Transient receptor potential Vanilloid 1-based gene therapy alleviates orthodontic pain in rats

Rui Guo , Yang Zhou , Hu Long , Di Shan , Jing Wen , Huimin Hu , Hong Yang , Zhouqiang Wu , Wenli Lai

International Journal of Oral Science ›› 2019, Vol. 11 ›› Issue (1) : 11

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International Journal of Oral Science ›› 2019, Vol. 11 ›› Issue (1) : 11 DOI: 10.1038/s41368-019-0044-3
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Transient receptor potential Vanilloid 1-based gene therapy alleviates orthodontic pain in rats

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Abstract

Gene therapy targeting a pain receptor in nerve cells carrying signals from the jaw could be an effective treatment for the pain associated with orthodontic treatment. Pain triggered by the movement of teeth is a common reason why patients terminate orthodontic treatment early. Previous studies have suggested that tooth movement is associated with an increase in the expression of transient receptor potential vanilloid 1 (TRPV1), a receptor which is activated by various physical and chemical stimuli, triggering pain. In this study, Wenli Lai at Sichuan University and colleagues confirm that TRPV1 expression increases in response to orthodontic forces which coincide with tooth movement pain in rats. They also show that a lentivirus vector can be used to deliver a small interfering RNA molecule that blocks the expression of TRPV1, alleviating pain.

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Rui Guo, Yang Zhou, Hu Long, Di Shan, Jing Wen, Huimin Hu, Hong Yang, Zhouqiang Wu, Wenli Lai. Transient receptor potential Vanilloid 1-based gene therapy alleviates orthodontic pain in rats. International Journal of Oral Science, 2019, 11(1): 11 DOI:10.1038/s41368-019-0044-3

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References

[1]

Banerjee S, Banerjee R, Shenoy U, Agarkar S, Bhattacharya S. Effect of orthodontic pain on quality of life of patients undergoing orthodontic treatment. Indian J. Dent. Res., 2018, 29: 4-9.

[2]

Campos MJ, Fraga MR, Raposo NR, Ferreira AP, Vitral RW. Assessment of pain experience in adults and children after bracket bonding and initial archwire insertion. Dent. Press J. Orthod., 2013, 18: 32-37.

[3]

Rakhshan H, Rakhshan V. Pain and discomfort perceived during the initial stage of active fixed orthodontic treatment. Saudi Dent. J., 2015, 27: 81-87.

[4]

Krishnan V. Orthodontic pain: from causes to management--a review. Eur. J. Orthod., 2007, 29: 170-179.

[5]

Bergius M, Berggren U, Kiliaridis S. Experience of pain during an orthodontic procedure. Eur. J. Oral. Sci., 2002, 110: 92-98.

[6]

Long H, . Current advances in orthodontic pain. Int. J. Oral. Sci., 2016, 8: 67-75.

[7]

Gupta M, . Controlling pain during orthodontic fixed appliance therapy with non-steroidal anti-inflammatory drugs (NSAID): a randomized, double-blinded, placebo-controlled study. J. Orofac. Orthop., 2014, 75: 471-476.

[8]

Yadav S, . Effect of low-frequency mechanical vibration on orthodontic tooth movement. Am. J. Orthod. Dentofac. Orthop., 2015, 148: 440-449.

[9]

Deana NF, Zaror C, Sandoval P, Alves N. Effectiveness of low-level laser therapy in reducing orthodontic pain: a systematic review and meta-analysis. Pain. Res. Manag., 2017, 2017: 8560652.

[10]

Sawada A, Usui N, Shimazaki K, Taira M, Ono T. The effects of cognitive behavioral therapy on experimental orthodontic pain. Orthod. Waves, 2015, 74: 10-14.

[11]

Prabhakar AR, Paul JM, Basappa N. Gene therapy and its implications in dentistry. Int. J. Clin. Pediatr. Dent., 2011, 4: 85-92.

[12]

Hussain AS, Al Toubity MJ, Elias WY. Methodologies in orthodontic pain management: a review. Open Dent. J., 2017, 11: 492-497.

[13]

Glorioso JC, Fink DJ. Gene therapy for pain: introduction to the special issue. Gene Ther., 2009, 16: 453-454.

[14]

Simonato M, . Progress in gene therapy for neurological disorders. Nat. Rev. Neurol., 2013, 9: 277-291.

[15]

Leung RK, Whittaker PA. RNA interference: from gene silencing to gene-specific therapeutics. Pharmacol. Ther., 2005, 107: 222-239.

[16]

Rohl T, Kurreck J. RNA interference in pain research. J. Neurochem., 2006, 99: 371-380.

[17]

Zychowska M, . Participation of pro- and anti-nociceptive interleukins in botulinum toxin A-induced analgesia in a rat model of neuropathic pain. Eur. J. Pharmacol., 2016, 791: 377-388.

[18]

Singh AK, Vinayak M. Anti-nociceptive effect of resveratrol during inflammatory hyperalgesia via differential regulation of pro-inflammatory mediators. Phytother. Res., 2016, 30: 1164-1171.

[19]

Gunthorpe MJ, Chizh BA. Clinical development of TRPV1 antagonists: targeting a pivotal point in the pain pathway. Drug Discov. Today, 2009, 14: 56-67.

[20]

Caterina MJ, . The capsaicin receptor: a heat-activated ion channel in the pain pathway. Nature, 1997, 389: 816-824.

[21]

Zheng J. Molecular mechanism of TRPchannels. Compr. Physiol., 2013, 3: 221-242.

[22]

Ghilardi JR, . Selective blockade of the capsaicin receptor TRPV1 attenuates bone cancer pain. J. Neurosci., 2005, 25: 3126-3131.

[23]

Honore P, . A-425619 [1-isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a novel transient receptor potential type V1 receptor antagonist, relieves pathophysiological pain associated with inflammation and tissue injury in rats. J. Pharmacol. Exp. Ther., 2005, 314: 410-421.

[24]

Qiao H, Gao Y, Zhang C, Zhou H. Increased expression of TRPV1 in the trigeminal ganglion is involved in orofacial pain during experimental tooth movement in rats. Eur. J. Oral. Sci., 2015, 123: 17-23.

[25]

Ohkura M, . Orthodontic force application upregulated pain-associated prostaglandin-I2/PGI2-receptor/TRPV1 pathway-related gene expression in rat molars. Odontology, 2018, 106: 2-10.

[26]

Gao Y, . Blocking of TRPV-1 in the parodontium relieves orthodontic pain by inhibiting the expression of TRPV-1 in the trigeminal ganglion during experimental tooth movement in rats. Neurosci. Lett., 2016, 628: 67-72.

[27]

Zhang CD, . Expression of TRPV1 and CGRP in rat trigeminal ganglion during orthodontic tooth movement. Shanghai Kou. Qiang. Yi. Xue., 2015, 24: 6-12.

[28]

Gunthorpe MJ, . Identification and characterisation of SB-366791, a potent and selective vanilloid receptor (VR1/TRPV1) antagonist. Neuropharmacology, 2004, 46: 133-149.

[29]

Gavva NR, . AMG 9810 [(E)-3-(4-t-butylphenyl)-N-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)acrylamide], a novel vanilloid receptor 1 (TRPV1) antagonist with antihyperalgesic properties. J. Pharmacol. Exp. Ther., 2005, 313: 474-484.

[30]

El Kouhen R, . A-425619 [1-isoquinolin-5-yl-3-(4-trifluoromethyl-benzyl)-urea], a novel and selective transient receptor potential type V1 receptor antagonist, blocks channel activation by vanilloids, heat, and acid. J. Pharmacol. Exp. Ther., 2005, 314: 400-409.

[31]

Behrendt HJ, Germann T, Gillen C, Hatt H, Jostock R. Characterization of the mouse cold-menthol receptor TRPM8 and vanilloid receptor type-1 VR1 using a fluorometric imaging plate reader (FLIPR) assay. Br. J. Pharmacol., 2004, 141: 737-745.

[32]

Wiskur BJ, . A novel Trpv1 receptor antagonist Jnj-17203212 attenuates colonic hypersensitivity in rats. Methods Find. Exp. Clin. Pharmacol., 2010, 32: 557-564.

[33]

Teramoto S, Ishii T, Matsuse T, Fukuchi Y. Recombinant adeno-associated virus vectors efficiently transduce foreign gene into bovine aortic endothelial cells: comparison with adenovirus vectors. Jpn. J. Pharmacol., 2000, 84: 206-212.

[34]

Delenda C. Lentiviral vectors: optimization of packaging, transduction and gene expression. J. Gene Med., 2004, 6: S125-S138.

[35]

Benavides OJ, Satlin L, Burrow C, Wilson P, Herold B. Herpes simplex virus (HSV) as a model vector for gene therapy for renal disease. J. Am. Soc. Nephrol., 2002, 13: 125a.

[36]

Daya S, Berns KI. Gene therapy using adeno-associated virus vectors. Clin. Microbiol. Rev., 2008, 21: 583-593.

[37]

Ogawa N, . Gene therapy for neuropathic pain by silencing of TNF-alpha expression with lentiviral vectors targeting the dorsal root ganglion in mice. PLoS One, 2014, 9: e92073.

[38]

Wang W, Cao XH, Liu CJ, Liu LJ. Cannabinoid WIN 55,212-2 inhibits TRPV1 in trigeminal ganglion neurons via PKA and PKC pathways. Neurol. Sci., 2012, 33: 79-85.

[39]

Sanz-Salvador L, Andres-Borderia A, Ferrer-Montiel A, Planells-Cases R. Agonist- and Ca2+-dependent desensitization of TRPV1 channel targets the receptor to lysosomes for degradation. J. Biol. Chem., 2012, 287: 19462-19471.

[40]

Lappin SC, Randall AD, Gunthorpe MJ, Morisset V. TRPV1 antagonist, SB-366791, inhibits glutamatergic synaptic transmission in rat spinal dorsal horn following peripheral inflammation. Eur. J. Pharmacol., 2006, 540: 73-81.

[41]

Christoph T, . Investigation of TRPV1 loss-of-function phenotypes in transgenic shRNA expressing and knockout mice. Mol. Cell. Neurosci., 2008, 37: 579-589.

[42]

Nakamura A, . G protein-gated inwardly rectifying potassium (KIR3) channels play a primary role in the antinociceptive effect of oxycodone, but not morphine, at supraspinal sites. Br. J. Pharmacol., 2014, 171: 253-264.

[43]

Kilkenny C, Browne WJ, Cuthill IC, Emerson M, Altman DG. Improving bioscience research reporting: the ARRIVE guidelines for reporting animal research. J. Pharmacol. Pharmacother., 2010, 1: 94-99.

[44]

Liao L, . Evaluation of pain in rats through facial expression following experimental tooth movement. Eur. J. Oral. Sci., 2014, 122: 121-124.

Funding

National Natural Science Foundation of China (National Science Foundation of China)(81571004, 81500884, 81571004, 81500884, 81571004, 81500884, 81571004, 81500884, 81571004, 81500884, 81571004, 81500884, 81571004, 81500884, 81571004, 81500884, 81571004, 81500884)

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