Introduction of calcium chelators into isolated rat pancreatic acini inhibits amylase release in response to carbamylcholine |
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Authors: | R L Dormer |
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Affiliation: | Department of Medical Biochemistry, Welsh National School of Medicine, Heath Park, Cardiff, U.K. |
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Abstract: | The Ca2+ chelators, EGTA and BAPTA, have been introduced into intact, isolated rat pancreatic acini using a hypotonic swelling method. This resulted in complete inhibition of amylase release, stimulated by carbamylcholine at a submaximal concentration and 82 - 85% inhibition at maximal concentrations. Acini swollen in the absence of Ca2+ chelators showed similar secretory responses to those of unswollen acini. Treatment of unswollen acini with chelators inhibited the maximum response to carbamylcholine by only 23%. The inhibitory effect of intracellular chelators was not due to ATP depletion or a lowering of the total cell Ca2+ content. Thus, these results provide the first direct demonstration that an increase in intracellular Ca2+ concentration is necessary for the stimulation of enzyme release from pancreatic acinar cells. |
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Keywords: | EGTA ethylene glycol bis (β-aminoethyl ether) NNN′,N′-tetra-acetic acid BAPTA 1,2-bis(2-aminophenoxy) ethane-NNN′,N′-tetra-acetic acid TES N-Tris-(hydroxymethyl)-methyl-2-amino-ethanesulphonic acid HEPES N-2-hydroxyethyl-piperazine-N′-2-ethanesulphonic acid |
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