The unequivocal incorporation of radioactive phosphate (32p) into the nucleic acids of brain slices has not as yet been demonstrated. Because of the great interest in the nucleic acids of the nervous system aroused by the work of Caspersson (1947)
The metabolic activity (as gauged by glycogen synthesis, glucose uptake and oxygen consumption per gram of wet tissue) was found to be increased in diaphragms taken from rats maintained on a low-protein diet compared to normal controls. There was no significant difference in these indices of metabolic activity when they were expressed on a per cell basis (calculated on the content of desoxyribonucleic acid phosphorus). In protein deprivation, the mass of the diaphragm cell was dependent upon the protein intake rather than the total caloric intake but the metabolic activity of the cell was independent of its mass. These findings suggest that the metabolic activity of a tissue may, under certain experimental conditions, be more suitably expressed on a per cell basis than on the more usual basis of wet weight of tissue.
A method for the determination of protein-bound iodine in plasma is described. It is based essentially on the method of Barker, Humphrey, and Soley, which makes use of the catalytic effect of iodide on the reduction of ceric ion by arsenious acid. A number of improvements have been made in the direction of ease of manipulation and an over-all saving of time.
In confirmation of the work of others, the concentration of inorganic phosphate (P) in the plasma of hypophysectomized rats was found to be less than that in the plasma of control animals. Hypophysectomy caused no significant change in the concentration of inorganic P in the adrenal gland or liver. A single intraperitoneal injection of each of two preparations of ACTH failed to cause any significant change in the concentrations of inorganic P in plasma, adrenal, or liver.The specific activity of the inorganic P in the plasma of hypophysectomized rats after an intraperitoneal injection of inorganic P labelled with P32 was greater than that in the control animals. Hypophysectomy caused a decrease in the specific activity of the inorganic P of the adrenal gland relative to that of the inorganic P of the plasma. Each of the two preparations of ACTH, given to the hypophysectomized animals as a single intraperitoneal injection 20 hr. before killing, restored the relative specific activity of the inorganic P of the adrenals to normal values. When the ACTH was administered six hours before killing, one of the preparations (ACTH A) caused an increase in the relative specific activity of the inorganic P of the adrenals, but a second preparation (ACTH C) was without significant effect.The increase in the specific activity of the inorganic P of the plasma comes on slowly (quite small two days after hypophysectomy), whereas the decrease in the relative specific activity of the inorganic P of the adrenal gland comes on rapidly (maximal two days after hypophysectomy). For this reason, at longer time intervals after hypophysectomy (greater than six days) the absolute activity of the acid-soluble P of the adrenal, i.e. the activity not referred to that of the inorganic P of the plasma, was greater in hypophysectomized animals, and not less, as reported by other workers. The activity of this fraction is less in hypophysectomized animals only if the observations are made at short time intervals after removal of the pituitary. Evidence is presented for the view that the increase in the specific activity of the inorganic P of the plasma is the result of changes brought about by a deficiency of growth hormone, whereas the decrease in the relative specific activity of the adrenal is due to a deficiency of ACTH.
In confirmation of the work of others, the concentration of inorganic phosphate (P) in the plasma of hypophysectomized rats was found to be less than that in the plasma of control animals. Hypophysectomy caused no significant change in the concentration of inorganic P in the adrenal gland or liver. A single intraperitoneal injection of each of two preparations of ACTH failed to cause any significant change in the concentrations of inorganic P in plasma, adrenal, or liver.The specific activity of the inorganic P in the plasma of hypophysectomized rats after an intraperitoneal injection of inorganic P labelled with P32 was greater than that in the control animals. Hypophysectomy caused a decrease in the specific activity of the inorganic P of the adrenal gland relative to that of the inorganic P of the plasma. Each of the two preparations of ACTH, given to the hypophysectomized animals as a single intraperitoneal injection 20 hr. before killing, restored the relative specific activity of the inorganic P of the adrenals to normal values. When the ACTH was administered six hours before killing, one of the preparations (ACTH A) caused an increase in the relative specific activity of the inorganic P of the adrenals, but a second preparation (ACTH C) was without significant effect.The increase in the specific activity of the inorganic P of the plasma comes on slowly (quite small two days after hypophysectomy), whereas the decrease in the relative specific activity of the inorganic P of the adrenal gland comes on rapidly (maximal two days after hypophysectomy). For this reason, at longer time intervals after hypophysectomy (greater than six days) the absolute activity of the acid-soluble P of the adrenal, i.e. the activity not referred to that of the inorganic P of the plasma, was greater in hypophysectomized animals, and not less, as reported by other workers. The activity of this fraction is less in hypophysectomized animals only if the observations are made at short time intervals after removal of the pituitary. Evidence is presented for the view that the increase in the specific activity of the inorganic P of the plasma is the result of changes brought about by a deficiency of growth hormone, whereas the decrease in the relative specific activity of the adrenal is due to a deficiency of ACTH.
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