Lysophosphatidic acid as the initiator of neuropathic pain.

Hiroshi Ueda

Division of Molecular Pharmacology and Neuroscience, Graduate School of Biomedical Sciences, Nagasaki University, Japan.

Journal Article: Biological & Pharmaceutical Bulletin (impact factor: 1.81). 01/2011; 34(8):1154-8.

Abstract

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.

Source: PubMed

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Keywords

A-type
 
feed-forward system
 
ganglion
 
initiation step
 
injury-induced intense stimulation
 
key roles
 
myelinated sensory
 
spinal cord neurons causes lysophosphatidic acid
 
synaptic reorganization
 
tactile