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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Physiology</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Physiology</journal-title><trans-title-group xml:lang="ru"><trans-title>Российский физиологический журнал им. И.М. Сеченова</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0869-8139</issn><issn publication-format="electronic">2658-655X</issn><publisher><publisher-name xml:lang="en">The Russian Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">698259</article-id><article-id pub-id-type="doi">10.7868/S2658655X25110117</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>EXPERIMENTAL ARTICLES</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Colonic Segment-Specific Effect of Lipopolysaccharide on TRPV1 and TRPA1 Levels in Rats</article-title><trans-title-group xml:lang="ru"><trans-title>СЕГМЕНТ-СПЕЦИФИЧЕСКОЕ ДЕЙСТВИЕ ЛИПОПОЛИСАХАРИДА НА УРОВЕНЬ КАНАЛОВ TRPV1 И TRPA1 В ТОЛСТОЙ КИШКЕ КРЫСЫ</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Dvornikova</surname><given-names>K. A</given-names></name><name xml:lang="ru"><surname>Дворникова</surname><given-names>К. А</given-names></name></name-alternatives><email>email@example.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Bystrova</surname><given-names>E. Yu</given-names></name><name xml:lang="ru"><surname>Быстрова</surname><given-names>Е. Ю</given-names></name></name-alternatives><email>email@example.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Platonova</surname><given-names>O. N</given-names></name><name xml:lang="ru"><surname>Платонова</surname><given-names>О. Н</given-names></name></name-alternatives><email>email@example.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Fedorova</surname><given-names>A. A</given-names></name><name xml:lang="ru"><surname>Федорова</surname><given-names>А. А</given-names></name></name-alternatives><email>email@example.com</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Markov</surname><given-names>A. G</given-names></name><name xml:lang="ru"><surname>Марков</surname><given-names>А. Г</given-names></name></name-alternatives><email>markovag@infran.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Pavlov Institute of Physiology of the Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">Институт физиологии им. И.П. Павлова РАН</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">St. Petersburg State University</institution></aff><aff><institution xml:lang="ru">Санкт-Петербургский государственный университет</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2025-11-15" publication-format="electronic"><day>15</day><month>11</month><year>2025</year></pub-date><volume>111</volume><issue>11</issue><issue-title xml:lang="en">VOL 111, NO11 (2025)</issue-title><issue-title xml:lang="ru">ТОМ 111, №11 (2025)</issue-title><fpage>1860</fpage><lpage>1874</lpage><history><date date-type="received" iso-8601-date="2025-12-09"><day>09</day><month>12</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2025, Russian Academy of Sciences</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2025, Российская академия наук</copyright-statement><copyright-year>2025</copyright-year><copyright-holder xml:lang="en">Russian Academy of Sciences</copyright-holder><copyright-holder xml:lang="ru">Российская академия наук</copyright-holder></permissions><self-uri xlink:href="https://journals.eco-vector.com/0869-8139/article/view/698259">https://journals.eco-vector.com/0869-8139/article/view/698259</self-uri><abstract xml:lang="en"><p>One of the most pressing issues in visceral physiology is the investigation of the molecular mechanisms behind pain signal interoception. Chronic abdominal pain is a type of pain sensitivity that arises during gastrointestinal disorders and frequently persists after they are healed. Abdominal pain syndrome is caused by molecular alterations in the intestinal wall, the specifics of which are still unknown. TRPV1 and TRPA1 are transient receptor potential (TRP) channels found in enteric nervous system nerve cells that contribute to the development of visceral pain and hypersensitivity perception. The rat colon's uneven distribution of channels along its proximal-distal axis suggests they may be involved in the initial stages of abdominal pain sensitivity. The goal of the present study was to evaluate segment-specific alterations in TRPV1 and TRPA1 channel levels after inflammation is initiated by a single lipopolysaccharide (LPS) dose. The study used the "cold and hot plate" pain sensitivity test, morphometric analysis methods, recording of electrophysiological parameters in the USsing chamber, and Western blotting to assess the TRPA1 and TRPV1 protein expression. The results of this research show that a unitary administration of LPS leads to diminished TRPA1 levels in both the ascending and descending colons. No variations in TRPV1 levels were found in the ascending colon, but a significant rise was recorded in the descending colon. There were no observed changes in nociception in "cold and hot plate" test. Thus, a segment-specific alteration in the levels of TRPA1 and TRPV1 channels was established in the direct model of LPS toxicity.</p></abstract><trans-abstract xml:lang="ru"><p>Исследование молекулярных механизмов интероцепции болевых сигналов остается актуальной проблемой висцеральной физиологии. Одним из видов болевой чувствительности являются хронические абдоминальные боли, возникающие при заболеваниях желудочно-кишечного тракта и часто продолжающиеся после их завершения. Развитие абдоминального болевого синдрома инициируется запуском молекулярных изменений в стенке кишки, детали которого остаются не исследованными. Каналы транзиторного рецепторного потенциала (TRP), а именно TRPV1 и TRPA1, расположены в нервных клетках энтеральной нервной системы и участвуют в формировании ощущения висцеральной боли и гиперчувствительности. Толстая кишка крыс имеет неравномерное распределение этих каналов на протяжении своей проксимально-дистальной оси. Предполагается, что эти каналы могут быть вовлечены в начальные этапы формирования абдоминальной болевой чувствительности. Целью данного исследования было изучение сегмент-специфического изменения уровня каналов TRPV1 и TRPA1 при инициации воспаления однократным введении липополисахарида (ЛПС). В исследовании использовали тест на болевую чувствительность "холодная и горячая пластина", методы морфометрического анализа, регистрацию электрофизиологических параметров в камере Уссинга и вестерн-блот для оценки уровня белков TRPA1 и TRPV1. Однократное введение ЛПС приводит к уменьшению уровня TRPA1 в восходящем и в нисходящем отделах толстой кишки. В восходящем отделе изменения уровня TRPV1 не выявлено, в то же время в нисходящем отделе зарегистрировано значительное увеличение уровня TRPV1. В тесте "горячая и холодная пластина" изменения ноцицепции не наблюдалось. Таким образом, в прямой модели ЛПС-токсичности было установлено сегмент-специфическое изменение уровня TRPV1- и TRPA1-каналов.</p></trans-abstract><kwd-group xml:lang="en"><kwd>interoception</kwd><kwd>visceral sensitivity</kwd><kwd>lipopolysaccharide</kwd><kwd>inflammation</kwd><kwd>colon</kwd><kwd>TRPV1</kwd><kwd>TRPA1</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>интероцепция</kwd><kwd>висцеральная чувствительность</kwd><kwd>липополисахарид</kwd><kwd>воспаление</kwd><kwd>толстая кишка</kwd><kwd>TRPV1</kwd><kwd>TRPA1</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена при поддержке Российского научного фонда (проект № 24-25-00267)</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>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.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>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</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>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</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>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</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>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 &amp; Francis, Boca Raton (FL), pp 125–148.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>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.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>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</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>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</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>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</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Mazgaeen L, Gurung P (2020) Recent Advances in Lipopolysaccharide Recognition Systems. Int J Mol Sci 21: 379. https://doi.org/10.3390/ijms21020379</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>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</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Korneev KV (2019) Mouse Models of Sepsis and Septic Shock. Mol Biol (Mosk) 53: 799–814. https://doi.org/10.1134/S0026898419050100</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>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</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>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</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>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</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>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</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>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</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>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</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>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</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>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</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>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</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>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</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>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</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>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</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>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</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>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</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>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</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>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</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Fischer MJ, Edwardson JM (2014) V2A2lidating TRP channel heteromers. Temperature (Austin) 1: 26–27. https://doi.org/10.4161/temp.29548</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>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</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>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</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>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</mixed-citation></ref></ref-list></back></article>
