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Transient receptor potential (TRP) channels: a clinical perspective
Open accessAbstract
Transient receptor potential (TRP) channels are important mediators of sensory signals with marked effects on cellular functions and signalling pathways. Indeed, mutations in genes encoding TRP channels are the cause of several inherited diseases in humans (the so‐called ‘TRP channelopathies’) that affect the cardiovascular, renal, skeletal and nervous systems.TRP channels are also promising targets for drug discovery. The initial focus of research was on TRP channels that are expressed on nociceptive neurons. Indeed, a number of potent, small‐molecule TRPV 1,TRPV 3 and TRPA 1 antagonists have already entered clinical trials as novel analgesic agents. There has been a recent upsurge in the amount of work that expands TRP channel drug discovery efforts into new disease areas such as asthma, cancer, anxiety, cardiac hypertrophy, as well as obesity and metabolic disorders. A better understanding of TRP channel functions in health and disease should lead to the discovery of first‐in‐class drugs for these intractable diseases. With this review, we hope to capture the current state of this rapidly expanding and changing field. Linked Articles: This article is part of a themed section on the pharmacology of TRP channels. To view the other articles in this section visit http://dx.doi.org/10.1111/bph.2014.171.issue‐10
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TRPM8: From Cold to Cancer, Peppermint to Pain
Knowlton, W., & McKemy, D. D. (2010) · Current Pharmaceutical Biotechnology · doi:10.2174/138920111793937961 · Cited by 85
Heteromerization of TRP channel subunits: extending functional diversity
Cheng, W., Sun, C., & Zheng, J. (2010) · Protein & Cell · doi:10.1007/s13238-010-0108-9 · Cited by 85
Fischer, M. J. M., Btesh, J., & McNaughton, P. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3721-12.2013 · Cited by 85
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Transient Receptor Potential A1 Channels
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TRP channels as therapeutic targets in airway disorders: a patent review
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TRPA1 receptor modulation attenuates bladder overactivity induced by spinal cord injury
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An Inhibitor of TRPV1 Channels Isolated from Funnel Web Spider Venom
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Pregnenolone sulphate-independent inhibition of TRPM3 channels by progesterone
Majeed, Y., Tumova, S., Green, B. L., Seymour, V. A. L., Woods, D., Agarwal, A. K., Naylor, J., Jiang, S., Picton, H. M., Porter, K. E., et al. (2011) · Cell Calcium · doi:10.1016/j.ceca.2011.09.005 · Cited by 76
Apigenin, a plant‐derived flavone, activates transient receptor potential vanilloid 4 cation channel
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Blockade of TRPM7 Channel Activity and Cell Death by Inhibitors of 5-Lipoxygenase
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TRP channels and their implications in metabolic diseases
Zhu, Z., Luo, Z., Ma, S., & Liu, D. (2010) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-010-0902-5 · Cited by 73
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Targeting ion channels for drug discovery.
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Effects of TRPV4 cation channel activation on the primary bladder afferent activities of the rat
Aizawa, N., Wyndaele, J., Homma, Y., & Igawa, Y. (2011) · Neurourology and Urodynamics · doi:10.1002/nau.21212 · Cited by 71
Inhibition of the human epithelial calcium channel TRPV6 by 2-aminoethoxydiphenyl borate (2-APB)
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‘Sensing’ autoimmunity in type 1 diabetes
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Evodiamine functions as an agonist for the vanilloid receptor TRPV1
Pearce, L. V., Petukhov, P. A., Szabó, T. G., Kedei, N., Bizik, F., Kozikowski, A. P., & Blumberg, P. M. (2004) · Organic & Biomolecular Chemistry · doi:10.1039/b404506h · Cited by 67
Activation of transient receptor potential A1 by a non‐pungent capsaicin‐like compound, capsiate
Shintaku, K., Uchida, K., Suzuki, Y., Zhou, Y., Fushiki, T., Watanabe, T., Yazawa, S., & Tominaga, M. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01634.x · Cited by 65
Puttfarcken, P. S., Han, P., Joshi, S. K., Neelands, T. R., Gauvin, D. M., Baker, S. J., Lewis, L. G. R., Bianchi, B. R., Mikusa, J. P., Koenig, J. R., et al. (2010) · Pain · doi:10.1016/j.pain.2010.05.015 · Cited by 64
TRPA1 and TRPV1 are differentially involved in heat nociception of mice
Hoffmann, T., Kistner, K., Miermeister, F., et al. (2013) · European Journal of Pain · doi:10.1002/j.1532-2149.2013.00331.x · Cited by 63
Resiniferatoxin for Pain Treatment: An Interventional Approach to Personalized Pain Medicine
Iadarola, M. J., & Gonnella, G. L. (2013) · The Open Pain Journal · doi:10.2174/1876386301306010095 · Cited by 62
Delescluse, I., Mace, H., & Adcock, J. J. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2012.01891.x · Cited by 60
Increased expression of TRPV1 channel in intrinsically aged and photoaged human skin in vivo
Lee, Y., Kim, Y. K., & Chung, J. H. (2008) · Experimental Dermatology · doi:10.1111/j.1600-0625.2008.00806.x · Cited by 60
Nociceptive and pro‐inflammatory effects of dimethylallyl pyrophosphate via TRPV4 activation
Bang, S., Yoo, S., Yang, T., Cho, H., & Hwang, S. W. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2012.01884.x · Cited by 59
Tamayo, N. A., Bo, Y. Y., Gore, V., Ma, V., Nishimura, N., Tang, P., Deng, H. X., Klionsky, L., Lehto, S. G., Wang, W., et al. (2012) · Journal of Medicinal Chemistry · doi:10.1021/jm2013634 · Cited by 56
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Inhibitory effects of TRPV1 blocker on UV-induced responses in the hairless mice
Lee, Y., Kang, S. M., Lee, S. R., Kong, K. H., Lee, J. Y., Kim, E. J., & Chung, J. H. (2011) · Archives of Dermatological Research · doi:10.1007/s00403-011-1153-9 · Cited by 53
Keszthelyi, D., Troost, F. J., Jonkers, D. M. A. E., Helyes, Z., Hamer, H. M., Ludidi, S., Vanhoutvin, S. A. L. W., Venema, K., Dekker, J. P., Szolcsányi, J., et al. (2013) · European Journal of Pain · doi:10.1002/j.1532-2149.2013.00309.x · Cited by 53
Capasso, R., Aviello, G., Romano, B., Borrelli, F., PETROCELLIS, L. D., Marzo, V. D., & Izzo, A. A. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01703.x · Cited by 51
Effect of Menthol on Detrusor Smooth-Muscle Contraction and the Micturition Reflex in Rats
Nomoto, Y., Yoshida, A., Ikeda, S., Kamikawa, Y., Harada, K., Ohwatashi, A., & Kawahira, K. (2008) · Urology · doi:10.1016/j.urology.2007.11.137 · Cited by 51
Production of a specific extracellular inhibitor of TRPM3 channels
Naylor, J., Milligan, C. J., Zeng, F., Jones, C. A., & Beech, D. J. (2008) · British Journal of Pharmacology · doi:10.1038/bjp.2008.283 · Cited by 51
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Mapping the Binding Site of TRPV1 on AKAP79: Implications for Inflammatory Hyperalgesia
Btesh, J., Fischer, M. J. M., Stott, K. M., & McNaughton, P. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4991-12.2013 · Cited by 48
Schwarz, E. C., Wolfs, M., Tonner, S., Wenning, A. S., Quintana, A., Griesemer, D., & Hoth, M. (2007) · Springer eBooks · doi:10.1007/978-3-540-34891-7_26 · Cited by 47
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Attenuation of acid induced oesophagitis in VR-1 deficient mice
Fujino, K., de la Fuente, S. G., Takami, Y., Takahashi, T., & Mantyh, C. R. (2005) · Gut · doi:10.1136/gut.2005.066795 · Cited by 47
Tanaka, H., Shimaya, A., Kiso, T., Kuramochi, T., Shimokawa, T., & Shibasaki, M. (2011) · Life Sciences · doi:10.1016/j.lfs.2011.01.016 · Cited by 46
Transient receptor potential channels in bladder function
Avelino, A., Charrua, A., Frias, B., Cruz, C. D., Boudes, M., Ridder, D. J. M. K. D., & Cruz, F. (2012) · Acta Physiologica · doi:10.1111/apha.12021 · Cited by 45
TRP Channels: New Potential Therapeutic Approaches in CNS Neuropathies
Morelli, M. B., Amantini, C., Liberati, S., Santoni, M., & Nabissi, M. (2013) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/18715273113129990056 · Cited by 44
Methylglyoxal activates the human transient receptor potential ankyrin 1 channel
Ohkawara, S., Tanaka‐Kagawa, T., Furukawa, Y., & Jinno, H. (2012) · The Journal of Toxicological Sciences · doi:10.2131/jts.37.831 · Cited by 42
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Transient receptor proteins illuminated: Current views on TRPs and disease
Nelson, P. L., Beck, A., & Cheng, H. (2010) · The Veterinary Journal · doi:10.1016/j.tvjl.2010.01.020 · Cited by 37
Apomorphine Is a Bimodal Modulator of TRPA1 Channels
Schulze, A., Oehler, B., Urban, N. D., Schaefer, M., & Hill, K. (2012) · Molecular Pharmacology · doi:10.1124/mol.112.081976 · Cited by 37
Oncogenic and Anti-Oncogenic Effects of Transient Receptor Potential Channels
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Thapsigargin binds to and inhibits the cloned vanilloid receptor-1
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TRPM4 channel: a new player in urinary bladder smooth muscle function in rats
Smith, A. C., Parajuli, S. P., Hristov, K. L., Cheng, Q., Soder, R. P., Afeli, S. A. Y., Earley, S., Xin, W., Malysz, J., & Petkov, G. V. (2013) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00417.2012 · Cited by 35
Mucolipidosis type IV: The importance of functional lysosomes for efficient autophagy
Vergarajauregui, S., & Puertollano, R. (2008) · Autophagy · doi:10.4161/auto.6567 · Cited by 33
5-Benzyloxytryptamine as an antagonist of TRPM8
DeFalco, J., Steiger, D., Dourado, M., Emerling, D. E., & Duncton, M. A. J. (2010) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2010.09.099 · Cited by 26
Transient Receptor Potential (TRP) Cation Channels in Diabetes
Colsoul, B., Nilius, B., & Vennekens, R. (2013) · Current Topics in Medicinal Chemistry · doi:10.2174/1568026611313030004 · Cited by 24
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Regulating cough through modulation of sensory nerve function in the airways
Spina, D., & Page, C. P. (2013) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2013.03.011 · Cited by 21
Effects of Topical Capsaicin on Cutaneous Innervation: Implications for Pain Management
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‘Sensing’ the link between type 1 and type 2 diabetes
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Capsaicin impairs preoptic serotonin-sensitive structures mediating hypothermia in rats
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Teitelbaum, J. E. (2012) · The Open Pain Journal · doi:10.2174/1876386301205010032 · Cited by 14
Capsaicin Induces Reflex Scratching in Inflamed Skin
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Transient Receptor Potential Channels in Chemotherapy-Induced Neuropathy
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Capsaicin provocation using two different inhalation devices
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Jiménez‐Andrade, J. M., & Mantyh, P. W. (2010) · Wiley eBooks · doi:10.1002/9780470588284.ch7 · Cited by 2
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Joshi, S. K., & Honoré, P. (2010) · Wiley eBooks · doi:10.1002/9780470588284.ch6 · Cited by 1
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TRPV4: molecular conductor of a diverse orchestra
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Physiology and Pathophysiology of Itch
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Garami, A., Shimansky, Y. P., Rumbus, Z., Vizin, R. C. L., Farkas, N., Hegyi, J., Szakacs, Z., Solymar, M., Csenkey, A., Chiche, D. A., et al. (2020) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2020.107474 · Cited by 159
The impact of temperature on the skin barrier and atopic dermatitis
Hui-Beckman, J. W., Goleva, E., Leung, D. Y. M., & Kim, B. E. (2023) · Annals of Allergy, Asthma & Immunology · doi:10.1016/j.anai.2023.08.007 · Cited by 58
Metadata
- Authors
- Kaneko, Y., & Szallasi, A.
- Venue
- British Journal of Pharmacology
- Publisher
- Wiley
- Published
- 2014-04-28
- Volume
- 171
- Issue
- 10
- Pages
- 2474-2507
- ISSN
- 0007-1188 (ISSN-L)
- 1476-5381
- OpenAlex
- W1571837352
- Cited by
- 370
- References
- 369
- FWCI
- 13.80
- Type
- journal article
- Language
- en
- Open access
- bronze
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