{"id":210,"date":"2025-12-09T00:30:26","date_gmt":"2025-12-08T15:30:26","guid":{"rendered":"https:\/\/website.jikei-neuroscience.com\/?page_id=210"},"modified":"2025-12-10T09:29:00","modified_gmt":"2025-12-10T00:29:00","slug":"%e4%b8%89%e5%8f%89%e7%a5%9e%e7%b5%8c-vs-%e8%84%8a%e9%ab%84%e7%a5%9e%e7%b5%8c","status":"publish","type":"page","link":"https:\/\/website.jikei-neuroscience.com\/?page_id=210","title":{"rendered":"\u4e09\u53c9\u795e\u7d4c vs. \u810a\u9ac4\u795e\u7d4c\u3000\u8ad6\u6587\u30ea\u30b9\u30c8\uff08Pain Week 2025\u30b7\u30f3\u30dd\u30b8\u30a6\u30e017\uff09"},"content":{"rendered":"\n<p>Aicher, S. A., Hegarty, D. M., &amp; Hermes, S. M. (2014). Corneal pain activates a trigemino-parabrachial pathway in rats. <em>Brain Research<\/em>, <em>1550<\/em>, 18\u201326. https:\/\/doi.org\/10.1016\/j.brainres.2014.01.002<\/p>\n\n\n\n<p>An, S. Bin, Cho, Y. S., Park, S. K., Kim, Y. S., &amp; Bae, Y. C. (2023). Synaptic connectivity of the TRPV1-positive trigeminal afferents in the rat lateral parabrachial nucleus. <em>Frontiers in Cellular Neuroscience<\/em>, <em>17<\/em>. https:\/\/doi.org\/10.3389\/fncel.2023.1162874<\/p>\n\n\n\n<p>Asquini, G., Devecchi, V., Viscuso, D., Bucci, R., Michelotti, A., Liew, B. X. W., &amp; Falla, D. (2025). An exploratory data-driven approach to classify subgroups of patients with temporomandibular disorders based on pain mechanisms. <em>Journal of Pain<\/em>, <em>26<\/em>. https:\/\/doi.org\/10.1016\/j.jpain.2024.104721<\/p>\n\n\n\n<p>Baker, C. V. H., &amp; Bronner-Fraser, M. (2001). Vertebrate cranial placodes. I. Embryonic induction. In <em>Developmental Biology<\/em> (Vol. 232, Issue 1, pp. 1\u201361). https:\/\/doi.org\/10.1006\/dbio.2001.0156<\/p>\n\n\n\n<p>Cavanaugh, D. J., Chesler, A. T., Br\u00e1z, J. M., Shah, N. M., Julius, D., &amp; Basbaum, A. I. (2011). Restriction of transient receptor potential vanilloid-1 to the peptidergic subset of primary afferent neurons follows its developmental downregulation in nonpeptidergic neurons. <em>Journal of Neuroscience<\/em>, <em>31<\/em>(28), 10119\u201310127. https:\/\/doi.org\/10.1523\/JNEUROSCI.1299-11.2011<\/p>\n\n\n\n<p>Condon, L. F., Yu, Y., Park, S., Cao, F., Pauli, J. L., Nelson, T. S., &amp; Palmiter, R. D. (2024). Parabrachial Calca neurons drive nociplasticity. <em>Cell Reports<\/em>, <em>43<\/em>(4). https:\/\/doi.org\/10.1016\/j.celrep.2024.114057<\/p>\n\n\n\n<p>Flegel, C., Sch\u00f6bel, N., Altm\u00fcller, J., Becker, C., Tannapfel, A., Hatt, H., &amp; Gisselmann, G. (2015). RNA-Seq analysis of human trigeminal and dorsal root ganglia with a focus on chemoreceptors. <em>PLoS ONE<\/em>, <em>10<\/em>(6). https:\/\/doi.org\/10.1371\/journal.pone.0128951<\/p>\n\n\n\n<p>Kaya, B., Khalil, O., Abssy, S. S., Cioffi, I., &amp; Moayedi, M. (2025). Delineation of the trigeminal-lateral parabrachial-central amygdala tract in humans. <em>Imaging Neuroscience<\/em>, <em>3<\/em>. https:\/\/doi.org\/10.1162\/imag_a_00567<\/p>\n\n\n\n<p>Maric, S., Hasan, M., Pounder, M. L., Graham, B. A., &amp; Browne, T. J. (2025). A Viral Labelling Study of Spinal Trigeminal Nucleus Caudalis Projection Neurons Targeting the Parabrachial Nucleus. <em>Journal of Neurochemistry<\/em>, <em>169<\/em>(3). https:\/\/doi.org\/10.1111\/jnc.70028<\/p>\n\n\n\n<p>Megat, S., Ray, P. R., Tavares-Ferreira, D., Moy, J. K., Sankaranarayanan, I., Wanghzou, A., Lou, T. F., Barragan-Iglesias, P., Campbell, Z. T., Dussor, G., &amp; Price, T. J. (2019). Differences between dorsal root and trigeminal ganglion nociceptors in mice revealed by translational profiling. <em>Journal of Neuroscience<\/em>, <em>39<\/em>(35), 6829\u20136847. https:\/\/doi.org\/10.1523\/JNEUROSCI.2663-18.2019<\/p>\n\n\n\n<p>Meier, M. L., de Matos, N. M. P., Br\u00fcgger, M., Ettlin, D. A., Lukic, N., Cheetham, M., J\u00e4ncke, L., &amp; Lutz, K. (2014). Equal pain &#8211; Unequal fear response: Enhanced susceptibility of tooth pain to fear conditioning. <em>Frontiers in Human Neuroscience<\/em>, <em>8<\/em>(JULY). https:\/\/doi.org\/10.3389\/fnhum.2014.00526<\/p>\n\n\n\n<p>Okuda, T., Uchiyama, S., Sato, N., Sugimura, Y. K., Takahashi, Y., Tsuda, M., &amp; Kato, F. (2025). The posterior-capsular central amygdala (pCeC) showing synaptic coactivation with nociplastic pain-associated parabrachial neurons in mice. <em>IScience<\/em>, 113001. https:\/\/doi.org\/10.1016\/j.isci.2025.113001<\/p>\n\n\n\n<p>Palmiter, R. D. (2024). Parabrachial neurons promote nociplastic pain. <em>Trends in Neurosciences<\/em>. https:\/\/doi.org\/10.1016\/j.tins.2024.07.002<\/p>\n\n\n\n<p>Panneton, W. M., &amp; Gan, Q. (2014). Direct reticular projections of trigeminal sensory fibers immunoreactive to CGRP: Potential monosynaptic somatoautonomic projections. <em>Frontiers in Neuroscience<\/em>, <em>8 JUN<\/em>. https:\/\/doi.org\/10.3389\/fnins.2014.00136<\/p>\n\n\n\n<p>Rodriguez, E., Sakurai, K., Xu, J., Chen, Y., Toda, K., Zhao, S., Han, B. X., Ryu, D., Yin, H., Liedtke, W., &amp; Wang, F. (2017). A craniofacial-specific monosynaptic circuit enables heightened affective pain. <em>Nature Neuroscience<\/em>, <em>20<\/em>(12), 1734\u20131743. https:\/\/doi.org\/10.1038\/s41593-017-0012-1<\/p>\n\n\n\n<p>Schmidt, K., Forkmann, K., Sinke, C., Gratz, M., Bitz, A., &amp; Bingel, U. (2016). The differential effect of trigeminal vs. peripheral pain stimulation on visual processing and memory encoding is influenced by pain-related fear. <em>NeuroImage<\/em>, <em>134<\/em>, 386\u2013395. https:\/\/doi.org\/10.1016\/j.neuroimage.2016.03.026<\/p>\n\n\n\n<p>Sugimoto, M., Takahashi, Y., Sugimura, Y. K., Tokunaga, R., Yajima, M., &amp; Kato, F. (2021). Active role of the central amygdala in widespread mechanical sensitization in rats with facial inflammatory pain. <em>Pain<\/em>, <em>162<\/em>(8), 2273\u20132286. https:\/\/doi.org\/10.1097\/j.pain.0000000000002224<\/p>\n\n\n\n<p>Svensson, P. (2024). Could painful temporomandibular disorders be nociplastic in nature? A critical review and new proposal. In <em>Acta Odontologica Scandinavica<\/em> (Vol. 83, pp. 144\u2013150). Medical Journals Sweden AB. https:\/\/doi.org\/10.2340\/aos.v83.40586<\/p>\n\n\n\n<p>Uddin, O., Anderson, M., Smith, J., Masri, R., &amp; Keller, A. (2021). Parabrachial complex processes dura inputs through a direct trigeminal ganglion-to-parabrachial connection. <em>Neurobiology of Pain<\/em>, <em>9<\/em>. https:\/\/doi.org\/10.1016\/j.ynpai.2021.100060<\/p>\n\n\n\n<p>Vermeiren, S., Bellefroid, E. J., &amp; Desiderio, S. (2020). Vertebrate Sensory Ganglia: Common and Divergent Features of the Transcriptional Programs Generating Their Functional Specialization. In <em>Frontiers in Cell and Developmental Biology<\/em> (Vol. 8). Frontiers Media S.A. https:\/\/doi.org\/10.3389\/fcell.2020.587699<\/p>\n\n\n\n<p>Yajima, M., Sugimoto, M., Sugimura, Y. K., Takahashi, Y., &amp; Kato, F. (2022). Acetaminophen and pregabalin attenuate central sensitization in rodent models of nociplastic widespread pain. <em>Neuropharmacology<\/em>, <em>210<\/em>, 109029. https:\/\/doi.org\/10.1016\/j.neuropharm.2022.109029<\/p>\n\n\n\n<p>Yajima, M., Takahashi, Y., Sugimura, Y. K., &amp; Kato, F. (2023). Pregabalin attenuates long-lasting post-inflammatory nociplastic mechanical sensitization in mice. <em>Neurobiology of Pain<\/em>, <em>13<\/em>, 100131. https:\/\/doi.org\/10.1016\/j.ynpai.2023.100131<\/p>\n\n\n\n<p>Yajima, M., Takahashi, Y., Uezono, Y., &amp; Kato, F. (2025). Mirogabalin and pregabalin alleviate nociplastic sensitization induced by chemogenetic activation of the central amygdala neurons in rodents. <em>Journal of Pharmacological Sciences<\/em>, <em>158<\/em>(2), 77\u201383. https:\/\/doi.org\/10.1016\/j.jphs.2025.03.004<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Aicher, S. A., Hegarty, D. 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