scholarly journals β-l-Aspartyl-l-histidine, a Normal Constituent of Human Urine

1961 ◽  
Vol 236 (12) ◽  
pp. 3280-3282
Author(s):  
Yasuo Kakimoto ◽  
Marvin D. Armstrong
Nature ◽  
1955 ◽  
Vol 176 (4495) ◽  
pp. 1217-1218 ◽  
Author(s):  
BERNARD WEISSMANN ◽  
PHILIP A. BROMBERG ◽  
ALEXANDER B. GUTMAN

1864 ◽  
Vol 13 ◽  
pp. 314-316

The object of the present communication is to describe the mode of ex­traction and the properties of an acid of a colloid nature which is always present in healthy human urine, and appears destined to become of great importance in Physiological Chemistry.


1865 ◽  
Vol 14 ◽  
pp. 1-9

In the autumn of 1862, feeling assured that, besides the known normal crystalloid compounds found in urine, this secretion contained colloid substances, I submitted samples of the healthy secretion, after concentration, first, to the process of dialysis, and then to the action of reagents, and finally succeeded in precipitating with alcohol a colloid substance exhibiting a faintly acid or neutral reaction, and containing a small proportion of ash. For a while my endeavours to obtain a definite compound from this amorphous mass were fruitless, until, on observing that basic acetate of lead produced a precipitate in its aqueous solution, I thought of examining this precipitate, and, by decomposing it with sulphuretted hydrogen, found it to consist of an organic acid combined with lead. This new acid is possessed of the properties of a colloid substance; it may be considered as having a definite combining proportion or equivalent weight, and is undoubtedly destined to become of great importance in physiological chemistry.


1867 ◽  
Vol 15 ◽  
pp. 259-260 ◽  

When ordinary healthy urine is passed through animal charcoal in the manner described in the preceding paper, several organic substances are separated and absorbed by the charcoal in addition to the fatty acid there referred to. The liquid obtained by treating the charcoal with boiling alcohol having been evaporated, the residue is treated with water, which leaves the fatty acid undissolved. The filtered liquid yields on evaporation a quantity of crystals, which, after being purified in the manner described by the author, are found to have the properties and composition of oxalurate of ammonia. The watery solution of the substance gives with acids a white crystalline precipitate of oxaluric acid; with nitrate of silver it produces a precipitate which dissolves without change in boiling water, the solution on cooling depositing white silky needles of oxalurate of silver. The lead compound produced by adding acetate of lead to the watery solution, forms well-defined prismatic crystals. With chloride of calcium the watery solution gives no precipitate, but on adding ammonia and boiling, there is an abundant precipitation of oxalate of lime. By treatment with strong acids the substance is decomposed, yielding oxalic acid and urea. Its composition was found to correspond with the formula C 6 H 7 N 3 O s , which is that of oxalurate of ammonia. The author’s experiments were not sufficiently numerous to decide the question whether this salt is a normal constituent of human urine or not. There is no doubt, however, that its presence, whether exceptional or not, affords an easy and satisfactory explanation of a phenomenon which has until now proved very puzzling, viz., the formation of oxalate of lime in urine long after its emission. It is doubtless owing to the decomposition of oxaluric acid, which takes up water and splits up into urea and oxalic acid; the latter then combines with lime, of which there is always a sufficient quantity present to saturate the acid. There can be little doubt also that oxaluric acid is derived in the animal frame, as in the laboratory, from uric acid, the oxidation of which is its only known source.


1979 ◽  
Vol 41 (04) ◽  
pp. 718-733 ◽  
Author(s):  
Preben Kok

SummaryThree types of plasminogen activator could be distinguished in extracts from human uterine tissue. The activators differed in thermostability or in mode of inhibition by EACA.All the extracts contained stable as well as labile activators. The saline extracts were uniformly inhibited by increasing concentrations of EACA. Extracts made with 2 M ammonium thiocyanate were either uniformly inhibited by EACA or showed deflections indicating contamination with an activator, which was inhibited in a biphasic manner. It was possible to distinguish between: (1) An activator, abundantly present in the tissue, which was uniformly inhibited and stable. (2) Another uniformly inhibited activator, which was labile. (3) An activator, inhibited in a biphasic manner, similar to urokinase, which was present in varying amounts in uteri with the endometrium in the proliferative phase.Gel filtration of the uterine extracts showed two major activity peaks corresponding to particle sizes of 60,000 dalton and about 10,000 dalton.Antiserum to purified plasminogen activator, prepared from porcine ovaries, inhibited the activity of the human uterine extracts, but not the activities of human urokinase or urine. Urokinase antiserum in a concentration completely inhibiting human urine or urokinase, inhibited only 10% or less of the activities of human uterine extracts.


1995 ◽  
Vol 73 (05) ◽  
pp. 805-811 ◽  
Author(s):  
Yasuo Takahashi ◽  
Yoshitaka Hosaka ◽  
Hiromi Niina ◽  
Katsuaki Nagasawa ◽  
Masaaki Naotsuka ◽  
...  

SummaryWe examined the anticoagulant activity of two major molecules of soluble thrombomodulin purified from human urine. The apparent molecular weights of these urinary thrombomodulins (UTMs) were 72,000 and 79,000, respectively. Both UTMs showed more potent cofactor activity for protein C activation [specific activity >5,000 thrombomodulin units (TMU)/mg] than human placental thrombomodulin (2,180 TMU/mg) and rabbit lung thrombomodulin (1,980 TMU/mg). The UTMs prolonged thrombin-induced fibrinogen clotting time (>1 TMU/ml), APTT (>5 TMU/ml), TT (>5 TMU/ml) and PT (>40 TMU/ml) in a dose-dependent fashion. These effects appeared in the concentration range of soluble thrombomodulins present in human plasma and urine. In the rat DIC model induced by thromboplastin, administration of UTMs by infusion (300-3,000 TMU/kg) restored the hematological abnormalities derived from DIC in a dose-dependent fashion. These results demonstrate that UTMs exhibit potent anticoagulant and antithrombotic activities, and could play a physiologically important role in microcirculation.


1982 ◽  
Vol 47 (03) ◽  
pp. 197-202 ◽  
Author(s):  
Kurt Huber ◽  
Johannes Kirchheimer ◽  
Bernd R Binder

SummaryUrokinase (UK) could be purified to apparent homogeneity starting from crude urine by sequential adsorption and elution of the enzyme to gelatine-Sepharose and agmatine-Sepharose followed by gel filtration on Sephadex G-150. The purified product exhibited characteristics of the high molecular weight urokinase (HMW-UK) but did contain two distinct entities, one of which exhibited a two chain structure as reported for the HMW-UK while the other one exhibited an apparent single chain structure. The purification described is rapid and simple and results in an enzyme with probably no major alterations. Yields are high enough to obtain purified enzymes for characterization of UK from individual donors.


1951 ◽  
Vol 7 (1) ◽  
pp. 240-256 ◽  
Author(s):  
G. F. MARRIAN ◽  
W. S. BAULD
Keyword(s):  

1965 ◽  
Vol 50 (2) ◽  
pp. 301-309 ◽  
Author(s):  
Jürg Müller

ABSTRACT An extract of human urine, which was previously shown to stimulate aldosterone production by rat adrenal sections, was further purified. Evidence was obtained that its aldosterone-stimulating effect was due to the presence of ammonium ions. Addition of ammonium chloride and of urine extract to the incubation medium caused identical increases in aldosterone production in vitro. In addition to ammonium ions, rubidium and caesium ions also stimulated aldosterone production up to 250% that of control values without a significant effect on corticosterone production. Similar dose-response curves were obtained when increasing concentrations of potassium, ammonium, rubidium and caesium ions were tested. Aldosterone production was maximal at concentrations of 7 mval/1 and was significantly lower at higher concentrations. When ammonium chloride and ACTH were simultaneously added to the incubation medium, the production of aldosterone and of corticosterone was lower than with ACTH alone. On the other hand, the stimulating activity on aldosterone and corticosterone production by »TPN« (NADP) and glucose-6-phosphate was enhanced by the simultaneous addition of ammonium chloride.


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