Abstract
The anterior tibial muscles of Rana pipiens were removed, sprinkled with powdered quinhydrone, and mounted between a platinum plate electrode and an agar-KCl bridge connected with a saturated KCl-ealomel half-cell. 1 The muscle and electrodes were inserted in a glass chamber through which known gas mixtures could be flushed. The potential differences were read in the usual way by means of a Type K potentiometer and galvanometer.
After the initial rapid acid shift, muscle macerated with quinhydrone slowly became more and more acid in 5% CO2 in O2. Intact muscle in 5% CO2 in O2 shifts rapidly acid in the first few minutes' exposure. This reaction is followed by a small alkaline drift, succeeded by a plateau which is maintained for 20 to 40 minutes. The secondary alkaline drift is attributed to the mobilization of base which is presumably a less rapid process than the inward diffusion of CO2. The plateau usually terminated in an acid drift.
If the plateau values are assumed to be the pH of the tissue at definite CO2 tensions and if these are compared with the hydrogen ion concentrations calculated from CO2 combining power data, 2 the agreement is found to be good between 36 and 100 mm. Hg. CO2 tensions. Above this range the electrometric method gives readings 0.1 to 0.2 pH higher. Below 36 mm. Hg. CO2 tension, plateau values were not obtained in one hour.
In the presence of tank N2 or tank O2 the pH of resting muscle became progressively more acid at a decreasingly rapid rate. Apparently at alkaline reactions (pH 7.3 to 8.0) pure O2 cannot prevent acid production, although the tissue reaction is maintained at a constant level in the presence of 5% CO2 in O2.
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