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Genetic analysis of neuropathic pain-like behavior following peripheral nerve injury suggests a role of the major histocompatibility complex in development of allodynia

Dominguez, Cecilia A (author)
Karolinska Institutet
Lidman, Olle (author)
Karolinska Institutet
Hao, Jing-Xia (author)
Karolinska Institutet
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Diez, Margarita (author)
Karolinska Institutet
Tuncel, Jonatan (author)
Karolinska Institutet,Lund University,Lunds universitet,Immunologi,Forskargrupper vid Lunds universitet,Immunology,Lund University Research Groups
Olsson, Tomas (author)
Karolinska Institutet
Wiesenfeld-Hallin, Zsuzsanna (author)
Karolinska Institutet
Piehl, Fredrik (author)
Karolinska Institutet
Xu, Xiao-Jun (author)
Karolinska Institutet
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 (creator_code:org_t)
Ovid Technologies (Wolters Kluwer Health), 2008
2008
English.
In: Pain. - : Ovid Technologies (Wolters Kluwer Health). - 1872-6623 .- 0304-3959. ; 136:3, s. 313-319
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Neuropathic pain is a common consequence of damage to the nervous system. We here report a genetic analysis of development of neuropathic pain-like behaviors after unilateral photochemically-induced ischemic sciatic nerve injury in a panel of inbred rat strains known to display different susceptibility to autoimmune neuroinflammation. Pain behavior was initially characterized in Dark-Agouti (DA; RT1(avl)), Piebald Virol Glaxo (PVG; RT1(c)), and in the major histocompatibility complex (MHC)-congenic strain PVG-RT1(avl). All strains developed mechanical hypersensitivity (allodynia) following nerve injury. However, the extent and duration of allodynia varied significantly among the strains, with PVG displaying more severe allodynia compared to DA rats. Interestingly, the response of PVG-RT1(avR1) was similar to that of DA, suggesting regulation by the MHC locus. This notion was subsequently confirmed in an F2 cohort derived from crossing of the PVG and PVG-RT1(avl) strains, where allodynia was reduced in homozygous or heterozygous carriers of the RT1(avl) allele in comparison to rats homozygous for the RT1(c) allele. These results indicate that certain allelic variants of the MHC could influence susceptibility to develop and maintain neuropathic pain-like behavior following peripheral nerve injury in rats.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)

Keyword

congenic
genetic
neuropathic pain
inbred strains
MHC
immune system

Publication and Content Type

art (subject category)
ref (subject category)

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