There is enthusiasm for the application of knowledge concerning neurot
rophins and other growth factors to human neurologic disease. New neur
otrophins and other growth factors or inflammatory mediators that infl
uence neurons and axons have been recently identified, Diabetic neurop
athy may be an ideal testing ground for these substances because speci
fic neurotrophins and growth factors could theoretically prevent loss
of diabetic dorsal root ganglion (DRG) cells or enhance regeneration o
f diabetic nerves, Several of the neurotrophins support DRG cells in c
ulture or prevent their loss during neonatal development, and a few he
lp prevent retrograde loss of adult DRG cells after axotomy, Early Pha
se I trials suggest that nerve growth factor, brain-derived neurotroph
ic factor, and neurotrophin-3 are reasonably safe agents as administer
ed in short-term trials to humans, but there are lingering experimenta
l doubts, For example, it has not been established whether DRG cells a
re targeted by diabetes, Additional work suggests that simultaneous an
d sequential cocktails of trophins are required to support and rescue
neurons and that the use of single agents may not be sufficient, Final
ly, it is uncertain whether trophins might act as a general tonic for
DRG cells to prevent diabetes-related injury or whether they are actua
lly deficient in human diabetic patients.