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Mammalian Transient Receptor Potential TRPA1 Channels: From Structure to Disease
Open accessAbstract
The transient receptor potential ankyrin (TRPA) channels are Ca 2+ -permeable nonselective cation channels remarkably conserved through the animal kingdom. Mammals have only one member, TRPA1, which is widely expressed in sensory neurons and in non-neuronal cells (such as epithelial cells and hair cells). TRPA1 owes its name to the presence of 14 ankyrin repeats located in the NH 2 terminus of the channel, an unusual structural feature that may be relevant to its interactions with intracellular components. TRPA1 is primarily involved in the detection of an extremely wide variety of exogenous stimuli that may produce cellular damage. This includes a plethora of electrophilic compounds that interact with nucleophilic amino acid residues in the channel and many other chemically unrelated compounds whose only common feature seems to be their ability to partition in the plasma membrane. TRPA1 has been reported to be activated by cold, heat, and mechanical stimuli, and its function is modulated by multiple factors, including Ca 2+ , trace metals, pH, and reactive oxygen, nitrogen, and carbonyl species. TRPA1 is involved in acute and chronic pain as well as inflammation, plays key roles in the pathophysiology of nearly all organ systems, and is an attractive target for the treatment of related diseases. Here we review the current knowledge about the mammalian TRPA1 channel, linking its unique structure, widely tuned sensory properties, and complex regulation to its roles in multiple pathophysiological conditions.
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Citations
Cites
Unravelling the pathogenesis of inflammatory bowel disease
Xavier, R. J., & Podolsky, D. K. (2007) · Nature · doi:10.1038/nature06005 · Cited by 4,364
Gut microbiota in health and disease
Sekirov, I., Russell, S. L., Antunes, L. C. M., & Finlay, B. B. (2010) · Physiological Reviews · doi:10.1152/physrev.00045.2009 · Cited by 4,182
Role of proinflammatory cytokines in the pathophysiology of osteoarthritis
Kapoor, M., Martel-Pelletier, J., Lajeunesse, D., Pelletier, J.-P., & Fahmi, H. (2011) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2010.196 · Cited by 2,778
ANKTM1, a TRP-like Channel Expressed in Nociceptive Neurons, Is Activated by Cold Temperatures
Story, G. M., Peier, A. M., Reeve, A. J., Eid, S. R., Mosbacher, J., Hricik, T. R., Earley, T. J., Hergarden, A. C., Andersson, D. A., Hwang, S. W., et al. (2003) · Cell · doi:10.1016/s0092-8674(03)00158-2 · Cited by 2,486
TRPA1 Mediates the Inflammatory Actions of Environmental Irritants and Proalgesic Agents
Bautista, D. M., Jordt, S.-E., Nikai, T., Tsuruda, P. R., Read, A. J., Poblete, J., Yamoah, E. N., Basbaum, A. I., & Julius, D. (2006) · Cell · doi:10.1016/j.cell.2006.02.023 · Cited by 1,932
Mustard oils and cannabinoids excite sensory nerve fibres through the TRP channel ANKTM1
Jordt, S.-E., Bautista, D. M., Chuang, H.-H., McKemy, D. D., Zygmunt, P. M., Högestätt, E. D., Meng, I. D., & Julius, D. (2004) · Nature · doi:10.1038/nature02282 · Cited by 1,899
Martel-Pelletier, J., Barr, A. J., Cicuttini, F. M., Conaghan, P. G., Cooper, C., Goldring, M. B., Goldring, S. R., Jones, G., Teichtahl, A. J., & Pelletier, J.-P. (2016) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2016.72 · Cited by 1,877
Noxious Cold Ion Channel TRPA1 Is Activated by Pungent Compounds and Bradykinin
Bandell, M., Story, G. M., Hwang, S. W., Viswanath, V., Eid, S. R., Petrus, M. J., Earley, T. J., & Patapoutian, A. (2004) · Neuron · doi:10.1016/s0896-6273(04)00150-3 · Cited by 1,827
The enteric nervous system and neurogastroenterology
Furness, J. B. (2012) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/nrgastro.2012.32 · Cited by 1,619
Kwan, K. Y., Allchorne, A. J., Vollrath, M. A., Christensen, A. P., Zhang, D.-S., Woolf, C. J., & Corey, D. P. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.042 · Cited by 1,267
TRPA1 mediates formalin-induced pain
McNamara, C. R., Mandel-Brehm, J., Bautista, D. M., Siemens, J., Deranian, K. L., Zhao, M., Hayward, N. J., Chong, J. A., Julius, D., Moran, M. M., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705924104 · Cited by 1,263
Atopic dermatitis and the atopic march
Spergel, J. M., & Paller, A. S. (2003) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2003.09.033 · Cited by 1,229
Julius, D. (2013) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-101011-155833 · Cited by 1,140
Noxious compounds activate TRPA1 ion channels through covalent modification of cysteines
Macpherson, L. J., Dubin, A. E., Evans, M. J., Marr, F., Schultz, P. G., Cravatt, B. F., & Patapoutian, A. (2007) · Nature · doi:10.1038/nature05544 · Cited by 1,116
An internal thermal sensor controlling temperature preference in Drosophila
Hamada, F. N., Rosenzweig, M., Kang, K., Pulver, S. R., Ghezzi, A., Jegla, T. J., & Garrity, P. A. (2008) · Nature · doi:10.1038/nature07001 · Cited by 1,075
Atopic dermatitis: a disease of altered skin barrier and immune dysregulation
Boguniewicz, M., & Leung, D. Y. M. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01027.x · Cited by 1,073
The principle of temperature-dependent gating in cold- and heat-sensitive TRP channels
Voets, T., Droogmans, G., Wissenbach, U., Janssens, A., Flockerzi, V., & Nilius, B. (2004) · Nature · doi:10.1038/nature02732 · Cited by 1,070
Self-citationThe Epithelial Cell-Derived Atopic Dermatitis Cytokine TSLP Activates Neurons to Induce Itch
Wilson, S. R., Thé, L., Batia, L. M., Beattie, K., Katibah, G. E., McClain, S. P., Pellegrino, M., Estandian, D. M., & Bautista, D. M. (2013) · Cell · doi:10.1016/j.cell.2013.08.057 · Cited by 987
De Petrocellis, L., Ligresti, A., Moriello, A. S., Allarà, M., Bisogno, T., Petrosino, S., Stott, C. G., & Di Marzo, V. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2010.01166.x · Cited by 946
TRPM8 Is Required for Cold Sensation in Mice
Dhaka, A., Murray, A. N., Mathur, J., Earley, T. J., Petrus, M. J., & Patapoutian, A. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.024 · Cited by 930
Enterochromaffin cells are gut chemosensors that couple to sensory neural pathways
Bellono, N. W., Bayrer, J. R., Leitch, D. B., Castro, J., Zhang, C., O’Donnell, T. A., Brierley, S. M., Ingraham, H. A., & Julius, D. (2017) · Cell · doi:10.1016/j.cell.2017.05.034 · Cited by 910
TRP channel activation by reversible covalent modification
Hinman, A., Chuang, H.-H., Bautista, D. M., & Julius, D. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0609598103 · Cited by 890
Pungent products from garlic activate the sensory ion channel TRPA1
Bautista, D. M., Movahed, P., Hinman, A., Axelsson, H. E., Sterner, O., Högestätt, E. D., Julius, D., Jordt, S.-E., & Zygmunt, P. M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505356102 · Cited by 860
Cevikbas, F., Wang, X., Akiyama, T., Kempkes, C., Savinko, T., Antal, A., Kukova, G., Buhl, T., Ikoma, A., Buddenkotte, J., et al. (2014) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2013.10.048 · Cited by 804
Attenuated Cold Sensitivity in TRPM8 Null Mice
Colburn, R. W., Lubin, M. L., Stone, D. J., Wang, Y., Lawrence, D., D'Andrea, M. R., Brandt, M. R., Liu, Y., Flores, C. M., & Qin, N. (2007) · Neuron · doi:10.1016/j.neuron.2007.04.017 · Cited by 771
Trevisani, M., Siemens, J., Materazzi, S., Bautista, D. M., Nassini, R., Campi, B., Imamachi, N., Andrè, E., Patacchini, R., Cottrell, G. S., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705923104 · Cited by 770
TRPA1 is a candidate for the mechanosensitive transduction channel of vertebrate hair cells
Corey, D. P., García-Añoveros, J., Holt, J. R., Kwan, K. Y., Lin, S.-Y., Vollrath, M. A., Amalfitano, A., Cheung, E. L.-M., Derfler, B. H., Duggan, A., et al. (2004) · Nature · doi:10.1038/nature03066 · Cited by 738
Kobayashi, K., Fukuoka, T., Obata, K., Yamanaka, H., Dai, Y., Tokunaga, A., & Noguchi, K. (2005) · Journal of Comparative Neurology · doi:10.1002/cne.20794 · Cited by 729
Transient Receptor Potential A1 Is a Sensory Receptor for Multiple Products of Oxidative Stress
Andersson, D. A., Gentry, C., Moss, S., & Bevan, S. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.5369-07.2008 · Cited by 718
Structure of the TRPA1 ion channel suggests regulatory mechanisms
Paulsen, C. E., Armache, J.-P., Gao, Y., Cheng, Y., & Julius, D. (2015) · Nature · doi:10.1038/nature14367 · Cited by 660
Nociceptor and Hair Cell Transducer Properties of TRPA1, a Channel for Pain and Hearing
Nagata, K., Duggan, A., Kumar, G., & García-Añoveros, J. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.0013-05.2005 · Cited by 644
Oregano, thyme and clove-derived flavors and skin sensitizers activate specific TRP channels
Xu, H., Delling, M., Jun, J. C., & Clapham, D. E. (2006) · Nature Neuroscience · doi:10.1038/nn1692 · Cited by 644
Obata, K. (2005) · Journal of Clinical Investigation · doi:10.1172/jci25437 · Cited by 630
Effect of garlic on cardiovascular disorders: a review
Banerjee, S. K., & Maulik, S. K. (2002) · Nutrition Journal · doi:10.1186/1475-2891-1-4 · Cited by 627
The Pungency of Garlic: Activation of TRPA1 and TRPV1 in Response to Allicin
Macpherson, L. J., Geierstanger, B. H., Viswanath, V., Bandell, M., Eid, S. R., Hwang, S., & Patapoutian, A. (2005) · Current Biology · doi:10.1016/j.cub.2005.04.018 · Cited by 612
TRPA1 is required for histamine-independent, Mas-related G protein–coupled receptor–mediated itch
Wilson, S. R., Gerhold, K. A., Bifolck-Fisher, A., Liu, Q., Patel, K. N., Dong, X., & Bautista, D. M. (2011) · Nature Neuroscience · doi:10.1038/nn.2789 · Cited by 599
Tolerance for Rectosigmoid Distention in Irritable Bowel Syndrome
Whitehead, W. E., Holtkotter, B., Enck, P., Hoelzl, R., Holmes, K. D., Anthony, J., Shabsin, H. S., & Schuster, M. M. (1990) · Gastroenterology · doi:10.1016/0016-5085(90)90332-u · Cited by 593
TRPA1 acts as a cold sensor in vitro and in vivo
Karashima, Y., Talavera, K., Everaerts, W., Janssens, A., Kwan, K. Y., Vennekens, R., Nilius, B., & Voets, T. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0808487106 · Cited by 585
Self-citation小林, 希. (2007) · Medical Entomology and Zoology · Cited by 575
Heat activation of TRPM5 underlies thermal sensitivity of sweet taste
Talavera, K., Yasumatsu, K., Voets, T., Droogmans, G., Shigemura, N., Ninomiya, Y., Margolskee, R. F., & Nilius, B. (2005) · Nature · doi:10.1038/nature04248 · Cited by 523
Self-citationDirect activation of the ion channel TRPA1 by Ca2+
Zurborg, S., Yurgionas, B., Jira, J. A., Caspani, O., & Heppenstall, P. A. (2007) · Nature Neuroscience · doi:10.1038/nn1843 · Cited by 505
Observations upon the reactions of the vessels of the human skin to cold
Lewis, T. (1930) · Medical Entomology and Zoology · Cited by 489
Molecular basis of infrared detection by snakes
Gracheva, E. O., Ingolia, N. T., Kelly, Y. M., Cordero-Morales, J. F., Hollopeter, G., Chesler, A. T., Sánchez, E. E., Perez, J. C., Weissman, J. S., & Julius, D. (2010) · Nature · doi:10.1038/nature08943 · Cited by 482
TRPA1 channels mediate acute neurogenic inflammation and pain produced by bacterial endotoxins
Meseguer, V., Alpizar, Y. A., Luis, E., Tajada, S., Denlinger, B., Fajardo, O., Manenschijn, J.-A., Fernández-Peña, C., Talavera, A., Kichko, T., et al. (2014) · Nature Communications · doi:10.1038/ncomms4125 · Cited by 479
Self-citationBimodal Action of Menthol on the Transient Receptor Potential Channel TRPA1
Karashima, Y., Damann, N., Prenen, J., Talavera, K., Segal, A., Voets, T., & Nilius, B. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2221-07.2007 · Cited by 477
Self-citationTRPA1 channels regulate astrocyte resting calcium and inhibitory synapse efficacy through GAT-3
Shigetomi, E., Tong, X., Kwan, K. Y., Corey, D. P., & Khakh, B. S. (2012) · Nature Neuroscience · doi:10.1038/nn.3000 · Cited by 472
A TRP channel trio mediates acute noxious heat sensing
Vandewauw, I., De Clercq, K., Mulier, M., Held, K., Pinto, S., Van Ranst, N., Segal, A., Voet, T., Vennekens, R., Zimmermann, K., et al. (2018) · Nature · doi:10.1038/nature26137 · Cited by 470
Light-avoidance-mediating photoreceptors tile the Drosophila larval body wall
Xiang, Y., Yuan, Q., Vogt, N., Looger, L. L., Jan, L. Y., & Jan, Y. N. (2010) · Nature · doi:10.1038/nature09576 · Cited by 462
TRPA1 is a major oxidant sensor in murine airway sensory neurons
Bessac, B. F., Sivula, M., von Hehn, C. A., Escalera, J., Cohn, L., & Jordt, S.-E. (2008) · Journal of Clinical Investigation · doi:10.1172/jci34192 · Cited by 449
Eid, S. R., Crown, E. D., Moore, E. L., Liang, H. A., Choong, K.-C., Dima, S., Henze, D. A., Kane, S. A., & Urban, M. O. (2008) · Molecular Pain · doi:10.1186/1744-8069-4-48 · Cited by 447
Peripheral thermosensation in mammals
Vriens, J., Nilius, B., & Voets, T. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3784 · Cited by 446
Self-citationA Gain-of-Function Mutation in TRPA1 Causes Familial Episodic Pain Syndrome
Kremeyer, B., Lopera, F., Cox, J. J., Momin, A., Rugiero, F., Marsh, S., Woods, C. G., Jones, N. G., Paterson, K. J., Fricker, F. R., et al. (2010) · Neuron · doi:10.1016/j.neuron.2010.04.030 · Cited by 443
Imamachi, N., Park, G. H., Lee, H., Anderson, D. J., Simon, M. I., Basbaum, A. I., & Han, S.-K. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0905605106 · Cited by 443
Breathtaking TRP Channels: TRPA1 and TRPV1 in Airway Chemosensation and Reflex Control
Bessac, B. F., & Jordt, S.-E. (2008) · Physiology · doi:10.1152/physiol.00026.2008 · Cited by 432
Sensitization of TRPA1 by PAR2 contributes to the sensation of inflammatory pain
Dai, Y., Wang, S., Tominaga, M., Yamamoto, S., Fukuoka, T., Higashi, T., Kobayashi, K., Obata, K., Yamanaka, H., & Noguchi, K. (2007) · Journal of Clinical Investigation · doi:10.1172/jci30951 · Cited by 432
Gouin, O., L’Herondelle, K., Lebonvallet, N., Le Gall-Ianotto, C., Sakka, M., Buhé, V., Plée-Gautier, E., Carré, J.-L., Lefeuvre, L., Misery, L., et al. (2017) · Protein & Cell · doi:10.1007/s13238-017-0395-5 · Cited by 425
Xu, H., Blair, N. T., & Clapham, D. E. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2574-05.2005 · Cited by 420
Transient Receptor Potential Channels in the Vasculature
Earley, S., & Brayden, J. E. (2015) · Physiological Reviews · doi:10.1152/physrev.00026.2014 · Cited by 420
TRP Ion Channel Function in Sensory Transduction and Cellular Signaling Cascades
(2006) · CRC Press eBooks · doi:10.1201/9781420005844 · Cited by 418
A Role of TRPA1 in Mechanical Hyperalgesia is Revealed by Pharmacological Inhibition
Petrus, M., Peier, A. M., Bandell, M., Hwang, S. W., Huynh, T., Olney, N., Jegla, T., & Patapoutian, A. (2007) · Molecular Pain · doi:10.1186/1744-8069-3-40 · Cited by 418
Asthma and Allergic Inflammation
Locksley, R. M. (2010) · Cell · doi:10.1016/j.cell.2010.03.004 · Cited by 408
More than cool: Promiscuous relationships of menthol and other sensory compounds
Macpherson, L. J., Hwang, S. W., Miyamoto, T., Dubin, A. E., Patapoutian, A., & Story, G. M. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.05.005 · Cited by 401
TRPA1 regulates gastrointestinal motility through serotonin release from enterochromaffin cells
Nozawa, K., Kawabata-Shoda, E., Doihara, H., Kojima, R., Okada, H., Mochizuki, S., Sano, Y., Inamura, K., Matsushime, H., Koizumi, T., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0805323106 · Cited by 399
Camilleri, M., Lasch, K., & Zhou, W. (2012) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00155.2012 · Cited by 396
Eberhardt, M., Dux, M., Namer, B., Miljkovic, J., Cordasic, N., Will, C., Kichko, T. I., de la Roche, J., Fischer, M., Suárez, S. A., et al. (2014) · Nature Communications · doi:10.1038/ncomms5381 · Cited by 379
Andrè, E., Campi, B., Materazzi, S., Trevisani, M., Amadesi, S., Massi, D., Creminon, C., Vaksman, N., Nassini, R., Civelli, M., et al. (2008) · Journal of Clinical Investigation · doi:10.1172/jci34886 · Cited by 372
Descoeur, J., Pereira, V., Pizzoccaro, A., Francois, A., Ling, B., Maffre, V., Couette, B., Busserolles, J., Courteix, C., Noel, J., et al. (2011) · EMBO Molecular Medicine · doi:10.1002/emmm.201100134 · Cited by 368
Expression and function of the ion channel TRPA1 in vagal afferent nerves innervating mouse lungs
Nassenstein, C., Kwong, K., Taylor‐Clark, T., Kollarik, M., MacGlashan, D. M., Braun, A., & Undem, B. J. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2007.148379 · Cited by 349
Cannabinoid CB2 receptor ligand profiling reveals biased signalling and off-target activity
Soethoudt, M., Grether, U., Fingerle, J., Grim, T. W., Fezza, F., de Petrocellis, L., Ullmer, C., Rothenhäusler, B., Perret, C., van Gils, N., et al. (2017) · Nature Communications · doi:10.1038/ncomms13958 · Cited by 349
A new gaseous signaling molecule emerges: Cardioprotective role of hydrogen sulfide
Lefer, D. J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709010104 · Cited by 347
Why we scratch an itch: the molecules, cells and circuits of itch
Bautista, D. M., Wilson, S. R., & Hoon, M. A. (2014) · Nature Neuroscience · doi:10.1038/nn.3619 · Cited by 338
De Petrocellis, L., Vellani, V., Schiano-Moriello, A., Marini, P., Magherini, P. C., Orlando, P., & Di Marzo, V. (2008) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.134809 · Cited by 336
The transient receptor potential channel TRPA1: from gene to pathophysiology
Nilius, B., Appendino, G., & Owsianik, G. (2012) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-012-1158-z · Cited by 335
Self-citationJaquemar, D., Schenker, T., & Trueb, B. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.11.7325 · Cited by 332
Ocular surface wetness is regulated by TRPM8-dependent cold thermoreceptors of the cornea
Parra, A., Madrid, R., Echevarria, D., del Olmo, S., Morenilla-Palao, C., Acosta, M. C., Gallar, J., Dhaka, A., Viana, F., & Belmonte, C. (2010) · Nature Medicine · doi:10.1038/nm.2264 · Cited by 324
Oxaliplatin elicits mechanical and cold allodynia in rodents via TRPA1 receptor stimulation
Nassini, R., Gees, M., Harrison, S., De Siena, G., Materazzi, S., Moretto, N., Failli, P., Preti, D., Marchetti, N., Cavazzini, A., et al. (2011) · Pain · doi:10.1016/j.pain.2011.02.051 · Cited by 324
Self-citationXiao, B., Dubin, A. E., Bursulaya, B., Viswanath, V., Jegla, T. J., & Patapoutian, A. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.2772-08.2008 · Cited by 321
TRPA1 Modulates Mechanotransduction in Cutaneous Sensory Neurons
Kwan, K. Y., Glazer, J. M., Corey, D. P., Rice, F. L., & Stucky, C. L. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5380-08.2009 · Cited by 321
Shigetomi, E., Jackson-Weaver, O., Huckstepp, R. T., O'Dell, T. J., & Khakh, B. S. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5779-12.2013 · Cited by 320
Transient Receptor Potential Channel A1 Is Directly Gated by Calcium Ions
Doerner, J. F., Gisselmann, G., Hatt, H., & Wetzel, C. H. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m607849200 · Cited by 320
Distribution and Function of the Hydrogen Sulfide–Sensitive TRPA1 Ion Channel in Rat Urinary Bladder
Streng, T., Axelsson, H. E., Hedlund, P., Andersson, D. A., Jordt, S.-E., Bevan, S., Andersson, K.-E., Högestätt, E. D., & Zygmunt, P. M. (2008) · European Urology · doi:10.1016/j.eururo.2007.10.024 · Cited by 308
Cinnamaldehyde in diabetes: A review of pharmacology, pharmacokinetics and safety
Zhu, R., Liu, H., Liu, C., Wang, L., Ma, R., Chen, B., Li, L., Niu, J., Fu, M., Zhang, D., et al. (2017) · Pharmacological Research · doi:10.1016/j.phrs.2017.05.019 · Cited by 307
Regulation of Pain and Itch by TRP Channels
Moore, C., Gupta, R., Jordt, S.-E., Chen, Y., & Liedtke, W. B. (2018) · Neuroscience Bulletin · doi:10.1007/s12264-017-0200-8 · Cited by 307
Chen, Y., Yang, C., & Wang, Z. J. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.06.085 · Cited by 302
Gating of TRP channels: a voltage connection?
Nilius, B., Talavera, K., Owsianik, G., Prenen, J., Droogmans, G., & Voets, T. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.088377 · Cited by 299
Self-citationThe Biology of Thymic Stromal Lymphopoietin (TSLP)
Ziegler, S. F., Roan, F., Bell, B. D., Stoklasek, T. A., Kitajima, M., & Han, H. (2013) · Advances in Pharmacology · doi:10.1016/b978-0-12-404717-4.00004-4 · Cited by 298
TRPA1 Contributes to Cold Hypersensitivity
del Camino, D., Murphy, S., Heiry, M., Barrett, L. B., Earley, T. J., Cook, C. A., Petrus, M. J., Zhao, M., D'Amours, M., Deering, N., et al. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2580-10.2010 · Cited by 287
Knowlton, W. M., Bifolck-Fisher, A., Bautista, D. M., & McKemy, D. D. (2010) · Pain · doi:10.1016/j.pain.2010.05.021 · Cited by 287
Wang, S., Dai, Y., Fukuoka, T., Yamanaka, H., Kobayashi, K., Obata, K., Cui, X., Tominaga, M., & Noguchi, K. (2008) · Brain · doi:10.1093/brain/awn060 · Cited by 285
Andersson, D. A., Gentry, C., Alenmyr, L., Killander, D., Lewis, S. E., Andersson, A., Bucher, B., Galzi, J.-L., Sterner, O., Bevan, S., et al. (2011) · Nature Communications · doi:10.1038/ncomms1559 · Cited by 283
Opposite thermosensor in fruitfly and mouse
Viswanath, V., Story, G. M., Peier, A. M., Petrus, M. J., Lee, V. M., Hwang, S. W., Patapoutian, A., & Jegla, T. (2003) · Nature · doi:10.1038/423822a · Cited by 283
De Logu, F., Nassini, R., Materazzi, S., Carvalho Gonçalves, M., Nosi, D., Rossi Degl’Innocenti, D., Marone, I. M., Ferreira, J., Li Puma, S., Benemei, S., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-01739-2 · Cited by 283
The Nociceptor Ion Channel TRPA1 Is Potentiated and Inactivated by Permeating Calcium Ions
Wang, Y. Y., Chang, R. B., Waters, H. N., McKemy, D. D., & Liman, E. R. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m803568200 · Cited by 282
Chen, J., Joshi, S. K., DiDomenico, S., Perner, R. J., Mikusa, J. P., Gauvin, D. M., Segreti, J. A., Han, P., Zhang, X.-F., Niforatos, W., et al. (2011) · Pain · doi:10.1016/j.pain.2011.01.049 · Cited by 276
TRPA1 Agonists Evoke Coughing in Guinea Pig and Human Volunteers
Birrell, M. A., Belvisi, M. G., Grace, M., Sadofsky, L., Faruqi, S., Hele, D. J., Maher, S. A., Freund-Michel, V., & Morice, A. H. (2009) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200905-0665oc · Cited by 275
Akopian, A. N., Ruparel, N. B., Jeske, N. A., & Hargreaves, K. M. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.133231 · Cited by 274
Akiyama, T., & Carstens, E. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.07.035 · Cited by 272
TRPA1 underlies a sensing mechanism for O2
Takahashi, N., Kuwaki, T., Kiyonaka, S., Numata, T., Kozai, D., Mizuno, Y., Yamamoto, S., Naito, S., Knevels, E., Carmeliet, P., et al. (2011) · Nature Chemical Biology · doi:10.1038/nchembio.640 · Cited by 272
In Search of the Hair-Cell Gating Spring
Sotomayor, M., Corey, D. P., & Schulten, K. (2005) · Structure · doi:10.1016/j.str.2005.03.001 · Cited by 269
Endothelium-Dependent Cerebral Artery Dilation Mediated by TRPA1 and Ca 2+ -Activated K + Channels
Earley, S., Gonzales, A. L., & Crnich, R. (2009) · Circulation Research · doi:10.1161/circresaha.108.189530 · Cited by 267
The Ion Channel TRPA1 Is Required for Normal Mechanosensation and Is Modulated by Algesic Stimuli
Brierley, S. M., Hughes, P. A., Page, A. J., Kwan, K. Y., Martin, C. M., O'Donnell, T. A., Cooper, N. J., Harrington, A. M., Adam, B., Liebregts, T., et al. (2009) · Gastroenterology · doi:10.1053/j.gastro.2009.07.048 · Cited by 266
General anesthetics activate a nociceptive ion channel to enhance pain and inflammation
Matta, J. A., Cornett, P. M., Miyares, R. L., Abe, K., Sahibzada, N., & Ahern, G. P. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0711038105 · Cited by 265
The multiple pathways for itch and their interactions with pain
Davidson, S., & Giesler, G. J. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.09.002 · Cited by 261
Habauzit, V., & Morand, C. (2012) · Therapeutic Advances in Chronic Disease · doi:10.1177/2040622311430006 · Cited by 261
Nicotine activates the chemosensory cation channel TRPA1
Talavera, K., Gees, M., Karashima, Y., Meseguer, V. M., Vanoirbeek, J. A. J., Damann, N., Everaerts, W., Benoit, M., Janssens, A., Vennekens, R., et al. (2009) · Nature Neuroscience · doi:10.1038/nn.2379 · Cited by 259
Self-citationBautista, D. M., Sigal, Y. M., Milstein, A. D., Garrison, J. L., Zorn, J. A., Tsuruda, P. R., Nicoll, R. A., & Julius, D. (2008) · Nature Neuroscience · doi:10.1038/nn.2143 · Cited by 258
Non-Neuronal Expression of Transient Receptor Potential Type A1 (TRPA1) in Human Skin
Atoyan, R., Shander, D., & Botchkareva, N. V. (2009) · Journal of Investigative Dermatology · doi:10.1038/jid.2009.58 · Cited by 257
The concept of neurogenic inflammation
Geppetti, P., Nassini, R., Materazzi, S., & Benemei, S. (2008) · BJU International · doi:10.1111/j.1464-410x.2008.07493.x · Cited by 257
TRPV1 Is Activated by Both Acidic and Basic pH
Dhaka, A., Uzzell, V., Dubin, A. E., Mathur, J., Petrus, M., Bandell, M., & Patapoutian, A. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.4901-08.2009 · Cited by 252
Molecular characterization of TRPA1 channel activation by cysteine-reactive inflammatory mediators
Takahashi, N., Mizuno, Y., Kozai, D., Yamamoto, S., Kiyonaka, S., Shibata, T., Uchida, K., & Mori, Y. (2008) · Channels · doi:10.4161/chan.2.4.6745 · Cited by 247
Transient receptor potential (TRP) channels as drug targets for diseases of the digestive system
Holzer, P. (2011) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2011.03.006 · Cited by 245
Pain-related electrical potentials of the human nasal mucosa elicited by chemical stimulation
Kobal, G. (1985) · Pain · doi:10.1016/0304-3959(85)90175-7 · Cited by 243
Zhong, L., Bellemer, A., Yan, H., Honjo, K., Robertson, J., Hwang, R. Y., Pitt, G. S., & Tracey, W. D. (2012) · Cell Reports · doi:10.1016/j.celrep.2011.11.002 · Cited by 242
TRPA1 and TRPM8 activation in humans: effects of cinnamaldehyde and menthol
Namer, B., Seifert, F., Handwerker, H. O., & Maih??fner, C. (2005) · NeuroReport · doi:10.1097/00001756-200506210-00015 · Cited by 241
Pretty painful: Why does tooth bleaching hurt?
Markowitz, K. (2010) · Medical Hypotheses · doi:10.1016/j.mehy.2009.11.044 · Cited by 239
Caenorhabditis elegans TRPA-1 functions in mechanosensation
Kindt, K. S., Viswanath, V., Macpherson, L., Quast, K., Hu, H., Patapoutian, A., & Schafer, W. R. (2007) · Nature Neuroscience · doi:10.1038/nn1886 · Cited by 238
Taylor‐Clark, T. E., McAlexander, M. A., Nassenstein, C., Sheardown, S. A., Wilson, S., Thornton, J., Carr, M. J., & Undem, B. J. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.153585 · Cited by 237
Nassini, R., Pedretti, P., Moretto, N., Fusi, C., Carnini, C., Facchinetti, F., Viscomi, A. R., Pisano, A. R., Stokesberry, S., Brunmark, C., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042454 · Cited by 237
He, R., & Geha, R. S. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.05128.x · Cited by 235
Modulation of TRPA1 thermal sensitivity enables sensory discrimination in Drosophila
Kang, K., Panzano, V. C., Chang, E. C., Ni, L., Dainis, A. M., Jenkins, A. M., Regna, K., Muskavitch, M. A. T., & Garrity, P. A. (2012) · Nature · doi:10.1038/nature10715 · Cited by 234
Cordero-Morales, J. F., Gracheva, E. O., & Julius, D. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1114124108 · Cited by 233
TRPA1 controls inflammation and pruritogen responses in allergic contact dermatitis
Liu, B., Escalera, J., Balakrishna, S., Fan, L., Caceres, A. I., Robinson, E., Sui, A., McKay, M. C., McAlexander, M. A., Herrick, C. A., et al. (2013) · The FASEB Journal · doi:10.1096/fj.13-229948 · Cited by 232
Species differences and molecular determinant of TRPA1 cold sensitivity
Chen, J., Kang, D., Xu, J., Lake, M., Hogan, J. O., Sun, C., Walter, K., Yao, B., & Kim, D. (2013) · Nature Communications · doi:10.1038/ncomms3501 · Cited by 231
Akilen, R., Tsiami, A., Devendra, D., & Robinson, N. (2010) · Diabetic Medicine · doi:10.1111/j.1464-5491.2010.03079.x · Cited by 230
Zinc activates damage-sensing TRPA1 ion channels
Hu, H., Bandell, M., Petrus, M. J., Zhu, M. X., & Patapoutian, A. (2009) · Nature Chemical Biology · doi:10.1038/nchembio.146 · Cited by 229
Regular review: Peripheral neuropathy
Hughes, R. A. C. (2002) · BMJ · doi:10.1136/bmj.324.7335.466 · Cited by 228
Nociceptive Signals Induce Trafficking of TRPA1 to the Plasma Membrane
Schmidt, M., Dubin, A. E., Petrus, M. J., Earley, T. J., & Patapoutian, A. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.030 · Cited by 225
Materazzi, S., Fusi, C., Benemei, S., Pedretti, P., Patacchini, R., Nilius, B., Prenen, J., Creminon, C., Geppetti, P., & Nassini, R. (2012) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-011-1071-x · Cited by 224
Self-citationda Costa, D. S. M., Meotti, F. C., Andrade, E. L., Leal, P. C., Motta, E. M., & Calixto, J. B. (2010) · Pain · doi:10.1016/j.pain.2009.12.002 · Cited by 223
TRPV1 and TRPA1 Mediate Peripheral Nitric Oxide-Induced Nociception in Mice
Miyamoto, T., Dubin, A. E., Petrus, M. J., & Patapoutian, A. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007596 · Cited by 223
Zygmunt, P. M., & Högestätt, E. D. (2014) · Handbook of Experimental Pharmacology · doi:10.1007/978-3-642-54215-2_23 · Cited by 223
Howard, J., & Bechstedt, S. (2004) · Current Biology · doi:10.1016/j.cub.2004.02.050 · Cited by 222
The Bile Acid Receptor TGR5 Activates the TRPA1 Channel to Induce Itch in Mice
Lieu, T., Jayaweera, G., Zhao, P., Poole, D. P., Jensen, D., Grace, M., McIntyre, P., Bron, R., Wilson, Y. M., Krappitz, M., et al. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.08.042 · Cited by 221
TRPA1 and Substance P Mediate Colitis in Mice
Engel, M. A., Leffler, A., Niedermirtl, F., Babes, A., Zimmermann, K., Filipović, M. R., Izydorczyk, I., Eberhardt, M., Kichko, T. I., Mueller–Tribbensee, S. M., et al. (2011) · Gastroenterology · doi:10.1053/j.gastro.2011.07.002 · Cited by 218
Hydrogen sulphide — a novel mediator of inflammation?
LI, L., BHATIA, M., & MOORE, P. (2006) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2005.10.007 · Cited by 218
Sandow, S. L., Neylon, C. B., Chen, M. X., & Garland, C. J. (2006) · Journal of Anatomy · doi:10.1111/j.1469-7580.2006.00647.x · Cited by 215
Katsura, H., Obata, K., Mizushima, T., Yamanaka, H., Kobayashi, K., Dai, Y., Fukuoka, T., Tokunaga, A., Sakagami, M., & Noguchi, K. (2006) · Experimental Neurology · doi:10.1016/j.expneurol.2006.01.031 · Cited by 213
TRPA1‐mediated responses in trigeminal sensory neurons: interaction between TRPA1 and TRPV1
Salas, M. M., Hargreaves, K. M., & Akopian, A. N. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06702.x · Cited by 211
TRPA1 channels: molecular sentinels of cellular stress and tissue damage
Viana, F. (2016) · The Journal of Physiology · doi:10.1113/jp270935 · Cited by 210
The TRPA1 Channel in Inflammatory and Neuropathic Pain and Migraine
Nassini, R., Materazzi, S., Benemei, S., & Geppetti, P. (2014) · Reviews of Physiology, Biochemistry and Pharmacology · doi:10.1007/112_2014_18 · Cited by 206
Hjerling-Leffler, J., AlQatari, M., Ernfors, P., & Koltzenburg, M. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5614-06.2007 · Cited by 205
TRPA1-Dependent Pruritus in IL-13–Induced Chronic Atopic Dermatitis
Oh, M.-H., Oh, S. Y., Lu, J., Lou, H., Myers, A. C., Zhu, Z., & Zheng, T. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1300300 · Cited by 205
Pharmacological Blockade of TRPM8 Ion Channels Alters Cold and Cold Pain Responses in Mice
Knowlton, W. M., Daniels, R. L., Palkar, R., McCoy, D. D., & McKemy, D. D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025894 · Cited by 203
Salazar, H., Llorente, I., Jara-Oseguera, A., García-Villegas, R., Munari, M., Gordon, S. E., Islas, L. D., & Rosenbaum, T. (2008) · Nature Neuroscience · doi:10.1038/nn2056 · Cited by 202
Trevisan, G., Benemei, S., Materazzi, S., De Logu, F., De Siena, G., Fusi, C., Fortes Rossato, M., Coppi, E., Marone, I. M., Ferreira, J., et al. (2016) · Brain · doi:10.1093/brain/aww038 · Cited by 202
Moran, M. M., & Szallasi, A. (2018) · British Journal of Pharmacology · doi:10.1111/bph.14044 · Cited by 199
Chemosensory properties of the trigeminal system
Viana, F. (2011) · ACS Chemical Neuroscience · doi:10.1021/cn100102c · Cited by 196
The ‘headache tree’ via umbellulone and TRPA1 activates the trigeminovascular system
Nassini, R., Materazzi, S., Vriens, J., Prenen, J., Benemei, S., De Siena, G., la Marca, G., Andrè, E., Preti, D., Avonto, C., et al. (2012) · Brain · doi:10.1093/brain/awr272 · Cited by 196
Self-citationTa, L. E., Bieber, A. J., Carlton, S. M., Loprinzi, C. L., Low, P. A., & Windebank, A. J. (2010) · Molecular Pain · doi:10.1186/1744-8069-6-15 · Cited by 193
Anand, U., Otto, W. R., Facer, P., Zebda, N., Selmer, I., Gunthorpe, M. J., Chessell, I. P., Sinisi, M., Birch, R., & Anand, P. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.04.007 · Cited by 192
Transient receptor potential (TRP) channels in the airway: role in airway disease
Grace, M. S., Baxter, M., Dubuis, E., Birrell, M. A., & Belvisi, M. G. (2014) · British Journal of Pharmacology · doi:10.1111/bph.12538 · Cited by 190
Methylglyoxal Activates Nociceptors through Transient Receptor Potential Channel A1 (TRPA1)
Eberhardt, M. J., Filipovic, M. R., Leffler, A., de la Roche, J., Kistner, K., Fischer, M. J., Fleming, T., Zimmermann, K., Ivanovic-Burmazovic, I., Nawroth, P. P., et al. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.328674 · Cited by 190
Camacho, S., Michlig, S., de Senarclens-Bezençon, C., Meylan, J., Meystre, J., Pezzoli, M., Markram, H., & le Coutre, J. (2015) · Scientific Reports · doi:10.1038/srep07919 · Cited by 189
Zhao, M., Isami, K., Nakamura, S., Shirakawa, H., Nakagawa, T., & Kaneko, S. (2012) · Molecular Pain · doi:10.1186/1744-8069-8-55 · Cited by 189
HTR7 Mediates Serotonergic Acute and Chronic Itch
Morita, T., McClain, S. P., Batia, L. M., Pellegrino, M., Wilson, S. R., Kienzler, M. A., Lyman, K., Olsen, A. S. B., Wong, J. F., Stucky, C. L., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.044 · Cited by 188
Inceoglu, B., Bettaieb, A., Trindade da Silva, C. A., Lee, K. S. S., Haj, F. G., & Hammock, B. D. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1510137112 · Cited by 184
McGaraughty, S., Chu, K. L., Perner, R. J., DiDomenico, S., Kort, M. E., & Kym, P. R. (2010) · Molecular Pain · doi:10.1186/1744-8069-6-14 · Cited by 183
Cold sensitivity of recombinant TRPA1 channels
Sawada, Y., Hosokawa, H., Hori, A., Matsumura, K., & Kobayashi, S. (2007) · Brain Research · doi:10.1016/j.brainres.2007.05.047 · Cited by 182
Trevisan, G., Materazzi, S., Fusi, C., Altomare, A., Aldini, G., Lodovici, M., Patacchini, R., Geppetti, P., & Nassini, R. (2013) · Cancer Research · doi:10.1158/0008-5472.can-12-4370 · Cited by 182
Tmem100 Is a Regulator of TRPA1-TRPV1 Complex and Contributes to Persistent Pain
Weng, H.-J., Patel, K. N., Jeske, N. A., Bierbower, S. M., Zou, W., Tiwari, V., Zheng, Q., Tang, Z., Mo, G. C. H., Wang, Y., et al. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.065 · Cited by 181
Taylor-Clark, T. E., Ghatta, S., Bettner, W., & Undem, B. J. (2009) · Molecular Pharmacology · doi:10.1124/mol.108.054445 · Cited by 180
Synergistic Role of TRPV1 and TRPA1 in Pancreatic Pain and Inflammation
Schwartz, E. S., Christianson, J. A., Chen, X., La, J., Davis, B. M., Albers, K. M., & Gebhart, G. F. (2011) · Gastroenterology · doi:10.1053/j.gastro.2010.12.033 · Cited by 178
Roles of TRPA1 and TRPV1 in cigarette smoke -induced airway epithelial cell injury model
Wang, M., Zhang, Y., Xu, M., Zhang, H., Chen, Y., Chung, K. F., Adcock, I. M., & Li, F. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.01.004 · Cited by 178
Bang, S., Yoo, S., Yang, T., Cho, H., Kim, Y., & Hwang, S. (2010) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2010.00909.x · Cited by 176
Baraldi, P. G., Preti, D., Materazzi, S., & Geppetti, P. (2010) · Journal of Medicinal Chemistry · doi:10.1021/jm100062h · Cited by 176
Maione, S., Piscitelli, F., Gatta, L., Vita, D., De Petrocellis, L., Palazzo, E., de Novellis, V., & Di Marzo, V. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2010.01063.x · Cited by 175
Fajardo, O., Meseguer, V., Belmonte, C., & Viana, F. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1696-08.2008 · Cited by 173
Schwartz, E. S., La, J.-H., Scheff, N. N., Davis, B. M., Albers, K. M., & Gebhart, G. F. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1806-12.2013 · Cited by 173
Babes, A., Zorzon, D., & Reid, G. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03695.x · Cited by 173
TRPA1 receptors mediate environmental irritant-induced meningeal vasodilatation
Kunkler, P. E., Ballard, C. J., Oxford, G. S., & Hurley, J. H. (2011) · Pain · doi:10.1016/j.pain.2010.08.021 · Cited by 172
Veldhuis, N. A., Poole, D. P., Grace, M., McIntyre, P., & Bunnett, N. W. (2015) · Pharmacological Reviews · doi:10.1124/pr.114.009555 · Cited by 172
Deuis, J. R., Zimmermann, K., Romanovsky, A. A., Possani, L. D., Cabot, P. J., Lewis, R. J., & Vetter, I. (2013) · Pain · doi:10.1016/j.pain.2013.05.032 · Cited by 171
Bessac, B. F., Sivula, M., von Hehn, C. A., Caceres, A. I., Escalera, J., & Jordt, S.-E. (2009) · The FASEB Journal · doi:10.1096/fj.08-117812 · Cited by 171
Cox-dependent fatty acid metabolites cause pain through activation of the irritant receptor TRPA1
Materazzi, S., Nassini, R., Andrè, E., Campi, B., Amadesi, S., Trevisani, M., Bunnett, N. W., Patacchini, R., & Geppetti, P. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802354105 · Cited by 170
A Comparison of Oral Sensory Effects of Three TRPA1 Agonists in Young Adult Smokers and Non-smokers
Hansen, E. Ø., Arendt-Nielsen, L., & Boudreau, S. A. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00663 · Cited by 170
Pharmacological Blockade of TRPA1 Inhibits Mechanical Firing in Nociceptors
Kerstein, P. C., del Camino, D., Moran, M. M., & Stucky, C. L. (2009) · Molecular Pain · doi:10.1186/1744-8069-5-19 · Cited by 169
Fernandes, E. S., Russell, F. A., Spina, D., McDougall, J. J., Graepel, R., Gentry, C., Staniland, A. A., Mountford, D. M., Keeble, J. E., Malcangio, M., et al. (2011) · Arthritis & Rheumatism · doi:10.1002/art.30150 · Cited by 168
Sullivan, M. N., Gonzales, A. L., Pires, P. W., Bruhl, A., Leo, M. D., Li, W., Oulidi, A., Boop, F. A., Feng, Y., Jaggar, J. H., et al. (2015) · Science Signaling · doi:10.1126/scisignal.2005659 · Cited by 167
Thymol and related alkyl phenols activate the hTRPA1 channel
Lee, S. P., Buber, M. T., Yang, Q., Cerne, R., Cortés, R. Y., Sprous, D. G., & Bryant, R. W. (2008) · British Journal of Pharmacology · doi:10.1038/bjp.2008.85 · Cited by 166
Riera, C., Menozzi‐Smarrito, C., Affolter, M., Michlig, S., Munari, C., Robert, F., Vogel, H., Simon, S., & Le Coutre, J. (2009) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2009.00307.x · Cited by 165
NGF Up-regulates TRPA1: Implications for Orofacial Pain
Diogenes, A., Akopian, A. N., & Hargreaves, K. M. (2007) · Journal of Dental Research · doi:10.1177/154405910708600612 · Cited by 163
Bráz, J. M., & Basbaum, A. I. (2010) · Pain · doi:10.1016/j.pain.2010.05.005 · Cited by 162
Urinary Biomarkers for Phthalates Associated with Asthma in Norwegian Children
Bertelsen, R. J., Carlsen, K. C. L., Calafat, A. M., Hoppin, J. A., Håland, G., Mowinckel, P., Carlsen, K.-H., & Løvik, M. (2013) · Environmental Health Perspectives · doi:10.1289/ehp.1205256 · Cited by 161
Spices: The Savory and Beneficial Science of Pungency
Nilius, B., & Appendino, G. (2013) · Reviews of Physiology, Biochemistry and Pharmacology · doi:10.1007/112_2013_11 · Cited by 160
Self-citationOsteoarthritis year in review 2015: biology
Malfait, A. M. (2016) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2015.09.010 · Cited by 160
Wei, H., Hämäläinen, M. M., Saarnilehto, M., Koivisto, A., & Pertovaara, A. (2009) · Anesthesiology · doi:10.1097/aln.0b013e3181a1642b · Cited by 159
Proton-gated Ca2+-permeable TRP channels damage myelin in conditions mimicking ischaemia
Hamilton, N. B., Kolodziejczyk, K., Kougioumtzidou, E., & Attwell, D. (2016) · Nature · doi:10.1038/nature16519 · Cited by 159
Paravicini, T. M., Chrissobolis, S., Drummond, G. R., & Sobey, C. G. (2004) · Stroke · doi:10.1161/01.str.0000112974.37028.58 · Cited by 156
Functional characterization of transient receptor potential channels in mouse urothelial cells
Everaerts, W., Vriens, J., Owsianik, G., Appendino, G., Voets, T., Ridder, D. J. M. K. D., & Nilius, B. (2009) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00599.2009 · Cited by 156
Self-citationHuman TRPA1 is a heat sensor displaying intrinsic U-shaped thermosensitivity
Moparthi, L., Kichko, T. I., Eberhardt, M. J., Högestätt, E. D., Kjellbom, P. O., Johanson, U., Reeh, P. W., Leffler, A., Filipović, M. R., & Zygmunt, P. M. (2016) · Scientific Reports · doi:10.1038/srep28763 · Cited by 156
The Molecular and Cellular Basis of Cold Sensation
McKemy, D. D. (2012) · ACS Chemical Neuroscience · doi:10.1021/cn300193h · Cited by 155
Redox Regulation of Transient Receptor Potential Channels
Kozai, D., Ogawa, N., & Mori, Y. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5616 · Cited by 155
TRPA1 Mediates Mechanical Currents in the Plasma Membrane of Mouse Sensory Neurons
Vilceanu, D., & Stucky, C. L. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012177 · Cited by 155
Moparthi, L., Survery, S., Kreir, M., Simonsen, C., Kjellbom, P. O., Högestätt, E. D., Johanson, U., & Zygmunt, P. M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1412689111 · Cited by 155
TRPA1 Is a Component of the Nociceptive Response to CO 2
Wang, Y. Y., Chang, R. B., & Liman, E. R. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2715-10.2010 · Cited by 155
Brierley, S. M., Castro, J., Harrington, A. M., Hughes, P. A., Page, A. J., Rychkov, G. Y., & Blackshaw, L. A. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.206789 · Cited by 153
TRPA1 antagonists as potential analgesic drugs
de Andrade, E. L., Meotti, F. C., & Calixto, J. Β. (2011) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2011.10.008 · Cited by 153
Hazari, M. S., Haykal-Coates, N., Winsett, D. W., Krantz, Q. T., King, C. J., Costa, D. L., & Farraj, A. K. (2011) · Environmental Health Perspectives · doi:10.1289/ehp.1003200 · Cited by 152
The TRPA1 channel in migraine mechanism and treatment
Benemei, S., Fusi, C., Trevisan, G., & Geppetti, P. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12512 · Cited by 151
TRPs in Taste and Chemesthesis
Roper, S. D. (2014) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-05161-1_5 · Cited by 150
Cited by
Zhang, M., Ma, Y., Ye, X., Zhang, N., Pan, L., & Wang, B. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01464-x · Cited by 522
TRPA1 rare variants in chronic neuropathic and nociplastic pain patients
Marchi, M., Salvi, E., Andelic, M., Mehmeti, E., D'Amato, I., Cazzato, D., Chiappori, F., Lombardi, R., Cartelli, D., Devigili, G., et al. (2023) · Pain · doi:10.1097/j.pain.0000000000002905 · Cited by 29
TRPA1 promotes melanosome phagocytosis in keratinocytes via PAR-2/CYLD axis
Wang, Y., Li, Z., Wu, W., Liu, Y., Xiao, Y., Qi, D., Zhao, G., Zhou, M., Wang, H., Liu, J., et al. (2022) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2022.05.005 · Cited by 12
Giacco, V., Flower, G., Artamonova, M., Hunter, J., Padilla Requerey, A., & Hamilton, N. B. (2023) · Glia · doi:10.1002/glia.24347 · Cited by 11
Metadata
- Authors
- Talavera, K., Startek, J. B., Alvarez-Collazo, J., Boonen, B., Alpizar, Y. A., Sanchez, A., Naert, R., & Nilius, B.
- Venue
- Physiological Reviews
- Publisher
- American Physiological Society
- Published
- 2020-04-01
- Volume
- 100
- Issue
- 2
- Pages
- 725-803
- ISSN
- 0031-9333 (ISSN-L)
- 1522-1210
- OpenAlex
- W2987691534
- Cited by
- 403
- References
- 728
- FWCI
- 6.62
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.