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Alkaline tide

Bicarbonate ion (production catalysed by carbonic anhydrase) exits the cell on the basolateral surface, in exchange for chloride. The outflow of hicarhonate into hlood results in a slight alkalinity of the blood, known as the alkaline tide . [Pg.67]

Although the urine is usually acid, an alkaline urine may be secreted by subjects whose diet contains large amounts of vegetables and fruit which produce alkaline salts in the body. A slight temporary increase in the alkalinity of the blood and urine may also accompany the secretion of gastric juice and is known as the alkaline tide. An alkaline urine contains bicarbonate and the Na2HP04/NaH2P04 ratio is increased. The excretion of ammonium salts is reduced. [Pg.397]

E. No. Secretion of acid into the lumen of the stomach leaves the gastric venous blood with a raised concentration of bicarbonate, hence the slight alkaline tide after feeding. [Pg.160]

On 11 December 1823, at the Royal Society, William Front presented his landmark paper On the Nature of Acid and Saline Matters Usually Existing in the Stomach of Animals ". This presentation was unique in two ways. First, Front had specifically identified hydrochloric acid in the gastric juice of many species (man, dog, rabbit, horse, calf and hare), and second, he was able to quantify the free and total hydrochloric acid and chloride present. The acid was measured by neutralization with potash solution of known strength and the chloride by titration with silver nitrate. He also proposed that chloride may be secreted from blood to lumen by electrical means and that, when gastric acid was secreted, the blood would become alkaline (now recognized as the postprandial alkaline tide). More than 100 years were to elapse before his subsequent proposal was confirmed. [Pg.23]

Appearance.— Fresh urine is usually transparent, but may be opaque after meals owing to the alkaline tide causing a precipitation of calcium and magnesium phosphate (p. 395). As urine cools, a cloudy suspension of mucoprotein from the urinary tract may appear in the body of the fluid. [Pg.392]

The precipitation of these phosphates when urine is boiled is a common fallacy in the heat-coagulation test for proteins in urine. They can be distinguished from proteins by their solubility in acids. Earthy phosphates tend to precipitate whenever the H-ion value of urine falls below pH 6, and thus they appear during the alkaline tide after meals. [Pg.395]

Dry environmental quality PetroKlenz must be reconstituted with water and made into a slurry. The organisms will be ineffective if they are applied as dry cultures over the oil. The effective use of PetroKlenz in a biotreatment program is dependent upon the environmental conditions present at the site. Adverse conditions such as cold temperatures, oxygen, nitrogen, or phosphorus-deficient water, chemical toxic load, highly acidic or alkaline conditions, or excessive dilution of biomass by tides and currents, may retard or prevent biodegradation. [Pg.360]

Markers of bone resorption can be measured in serum or urine, whereas bone formation markers, such as bone-specific alkaline phosphatase, are usually measured in serum. Measurement of bone markers allows for real-time assessment of bone resorption or formation and can be used to monitor therapy (Ravn et al., 2003). The pyridonolines (deoxypyridinoline and pyridinoline) and the N- and C-teleopep-tides are the most frequently measured markers of bone resorption. Pyridinoline and teleopep-tides (NTx and CTx) are increased in individuals with metabolic bone diseases associated... [Pg.332]

The principal lipid constituent of the tubercle bacilli was a wax-like substance. Anderson obtained this by chloroform extraction of fat-free bacilli. The preliminary removal of lipids with alcohol and other solvents served to dissolve the free fatty acids, neutral fat and phospha-tides. The crude wax was fractionated with alcohol or acetone. The purified derivative was a white amorphous powder containing 0.41% nitrogen and 0.77% phosphorus. The substance was very resistant to acid hydrolysis. Continuous treatment with acidified alcohol resulted in very slow hydrolysis. Alkaline hydrolysis proceeded very rapidly, with the formation of ether-soluble components together with a water-soluble polysaccharide. [Pg.327]

The full cubic symmetry of the NaCl structure is retained in (a) high temperature defect structures with random distribution of vacancies, (b) solid solutions in which there is random arrangement of ions of two or more kinds in the anion and/or cation positions, and (c) crystals containing complex ions either if the complex ions have full cubic symmetry, as in [Co(NH3)6] [Tide], or if there is rotation or random orientation of less symmetrical groups, as in the high-temperature forms of alkaline-earth carbides, KSH, and KCN. In the latter cases the low-temperature forms have lower symmetry. [Pg.195]

Partial alkaline degradations have been used for the release of glycopep-tides from the hydroxyproline-rich cell wall glycoprotein(s). Lamport... [Pg.111]

In slightly alkaline medium, the macromolecules of nucleic acids are broken into fragments named ohgonucleo-tides, or even mononucleotides (often simply referred as nucleotide ) by advanced hydrolysis. These mononucleotides are, in fact, the structural blocks of the nucleic acids. [Pg.1604]

Musculoskeletal In ASSERT, a multicenter, open, 96-week study, 385 antiretroviral drug-naive adults with HIV infections were randomized to either abacavir -I- lamivudine or tenofovir-I-emtricitabine with efavirenz [60 ]. There was reduced bone mineral density in both groups, but to a greater extent with the latter (hip 1.9% versus 3.6% lumbar spine 1.6% versus 2.4%). Loss of at least 6% was more common in those who took tenofovir-I-emtricitabine (13% versus 3%). Markers of bone turnover (osteocalcin, procollagen 1, N-terminal propeptide, bone-specific alkaline phosphatase, and type 1 collagen cross-linked C telopep-tide) increased in both groups during the first 24 weeks and stabilized or improved thereafter, but without complete resolution. [Pg.455]

Alkaline phosphodiesterase 1 (EC 3.1.4.1) hydrolyses polyribonucleotides or oligodeoxyribonucleo-tides which have a free 3 -OH group, sequentiaUy U-berating 5 -nucleoside monophosphate (Khorana 1961). This enzyme has been recognised as a component of the plasma membrane of rabbit alveolar... [Pg.257]

So advanced were his ideas that in addition he proposed that chloride may be secreted from blood to lumen by electrical means and that, when gastric add was secreted, the blood would become alkaline (now recognized as the postprandial alteiline tide). AAore than 100 years were to elapse before his latter proposal was confirmed. [Pg.11]

The interaction of bare monovalent (alkah metals and coinage metals) and divalent (alkaline earth and zinc group metals) cations with the N7 site of piuine NA bases was examined in gas phase using MP2/6-31G(d,p)//HF/6-31G(d,p) level of theory (Burda et al. 1996). A graphical illustration of the dependence of the coordination distance on the atomic number of the cations is displayed in O Fig- 36-1. The intermolecular M-N7 distance monotonicaUy increase with the atomic numbers for the alkali metals and metals of alkaline earths (cf. O Fig. 36-1). This increase of the distances is more pronounced for the alkali metals where it exceeds 1 A. The calculated M-N7 distances for both types of metals correlate well with the known ionic radii, e.g.. Tide (1977). The influence of the relativity for the 5s and 5p electrons (Cs, Ba ) is not as pronounced as for the 5d electrons (Au, Hg ) (Pyykko 1988). [Pg.1280]

Alkaline hydrolysis of RNA, however, does not release the 5 -phosphates, but rather a mixture of 2 - and 3 -phosphates. This mixture arises because an intermediary cyclic 2, 3 -phosphodiester forms during hydrolysis. (Deoxyribonucleo-tides, of course, cannot form such cyclic 2, 3 -phosphates.) The cyclic phosphate finally opens up either to the 3 -monoester or the 2 -monoester. These isomers can be separated successfully by ion-exchange chromatography or paper chromatography. For the discussion of enzymic hydrolysis of nucleic acids, see Section 9 of this chapter. [Pg.117]


See other pages where Alkaline tide is mentioned: [Pg.725]    [Pg.724]    [Pg.725]    [Pg.454]    [Pg.807]    [Pg.52]    [Pg.416]    [Pg.160]    [Pg.20]    [Pg.20]    [Pg.25]    [Pg.393]    [Pg.725]    [Pg.724]    [Pg.725]    [Pg.454]    [Pg.807]    [Pg.52]    [Pg.416]    [Pg.160]    [Pg.20]    [Pg.20]    [Pg.25]    [Pg.393]    [Pg.214]    [Pg.319]    [Pg.5]    [Pg.54]    [Pg.724]    [Pg.976]    [Pg.101]    [Pg.93]    [Pg.356]    [Pg.640]    [Pg.288]    [Pg.430]   
See also in sourсe #XX -- [ Pg.50 ]

See also in sourсe #XX -- [ Pg.724 ]

See also in sourсe #XX -- [ Pg.397 ]

See also in sourсe #XX -- [ Pg.393 ]




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