Colonic Segment-Specific Effect of Lipopolysaccharide on TRPV1 and TRPA1 Levels in Rats
- Autores: Dvornikova K.A1, Bystrova E.Y.1, Platonova O.N1, Fedorova A.A1,2, Markov A.G1,2
-
Afiliações:
- Pavlov Institute of Physiology of the Russian Academy of Sciences
- St. Petersburg State University
- Edição: Volume 111, Nº 11 (2025)
- Páginas: 1860-1874
- Seção: EXPERIMENTAL ARTICLES
- URL: https://journals.rcsi.science/0869-8139/article/view/355693
- DOI: https://doi.org/10.7868/S2658655X25110117
- ID: 355693
Citar
Resumo
Palavras-chave
Sobre autores
K. Dvornikova
Pavlov Institute of Physiology of the Russian Academy of SciencesSaint Petersburg, Russia
E. Bystrova
Pavlov Institute of Physiology of the Russian Academy of SciencesSaint Petersburg, Russia
O. Platonova
Pavlov Institute of Physiology of the Russian Academy of SciencesSaint Petersburg, Russia
A. Fedorova
Pavlov Institute of Physiology of the Russian Academy of Sciences; St. Petersburg State UniversitySaint Petersburg, Russia
A. Markov
Pavlov Institute of Physiology of the Russian Academy of Sciences; St. Petersburg State University
Email: markovag@infran.ru
Saint Petersburg, Russia; Saint Petersburg, Russia
Bibliografia
- Dekel R, Drossman DA, Sperber AD (2015) Abdominal Pain in Irritable Bowel Syndrome (IBS). In: Kapurai L (ed) Chronic Abdominal Pain: An Evidence-Based, Comprehensive Guide to Clinical Management. Springer, New York, pp. 59–67.
- Li Y-C, Zhang F-C, Xu TW, Weng R-X, Zhang H-H, Chen Q-Q, Hu S, Gao R, Li R, Xu G-Y (2024) Advances in the pathological mechanisms and clinical treatments of chronic visceral pain. Mol Pain 20: 17448069241305942. https://doi.org/10.1177/17448069241305942
- Ford AC, Yanner S, Kashyap PC, Nasser Y (2024) Chronic Visceral Pain: New Peripheral Mechanistic Insights and Resulting Treatments. Gastroenterology 166: 976–994. https://doi.org/10.1053/j.gastro.2024.01.045
- Zhang M, Ma Y, Ye X, Zhang N, Pan L, Wang B (2023) TRP (transient receptor potential) ion channel family: structures, biological functions and therapeutic interventions for diseases. Signal Transduct Target Ther 8: 261. https://doi.org/10.1038/s41392-023-01464-x
- González-Ramirez R, Chen Y, Liedtke WB, Morales-Lázaro SL (2017) TRP Channels and Pain. In: Emir TLR (ed) Neurobiology of TRP Channels. CRC Press/Taylor & Francis, Boca Raton (FL), pp 125–148.
- Bharucha AE, Camilleri M (2019) Physiology of the Colon and Its Measurement. In: Yeo CJ (ed) Shackelford’s Surgery of the Alimentary Tract, 2 Volume Set (Eighth Edition). Elsevier, Philadelphia, pp 1676–1688.
- Evans C, Howells K, Suzuki R, Brown AJH, Cox HM (2023) Regional characterisation of TRPV1 and TRPA1 signalling in the mouse colon mucosa. Eur J Pharmacol 954: 175897. https://doi.org/10.1016/j.ejphar.2023.175897
- Startek JB, Talavera K, Voets T, Alpizar YA (2018) Differential interactions of bacterial lipopolysaccharides with lipid membranes: implications for TRPA1-mediated chemosensation. Sci Rep 8: 12010. https://doi.org/10.1038/s41598-018-30534-2
- Boonen B, Alpizar YA, Sanchez A, López-Requena A, Voets T, Talavera K (2018) Differential effects of lipopolysaccharide on mouse sensory TRP channels. Cell Calcium 73: 72–81. https://doi.org/10.1016/j.ceca.2018.04.004
- Mazgaeen L, Gurung P (2020) Recent Advances in Lipopolysaccharide Recognition Systems. Int J Mol Sci 21: 379. https://doi.org/10.3390/ijms21020379
- Dickson K, Lehmann C (2019) Inflammatory Response to Different Toxins in Experimental Sepsis Models. Int J Mol Sci 20: 4341. https://doi.org/10.3390/ijms20184341
- Korneev KV (2019) Mouse Models of Sepsis and Septic Shock. Mol Biol (Mosk) 53: 799–814. https://doi.org/10.1134/S0026898419050100
- Yalcin I, Charlet A, Freund-Mercier M-J, Barrot M, Poisbeau P (2009) Differentiating thermal allodynia and hyperalgesia using dynamic hot and cold plate in rodents. J Pain 10: 767–773. https://doi.org/10.1016/j.jpain.2009.01.325
- Jain P, Materazzi S, De Logu F, Rossi Degl’Innocenti D, Fusi C, Li Puma S, Marone IM, Coppi E, Holzer P, Geppetti P, Nassini R (2020) Transient receptor potential ankyrin 1 contributes to somatic pain hypersensitivity in experimental colitis. Sci Rep 10: 8632. https://doi.org/10.1038/s41598-020-65618-5
- López-Estévez S, López-Torrellardona JM, Parera M, Martínez V (2022) Long-lasting visceral hypersensitivity in a model of DSS-induced colitis in rats. Neurogastroenterol Motil 34: e14441. https://doi.org/10.1111/nmo.14441
- Tranb RJ, Wang G (2004) Colonic inflammation decreases thermal sensitivity of the forepaw and hindpaw in the rat. Neurosci Lett 359: 81–84. https://doi.org/10.1016/j.neulet.2004.02.026
- Slesarenko N, Komiakova VA, Stepanishin VV (2019) The morphofunctional characteristic of rodenties’ intestine. Lab Anim Sci Rus 2. https://doi.org/10.29296/2618723X-2019-03-01
- Markov AG, Fedorova AA, Kravtsova VV, Bikmurzina AE, Okorokova LS, Matchkov VV, Cornelius V, Amasheh S, Krivoi II (2020) Circulating Ouabain Modulates Expression of Claudins in Rat Intestine and Cerebral Blood Vessels. Int J Mol Sci 21: 5067. https://doi.org/10.3390/ijms21145067
- Lyubashina OA, Sivachenko IB, Busygina II (2020) Neurophysiological features of visceral and somatic pain. Usp Fiz Nauk 53: 3–14. https://doi.org/10.31857/S0301179822020072
- Bekusova V, Fatyykhov I, Amasheh S, Markov A (2021) Heterogeneity of the barrier properties of the colon in rat. Biol Communicat 66: 160–170. https://doi.org/10.21638/spbu03.2021.207
- Di Vincenzo F, Del Gaudio A, Petito V, Lopetuso LR, Scaldaferr i F (2024) Gut microbiota, intestinal permeability, and systemic inflammation: a narrative review. Int Emerg Med 19: 275–293. https://doi.org/10.1007/s11739-023-03374-w
- Diogenes A, Ferraz CCR, Akopian AN, Henry MA, Hargreaves KM (2011) LPS sensitizes TRPV1 via activation of TLR4 in trigeminal sensory neurons. J Dent Res 90: 759–764. https://doi.org/10.1177/0022034511400225
- Meseguer V, Alpizar YA, Luis E, Tajada S, Denlinger B, Fajardo O, Manenschijn J-A, Fernández-Peña C, Talavera A, Kichko T, Navia B, Sánchez A, Señaris R, Reeh P, Pérez-García MT, López-López JR, Voets T, Belmonte C, Talavera K, Viana F (2014) TRPA1 channels mediate acute neurogenic inflammation and pain produced by bacterial endotoxins. Nat Commun 5: 3125. https://doi.org/10.1038/ncomms4125
- Devesa I, Planells-Cases R, Fernández-Ballester G, González-Ros JM, Ferrer-Montiel A, Fernández-Carvajal A (2011) Role of the transient receptor potential vanilloid 1 in inflammation and sepsis. J Inflamm Res 4: 67–81. https://doi.org/10.2147/JIR.S12978
- Engel MA, Leffler A, Niedermirth F, Babes A, Zimmermann K, Filipović MR, Izydorczyk I, Eberhardt M, Kichko TI, Mueller-Tribbensee SM, Khalil M, Siklosi N, Nau C, Ivanović-Burmazović I, Neuhuber WL, Becker C, Neurath MF, Reeh PW (2011) TRPA1 and substance P mediate colitis in mice. Gastroenterology 141: 1346–1358. https://doi.org/10.1053/j.gastro.2011.07.002
- Kun J, Szitter J, Kemény A, Perkecz A, Kereskai L, Pohóczky K, Vincze A, Gódi S, Szabó I, Szolcsányi J, Pintér E, Helyes Z (2014) Upregulation of the transient receptor potential ankyrin 1 ion channel in the inflamed human and mouse colon and its protective roles. PLoS One 9: e108164. https://doi.org/10.1371/journal.pone.0108164
- Bertin S, Aoki-Nonaka Y, Lee J, de Jong PR, Kim P, Han T, Yu T, To K, Takahashi N, Boland BS, Chang JT, Ho SB, Herdman S, Corr M, Franco A, Sharma S, Dong H, Akopian AN, Raz E (2017) The TRPA1 ion channel is expressed in CD4+ T cells and restrains T-cell-mediated colitis through inhibition of TRPV1. Gut 66: 1584–1596. https://doi.org/10.1136/guqjnl-2015-310710
- Schwartz ES, Christianson JA, Chen X, La J-H, Davis BM, Albers KM, Gebhart GF (2011) Synergistic role of TRPV1 and TRPA1 in pancreatic pain and inflammation. Gastroenterology 140: 1283–1291.e1–2. https://doi.org/10.1053/j.gastro.2010.12.033
- Fischer MJ, Edwardson JM (2014) V2A2lidating TRP channel heteromers. Temperature (Austin) 1: 26–27. https://doi.org/10.4161/temp.29548
- Nagpal R, Mishra SK, Deep G, Yadav H (2020) Role of TRP Channels in Shaping the Gut Microbiome. Pathogens 9: 753. https://doi.org/10.3390/pathogens9090753
- Zhang W, Lyu M, Bessman NJ, Xie Z, Arifazzaman M, Yano H, Parkhurst CN, Chu C, Zhou L, Putzel GG, Li T-T, Jin W-B, Zhou J, JRI Live Cell Bank, Hu H, Tsou AM, Guo C-J, Artis D (2022) Gut-innervating nociceptors regulate the intestinal microbiota to promote tissue protection. Cell 185: 4170–4189.e20. https://doi.org/10.1016/j.cell.2022.09.008
- Foppa C, Rizkala T, Repici A, Hassan C, Spinelli A (2024) Microbiota and IBD: Current knowledge and future perspectives. Dig Liver Dis 56: 911–922. https://doi.org/10.1016/j.dld.2023.11.015
Arquivos suplementares

