Calcium ion concentrations

The Ca(Il) coaceatratioa ia blood is closely coatroUed aormal values He betweea 2.1 and 2.6 mmol/L (8.5—10.4 mg/dL) of semm (21). The free calcium ion concentration is near 1.2 mmol/L the rest is chelated with blood proteias or, to a lesser extent, with citrate. It is the free Ca(Il) ia the semm that determines the calcium balance with the tissues. The mineral phase of bone is essentially ia chemical equiUbrium with calcium and phosphate ions present ia blood semm, and bone cells can easily promote either the deposition or dissolution of the mineral phase by localized changes ia pH or chelating... 

Figure 8.19 Transient pH, ( -potential and calcium ion concentration in an agitated reactor Jones etal., 1992a)...

FIGURE 2.19 Potentiation and modulation of response through control of cellular processes, (a) Potentiation of inotropic response to isoproterenol in guinea pig papillary muscle by the phosphodiesterase inhibitor isobutylmethylxanthine (IBMX). Ordinates percent of maximal response to isoproterenol. Abscissa percent receptor occupancy by isoproterenol (log scale). Responses shown in absence (open circles) and presence (filled circles) of IBMX. Data redrawn from [7], (b) Effect of reduction in calcium ion concentration on carbachol contraction of guinea pig ileum. Responses in the presence of 2.5 mM (filled circles) and l.5mM (open circles) calcium ion in physiological media bathing the tissue. Data redrawn from [8],... 

Rizzuto, R., et al. (1995). Photoprotein-mediated measurement of calcium ion concentration in mitochondria of living cells. Method. Enzymol. 260 417-428. 

Shimomura, O., Musicki, B., and Kishi, Y. (1988). Semi-synthetic aequorin an improved tool for the measurement of calcium ion concentration. Biochem. J. 251 405 410. 

Comparison of results for the first and last entries in Table 7 (AOS 2024 and IOS 2024) was for samples for which the hydrophobe linearity, hydrophobe carbon number, and relative disulfonate content were held nearly constant. The major differences in these surfactants were possible differences in the relative locations of the double bond and the sulfonate group in the alkenesulfonate and in the relative locations of the hydroxy group and the sulfonate group in the hydroxyalkanesulfonate. Analyses to determine these are quite difficult. At calcium ion concentrations below 100-250 ppm, AOS 2024 appeared to be more salt-tolerant than linear IOS 2024. At higher calcium concentrations, the calcium ion tolerance of the two surfactants was similar. 

Typical adsorption isotherms are shown in Figs. 16 and 17. Despite the large experimental scatter, a steep increase in adsorption can be seen at low concentrations, followed by a plateau at concentrations exceeding the CMC. Similar behavior has been observed before with model surfactants [49-54] and has also been predicted by modem theories of adsorption [54]. According to Fig. 16, adsorption increases modestly with salinity provided that the calcium ion concentration remains low. The calcium influence, shown in Fig. 17, cannot be explained by ionic strength effects alone but may be due to calcium-kaolinite interactions. 

Phase diagrams of a polyacrylate-phosphonate system with temperature and calcium ion concentration can be established with turbidimetric measurements [1830]. Conductometric titrations also are suitable to characterize the phase behavior of scale inhibitors [514] (Table 7-2). 

Radenti et al. reported the corrosion rate of a typical potassium chloride fluid of 247 mils/year at 212°F. In contrast, they found by substituting potassium carbonate for potassium chloride, the corrosion rate was reduced to 3 mils/year t10 . Unfortunately, potassium carbonate is not optimum as a drilling fluid additive because it can produce massive amounts of calcium precipitation, may elevate the pH to undesirable levels, and in all cases reduces the calcium ion concentration to such a low level as to promote destabililzing cation exchange with clay minerals. 

The results are shown in Figures 6-5 and 6-6. Figure 6-5 depicts how the system evolves from its initial conditions to a repeatable oscillation about annual average conditions. This evolution is clearest for the calcium ion concentration, which rises toward twice the seawater value. Calcium does not quite reach twice the seawater value because it is removed from the system by the precipitation of calcium carbonate. The rise in calcium is a consequence of the evaporative concentration of the water s dissolved constituents. 

On the other hand, mercuric chloride decreased both spontaneous and evoked transmitter liberation at the frog neuromuscular junction [98] as well as the release of vasopressin from the pituitary gland [99] it was suggested that these effects are mediated via changes in the intracellular calcium ion concentration. 

As is often the case, tissue-specific control mechanisms operate to optimise adaptation to particular conditions. For example, muscle contraction requires an increase in cytosolic calcium ion concentration (see Section 7.2.1, Figure 7.4). During exercise when energy generation needs to be increased, or from a more accurate metabolic point of view, when the ATP-to-ADP ratio falls rapidly, and the accompanying rise in [Ca2 + ] activate (i) glycogen phosphorylase which initates catabolism of... 

In addition to the displacement of caldesmon, smooth muscle cell contraction requires kinase-induced phosphorylation of myosin. Smooth muscle has a unique type of myosin filament called p-light chains which are the target (substrate) for MLCK, but MLCK is only active when complexed with CaCM. Myosin light chain phosphatase reverses the PKA-mediated process and when cytosolic calcium ion concentration falls, CDM is released from CaCM and re-associates with the actin. The central role of calcium-calmodulin in smooth muscle contraction is shown in Figure 7.4. 

Just as Class III agents can exhibit positive inotropy, some positive inotropic agents demonstrate Class III electrophysiologic activity. The increase in intracellular calcium-ion concentration produced by the inotropic... 

Note that equation 5.2 is irreversible and the product AMP will require two phosphorylation steps to reconstitute the high-energy adenosine triphosphate, ATP. Inositol 1,4,5-triphosphate is an important molecule in the cytosol, where it releases calcium ions from storage. It forms part of a series of inositol-phosphate species that mediate calcium ion concentrations inside and outside the cell. 

After equilibrium, filtration, and pH adjustment, the residual calcium ion concentration was then titrated by EDTA solution. A higher residual calcium ion concentration indicates better inhibition activity and, therefore, more effectiveness in controlling calcium carbonate deposition in the treated water. As shown in Table III, at dosages of 1 to 5 ppm, the polyacrylic acid was more effective than the acrylic acid/N-(hydroxyalkyl)-acrylamide copolymers. 

The negative decadic (Le., base 10) logarithm of the calcium ion concentration. 

Glende EA, Recknagel RO. 1991. An indirect method demonstrating that CCh-dependent hapatocyte injury is linked to a rise in intracellular calcium ion concentration. Res Common Chem Pathol Pharmacol 73 41-52. 

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