spacer gif spacer gif spacer gif spacer gif spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    

First published online February 1, 2008
Journal of Experimental Biology 211, 568-576 (2008)
Published by The Company of Biologists 2008
doi: 10.1242/jeb.010207
This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hille, C.
Right arrow Articles by Walz, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hille, C.
Right arrow Articles by Walz, B.

Characterisation of neurotransmitter-induced electrolyte transport in cockroach salivary glands by intracellular Ca2+, Na+ and pH measurements in duct cells

Carsten Hille* and Bernd Walz

University of Potsdam, Institute of Biochemistry and Biology, Department of Animal Physiology, 14476 Potsdam-Golm, Germany

* Author for correspondence at present address: University of Potsdam, Institute of Chemistry, Department of Physical Chemistry, 14476 Potsdam-Golm, Germany (e-mail: hille{at}uni-potsdam.de)

Accepted 10 December 2007

Ion-transporting acinar peripheral cells in cockroach salivary glands are innervated by dopaminergic and serotonergic fibres, but saliva-modifying duct cells are innervated only by dopaminergic fibres. We used microfluorometry to record intracellular Na+, Ca2+ and H+ concentrations ([Na+]i, [Ca2+]i and pHi) in duct cells of two types of preparation, viz `lobes' consisting of acini with their duct system and `isolated ducts' without acini, in order to obtain information about the transporters involved in saliva secretion and/or modification. Our results indicate that (1) stimulation of lobes by dopamine (DA) causes a strong drop of pHi and increases in [Na+]i and [Ca2+]i in duct cells; (2) in contrast, DA stimulation of isolated ducts produces only a small pHi drop and no changes in [Na+]i and [Ca2+]i; (3) pHi and [Ca2+]i changes are also induced in duct cells by serotonin (5-HT) stimulation of lobes, but not isolated ducts; (4) in the absence of CO2/HCO3, the DA-induced pHi drop is strongly reduced by removal of extracellular Cl or inhibition of the Na+–K+–2Cl cotransporter (NKCC); (5) in the presence of CO2/HCO3, the DA-induced pHi drop is not reduced by NKCC inhibition, but rather by inhibition of the Cl/HCO3 exchanger (AE), Na+/H+ exchanger (NHE) or carbonic anhydrase. We suggest that DA and 5-HT act predominantly on acinar peripheral cells. Their activity (secretion of primary saliva) seems to cause changes in ion concentrations in duct cells. NKCC and/or AE/NHE activities are necessary for pHi changes in duct cells; we consider that these transporters are involved in the secretion of the NaCl-rich primary saliva.

Key words: dopamine, serotonin, insect, salivary glands, ion transport, intracellular pH, sodium–potassium–chloride cotransporter, sodium–proton exchanger, anion exchanger







© The Company of Biologists Ltd 2008