Bhave G, Karim F, Carlton S M, Gereau R W
Division of Neuroscience, Baylor College of Medicine, 1 Baylor Plaza, Room S636, Houston, Texas 77030, USA.
Nat Neurosci. 2001 Apr;4(4):417-23. doi: 10.1038/86075.
The metabotropic glutamate receptors (mGluRs) are found throughout the central nervous system, where they modulate neuronal excitability and synaptic transmission. Here we report the presence of phospholipase C-coupled group I mGluRs (mGluR1 and mGluR5) outside the central nervous system on peripheral unmyelinated sensory afferents. Given their localization on predominantly nociceptive afferents, we investigated whether these receptors modulate nociceptive signaling, and found that agonist-induced activation of peripheral group I mGluRs leads to increased sensitivity to noxious heat, a phenomenon termed thermal hyperalgesia. Furthermore, group I mGluR antagonists not only prevent, but also attenuate established formalin-induced pain. Taken together, these results suggest that peripheral mGluRs mediate a component of hyperalgesia and may be therapeutically targeted to prevent and treat inflammatory pain.
代谢型谷氨酸受体(mGluRs)存在于整个中枢神经系统中,在那里它们调节神经元兴奋性和突触传递。在此,我们报告在外周无髓感觉传入神经上,即中枢神经系统之外,存在与磷脂酶C偶联的I组mGluRs(mGluR1和mGluR5)。鉴于它们主要定位于伤害性传入神经上,我们研究了这些受体是否调节伤害性信号传导,并发现外周I组mGluRs的激动剂诱导激活会导致对有害热的敏感性增加,这一现象称为热痛觉过敏。此外,I组mGluR拮抗剂不仅能预防,还能减轻已建立的福尔马林诱导的疼痛。综上所述,这些结果表明外周mGluRs介导了痛觉过敏的一部分,并且可能成为预防和治疗炎性疼痛的治疗靶点。