Previous studies have shown that Ca influx increased but Ca efflux did not change during the contracture of taenia coli induced in hypertonically added 40 mm potassium solution (1) and the results were supported by the others (2-6). Further, the movements of Ca in the muscle in high-K solution might be differently affected by ouabain and 2, 4-dinitrophenol during the abolition of the tonic tension by them (6, 7).The experiments reported here were carried out in purpose to find the nature of Ca distribution and exchange in guinea pig taenia coli in high-K solution using ouabain and 2, 4-dinitrophenol.
METHODSStrips of taenia coli isolated from white male guinea pigs were suspended in an organ bath containing Tyrode solution of the following composition (mm); NaCI 136.8, KCl 2.7, CaC1, 2.5, MgCl2 1.0, NaH2PO4 0.4, NaHCO, 11.9 and glucose 5.5, saturated with 95% 02 and 5% CO, mixture at 37'C. Isotonically added 40 mm K solution (iso-40 K-S.) was made by replacing 40 mm NaCI in Tyrode solution with equimolar KC1. Tension changes were isometrically recorded with a mechanoelectro-transducer. 45Ca uptake: After pretreatment , muscle strips were soaked in iso-40 K-S. for 30 minutes, then 2.5 x 10-6 M ouabain or 1 x 10-4 M 2, 4-dinitrophenol (DNP) was added. Thirty minutes after the addition of ouabain or DNP, corresponding to zero time of Fig. 1, 45Ca (1 x 106 counts/min-ml) was added to the medium for incubation. After 5, 15 or 30 minutes incubation period, the strips were removed from the bath and radioactivities in the muscle strips were counted (1, 4). Tissue Ca: Strips were treated in the same manner as that in the preceding para graph except that 45Ca was not used and Ca content of the tissue was determined using atomic absorption spectrophotometer (1, 4). 45Ca efflux: Muscle strips were incubated in iso -40 K-S. with 45Ca (200 pCi/ml) for 180 to 200 minutes and then washed by dipping into successive tubes containing iso