Excess salt loads in most non-mammalian vertebrates are dealt with by a var
iety of extra-renal salt-secreting structures collectively described as sal
t glands. The best studied of these are the supra-orbital nasal salt glands
of birds. Two distinct types of response tee osmoregulatory disturbances a
re shown by this structure: a progressive adaptive response on initial expo
sure to a salt load that results in the induction and enhancement of the se
cretory performance or capabilities of the gland; and the rapid activation
of existing osmoregulatory mechanisms in the adapted gland in response to i
mmediate osmoregulatory imbalance. Not only is the time-frame of these two
types of response very different, but the responses usually involve fundame
ntally different processes: e.g., the growth and differentiation of osmoreg
ulatory structures and their components in the former case, compared with t
he rapid activation of ion channels, pumps etc, in the latter. Despite mark
ed differences in the nature and time-frame of these responses, they both a
re apparently triggered by neuronally released acetylcholine, which acts at
muscarinic receptors on the secretory cells to induce an inositol phosphat
e-dependent increase in cytosolic-free calcium concentrations ([Ca2+](i)).
Therefore, the question arises as to how the cells produce the appropriate
distinct response using a single common signal (i.e., an increase in [Ca2+]
(i)). Examination of the features of this signaling pathway in the two cond
itions described, reveals that they each are uniquely tuned to generate a r
esponse with the characteristics appropriate for the cells' requirements. T
his tuning of the signal involves often rather subtle changes in the overal
l signaling pathway that are part of the adaptive differentiation process.
(C) 1999 Wiley-Liss, Inc.