Silver staining and high-resolution electrophoretic methods have been used
to compare the protein composition of rat parotid saliva evoked in response
to (i) parasympathetic stimulation (including the nonadrenergic, noncholin
ergic, atropine-associated secretion), (ii) sympathetic stimulation, or (ii
i) the infusion of neuropeptides with secretagogue activity (substance P, c
alcitonin gene-related peptide, neuropeptide Y, or vasoactive intestinal pe
ptide). The different stimuli influenced the protein concentration and flow
rate of the evoked secretion but had little effect upon the protein compos
ition of the saliva. In contrast to earlier studies using sodium dodecyl su
lfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Coomassie blue stai
ning, the combination of silver staining and two-dimensional electrophoresi
s (2-DE) revealed many newly detected proteins. The results indicate that t
he protein composition of rat parotid saliva is more complex than previousl
y reported but is unaffected by the mode of stimulation.