Epinephrine exacerbates arthritis by an action at presynaptic B2-adrenoceptors

Neuroscience. 1990;34(2):521-3. doi: 10.1016/0306-4522(90)90160-6.

Abstract

Sympathetic efferents contribute to the severity of joint injury in experimental arthritis in the rat, [Levine J. D. et al. (1986) J. Neurosci. 6, 3423-3429] and beta 2-adrenergic receptor antagonists suppress the disease [Levine J. D. et al. (1988) Proc. natn. Acad. Sci. U.S.A. 85, 4553-4556]. The present study was directed at determining the endogenous ligand for, and target of, the beta 2-receptor contribution to arthritis. We report that adrenal medullectomy significantly reduced joint injury in experimental arthritis, but that severe joint injury was re-established in adrenal medullectomized rats chronically treated with epinephrine or the beta 2-agonist, salbutamol. The ability of these two drugs to enhance joint injury in adrenal medullectomized rats was blocked by sympathectomy. These data suggest that adrenal medulla-derived epinephrine acts at beta 2-adrenoceptors on sympathetic efferent nerve terminals, to contribute to the severity of experimental arthritis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adrenal Medulla / metabolism*
  • Adrenal Medulla / physiopathology
  • Adrenergic Fibers / drug effects
  • Adrenergic Fibers / physiology*
  • Animals
  • Arthritis / metabolism*
  • Arthritis / physiopathology
  • Epinephrine / pharmacology
  • Epinephrine / physiology*
  • Male
  • Rats
  • Rats, Inbred Strains
  • Receptors, Adrenergic, beta / drug effects
  • Receptors, Adrenergic, beta / physiology*
  • Sympathectomy

Substances

  • Receptors, Adrenergic, beta
  • Epinephrine