Publicaciones científicas
Artículos publicados en revistas científicas con "peer-review".
Transporte de neurotransmisores
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Marvizón, J.C.G., F. Mayor, Jr., M.C. Aragón, C. Giménez and F. Valdivieso. L-Aspartate transport into plasma membrane vesicles derived from rat brain synaptosomes. J. Neurochem. 37: 1401-1406, 1981.
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Mayor, F., Jr., J.C.G. Marvizón, M.C. Aragón, C. Giménez and F. Valdivieso. Glycine transport into plasma membrane vesicles derived from rat brain synaptosomes. Biochem. J. 198: 534-541, 1981.
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Aragón, M.C., C. Giménez, F. Mayor, Jr., J.C.G. Marvizón and F. Valdivieso. Tyrosine transport by membrane vesicles isolated from rat brain. Biochim. Biophys. Acta 646: 465-470, 1981.
Receptores de neurotransmisores: glicina, GABA y NMDA
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Marvizón, J.C.G., J. Vázquez, M. García Calvo, F. Mayor, Jr., A. Ruiz Gómez, F. Valdivieso and J. Benavides. The glycine receptor: pharmacological studies and mathematical modeling of the allosteric interaction between the glycine- and the strychnine-binding sites. Mol. Pharmacol. 30: 590-597, 1986.
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Marvizón, J.C.G., M. García Calvo, J. Vázquez, F. Mayor, Jr., A. Ruiz Gómez, F. Valdivieso and J. Benavides. Activation and inhibition of [3H]strychnine binding to the glycine receptor by Eccles' anions: modulatory effect of cations. Mol. Pharmacol. 30: 598-602, 1986.
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Marvizón, J.C.G. and P. Skolnick. Enhancement of t-[35S]Butylbicyclophosphorothionate and [3H]strychnine binding by monovalent anions reveals similarities between g-aminobutyric acid- and glycine-gated chloride channels. J. Neurochem. 50: 1632-1639, 1988.
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Alonso, T., R.O. Morgan, J.C.G. Marvizón, H. Zarbl and E. Santos. Malignant transformation by ras and other oncogenes produces common alterations in phosphoinositide signaling pathways. Proc. Nat. Acad. Sci. USA 85: 4271-4275, 1988.
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Marvizón, J.C.G. and P. Skolnick. [3H]Glycine binding is modulated by Mg+2 and other ligands of the NMDA receptor-cation channel complex. Eur. J. Pharmacol. 151: 157-58, 1988.
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Marvizón, J.C.G. and P. Skolnick. Anion regulation of [3H]strychnine binding to glycine-gated chloride channels is explained by the presence of two anion binding sites. Mol. Pharmacol. 34: 806-813, 1988.
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Marvizón, J.C.G., A. Lewin and P. Skolnick. 1-Amino-cyclopropane carboxylic acid: a potent and selective ligand for the glycine modulatory site of the N-methyl-D-Aspartate receptor complex. J. Neurochem. 52: 992-994, 1989.
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Ruiz-Gómez, A., M. García-Calvo, J. Vázquez, J.C.G. Marvizón, F. Valdivieso and F. Mayor, Jr. Thermodynamics of agonist and antagonist interaction with the strychnine-sensitive glycine receptor. J. Neurochem. 52: 1775-1780, 1989.
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Skolnick, P., J.C.G. Marvizón, B. W. Jackson., J. A. Monn, K. C. Rice and A. Lewin. Blockade of N-methyl-D-aspartate induced convulsions by 1-aminocyclopropane-carboxylates. Life Sci. 45: 1647-1655, 1989.
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Marvizón, J.C.G., and P. Skolnick. An endogenous modulator of N-methyl-D-aspartate receptor-coupled glycine receptors. Eur. J. Pharmacol. Mol. Pharmacol. 188: 23-32, 1990.
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Ruiz-Gómez, A., C. Fernández-Shaw, E. Morato, J. C. G. Marvizón, J. Vázquez, F. Valdivieso, F. Mayor, Jr. Sulfydryl groups modulate the allosteric interaction between glycine binding sites at the inhibitory glycine receptor. J. Neurochem. 56: 1690-1697, 1991.
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Shahi, K., J.C.G. Marvizón and M. Baudry. High concentrations of glycine induce long-lasting changes in synaptic efficacy in rat hippocampal slices. Neurosci. Lett. 149: 185-188, 1993.
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Marvizón, J.C.G., and M. Baudry. NMDA receptor activation by spermine requires glutamate but not glycine. Eur. J. Pharmacol. Mol. Pharmacol. 244: 103-104, 1993.
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Lewin, A. H., P. Skolnick, J.C.G. Marvizón, I. A. Paul and J. P. Bowen. Requirements for high affinity binding of glycine analogs to the glycine site of the NMDA receptor complex. Eur. J. Pharmacol. Mol. Pharmacol. 247: 1-10, 1993.
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Marvizón, J.C.G., and M. Baudry. Receptor activation by two agonists: Analysis by non-linear regression and application to N-methyl-D-aspartate receptors. Anal. Biochem 213: 3-11, 1993.
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Marvizón, J.C.G., and M. Baudry. [3H]Dizocilpine association kinetics distinguish stimulatory and inhibitory polyamine sites of N-Methyl-D-Aspartate receptors. J. Neurochem. 63: 963-971, 1994.
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Marvizón, J.C.G., and M. Baudry. Allosteric interactions and modulator requirement for NMDA receptor function. Eur. J. Pharmacol. Mol. Pharmacol. 269: 165-175, 1994.
Neuropéptidos que regulan el dolor: substancia P, CGRP, BDNF y endorfinas
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Marvizón, J.C.G., V. Martínez, E.F. Grady, N.W. Bunnett and E.A. Mayer. Neurokinin 1 receptor internalization in spinal cord slices induced by dorsal root stimulation is mediated by NMDA receptors. J. Neurosci. 17: 8129-8136, 1997.
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Marvizón, J.C.G., S. Eskandari, H. Ennes and E.A. Mayer. Substance P induces brief, localized increases in [Ca2+]i in dorsal horn neurons. NeuroReport 9 (15): 3369-3374, 1998.
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Marvizón, J.C.G., E.F. Grady, E. Stefani, N.W. Bunnett and E.A. Mayer. Substance P release in the dorsal horn assessed by receptor internalization: NMDA receptors counteract a tonic inhibition by GABAB receptors. Eur. J. Neurosci. 11: 417-426, 1999.
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Marvizón, J.C.G., E.F. Grady, J. Wazsak-McGee and E. Mayer. Internalization of m-opioid receptors in rat spinal cord slices. NeuroReport 10 (11): 2329-2334, 1999.
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McRoberts, J.A., S.V. Coutinho, J.C.G. Marvizon, E.F. Grady, M. Tognetto, J.N. Sengupta, H.S. Ennes, V.V. Chaban, S. Amadesi, Ch. Creminon, T. Lanthorn, P. Geppetti, N.W. Bunnett, and E.A. Mayer. Role of peripheral N-methyl-D-aspartate (NMDA) receptors in visceral nociception in rats. Gastroenterology 120: 1737-1748, 2001.
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I.J. Lever, E.J. Bradbury, J.R. Cunningham, D.W. Adelson, M.G. Jones, S.B. McMahon, J.C.G. Marvizon and M. Malcangio. Brain-derived neurotrophic factor is released in the dorsal horn by distinctive patterns of nociceptor stimulation. J. Neurosci. 21 (12): 4469-4477, 2001.
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Marvizón, J.C.G., J. McRoberts, H.S. Ennes, B. Song, X. Wang, L. Jinton, B. Corneliussen and E. A. Mayer. Two NMDA receptors in rat dorsal root ganglia with different subunit composition and localization. J. Comp. Neurol. 446: 325-341, 2002.
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Wang, X., and J.C.G. Marvizón. Time-course of the internalization and recycling of neurokinin 1 receptors in rat dorsal horn neurons. Brain Res. 944: 239-247, 2002.
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Marvizón, J.C.G., X. Wang, Y. Matsuka, J.K. Neubert and I. Spigelman. Relationship between capsaicin-evoked substance P release and NK1 receptor internalization in the rat dorsal horn. Neuroscience 118 (2): 535-545, 2003.
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Song, B., and J.C.G. Marvizon. Peptidases prevent mu-opioid receptor internalization in dorsal horn neurons by endogenously released opioids. J. Neurosci. 23: 1847-1858, 2003.
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Song, B., and J.C.G. Marvizón. Dorsal horn neurons firing at high frequency, but not primary afferents, release opioid peptides that produce mu-opioid receptor internalization in the rat spinal cord. J. Neurosci. 23: 9171-9184, 2003.
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Lao, L.J., Song, B. and J.C.G. Marvizón. Neurokinin release produced by capsaicin acting on the central terminals and axons of primary afferents: relationship with NMDA and GABAB receptors. Neuroscience 121: 667-680, 2003.
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Marvizón, J.C.G., X. Wang, L. Lao and B. Song. Effect of peptidases on the ability of exogenous and endogenous neurokinins to produce neurokinin 1 receptor internalization in the rat spinal cord. Br. J. Pharmacol. 140: 1389-1398, 2003.
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Lao L., and J.C.G. Marvizón. GABAA receptor facilitation of neurokinin release from primary afferent terminals in the rat spinal cord. Neuroscience 130: 1013-1027, 2005.
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Kondo, I., J.C.G. Marvizón, B. Song, F. Salgado, S. Codeluppi, X.-Y. Hua and T. Yaksh. Inhibition by spinal m- and d-opioid agonists of afferent-evoked substance P release. J. Neurosci. 25: 3651-3660, 2005.
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Cottrell,G.S., D. Roosterman, J.C. Marvizon, B. Song, E. Wick, S. Pikios, H. Wong, C. Berthelier, Y. Tang, C. Sternini, C.W. Tam, S.D. Brain, N.W. Bunnett, E. Grady. Localization of calcitonin receptor-like receptor and receptor activity modifying protein 1 in enteric neurons, dorsal root ganglia, and the spinal cord of the rat. J. Comp. Neurol. 490: 235-255, 2005.
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Song, B., and J.C.G. Marvizón. NMDA receptors and large conductance calcium-sensitive potassium channels inhibit the release of opioid peptides that induce m-opioid receptor internalization in the rat spinal cord. Neuroscience 136: 549-562, 2005.
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Bradesi, S. , E. Kokkotou, S. Simeonidis, S. Patierno, H.S. Ennes, Y. Mittal, J.A. McRoberts, G. Ohning, J.C.G. Marvizon, C. Sternini, C. Pothoulakis and E.A. Mayer. The role of neurokinin 1 receptors in the maintenance of visceral hyperalgesia induced by repeated stress in rats. Gastroenterology 130: 1729-1742, 2006.
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Song, B., W. Chen and J.C.G. Marvizon. Inhibition of opioid release in the rat spinal cord by serotonin 5-HT1A receptors. Brain Res. 1158: 57-62, 2007.
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Marvizon, J.C.G., O.A. Perez, B. Song, W. Chen, N.W. Bunnett, E.F. Grady and A.J. Todd. Calcitonin Receptor-Like Receptor and Receptor Activity Modifying Protein 1 in the rat dorsal horn: localization in excitatory presynaptic terminals containing opioids and adrenergic α2C receptors. Neuroscience 148: 250-265, 2007.
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Chen, W., B. Song, L. Lao, O.A. Perez, W. Kim and J.C.G. Marvizon. Comparing analgesia and µ-opioid receptor internalization produced by intrathecal enkephalin: Requirement for peptidase inhibition. Neuropharmacology 53: 664-667, 2007.
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Lao, L., B. Song, W. Chen and J.C.G. Marvizon. Noxious mechanical stimulation evokes the segmental release of opioid peptides that induce µ-opioid receptor internalization. Brain Res. 1197: 85-93, 2008.
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Chen, W., B. Song, G. Zhang and J.C.G. Marvizon. Effects of veratridine and high potassium on µ-opioid receptor internalization in the rat spinal cord: stimulation of opioid release versus inhibition of internalization. J. Neurosci. Methods 170: 285-293, 2008.
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Chen, W., B. Song and J.C.G. Marvizón. Inhibition of opioid release in the rat spinal cord by α2C adrenergic receptors. Neuropharmacology 54: 944-953, 2008.
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Chen, W., and J.C.G. Marvizón. Acute inflammation induces segmental, bilateral, supraspinally mediated opioid release in the rat spinal cord, as measured by µ-opioid receptor internalization. Neuroscience 161: 157-172, 2009.
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Adelson, D.W., L. Lao, G. Zhang, W. Kim and J.C.G. Marvizón. Substance P release and neurokinin 1 receptor activation in the rat spinal cord increases with the firing frequency of C-fibers. Neuroscience 161: 538-553, 2009. PMC2692762
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Marvizon, J.C.G., W. Chen, and N. Murphy. Enkephalins, dynorphins and β-endorphin in the rat dorsal horn: an immunofluorescence colocalization study. J. Comp. Neurol. 517: 51-68, 2009. PMC2924145
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Zhang G., W. Chen, L. Lao and J.C.G. Marvizon. Cannabinoid CB1 receptor facilitation of substance P release in the rat spinal cord, measured as neurokinin 1 receptor internalization. Eur. J. Neurosci. 31: 225-237, 2010. PMC2857979
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Chen W., G. Zhang and J.C.G. Marvizon. NMDA receptors in primary afferents require phosphorylation by Src family kinases to induce substance P release in the rat spinal cord. Neuroscience 166: 924-934, 2010. PMC2837134
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Ao Y, M. Ko, A. Chen, J.C. Marvizon, D.W. Adelson, M.K. Song, L.W. Go, L.L. Liu, H. Yang. Potent hyperglycemic and hyperinsulinemic effects of thyrotropin-releasing hormone microinjected into the rostroventrolateral medulla and abnormal responses in type 2 diabetic rats. Neuroscience 169: 706-719, 2010. PMC3896326
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Chen, W., G. Zhang and J.C.G. Marvizon. Src family kinases mediate the inhibition of substance P release in the spinal cord by µ-opioid receptors and GABAB receptors, but not α2 adrenergic receptors. Eur. J. Neurosci. 32: 963-973, 2010. PMC2942982
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McRoberts J.A., Ennes H., Marvizon J.C.G., Fanselow M., Mayer E.A., Vissel B. Selective knockdown of NMDA receptors in primary afferent neurons decreases pain during phase 2 of the formalin test. Neuroscience 172: 474-482, 2011. PMC3010451
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Taylor B. K., W. Fu, K.E. Kuphal, C.-O. Stiller, M.K. Winter, W. Chen, G.F. Corder, J.H. Urban, K.E. McCarson, and J.C. Marvizon. Inflammation enhances Y1 receptor signaling, neuropeptide Y-mediated inhibition of hyperalgesia, and substance P release from primary afferent neurons. Neuroscience 256:178-194, 2014. PMC4363128
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Chen W, J. A. McRoberts, J.C.G. Marvizón. µ-Opioid receptor inhibition of substance P release from primary afferents disappears during neuropathic pain but not inflammatory pain. Neuroscience 267: 67-82, 2014. PMC3998911
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Chen W., W. Walwyn, H. Ennes, J.A. McRoberts, J.C.G. Marvizón. BDNF released by microglia during neuropathic pain potentiates NMDA receptors in primary afferent terminals. Eur. J. Neurosci. 39: 1439-1454, 2014. PMC4122572
Dolor crónico
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Marvizón JC, Walwyn W, Minasayan A, Chen W, Taylor BK. Latent Sensitization: a model for stress-sensitive chronic pain. Current Protocols in Neuroscience 71: 9.50.1-9.50.14, 2015. PMC4532319
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Walwyn W., W. Chen, H. Kim, A. Minasayan, H. Ennes, J.A. McRoberts, J.C. Marvizón. Sustained suppression of hyperalgesia during latent sensitization by µ, δ and κ opioid receptors and α2A adrenergic receptors - role of constitutive activity. J. Neurosci. 36: 204-221, 2016. PMC4701961
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Chen W., H.S. Ennes, J.A. McRoberts, J.C. Marvizón. Mechanisms of µ-opioid receptor inhibition of NMDA receptor-induced substance P release in the rat spinal cord. Neuropharmacology 128: 255-268, 2018. PMC5726399
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Chen W, Taché Y, Marvizon JCG. Corticotropin Releasing Factor in the brain and blocking spinal descending signals induce hyperalgesia in the latent sensitization model of chronic pain. Neuroscience 381: 149-158, 2018. PMC5962032
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Severino, A, W Chen, J K Hakimian, B Kieffer, C Gaveriaux-Ruff, W Walwyn, J C Marvizon. Mu-opioid receptors in nociceptive afferents produce a sustained suppression of hyperalgesia in chronic pain. Pain 159: 1607-1620, 2018. PMC6053329 Full text
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Marvizon, J C, W Chen, W Fu and B K Taylor. Neuropeptide Y release in the rat spinal cord measured with Y1 receptor internalization is increased after nerve injury. Neuropharmacology 158: 107732, 2019.
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Chen, W, J C Marvizón. A Src family kinase maintains latent sensitization in rats, a model of inflammatory and neuropathic pain. Brain Res 1746: 146999 (2020). Biorxiv
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Chen, W, J C Marvizón. Neurokinin 1 receptor activation in the rat spinal cord maintains latent sensitization, a model of inflammatory and neuropathic chronic pain. Neuropharmacology 177: 108253 (2020). Biorxiv
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Chen, W, J A McRoberts, H S Ennes, J C Marvizon. cAMP signaling through protein kinase A and Epac2 induces substance P release in the rat spinal cord. Neuropharmacology 189: 108533 (2021) PMC8577816