TY - JOUR
T1 - Therapeutic efficacy of sonic hedgehog protein in experimental diabetic neuropathy
AU - Calcutt, Nigel A.
AU - Allendoerfer, Karen L.
AU - Mizisin, Andrew P.
AU - Middlemas, Alicia
AU - Freshwater, Jason D.
AU - Burgers, Monica
AU - Ranciato, Rigel
AU - Delcroix, Jean Dominique
AU - Taylor, Frederick R.
AU - Shapiro, Renee
AU - Strauch, Kathy
AU - Dudek, Henryk
AU - Engber, Thomas M.
AU - Galdes, Alphonse
AU - Rubin, Lee L.
AU - Tomlinson, David R.
PY - 2003/2
Y1 - 2003/2
N2 - Hedgehog proteins modulate development and patterning of the embryonic nervous system. As expression of desert hedgehog and the hedgehog receptor, patched-1, persist in the postnatal and adult peripheral nerves, the hedgehog pathway may have a role in maturation and maintenance of the peripheral nervous system in normal and disease states. We measured desert hedgehog expression in the peripheral nerve of maturing diabetic rats and found that diabetes caused a significant reduction in desert hedgehog mRNA. Treating diabetic rats with a sonic hedgehog-IgG fusion protein fully restored motor- and sensory-nerve conduction velocities and maintained the axonal caliber of large myelinated fibers. Diabetes-induced deficits in retrograde transport of nerve growth factor and sciatic-nerve levels of calcitonin gene-related product and neuropeptide Y were also ameliorated by treatment with the sonic hedgehog-IgG fusion protein, as was thermal hypoalgesia in the paw. These studies implicate disruption of normal hedgehog function in the etiology of diabetes-induced peripheral-nerve dysfunction and indicate that delivery of exogenous hedgehog proteins may have therapeutic potential for the treatment of diabetic neuropathy.
AB - Hedgehog proteins modulate development and patterning of the embryonic nervous system. As expression of desert hedgehog and the hedgehog receptor, patched-1, persist in the postnatal and adult peripheral nerves, the hedgehog pathway may have a role in maturation and maintenance of the peripheral nervous system in normal and disease states. We measured desert hedgehog expression in the peripheral nerve of maturing diabetic rats and found that diabetes caused a significant reduction in desert hedgehog mRNA. Treating diabetic rats with a sonic hedgehog-IgG fusion protein fully restored motor- and sensory-nerve conduction velocities and maintained the axonal caliber of large myelinated fibers. Diabetes-induced deficits in retrograde transport of nerve growth factor and sciatic-nerve levels of calcitonin gene-related product and neuropeptide Y were also ameliorated by treatment with the sonic hedgehog-IgG fusion protein, as was thermal hypoalgesia in the paw. These studies implicate disruption of normal hedgehog function in the etiology of diabetes-induced peripheral-nerve dysfunction and indicate that delivery of exogenous hedgehog proteins may have therapeutic potential for the treatment of diabetic neuropathy.
KW - Animals
KW - drug therapy: Diabetic Neuropathies
KW - Human
KW - genetics: Immunoglobulin G
KW - Male
KW - drug effects: Neural Conduction
KW - genetics: RNA, Messenger
KW - Rats
KW - Rats, Wistar
KW - genetics: Recombinant Fusion Proteins
KW - drug effects: Sciatic Nerve
KW - Support, Non-U.S. Gov't
KW - Support, U.S. Gov't, P.H.S.
KW - genetics: Trans-Activators
U2 - 10.1172/JCI200315792
DO - 10.1172/JCI200315792
M3 - Article
SN - 0021-9738
VL - 111
SP - 507
EP - 514
JO - Journal of Clinical Investigation
JF - Journal of Clinical Investigation
IS - 4
ER -