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Biomedical subjects

B R Cirne

Publications and source records attributed to B R Cirne.

2 recordsLinked to original sources

Characteristics of toad bladder urinary acidification.

1. The urinary acification system present in the bladder of the toad Bufo marinus ictericus was investigated by means of an improved technique of mounting the membrane that minimizes the edge damage when the bladder is placed as a sheet between lucite half chambers. 2. In ouabain-treated bladders in the absence of exogenous CO2, acidification rates were similar to those observed for turtle bladder. 3. The presence of 1% CO2 at the serosal gas phase increased proton secretion (JH). Stimulation of JH was also observed when the cell pH was decreased by back diffusion of salicylic acid added to the mucosal (M) compartment. 4. The estimate of the passive proton permeability of this epithelium as a whole yielded values around 1 x 10(-4) cm/s. The maximum pH gradient that could be established across the membrane in the short circuit condition (about 3 pH units) was taken as the apparent proton-motive force (PMF') of the system and these values were similar to those observed in the turtle bladder. 5. Luminal membrane depolarization caused by substitution of NaCl by KCl in Ringer solution led to an increase in JH at M pH = 7.3 without altering the PMF', which suggests that the electrical potential difference across the luminal membrane in ouabain-treated bladders is negligible when M pH is sufficiently acid to abolish H+ secretion.

Acid-Base Equilibrium↗

The in vivo electrical parameters of toad skin.

Open-circuit voltage (PD) and short-circuit current (SCC) across toad skin were studied in in vivo conditions. An improved technique for fastening a lucite chamber on the abdominal region of the animal was developed. Saline bridges (230 mM NaCl in 4% agar solution) were placed subcutaneously to make the connections between the extracellular fluid and the half-cells. A clear relationship was observed between the electrical parameters and sodium transport by the skin, since PD and SCC were related to the sodium concentration of the bathing solution, and abolished by the presence of amiloride--a specific sodium transport inhibitor in epithelia. The initial control values of SCC in vivo were higher than those in vitro, which was attributed to hormonal stimulation. However, these high initial control values of SCC in vivo fell with time, reaching steady levels after a 2 hr period. Vasopressin failed to increase SCC in vivo when the external sodium concentration was 115 mM, being effective only when the sodium concentration was low (5 mM). On the other hand, in isolated preparations vasopressin significantly promoted an increase in both PD and SCC.

Animals↗