The distribution of binding sites for NTE-biotinyl-[Arg3]-substance P
(SPB) was demonstrated in neonatal. foreskin using a conjugate of stre
ptavidin with horseradish peroxidase. The observed binding is reversib
le, and may be abrogated by either the non-peptide substance P recepto
r antagonist, CP-96,345, or by unlabelled substance P. The generalized
epidermal distribution and focal dermal localization of SPB binding s
uggest that although NK-1 receptors are abundant in human neonatal for
eskin, neuromodulatory mechanisms may play a significant role in epide
rmal physiology.