Effects of 18-hydroxycorticosterone and of aldosterone on acid-base parameters in the arterial blood of adrenalectomized rats.

Adrenalectomized rats were injected twice with either 2 micrograms aldosterone or 6 micrograms 18-hydroxycorticosterone (18-OH-B) and were then kept either under normal, or high-CO2 respiratory conditions. Arterial blood samples were withdrawn sequentially from T1 (i.e., 70 minutes after the first injection) on, and were then submitted to determinations of pH and PCO2. Bicarbonate levels were calculated from these data. 18-OH-B: 1) increased pH under both conditions; 2) had a tendency to decrease PCO2 in both conditions; the decrease was significant at 130 minutes after injection, under normal conditions; 3) increased CO3H levels at T1 under high-CO2 atmospheres. Aldosterone did not produce changes in pH values, even if injected in doses equimolar to those of 18-OH-B, but showed a tendency--at these higher doses--to decrease PCO2 values.

Effects of 18-hydroxycorticosterone and of aldosterone on acid-base parameters in the arterial blood of adrenalectomized rats.

Adrenalectomized rats were injected twice with either 2 micrograms aldosterone or 6 micrograms 18-hydroxycorticosterone (18-OH-B) and were then kept either under normal, or high-CO2 respiratory conditions. Arterial blood samples were withdrawn sequentially from T1 (i.e., 70 minutes after the first injection) on, and were then submitted to determinations of pH and PCO2. Bicarbonate levels were calculated from these data. 18-OH-B: 1) increased pH under both conditions; 2) had a tendency to decrease PCO2 in both conditions; the decrease was significant at 130 minutes after injection, under normal conditions; 3) increased CO3H levels at T1 under high-CO2 atmospheres. Aldosterone did not produce changes in pH values, even if injected in doses equimolar to those of 18-OH-B, but showed a tendency--at these higher doses--to decrease PCO2 values.

Acute effects of three natural corticosteroids on the acid-base and electrolyte composition of urine in adrenalectomized rats.

In acute experiments, aldosterone (aldo), 18-hydroxycorticosterone (18 OH B) or corticosterone (B) were administered to adrenalectomized rats and parameters related to acid-base balance measured in urine samples collected for 3.5 hours after injection. Aldo reduced sodium excretion but did not affect pH nor the outputs of K, NH4+, CO3H-, phosphates nor titratable acidity. 18 OH B increased the excretion of titratable acidity and reduced drastically that of CO3H-. The lowest effective dose (3 micrograms) promoted Na excretion while the highest dose employed (6 micrograms) reduced pH and Na excretion. B increased the excretions of phosphates and ammonium, the former drastically. Potassium output either increased or did not change, and pH augmented marginally. It is postulated that a) 18 OH B is a naturally occurring steroid eliciting urine-acidification not necessarily accompanied by sodium retention; and b) at least B and 18 OH B in the rat, possess hormonal roles according to which the latter promotes the presence of protons, and the former, that of acute proton-acceptors in the lumen of tubuli.

Acute effects of three natural corticosteroids on the acid-base and electrolyte composition of urine in adrenalectomized rats.

In acute experiments, aldosterone (aldo), 18-hydroxycorticosterone (18 OH B) or corticosterone (B) were administered to adrenalectomized rats and parameters related to acid-base balance measured in urine samples collected for 3.5 hours after injection. Aldo reduced sodium excretion but did not affect pH nor the outputs of K, NH4+, CO3H-, phosphates nor titratable acidity. 18 OH B increased the excretion of titratable acidity and reduced drastically that of CO3H-. The lowest effective dose (3 micrograms) promoted Na excretion while the highest dose employed (6 micrograms) reduced pH and Na excretion. B increased the excretions of phosphates and ammonium, the former drastically. Potassium output either increased or did not change, and pH augmented marginally. It is postulated that a) 18 OH B is a naturally occurring steroid eliciting urine-acidification not necessarily accompanied by sodium retention; and b) at least B and 18 OH B in the rat, possess hormonal roles according to which the latter promotes the presence of protons, and the former, that of acute proton-acceptors in the lumen of tubuli.

Acute effects of three natural corticosteroids on the acid-base and electrolyte composition of urine in adrenalectomized rats

In acute experiments, aldosterone (aldo), 18-hydroxycorticosterone (18 OH B) or corticosterone (B) were administered to adrenalectomized rats and parameters related to acid-base balance measured in urine samples collected for 3.5 hours after injection. Aldo reduced sodium excretion but did not affect pH nor the outputs of K, NH4+, CO3H-, phosphates nor titratable acidity. 18 OH B increased the excretion of titratable acidity and reduced drastically that of CO3H-. The lowest effective dose (3 micrograms) promoted Na excretion while the highest dose employed (6 micrograms) reduced pH and Na excretion. B increased the excretions of phosphates and ammonium, the former drastically. Potassium output either increased or did not change, and pH augmented marginally. It is postulated that a) 18 OH B is a naturally occurring steroid eliciting urine-acidification not necessarily accompanied by sodium retention; and b) at least B and 18 OH B in the rat, possess hormonal roles according to which the latter promotes the presence of protons, and the former, that of acute proton-acceptors in the lumen of tubuli.

Determination of ammonium ions in small urine volumes from laboratory animals.

A method based on the indophenol reaction for the determination of ammonium ions in small urine samples from research animals is described. The method is precise and specific. Sensitivity (epsilon 630 molar = 174 X 10(3)) is far beyond needs. Interference by blood in hematuric samples can be avoided.

Determination of ammonium ions in small urine volumes from laboratory animals.

A method based on the indophenol reaction for the determination of ammonium ions in small urine samples from research animals is described. The method is precise and specific. Sensitivity (epsilon 630 molar = 174 X 10(3)) is far beyond needs. Interference by blood in hematuric samples can be avoided.

Determination of ammonium ions in small urine volumes from laboratory animals

A method based on the indophenol reaction for the determination of ammonium ions in small urine samples from research animals is described. The method is precise and specific. Sensitivity (epsilon 630 molar = 174 X 10(3)) is far beyond needs. Interference by blood in hematuric samples can be avoided.