scholarly journals The effect of tungstate ingestion on xanthine oxidase in milk and liver

1968 ◽  
Vol 22 (3) ◽  
pp. 331-340 ◽  
Author(s):  
E. C. Owen ◽  
R. Proudfoot
Keyword(s):  
Body Weight ◽  
Xanthine Oxidase ◽  
Sodium Tungstate ◽  
Early Lactation ◽  
Triphenyl Tetrazolium Chloride ◽  
Anaerobic Conditions ◽  
Hydrogen Acceptor ◽  
Tetrazolium Chloride ◽  
Conventional Diet

1. The ingestion of doses of up to 6 g sodium tungstate (56 mg W/kg body-weight) by goats was found to diminish the amount of xanthine oxidase secreted in their milk so that, in some samples, the enzyme became undetectable. This effect occurred whether the goats were eating a semi-synthetic or a conventional diet.2. Tungstate ingestion by goats did not affect the concentration of riboflavine in their milk.3. The ingestion of sodium tungstate by young goats for 3–5 months diminished the amount of xanthine oxidase in their livers.4. When given in early lactation to two cows, doses of sodium tungstate (up to 20 g) diminished the titre of xanthine oxidase in their milk with no concomitant effect on the yields.5. Much later in lactation the milk phosphatase of these two cows was poorly correlated with milk xanthine oxidase. Reasons for this are discussed.6. Under anaerobic conditions, with xanthine as substrate and triphenyl-tetrazolium chloride as hydrogen acceptor, neither molybdate nor tungstate affected the xanthine oxidase activity of cow's or goat's milk in vitro. Molybdate in vitro did not enhance the very low titre of human milk.

scholarly journals In VitroPollen Viability and Pollen Germination in Cherry Laurel (Prunus laurocerasusL.)

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Melekber Sulusoglu ◽  
Aysun Cavusoglu
Keyword(s):  
Pollen Germination ◽  
Culture Media ◽  
Pollen Viability ◽  
Second Step ◽  
Triphenyl Tetrazolium Chloride ◽  
Tetrazolium Chloride ◽  
Germinated Pollen ◽  
Cherry Laurel ◽  
Better Than

Pollen quality is important for growers and breeders. This study was carried out to determinein vitropollen viability and pollen germination in seven genotypes of cherry laurel (Prunus laurocerasusL.). Two pollen viability tests, TTC (2,3,5-triphenyl tetrazolium chloride) and IKI (iodine potassium iodide), were used. Pollen traits of genotypes were studied using anin vitromedium containing 0%, 5%, 10%, 15%, and 20% sucrose to determine the best sucrose concentrations for germination. In the second step, the germinated pollen was counted 1, 4, 6, 10, 12, 24, and 48 hours later until there was no further germination. The viability rates were different according to genotypes and tests used. The IKI and TTC staining tests and pollen germination had low correlation (r2= 0.0614 andr2= 0.0015, resp.). Painted pollen rate was higher and pollen was well-stained with IKI test and pollen viability estimated with TTC staining test was better than that estimated with the IKI staining test. 15% sucrose gave the best germination rates in most of the genotypes. Pollen germination rates were recorded periodically from one hour to 48 hours in 15% sucrose and the results showed that pollen germination rates increased after 6 hours of being placed in culture media.

Valine, malic, and pyruvic dehydrogenase tests in the differentiation of Bacteroides

1975 ◽  
Vol 21 (9) ◽  
pp. 1369-1371
Author(s):  
Noel R. Funderburk ◽  
A. S. Kester
Keyword(s):  
Amino Acids ◽  
Organic Acids ◽  
Dehydrogenase Activity ◽  
Rapid Method ◽  
Pyruvic Acid ◽  
Triphenyl Tetrazolium Chloride ◽  
Hydrogen Acceptor ◽  
Tetrazolium Chloride

Fifteen isolates of Bacteroides were tested for their ability to dehydrogenate a variety of amino acids and organic acids. A simple and rapid method was developed for detecting dehydrogenase activity using 2,3,5-triphenyl tetrazolium chloride as a hydrogen acceptor and indicator. The results indicate that the tests for valine, malic, and pyruvic acid dehydrogenases have value in differentiating organisms in this genus.

scholarly journals THE QUANTITATIVE REDUCTION OF 2,3,5-TRIPHENYL TETRAZOLIUM CHLORIDE BY SKIN IN VITRO

1958 ◽  
Vol 6 (3) ◽  
pp. 191-196 ◽  
Author(s):  
FALLS B. HERSHEY ◽  
C. N. D. CRUICKSHANK ◽  
L. I. MULLINS
Keyword(s):  
Triphenyl Tetrazolium Chloride ◽  
Tetrazolium Chloride

scholarly journals Determination of Xanthine Oxidase in Milk with Triphenyl Tetrazolium Chloride

1956 ◽  
Vol 39 (5) ◽  
pp. 522-527 ◽  
Author(s):  
C.A. Zittle ◽  
E.S. Dellamonica ◽  
J.H. Custer ◽  
R.K. Rudd
Keyword(s):  
Xanthine Oxidase ◽  
Triphenyl Tetrazolium Chloride ◽  
Tetrazolium Chloride

Pollen viability of some Populus species as indicated by in vitro pollen germination and tetrazolium chloride staining

1986 ◽  
Vol 64 (6) ◽  
pp. 1086-1088 ◽  
Author(s):  
Om P. Rajora ◽  
Louis Zsuffa
Keyword(s):  
Seed Set ◽  
Populus Deltoides ◽  
Agar Medium ◽  
Pollen Viability ◽  
Triphenyl Tetrazolium Chloride ◽  
Breeding Programs ◽  
Tetrazolium Chloride ◽  
Staining Techniques ◽  
Populus Species

The viability of pollen of Populus deltoides, P. maximowiczii, and P. nigra was assessed by in vitro germination and by use of 0.5% 2,3,5-triphenyl tetrazolium chloride (TTC) staining techniques. An agar medium with 10% sucrose resulted in maximum germination of P. deltoides and P. nigra pollen, while the medium with 20% sucrose was a optimal fo P. maximowiczii. Pollen staining in TTC for 1 h at 30 °C gave a good indication of pollen viability as determined by germination and seed set in poplar breeding programs. Significant differences in viability were observed among species, but not among clones and replications.

Superoxide, Xanthine Oxidase and Platelet Reactions: Further Studies on Mechanisms by which Oxidants Influence Platelets

1981 ◽  
Vol 45 (03) ◽  
pp. 290-293 ◽  
Author(s):  
Peter H Levine ◽  
Danielle G Sladdin ◽  
Norman I Krinsky
Keyword(s):  
Superoxide Dismutase ◽  
Cytochrome C ◽  
Xanthine Oxidase ◽  
Direct Effect ◽  
Platelet Function ◽  
Experimental Conditions ◽  
Release Reaction

SummaryIn the course of studying the effects on platelets of the oxidant species superoxide (O- 2), Of was generated by the interaction of xanthine oxidase plus xanthine. Surprisingly, gel-filtered platelets, when exposed to xanthine oxidase in the absence of xanthine substrate, were found to generate superoxide (O- 2), as determined by the reduction of added cytochrome c and by the inhibition of this reduction in the presence of superoxide dismutase.In addition to generating Of, the xanthine oxidase-treated platelets display both aggregation and evidence of the release reaction. This xanthine oxidase induced aggreagtion is not inhibited by the addition of either superoxide dismutase or cytochrome c, suggesting that it is due to either a further metabolite of O- 2, or that O- 2 itself exerts no important direct effect on platelet function under these experimental conditions. The ability of Of to modulate platelet reactions in vivo or in vitro remains in doubt, and xanthine oxidase is an unsuitable source of O- 2 in platelet studies because of its own effects on platelets.

The Effect of Adrenaline Infusions on Blood Coagulation in Normal and Haemophilia B Dogs

1966 ◽  
Vol 15 (03/04) ◽  
pp. 349-364 ◽  
Author(s):  
A.H Özge ◽  
H.C Rowsell ◽  
H.G Downie ◽  
J.F Mustard
Keyword(s):  
Body Weight ◽  
Factor Viii ◽  
Factor Ix ◽  
Clotting Factor ◽  
Blood Ph ◽  
Order Of Magnitude ◽  
Dose Dependent ◽  
Generation Test ◽  
Plasma Activity

SummaryThe addition of trace amounts of adrenaline to whole blood in plasma in vitro increased factor VIII, factor IX and whole plasma activity in the thromboplastin generation test. This was dose dependent.Adrenaline infusions less than 22 (μg/kg body weight in normal dogs accelerated clotting, increased factor IX, factor VIII and whole plasma activity in the thromboplastin generation test and caused a fall in blood pH. In a factor IX deficient dog, there was no increase in factor IX activity. After adrenaline infusions, however, the other changes occurred and were of the same order of magnitude as in the normal. Adrenaline in doses greater than 22 μg/kg body weight did not produce as great an effect on clotting in normal or factor IX deficient dogs. The platelet count in the peripheral blood was increased following the infusion of all doses of adrenaline. These observations suggest that the accelerating effect of adrenaline on clotting is not mediated through increase in activity of a specific clotting factor.

Evaluation of a New Preparation of Urokinase

1973 ◽  
Vol 30 (01) ◽  
pp. 114-122
Author(s):  
C.R.M Prentice ◽  
K.M Rogers ◽  
G.P McNicol
Keyword(s):  
Body Weight ◽  
Maintenance Therapy ◽  
Initial Dose ◽  
Fibrinolytic Activity ◽  
Pharmacological Effect ◽  
Whole Body ◽  
Fibrinolytic Agent ◽  
Thromboplastic Activity

SummaryThe pharmacological effect of a new preparation of urokinase (Leo) has been studied, both in vitro and in six patients suffering from thrombo-embolic disorders. It was a non-toxic, effective fibrinolytic agent if given in sufficient dosage. A regimen consisting of an initial dose of 7,200 ploug units per kg body weight, followed by hourly maintenance therapy with 3,600 ploug units per kg intravenously, gave satisfactory evidence of whole body fibrinolytic activity. The preparation had minor but insignificant thromboplastic activity both when assayed in the laboratory and when given to patients.

The Effect of Dextran of Various Molecular Weight on the Coagulation in Dogs

1961 ◽  
Vol 06 (01) ◽  
pp. 015-024 ◽  
Author(s):  
Sven Erik Bergentz ◽  
Oddvar Eiken ◽  
Inga Marie Nilsson
Keyword(s):  
Molecular Weight ◽  
Body Weight ◽  
High Molecular Weight ◽  
Bleeding Time ◽  
Factor Vii ◽  
Low Molecular Weight ◽  
Factor V ◽  
Coagulation Mechanism ◽  
Coagulation Defects

Summary1. Infusions of low molecular weight dextran (Mw = 42 000) to dogs in doses of 1—1.5 g per kg body weight did not produce any significant changes in the coagulation mechanism.2. Infusions of high molecular weight dextran (Mw = 1 000 000) to dogs in doses of 1—1.5 g per kg body weight produced severe defects in the coagulation mechanism, namely prolongation of bleeding time and coagulation time, thrombocytopenia, pathological prothrombin consumption, decrease of fibrinogen, prothrombin and factor VII, factor V and AHG.3. Heparin treatment of the dogs was found to prevent the decrease of fibrinogen, prothrombin and factor VII, and factor V otherwise occurring after injection of high molecular weight dextran. Thrombocytopenia was not prevented.4. In in vitro experiments an interaction between fibrinogen and dextran of high and low molecular weight was found to take place in systems comprising pure fibrinogen. No such interaction occurred in the presence of plasma.5. It is concluded that the coagulation defects induced by infusions of high molecular weight dextran are due to intravascular coagulation.

Effect of [Asu,]eel calcitonin on prolactin release in normal subjects and patients with prolactinoma

1985 ◽  
Vol 108 (3) ◽  
pp. 297-304 ◽  
Author(s):  
Hidesuke Kaji ◽  
Kazuo Chihara ◽  
Naoto Minamitani ◽  
Hitoshi Kodama ◽  
Tetsuya Kita ◽  
...  
Keyword(s):  
Body Weight ◽  
Bolus Injection ◽  
Normal Subjects ◽  
Regular Insulin ◽  
Prolactin Release ◽  
Saline Administration ◽  
The Central Nervous System ◽  
Plasma Prl ◽  
Male Subjects

Abstract. The effect of [Asu]eel calcitonin (ECT), an equipotent analogue of eel CT, on prolactin (Prl) secretion was examined in 12 healthy male subjects and in 6 patients with prolactinoma. In healthy subjects, ECT (0.5 μg/kg body weight · h) or saline was infused for 2 h and TRH was injected iv as a bolus of 500 μg at 1 h of ECT or saline administration. ECT did not affect basal Prl levels during 1 h of infusion. TRH caused a significant increase of plasma Prl with peak values of 75.2 ± 11.6 ng/ml in ECT-infused subjects, which did not differ from those infused with saline (68.5 ± 8.3 ng/ml). Next, an iv bolus injection of regular insulin (0.1 U/kg body weight) was followed by an infusion of ECT or saline alone. Plasma Prl peaks after hypoglycaemic stress were significantly lower in ECT-infused subjects than those in saline-injected controls (ECT, 16.5 ± 3.1 vs 33.5 ± 9.6 ng/ml, P < 0.05). In patients with prolactinoma, basal levels of plasma Prl ranging from 42.0–4130 ng/ml failed to change during iv infusion of ECT. Moreover, ECT (10−9–10−6m) did not affect Prl release from prolactinoma tissues perifused in vitro. These findings suggest that ECT may not act directly on the pituitary to modify Prl release. Rather, peripherally administered ECT appears to suppress Prl release via the central nervous system.

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