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Collagen antibody-induced arthritis evokes persistent pain with spinal glial involvement and transient prostaglandin dependency

Bas, D. B. (author)
Karolinska Institutet,Karolinska Institutet, Stockholm, Sweden
Su, J. (author)
Karolinska Institutet,Karolinska Institutet, Stockholm, Sweden
Sandor, K. (author)
Karolinska Institutet,Karolinska Institutet, Stockholm, Sweden
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Agalave, N. M. (author)
Karolinska Institutet,Karolinska Institutet, Stockholm, Sweden
Lundberg, J. (author)
Karolinska Institutet, Stockholm, Sweden
Codeluppi, S. (author)
Karolinska Institutet,Karolinska Institutet, Stockholm, Sweden
Baharpoor, A. (author)
Karolinska Institutet,Karolinska Institutet, Stockholm, Sweden
Nandakumar, Kutty Selva, 1965- (author)
Karolinska Institutet, Stockholm, Sweden
Holmdahl, R. (author)
Karolinska Institutet,Karolinska Institutet, Stockholm, Sweden
Svensson, C. I. (author)
Karolinska Institutet, Stockholm, Sweden
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 (creator_code:org_t)
2012-11-28
2012
English.
In: Arthritis & Rheumatology. - : Wiley. - 2326-5191 .- 2326-5205. ; 64:12, s. 3886-3896
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • ObjectivePain is one of the most debilitating symptoms reported by rheumatoid arthritis (RA) patients. While the collagen antibody–induced arthritis (CAIA) model is used for studying the effector phase of RA pathologic progression, it has not been evaluated as a model for studies of pain. Thus, this study was undertaken to examine pain-like behavior induced by anticollagen antibodies and to assess the effect of currently prescribed analgesics for RA. In addition, the involvement of spinal glia in antibody-induced pain was explored.MethodsCAIA was induced in mice by intravenous injection of a collagen antibody cocktail, followed by intraperitoneal injection of lipopolysaccharide. Disease severity was assessed by visual and histologic examination. Pain-like behavior and the antinociceptive effect of diclofenac, buprenorphine, gabapentin, pentoxifylline, and JNK-interacting protein 1 were examined in mechanical stimulation experiments. Spinal astrocyte and microglia reactivity were investigated by real-time polymerase chain reaction and immunohistochemistry.ResultsFollowing the induction of CAIA, mice developed transient joint inflammation. In contrast, pain-like behavior was observed prior to, and outlasted, the visual signs of arthritis. Whereas gabapentin and buprenorphine attenuated mechanical hypersensitivity during both the inflammatory and postinflammatory phases of arthritis, diclofenac was antinociceptive only during the inflammatory phase. Spinal astrocytes and microglia displayed time-dependent signs of activation, and inhibition of glial activity reversed CAIA-induced mechanical hypersensitivity.ConclusionCAIA represents a multifaceted model for studies exploring the mechanisms of pain induced by inflammation in the articular joint. Our findings of a time-dependent prostaglandin and spinal glial contribution to antibody-induced pain highlight the importance of using appropriate disease models to assess joint-related pain.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Reumatologi och inflammation (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Rheumatology and Autoimmunity (hsv//eng)

Keyword

Amines/therapeutic use
Analgesics/therapeutic use
Animals
Arthralgia/drug therapy/*etiology/metabolism
Arthritis
Experimental/*complications/metabolism/pathology
Buprenorphine/therapeutic use
Cyclohexanecarboxylic Acids/therapeutic use
Diclofenac/therapeutic use
Disease Models
Animal
Gabapentin
Male
Mice
Mice
Inbred BALB C
Mice
Inbred CBA
Neuroglia/metabolism/*pathology
Prostaglandins/*metabolism
Spine/metabolism/*pathology
Time Factors
Treatment Outcome
gamma-Aminobutyric Acid/therapeutic use

Publication and Content Type

ref (subject category)
art (subject category)

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