Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0085631 (agitation)
 12,064 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The unique of CO-cytochrome oxidase as first noted by Yonetani et al. (22) is that after its photodissociation at low temperatures recombination occurs as the sample temperature is raised, but at temperatures considerably higher than those for other CO-heme and CO-hemoprotein complexes; that is, the half recombination temperature is 180 K contrary to 25-30 K for other CO complexes. The photodissociability, however, disappeared when monomeric cytochrome oxidase was treated with pCMB to remove an intrinsic copper, the significance of which in CO complex formation was thus demonstrated. It is proposed that the copper is situated close to heme a and traps the photodissociated CO. The access of the trapped CO to the heme a to resume the original binding is effected only when sufficient energy for thermal agitation is provided by elevating the sample temperature. During the course of this study, new photo- and thermochromic properties were observed with the reduced enzyme by cooling it in liquid nitrogen after preincubation at pH 8.6 to 10.5. The characteristic bands appeared at 575 and 428 nm and diminished when this ample was illuminated at 26 K. As the sample temperature was raised these bands were restored with a half transition temperature of 80 K. When the reduced oxidase had been complexed with CO, cyanide or azide, or treated with pCMB, such a unique species did not appear. The enthalpy change of 1.16 kcal/mol for the formation of this species as well as the above-described properties suggests that the hydrogen bond between the formyl side group of heme a and one of seven sulfhydryl groups in cytochrome oxidase is responsible for the appearance and disappearance of this new species. Based on these results a schematic model has been proposed for the photo- and thermochromism of cytochrome oxidase at cryogenic temperatures and for the microenvironment of the prosthetic heme a and copper in this enzyme. On the other hand, contrary to the central dogma of Warburg that all CO-heme and CO-hemoprotein complexes are photodissociable, we observed little photodissociability with some CO-heme complexes, especially at very low temperatures, and presented a view that depending on the bond type between CO and heme iron the efficiency of photodissociation is so varied that under certain conditions practically no photodissociation occurs. According to this view a tilted arrangement of the ligated CO towards the heme plane accompanying a large extent of overlapping of the dpi(Fe) and the pi* antibonding orbital on the CO facilitates photodissociation. In addition to our own observations of photochemical properties of cytochrome oxidase and heme model compounds, recent photodynamic studies carried out by other investigator on CO-heme and CO-hemoproteins are summarized and the validity and limitation of their models are discussed.
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PMID:Photochemical reactions of cytochrome oxidase at low temperatures. 20 71

Dog platelets are refractory to aggregation by arachidonic acid (AA) but generate an unstable activity that aggregates rabbit platelets. Formation of this activity is inhibited by indomethacin, by the peroxide scavenging enzyme catalase, by two chelating agents that bind Cu+ and Cu2+ ions, by the -SH agent dithiothreitol and is stimulated by cysteine. Agitation of dog platelets is followed by spontaneous aggregation and uncovers aggregation by AA, which is blocked by indomethacin. Neither indomethacin nor apyrase prevent spontaneous aggregation, ruling out both activation of prostaglandin synthetase and leakage of ADP as possible explanations. Complexation of plasma Ca2+ by citrate as an explanation for refractoriness to AA was ruled out by replacing citrate with heparin. Dog platelets are also refractory to PGH2 formed from AA by the cyclo oxygenase component of prostaglandin synthetase. Aggregation of rabbit platelets by PGH2 is not inhibited by indomethacin, by catalase, by dithiothreitol or by metal chelating agents and is not potentiated by cysteine. This confirms that the reagents act before PGH2 is formed. Aggregating activity generated by dog platelets is probably due to an unstable lipoperoxide whose generation involves mechanisms similar to those responsible for aggregation of rabbit platelets, since similar antagonists block both processes.
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PMID:Dog platelets fail to aggregate when they form aggregating substances upon stimulation with arachidonic acid. 95 35

Total mercury release from a high-copper and a low-copper amalgam was measured in a study in vitro using atomic absorption spectrophotometry. Conditions of mechanical agitation and sealant coverage were evaluated over time. Mercury release was found under agitation and no-agitation conditions to increase shortly after preparation and then to level off after 24 to 48 hours. No difference in mercury release was observed for either amalgam type. Sealant coverage of amalgam significantly reduced mercury release under agitation conditions. In an experiment in vivo mercury vapor was measured at different times for patients receiving their first amalgam restoration. Sealant coverage was found to significantly reduce mercury vapor after chewing on this restoration compared to a nonsealant-covered amalgam.
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PMID:Mercury release from amalgam: a study in vitro and in vivo. 209 33

Complementary replicas of samples prepared for electron microscopy by the freeze-fracture/etch technique are extremely valuable in the interpretation of the exposed surfaces, the nature and location of the membrane fracture plane, and as an aid in the recognition of the potential artefacts of this technique. This paper describes a procedure for the preparation of complementary replicas of thin samples sandwiched between copper foil strips and frozen ultra-rapidly in the absence of chemical pretreatments. In this procedure, the copper foil support bearing the replica is floated on the surface of a chromic acid solution, resulting in the controlled dissolution of the copper metal. The replica which remains at the surface of the chromic acid is then stabilized against fragmentation during subsequent cleaning and rinsing steps by placing a 50 mesh gold grid on top of the replica. To minimize agitation of the replica/grid, all cleaning steps are performed in a single depression plate well. The clean replica/grid is picked up from below on a thin Formvar film, dried, and then separated from the extra film. Careful placement of the gold grid on the replicas and low magnification electron micrograph montages of the complementary grids facilitate the location of complementary regions and simplify examination of complementary specimen areas at higher magnification.
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PMID:A procedure for obtaining complementary replicas of ultra-rapidly frozen sandwiched samples. 351 48

The concentrations of soluble copper and tin which were generated by the corrosion of a number of different amalgams in both an artificial saliva and Ringer's solution are reported. Besides variations in solution composition, the effects of solution agitation and abrasive particle wear upon the release of soluble species are studied. Immersion only, moderate solution agitation, vigorous solution agitation with abrasive particle wear, and accelerated corrosion by both constant currents and cyclic voltammetry are included. The results indicate that an artificial saliva but not Ringer's solution is capable of generating high levels of soluble tin. With artificial saliva, agitation increases the amalgam weight losses and increases soluble copper and tin concentrations, whereas agitation with Ringer's solution decreases sample weight losses and decreases levels of soluble copper and tin. This latter effect is believed to be due to the increased oxygen supply to the amalgam surfaces with agitation and the greater ability for producing protective passivating films of the basic hydroxide and copper chlorides in solutions of higher chloride ion concentrations e.g. Ringer's solution. Abrasive particle wear, including pumice, alumina, glass beads, and silica gel had varied effects upon the release of soluble species. Depending upon the amalgam, the solution, and the abrasive combination, either larger increases in copper or in tin occurred or reduced concentrations.
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PMID:The effect of exposure conditions upon the release of soluble copper and tin from dental amalgams. 648

The behaviour of five non-ionic surfactants of different chain lengths was studied in relation to the improvement in sensitivity that their use affords as a sample pre-treatment procedure for the determination of calcium, magnesium, copper and zinc in real samples by flow injection flame atomic absorption spectrometry. The results show that the sensitivity changed with surfactant concentration, length of the hydrophobic chain and ultrasonic agitation time. Higher outputs were obtained with Triton X-100, which is the surfactant with the shortest chain length. In this case, the sensitivity of the atomic absorption signal increased 2.2, 2.2, 2.3 and 2.5-fold for aqueous solutions of calcium, magnesium, copper and zinc, respectively. The data also showed that ultrasonic agitation of the sample probe considerably improved the sensitivity, regardless of the element under evaluation. A relative precision between 0.6 and 3.3% was achieved with a smaller sample consumption than by the conventional atomic absorption method. The results obtained from the proposed sample pre-treatment procedure for the analysis of the elements under study were in good agreement with those obtained by microwave-assisted mineralization and flow injection AAS (for zinc and copper) and flame AAS (for calcium and magnesium).
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PMID:Effect of surfactants and of ultrasonic mixing in the determination of calcium, magnesium, copper and zinc in whole blood by flow injection flame atomic absorption spectrometry. 884 58

Copper can induce acute and chronic intoxications in humans. Copper in tap water has caused a series of severe systemic diseases in Germany in recent years (copper induced liver cirrhosis). Besides cirrhosis, another type of disease with predominantly gastrointestinal symptoms has occurred which likewise appeared to be induced by copper in tap water. - In a retrospective investigation we looked for additional indications and proof that chronic copper poisoning has been the cause of the observed gastrointestinal diseases. All patients suffering from this type of disease had copper plumbing in their houses. - The patients (children and adults) suffered from nausea, vomiting, colic, and diarrhoea. In the group of infants, one refused formula milk (prepared with tap water) and the others suffered from persistent restlessness, unexplainable screaming (especially at night) and/or long lasting diaper rash. - We accept the diagnosis of chronic copper intoxication as the cause of the gastrointestinal symptoms when at least one of the following criteria were fulfilled: 1. first manifestation, remission and relapse of the disease depend on intake and a non-intake of water containing copper, respectively. 2. hypercupric state of the patients (i.e. pathological high concentrations of the non-ceruloplasmin-bound copper in serum and/or elevated copper levels in urine) 3. signs of systemic copper intoxication in the same patient 4. signs of systemic copper intoxication or hypercupric states in members of the patient s family or in his neighbourhood (non-relatives) - We found that the disease can even be caused by copper concentrations below the allowed concentration given by the German Guidelines for Drinking Water (Trinkwasserverordnung). - The data prove that copper in drinking water can cause gastrointestinal diseases and not only the better known systemic diseases (i.e. copper induced liver cirrhosis). Copper poisoning must be considered as a possible cause of chronic gastrointestinal diseases in those countries in which copper plumbing is common.
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PMID:Chronic poisoning by copper in tap water: I. Copper intoxications with predominantly gastointestinal symptoms. 1057 26

Ultrasound has been shown to improve the cathodic current efficiency of copper electrodeposited from a dilute acidic sulphate bath and also zinc from a dilute alkaline zincate bath. Depending upon the plating parameters the metal may be plated with an enhanced value as a foil, sheet or powder. This agitation may be utilised in the recovery of metal from waste solutions and also in the recycling of acids and alkalies.
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PMID:Ultrasound improves electrolytic recovery of metals. 1123 23

Ultrasound is gaining importance in metal extraction process. In the previous laboratory scale investigation the authors have established the positive influence of ultrasound on copper recovery from oxide ores of Malanjkhand, Madhya Pradesh, India in an ammonical media. The process parameters in a conventional agitation method were optimized and a maximum recovery of approximately 32% in 20 min was obtained without sonication. The recovery was increased to approximately 78% by the application of ultrasound over the same period with several advantages like decrease in leaching time and the reagent consumption. In the present study the leaching process is intensified by studying the metal recovery variation at different ultrasonic frequencies (20, 40, 43 and 720 kHz) and intensities (up to 8 W cm-2) with sonication time. The results show that sinusoidal ultrasound even at larger intensity has some limitations with single frequency. However, simultaneous application of dual frequency 20 and 40 kHz ultrasound enhanced extraction rates along with increased yield. While conventional single frequency exposure at either one of the two frequencies at the same acoustic power level did not yield similar results, application of two wave sources, as used in the study revealed that it is possible to save energy through lowering of time of operation process.
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PMID:Intensification of leaching process by dual-frequency ultrasound. 1151 Feb 17

A sonotrode consisting of a disc shaped glassy carbon electrode attached to a quartz rod and inserted into a drilled ultrasonic probe tip has been designed and used as a novel alternative to the traditional 'face on' cell arrangement where an ultrasonic micro-tip probe is placed opposite a glassy carbon working electrode. The 'single probe' arrangement is both convenient and optimised for electroanalysis. We first report how under ultrasonic agitation of the sonotrode the mass transport to the electrode surface is enhanced compared to that observed under silent conditions and also how the sonotrode cell geometry compares with the well-established 'face on' cell geometry for cobalt electrodeposition. Second, we will show that the new sonotrode can be used in the application for the determination of copper in a series of fouling media in which conventional silent electroanalysis fails. The passivation of the electrodes surface by surfactant species can be overcome by cavitationally induced streaming and/or erosion at the sonotrode surface with recoveries of 100% and 93.8% achieved at 42 W cm-2 for Triton X-100 and sodium dodecyl sulfate (SDS), respectively. Other data indicates that the sonotrode can be successfully employed for the detection of copper in beer (Marston's bitter), a system known to be complex and highly electrode fouling and difficult to analyse using standard, silent electroanalytical techniques.
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PMID:A sonotrode for electroanalysis: the determination of copper in passivating media. 1219 52


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