Best Practice & Research Clinical Rheumatology
Volume 22, Issue 2 , Pages 285-297, April 2008

Neuroendocrine immune pathways in chronic arthritis

    Dr
  • Silvia Capellino, PhD
  • , Dr
  • Rainer H. Straub, MD (Professor)

      Affiliations

    • Corresponding Author InformationCorresponding author. Laboratory of Experimental Rheumatology and Neuroendocrino-Immunology, Department of Internal Medicine I, University Hospital Regensburg, 93042 Regensburg, Germany. Tel.: +49 941 944 7120; Fax: +49 941 944 7121.

Laboratory of Experimental Rheumatology and Neuroendocrino-Immunology, Department of Internal Medicine I, University Hospital, 93042 Regensburg, Germany

The analysis and understanding of the complex effects of endocrine and nervous system alterations on the inflammatory process in human arthritis is far from complete. Such alterations are observed as decreased responsiveness of the hypothalamic–pituitary–adrenal axis, an inadequate production of cortisol in relation to inflammation, and – consequently – elevated sympathetic activity, alterations of sex hormone metabolism (loss of androgens), psychological alterations (with chronic fatigue and symptoms of depression due to elevated circulating cytokines), local reduction of synovial sympathetic innervation, altered metabolism of estrogens in the synovium, and high expression of estrogen receptors in synovial cells. An understanding of these alterations will help to identify the different neuroendocrine immune mechanisms involved in the pathophysiology of rheumatoid arthritis and could trigger research into novel therapeutic targets for the treatment of patients with rheumatoid arthritis.

Key words: androgens, cortisol, estrogen receptors, estrogens, fatigue, hypothalamic–pituitary–adrenal axis, stress, sympathetic nervous system

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S1521-6942(08)00010-7

doi:10.1016/j.berh.2008.01.010

Best Practice & Research Clinical Rheumatology
Volume 22, Issue 2 , Pages 285-297, April 2008