Biomedical subjects
M Nagasaka
Publications and source records attributed to M Nagasaka.
[Studies on longitudinal changes of the form and the amount of growth of the maxilla (author's transl)].
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[Simulation of osmoregulation].
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[Longitudinal studies on the form and the amount of growth of the mandible (author's transl)].
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[Mineralocorticoids and sodium regulation].
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[Guyton's model of hypertension].
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[Symposium on edema (1)Pathogenesis. I)Systemic factors--Na regulatory system and edema (author's transl)].
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Quantitative relationship between serum Ca and inorganic phosphate concentrations in uremic patients.
Sixty four blood samples from 28 uremic patients were analyzed for total calcium (Ca), inorganic phosphate (P), total protein (TP), and albumin in the serum. In these patients Ca had no significant correlation with either TP or albumin as was generally postulated, but showed significant correlation only with P. The regression analysis revealed that the residuals were of the same order of magnitude in both linear and non-linear formation. It was also found that the product, CaxP, increased along with BUN in uremic patients.
[The cephalometric analyses with a function correcting the reference plane--review and improvement based on the six-years clinical application (author's transl)].
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Sodium excretion in volume-expanded dogs. I. Comparison of the effects of physiological saline and 5% glucose solution.
Dogs were subjected to volume expansion with physiological saline and 5% glucose solution. During the infusion Na excretion was significantly increased only when saline was given. Maintenance of the volume expansion with 5% glucose solution immediately following saline infusion was ineffective in preventing the decline of Na excretion rate after the cessation of saline loading. Although the indices of hemodilution such as plasma total protein concentration and peripheral venous hematocrit were reduced along with natriuresis, these values also correlated with the total amount of Na retained during saline infusion. And this amount of retained Na has also a good correlation with the natriuresis. It is concluded that hemodilution is not the essential cause of natriuresis in the present volume expansion experiments, and that the amount of Na retained during saline loading determines the Na excretion rate in some unknown manner. The implication of regression coefficient between Na retention and Na excretion is discussed as a characteristic value in the Na homeostatic mechanism of the organism.
[General pharmacological actions of l-(m-chlorophenyl)-3-N,N-dimethylcarbamoyl-5-methoxypyrazole (PZ-177)].
PZ-177 was found to have potent analgesic, anti-inflammatory and mild central depressive actions. In the present work, the general pharmacological actions of PZ-177 were tested in order to investigate other significant actions and to determine the side effects. PZ-177 showed no significant pharmacological activities on the respiratory and cardiovascular system, on the renal function, on the autonomic nervous system, on the sugar level and coagulation in blood and on local irritation. Volume and acidity of gastric juice were decreased and turn over was not inhibited in the connective tissure. Thus PZ-177 was considered to have no ulcerogenic action on the gastric mucosa. The compound relaxed the tonus of isolated small intestine, tracheal muscles and uterus and stopped spontaneous movement. Moreover the contraction of those smooth muscles by such spasmogens as acetylcholine, histamine serotonin, BaCl2 and oxytocin was inhibited by PZ-177 and the activity was almost the same with each spasmogen. It was found therefore to have spasmolytic activity and no specific antagonistic action on the chemical mediators. PZ-177 showed also wear relaxant activity on the skeletal muscle. Those actions on the muscles may have a curative effect on inflammation in bronchotracheal and gastrointestinal tracts or on pain with contraction of skeletal muscle. From the above results, it may be considered that PZ-177 is a relatively safe and useful analgesic and anti-inflammatory compound.
[Problems of the regional medical system - physicians' point of view].
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[Studies on diphenylmethane derivatives. V. Synthesis and pharmacology of N-alkylaminopropyl-1,1-diphenylmethylamine and N-alkylaminopropyl-1,2-diphenylethylamine derivatives (author's transl)].
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[Water-electrolyte imbalance in myxedema - analysis based on the feedback loop theory].
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[Symposium on pathophysiology of congestive heart failure. 6. A simulation study of Na metobolism. Three types of body fluid volume regulation (author's transl)].
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[Pharmacological study of 1,1-diphenylmethylamine derivatives. I. Local anesthetic activity of N-alkyl-1,1-diphenylmethylamine derivatives].
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QT duration and plasma electrolytes (Ca, Na, and K) in uremic patients.
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