Division of Molecular Pharmacology and Neuroscience, Graduate School of Biomedical Sciences, Nagasaki University, Japan.
Biol Pharm Bull. 2011;34(8):1154-8. doi: 10.1248/bpb.34.1154.
The injury-induced intense stimulation of spinal cord neurons causes lysophosphatidic acid (LPA) biosynthesis. LPA(1) receptor activation causes demyelination and sprouting of dorsal root fibers, leading to an induction of synaptic reorganization underlying allodynia, in which innocuous (tactile) stimuli cause intense pain. The LPA(1) signal also initiates the up-regulation of Ca(v)α2δ1 in dorsal root ganglion and PKCγ in the dorsal horn, underlying mechanisms for characteristic neuropathic hyperalgesia in myelinated sensory (A-type) fibers. On the other hand, the LPA(3) receptor mediates microglia activation at the early stage after nerve injury and LPA-induced LPA biosynthesis. Thus, both the LPA(1) and LPA(3) receptors play key roles in the initiation step using a feed-forward system for neuropathic pain.
脊髓神经元的损伤诱导性强烈刺激导致溶血磷脂酸(LPA)的生物合成。LPA(1)受体的激活导致背根纤维的脱髓鞘和发芽,导致痛觉过敏的突触重组诱导,其中无害(触觉)刺激引起强烈疼痛。LPA(1)信号还启动背根神经节中 Ca(v)α2δ1 和背角中 PKCγ 的上调,这是有髓感觉(A型)纤维特征性神经病理性痛觉过敏的潜在机制。另一方面,LPA(3)受体在神经损伤后早期介导小胶质细胞的激活,以及 LPA 诱导的 LPA 生物合成。因此,LPA(1)和 LPA(3)受体都在使用神经病理性疼痛的前馈系统的起始步骤中发挥关键作用。