Changes in electrolytes of pig pancreatic acinar cells following appli
cation of gastrin-cholecystokinin (CCK) were investigated using the te
chnique of X-ray microanalysis of hydrated and dehydrated sections of
freshly frozen pancreas. After stimulation by CCK (10(-9) M), Na and C
l increased significantly in the cytoplasm [Na, from 10 mmol/kg wet st
. (48 mmol/kg dry wt.) to 19 mmol/kg (95 mmol/kg); Cl, from 22 mmol/kg
(105 mmol/kg) to 49 mmol/kg (245 mmol/kg)] as well as in the luminal
interspace [Na, from 53 mmol/kg (189 mmol/kg) to 65 mmol/kg (283 mmol/
kg); Cl, from 65 mmol/kg (232 mmol/kg) to 102 mmol/kg (443 mmol/kg)].
In the secretory granules Cl increased significantly from 30 mmol/kg (
86 mmol/kg) to 67 mmol/kg (203 mmol/kg). K decreased significantly fro
m 120 mmol/kg (571 mmol/kg) to 81 mmol/kg (405 mmol/kg) in the cytopla
sm, while both increased from 38 mmol/kg (109 mmol/kg) to 58 mmol/kg (
176 mmol/kg) in the granules and from 46 mmol/kg (164 mmol/kg) to 48 m
mol/kg (209 mmol/kg) in the luminal interspace. Ca increased significa
ntly in the cytoplasm as well as in the luminal interspace, and decrea
sed significantly in the secretory granules. CCK evoked Ca release fro
m secretory granules in the secretory pole of acinar cells. The values
were measured from dehydrated sections, and agreed well with those fr
om hydrated sections. The effect of furosemide, an inhibitor of the Na
+-K+-2Cl(-) co-transporter, on the ion transport of acinar cell was st
udied. When furosemide (10(-5) M) was added to the external solution,
the cytoplasmic Cl and Ca concentrations decreased significantly, whil
e there was a little decrease in Na and K concentrations under the sec
retory condition. These results indicate that Na+-K+-2Cl(-) co-transpo
rt, and Na+, Cl- and K+ exits into the lumen are involved in the mecha
nism of ion secretion in pig pancreatic acinar cells.