Faculty of Dentistry, Department of Oral Physiology, University of Toronto, Toronto, Ontario, Canada.
Neurosci Lett. 2012 Sep 27;526(2):160-3. doi: 10.1016/j.neulet.2012.08.007. Epub 2012 Aug 14.
Central sensitization and purinergic receptor mechanisms have been implicated as important processes in acute and chronic pain conditions following injury or inflammation of peripheral tissues. This study has documented that application of the P2X(1,2/3,3) receptor agonist αβ-meATP (100mM) to the rat tooth pulp induces central sensitization in medullary dorsal horn nociceptive neurons that is reflected in significant increases in mechanoreceptive field size and responses to noxious stimuli and decreased mechanical activation threshold. Furthermore, these responses can be blocked by pulp application of the P2X(1,2/3,3) antagonist TNP-ATP and also attenuated by medullary application of TNP-ATP. These results suggest that activation of P2X(1,2/3,3) receptors in orofacial tissues plays a critical role in producing central sensitization in medullary dorsal horn nociceptive neurons.
中央敏化和嘌呤能受体机制被认为是外周组织损伤或炎症后急性和慢性疼痛状态的重要过程。本研究证明,将 P2X(1,2/3,3) 受体激动剂 αβ-meATP(100mM)应用于大鼠牙髓会导致背角伤害感受神经元的中枢敏化,这反映在机械感受野大小和对有害刺激的反应显著增加,机械激活阈值降低。此外,这些反应可以通过牙髓应用 P2X(1,2/3,3) 拮抗剂 TNP-ATP 阻断,并且也可以通过 TNP-ATP 在延髓中的应用减弱。这些结果表明,口腔组织中 P2X(1,2/3,3) 受体的激活在背角伤害感受神经元的中枢敏化中起着关键作用。