In parasympathetic saliva from rat submandibular glands the relative p
roportions of the various tissue kallikreins differ from those in symp
athetic saliva. Kallikreins in sympathetic saliva arise from exocytosi
s of prepackaged granules in granular tubules, so the kallikreins in p
arasympathetic saliva must come from a non-granular pool, and are like
ly to be secreted through a constitutive vesicular route. During perio
ds devoid of stimulation in anaesthetised rats, the kallikreins have b
een found to accumulate progressively in glandular lumina. in parasymp
athetic-like proportions. As this transport of kallikrein into lumina
occurs continuously in vivo, independently of any stimulation or any s
ecretion of fluid, it must arise by constitutive vesicular secretion.
During parasympathetic stimulation, the kallikreins are secreted into
the saliva at a greater rate than in the resting state but their propo
rtions remain the same and the means by which this increase occurs is
open to debate. Constitutively secreted true tissue kallikrein (rK1) h
as been found to have a different molecular form from that in secretor
y granules. The submandibular glands also contribute to the kallikrein
s normally circulating in the blood. Serum levels of kallikrein increa
sed equally during tither parasympathetic or sympathetic stimulation a
nd were independent of the amounts secreted into the saliva, so are li
kely to have arisen from constitutive secretion via the basal sides of
the cells, morphological evidence for which has been found in the mou
se (Penschow & Coghlan, 1993).