Oto Tatsuki, Urata Kentaro, Hayashi Yoshinori, Hitomi Suzuro, Shibuta Ikuko, Iwata Koichi, Iinuma Toshimitsu, Shinoda Masamichi
Department of Complete Denture Prosthodontics, Nihon University School of Dentistry.
Department of Physiology, Nihon University School of Dentistry.
Tohoku J Exp Med. 2022 Apr 20;256(4):283-290. doi: 10.1620/tjem.2022.J004. Epub 2022 Mar 17.
Aging affects various sensory functions of the body. However, the effect on the oral mucosal nociception has remain unclear, so this elucidation is very important. Therefore, this study aimed to evaluate the effect of age-related changes in transient receptor potential vanilloid 1 (TRPV1) and TRPV2 expression in the trigeminal ganglion (TG) neurons on intraoral mucosal heat sensitivity in the senescence-accelerated mouse prone 8 (SAMP8) model. We used 23-week-old (aged) and 7-week-old (young) SAMP8 mice. Heat stimulation was applied to the palatal mucosa under light anesthesia; moreover, the heat head withdrawal threshold (HHWT) was measured. We counted the number of TRPV1-immunoreactive (IR) and TRPV2-IR TG neurons innervating the palatal mucosa. Additionally, we investigated changes in HHWT when TRPV1 or TRPV2 antagonists (SB366791 or Tranilast) were administered to the palatal mucosa. Aged SAMP8 mice showed a higher HHWT than young SAMP8 mice. Compared with the aged SAMP8 mice, young SAMP8 mice showed a larger number of TRPV1-IR small-diameter neurons and a smaller number of TRPV2-IR medium-sized neurons innervating the palatal mucosa. SB366791 administration increased the HHWT in young, but not aged SAMP8 mice. Contrastingly, Tranilast administration increased the HHWT in aged, but not young SAMP8 mice. These results suggest that the modulation of heat pain sensitivity in the oral mucosa due to aging is dependent on changes in the TRPV1 and TRPV2 expression patterns in the TG neurons innervating the palatal mucosa.
衰老会影响身体的各种感觉功能。然而,衰老对口腔黏膜伤害感受的影响尚不清楚,因此阐明这一点非常重要。因此,本研究旨在评估衰老加速小鼠8型(SAMP8)模型中三叉神经节(TG)神经元瞬时受体电位香草酸受体1(TRPV1)和TRPV2表达的年龄相关变化对口腔黏膜热敏感性的影响。我们使用了23周龄(老年)和7周龄(年轻)的SAMP8小鼠。在轻度麻醉下对腭黏膜进行热刺激;此外,测量热头撤离阈值(HHWT)。我们计算了支配腭黏膜的TRPV1免疫反应性(IR)和TRPV2-IR TG神经元的数量。此外,我们研究了向腭黏膜施用TRPV1或TRPV2拮抗剂(SB366791或曲尼司特)时HHWT的变化。老年SAMP8小鼠的HHWT高于年轻SAMP8小鼠。与老年SAMP8小鼠相比,年轻SAMP8小鼠支配腭黏膜的TRPV1-IR小直径神经元数量更多,TRPV2-IR中直径神经元数量更少。施用SB366791可提高年轻SAMP8小鼠的HHWT,但对老年SAMP8小鼠无效。相反,施用曲尼司特可提高老年SAMP8小鼠的HHWT,但对年轻SAMP8小鼠无效。这些结果表明,衰老导致的口腔黏膜热痛敏感性调节取决于支配腭黏膜的TG神经元中TRPV1和TRPV2表达模式的变化。