Vascular changes and demyelination induced by the intraneural injection of tumour necrosis factor

• Published in: Brain (London, England : 1878) Vol. 118 ( Pt 4); p. 869
• Main Authors: Redford, E J, Hall, S M, Smith, K J
• Format: Journal Article
• Language: English
• Published: England 01-08-1995
• Subjects: Animals; Demyelinating Diseases - etiology; Demyelinating Diseases - pathology; Male; Mice; Myelin Sheath - drug effects; Myelin Sheath - pathology; Neuritis - etiology; Neuritis - pathology; Rats; Rats, Sprague-Dawley; Sciatic Nerve - blood supply; Sciatic Nerve - pathology; Tumor Necrosis Factor-alpha - pharmacology; Tumor Necrosis Factor-alpha - physiology
• ISSN: 0006-8950
• DOI: 10.1093/brain/118.4.869

Several observations suggest that tumour necrosis factor (TNF) plays a role in demyelination, although direct evidence for this is lacking. We have examined ultrastructurally rat sciatic nerves injected with TNF-alpha or TNF-beta: the effects of the two cytokines were found to be qualitatively similar. One day after injection nerves were oedematous and contained many inflammatory cells. Leucocytes were adherent to the walls of endoneurial vessels and sometimes were packed into the sub-endothelial layer apparently occluding the vascular lumen. Occasional myelinated axons were associated with macrophages and showed signs of myelin damage. By 3 days the inflammatory changes had diminished: some axons were degenerating or demyelinating. By 6-7 days, the vascular changes had resolved, and the endoneurium contained significant numbers of demyelinating and degenerating axons. Control nerves, which received injections of vehicle, showed no vascular changes and either no, or significantly fewer, degenerating or demyelinating axons. We conclude that the intraneural injection of TNF produces inflammatory vascular changes within the endoneurium, together with demyelination and axonal degeneration. We have also observed demyelination and degeneration in a preliminary study of the effects of TNF-alpha in mice. These findings may be relevant to the pathogenesis of demyelinating diseases such as Guillain-Barré syndrome.