapy : the journal of the American Society of Gene Therapy.

Subcutaneous formalin enhances outflow of met-enkephalin- and cholecystokinin-like materials in the rat nucleus accumbens

M. Hamon, A. Mauborgne, S. Bourgoin, 2001, Naunyn-Schmiedeberg's Archives of Pharmacology.

The Dual Peptidase Inhibitor RB101 Induces a Long‐Lasting Increase in the Extracellular Level of Met‐Enkephalin‐Like Material in the Nucleus Accumbens of Freely Moving Rats

B. Roques, A. Mauborgne, M. Fournié-Zaluski, 1996, Journal of neurochemistry.

The neuropeptide FF analogue, 1DMe, reduces in vivo dynorphin release from the rat spinal cord

M. Hamon, S. Ballet, A. Mauborgne, 2002, Journal of neurochemistry.

COMMUNICATION The neuropeptide FF analogue, 1DMe, reduces in vivo dynorphin release from the rat spinal cord

M. Hamon, A. Mauborgne, S. Bourgoin, 2002 .

SOCS3-Mediated Blockade of JAK/STAT3 Signaling Pathway Reveals Its Major Contribution to Spinal Cord Neuroinflammation and Mechanical Allodynia after Peripheral Nerve Injury

J. Mallet, A. Mauborgne, M. Pohl, 2010, The Journal of Neuroscience.

Opioid control of the release of Met-enkephalin-like material from the rat spinal cord

M. Hamon, A. Mauborgne, M. Pohl, 1991, Brain Research.

[Interactions between central opioidergic and cholecystokininergic systems in rats: possible significance for the development of of opioid tolerance].

M. Hamon, A. Mauborgne, S. Bourgoin, 1998, Bulletin de l'Academie nationale de medecine.

Adenosine receptor-mediated control of in vitro release of pain-related neuropeptides from the rat spinal cord.

M. Hamon, A. Mauborgne, S. Bourgoin, 2002, European journal of pharmacology.

KAPPA-/MU-receptor interactions in the opioid control of the in vivo release of substance P-like material from the rat spinal cord

M. Hamon, A. Mauborgne, L. Ferhat, 1992, Neuroscience.

Opioid Control of the In Vitro Release of Cholecystokinin‐Like Material from the Rat Substantia Nigra

M. Hamon, A. Mauborgne, S. Bourgoin, 1992, Journal of neurochemistry.

Opposite Effects of δ and μ Opioid Receptor Agonists on the In Vitro Release of Substance P‐Like Material from the Rat Spinal Cord

M. Hamon, A. Mauborgne, J. Legrand, 1987 .

Freezing of Enkephalinergic Functions by Multiple Noxious Foci: A Source of Pain Sensitization?

M. Hamon, A. Mauborgne, S. Bourgoin, 2009, PloS one.

The neuropeptide FF analogue, 1DMe, acts as a functional opioid autoreceptor antagonist in the rat spinal cord.

A. Mauborgne, S. Bourgoin, F. Cesselin, 2001, European journal of pharmacology.

Opioid receptors and neuropeptides in the CNS in rats treated chronically with amoxapine or amitriptyline

M. Hamon, A. Mauborgne, J. Micó, 1987, Neuropharmacology.

Ethanol and opiate decrease the axonal transport of substance-P like immunoreactive material in rat vagus-nerves

M. Hamon, A. Mauborgne, P. Laduron, 1990, Neuropeptides.

Enkephalinase is involved in the degradation of endogenous substance P released from slices of rat substantia nigra.

M. Hamon, A. Mauborgne, S. Bourgoin, 1987, The Journal of pharmacology and experimental therapeutics.

Lentiviral-mediated targeted NF-kappaB blockade in dorsal spinal cord glia attenuates sciatic nerve injury-induced neuropathic pain in the rat.

J. Mallet, M. Hamon, Alban Latremoliere, 2007, Molecular therapy : the journal of the American Society of Gene Therapy.

γ-Aminobutyric acid, through GABAA receptors, inhibits the potassium-stimulated release of calcitonin gene-related peptide-but not that of substance P-like material from rat spinal cord slices

M. Hamon, A. Mauborgne, M. Pohl, 1992, Brain Research.

gamma-Aminobutyric acid, through GABAA receptors, inhibits the potassium-stimulated release of calcitonin gene-related peptide- but not that of substance P-like material from rat spinal cord slices.

M. Hamon, A. Mauborgne, M. Pohl, 1992, Brain research.

Opioid control of the in vitro release of calcitonin gene-related peptide from primary afferent fibres projecting in the rat cervical cord

A. Carayon, M. Hamon, A. Mauborgne, 1989, Neuropeptides.

Implication of the chemokine CCL2 in trigeminal nociception and traumatic neuropathic orofacial pain

Y. Boucher, J. Molet, A. Mauborgne, 2014, European journal of pain.

Decrease of substance P-like immunoreactivity in the substantia nigra and pallidum of parkinsonian brains

Y. Agid, F. Javoy‐Agid, A. Mauborgne, 1983, Brain Research.

Mycolactone displays anti-inflammatory effects on the nervous system

C. Limatola, C. Demangel, Y. Boucher, 2017, PLoS neglected tropical diseases.

Social interaction increases the extracellular levels of [Met]enkephalin in the nucleus accumbens of control but not of chronic mild stressed rats.

B. Roques, A. Mauborgne, C. Smadja, 1997, Neuroscience.

Levels of MET-enkephalin, LEU-enkephalin, substance P and cholecystokinin in the brain of the common marmoset following long term 1-methyl-4-phenyl-1,2,3,6,-tetrahydropyridine treatment

C. Marsden, Y. Agid, M. Hamon, 1988, Neuropeptides.

Morphine reduces the release of met-enkephalin-like material from the rat spinal cord in vivo by acting at ∂ opioid receptors

M. Hamon, A. Mauborgne, S. Bourgoin, 1994, Neuropeptides.

Lentiviral-mediated targeted transgene expression in dorsal spinal cord glia: Tool for the study of glial cell implication in mechanisms underlying chronic pain development

J. Mallet, A. Mauborgne, M. Pohl, 2008, Journal of Neuroscience Methods.

Sumatriptan inhibits the release of CGRP and substance P from the rat spinal cord.

M. Hamon, C. Oliver, A. Mauborgne, 1996, Neuroreport.

Lipopolysaccharide-mediated inflammatory priming potentiates painful post-traumatic trigeminal neuropathy

Y. Boucher, A. Mauborgne, N. Moreau, 2018, Physiology & Behavior.

Opposite effects of delta and mu opioid receptor agonists on the in vitro release of substance P-like material from the rat spinal cord.

M. Hamon, A. Mauborgne, J. Legrand, 1987, Journal of neurochemistry.

Presynaptic Autoreceptors May Control the Release of Metenkephalin from the Rat Spinal Cord

M. Hamon, A. Mauborgne, S. Bourgoin, 1991 .

Could an endoneurial endothelial crosstalk between Wnt/β-catenin and Sonic Hedgehog pathways underlie the early disruption of the infraorbital blood–nerve barrier following chronic constriction injury?

P. Couraud, Y. Boucher, I. Romero, 2017, Molecular pain.