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   <subfield code="a">Phorbol ester attenuates inositol 1,4,5-trisphosphate-induced Ca2+ release in electropermeabilized rat pancreatic acini</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Y. Arita, T. Kimura, Y. Ogami, H. Nawata]</subfield>
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   <subfield code="a">Summary: To investigate the mechanism of inositol trisphosphate (IP3)-induced Ca2+ release from the internal Ca2+ store, we examined the effects of heparin, phorbol ester and cyclic nucleotides on Ca2+ release induced by carbachol or inositol 1,4,5-trisphosphate (1,4,5-IP3). For monitoring changes of Ca2+ we used the fluorescent indicator, fura-2, in electropermeabilized rat pancreatic acini. An amount of 100 μg/ml heparin inhibited the Ca2+ release induced by 1 μM 1,4,5-IP3 in permeabilized acini. Pretreatment with 12-O-tetradecanoyl-phorbol-13-acetate (TPA) for 10 min reduced the release of Ca2+ induced by 10 μM carbachol and 1 μM 1,4,5-IP3 in permeabilized acini. Staurosporine, a protein kinase C inhibitor, blocked the inhibitory effect of TPA. Cytosolic calcium concentration was restored by staurosporine in TPA-treated acini. Although cyclic AMP exaggerated the amylase release induced by carbachol, cyclic AMP and cyclic GMP had no effect on the carbachol-induced release of Ca2+ in permeabilized acini. These findings suggest that protein kinase C may act at the level of the IP3 receptors or the IP3-operated Ca2+ channels of the internal Ca2+ store and indicate that cyclic nucleotides do not affect the IP3-induced release of Ca2+ in rat pancreatic acini.</subfield>
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   <subfield code="a">Springer-Verlag, 1992</subfield>
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   <subfield code="a">Exocrine pancreas</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Calcium mobilization</subfield>
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   <subfield code="a">Permeabilized cell</subfield>
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   <subfield code="a">Arita</subfield>
   <subfield code="D">Y.</subfield>
   <subfield code="u">The Third Department of Internal Medicine, Faculty of Medicine, Kyushu University, 812, Fukuoka, Japan</subfield>
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   <subfield code="a">Kimura</subfield>
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   <subfield code="a">Ogami</subfield>
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   <subfield code="u">The Third Department of Internal Medicine, Faculty of Medicine, Kyushu University, 812, Fukuoka, Japan</subfield>
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   <subfield code="t">Research in Experimental Medicine</subfield>
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