Peripheral demyelination and neuropathic pain behavior in periaxin-deficient mice.

Abstract:

:The Prx gene in Schwann cells encodes L- and S-periaxin, two abundant PDZ domain proteins thought to have a role in the stabilization of myelin in the peripheral nervous system (PNS). Mice lacking a functional Prx gene assemble compact PNS myelin. However, the sheath is unstable, leading to demyelination and reflex behaviors that are associated with the painful conditions caused by peripheral nerve damage. Older Prx-/- animals display extensive peripheral demyelination and a severe clinical phenotype with mechanical allodynia and thermal hyperalgesia, which can be reversed by intrathecal administration of a selective NMDA receptor antagonist We conclude that the periaxins play an essential role in stabilizing the Schwann cell-axon unit and that the periaxin-deficient mouse will be an important model for studying neuropathic pain in late onset demyelinating disease.

journal_name

Neuron

journal_title

Neuron

authors

Gillespie CS,Sherman DL,Fleetwood-Walker SM,Cottrell DF,Tait S,Garry EM,Wallace VC,Ure J,Griffiths IR,Smith A,Brophy PJ

doi

10.1016/s0896-6273(00)81184-8

subject

Has Abstract

pub_date

2000-05-01 00:00:00

pages

523-31

issue

2

eissn

0896-6273

issn

1097-4199

pii

S0896-6273(00)81184-8

journal_volume

26

pub_type

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