We describe a technique using the water-soluble polymer polyethylene glycol
(PEG) to reconnect the two segments of completely transected mammalian spi
nal axons within minutes. This was accomplished by fusing completely severe
d strips of isolated guinea pig thoracic white matter maintained in vitro i
n a double sucrose gap recording chamber, The faces of the severed segments
were pressed together, and PEG (MW 1,400-3,500 d; similar to 50% by weight
in distilled water) was applied directly to this region through a micropip
ette and removed by aspiration within 2 min. Successful fusion was document
ed by the immediate restored conduction of compound action potentials throu
gh the original transection and by the variable numbers of fused axons in w
hich anatomical continuity was shown to be restored by high-resolution ligh
t microscopy and by the diffusion of intracellular fluorescent dyes through
fused axons, These data support the conclusion that some severed and subse
quently PEG-fused spinal axons both demonstrate restored anatomical continu
ity and also are physiologically competent to conduct action potentials. Th
is work adds to our previous demonstration that PEG application can immedia
tely repair severely crushed, rather than cut, spinal cord white matter, an
d may lead to novel treatments for acute trauma to the central and peripher
al nervous systems.