Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound   Target Concepts: Gene/Protein Disease Symptom Drug Enzyme Compound

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Query: EC:3.1.3.1 (alkaline phosphatase)
47,916 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Osteoclasts were isolated from the long bones of chicks by a nylon mesh filtering system. The cell purity, in terms of area of the slide occupied, was on the average 77.5% osteoclasts, 22% aggregated osteoblasts and matrix debris, and 1.5% individual blood and marrow cells. Viability, as measured by cytochalasin-blockable phagocytosis, of up to 99% was obtained. Electron microscopic examination revealed good retention of ultrastructural features. The presence of carbonic anhydrase and acid phosphatase in osteoclasts was verified by selective staining methods; the aggregates were positive for alkaline phosphatase. Carbonic anhydrase activity was 0.89 +/- 0.13 X 10(-4) micro Wilbur-Anderson units per osteoclast, and red blood cells had 0.12 +/- 0.03 X 10(-4) units/cell. Neither calcitonin nor parathyroid hormone influenced the activity of carbonic anhydrase. A review of other hormonal effects on carbonic anhydrase is provided.
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PMID:Carbonic anhydrase activity in isolated osteoclasts. 642 28

Zinc in granulocytes, erythrocytes, serum, urine and zinc-dependent enzymes (alkaline phosphatase in serum and granulocytes, carbonic anhydrase in erythrocytes) were measured in patients with rheumatoid arthritis before and during penicillamine therapy for 6 months. The zinc concentration in serum, urine and erythrocytes increased, while granulocyte zinc decreased. Alkaline phosphatase activity in plasma remained unchanged, while alkaline phosphatase in granulocytes decreased. Carbonic anhydrase activity in erythrocytes decreased. None of the changes could be related to the activity of the disease.
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PMID:Changes in zinc and zinc-dependent enzymes in rheumatoid patients during penicillamine treatment. 643 44

The genetic structure of three Asiatic eskimos subpopulations (402 individuals), five coast chuckchies subpopulations (1793 individuals) and three reindeer chuckchies subpopulations (559 individuals) have been studied for 26 electrophoretic protein systems (33 loci). These are: adenilate-kinase (AK), diaphorase NAD X H (Dia), glyoxalase-1 (GLO-1), glucose-6-phosphate dehydrogenase (6GPT), glutamatpyruvate transaminase (GPT), glutamicoxalate transaminase (GOT), carbonic anhydrase-1 (Ca-1), catalase (Ct), acid phosphatase (AcP), lactate dehydrogenase (loci LDH-A and LDH-B), leucine aminopeptidase (Lap), malatedehydrogenase (MDH), purine nucleoside phosphorylase (PNP), superoxide dismutase (Sod), 6-phosphogluconate dehydrogenase (PGD), phosphoglucomutase (loci PGM1 and PGM2), cholinesterase (loci c1--c5), alkaline phosphatase (Pp), esterase D (EsD), red cell esterase (Est) - 4 loci, albumin (Alb), haptoglobin (Hp), hemoglobine (Hb A and B), group-specific component (Gc), transferrin (Tf), ceruloplasmin (Cp). In addition, AB0 and Rh system blood groups and phenyl thiocarbamide taste sensitivity (PTC) have been studied. 12 of 36 loci are polymorphic (33.33%), heterozygosity for all loci in eskimos, coastal and reindeer chuckchies being 0.118 +/- 0.005, 0.130 +/- 0.002 and 0.120 +/- 0.004, respectively. These estimates do not differ essentially from heterozygosity at these loci for mongoloid groups living further south. The test for interpopulation heterogeneity has permitted to estimate contribution of the loci to the differentiation of these populations. The least heterogeneity has been found at loci where gene frequency distribution is the most specific for these ethnic groups.
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PMID:[Genetic structure of the populations of native inhabitants in the northeastern USSR. III. Asiatic Eskimos and the coast and reindeer Chukchi]. 643 3

The ability of rat liver zinc-thionein to donate its metal to the apo-enzymes of the zinc enzymes horse liver alcohol dehydrogenase, yeast aldolase, thermolysin, Escherichia coli alkaline phosphatase and bovine erythrocyte carbonic anhydrase was investigated. Zinc-thionein was as good as, or better than, ZnSO(4), Zn(CH(3)CO(2))(2) or Zn(NO(3))(2) in donating its zinc to these apo-enzymes. Apo-(alcohol dehydrogenase) could not be reactivated by zinc salts or by zinc-thionein. Incubation of the other apo-enzymes with near-saturating amounts of zinc as ZnSO(4), Zn(CH(3)CO(2))(2), Zn(NO(3))(2), or zinc-thionein resulted in reactivation of the apo-enzymes. With apo-aldolase zinc-thionein gave 100% reactivation within 30min. Reactivation by ZnSO(4) and Zn(CH(3)CO(2))(2) was complete and instantaneous. Zinc-thionein was somewhat better than Zn(NO(3))(2) in completely reactivating apo-thermolysin. With apo-(alkaline phosphatase) 43% reactivation was obtained with Zn(CH(3)CO(2))(2) and 18% with zinc-thionein. With apo-(carbonic anhydrase) zinc-thionein was better than ZnSO(4), Zn(CH(3)CO(2))(2) or Zn(NO(3))(2), with a maximal reactivation of 54%. That zinc was really being transferred from zinc-thionein to apo-(carbonic anhydrase) was shown by the fact that 2,6-pyridine dicarboxylic acid and 1,10-phenanthroline had minimal effects on the reactivation of apo-(carbonic anhydrase) when added after the incubation {[apo-(carbonic anhydrase)+zinc thionein]+chelator}, but inhibited reactivation when added before the incubation {apo-(carbonic anhydrase)+[zinc-thionein+chelator]}. These observations support the idea that zinc-thionein can function in zinc homeostasis as a reservoir of zinc, releasing the metal to zinc-requiring metalloenzymes according to need.
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PMID:Reactivation in vitro of zinc-requiring apo-enzymes by rat liver zinc-thionein. 677 58

After application of SnCl2 and tin incorporated into baker's yeast, the effects on carbonic anhydrase (CA), glutathione peroxidase (GPx), lactate dehydrogenase (LDH), alkaline phosphatase (AP) and leucine aminopeptidase (LAP) were measured. The tin contents of liver and kidneys were determined. CA and GPx are not affected. AP and LAP are inhibited by high concentrations of tin (as SnCl2). Tin incorporated into yeast exerts no effect. Inorganic tin produces increases in liver and kidneys.
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PMID:[Effects of tin on rats. II. Comparison of the effects of tin (II) chloride and yeast-incorporated tin]. 677 55

A method of diagnosing trace metal deficiency is proposed. Measurement of an appropriate metalloprotein before and after administration of a physiological replenishment dose of the metal should distinguish low levels due to metal deficiency from those due to other mechanisms. Serum ceruloplasmin is the logical protein for copper assessment; serum alkaline phosphatase and red cell carbonic anhydrase should be considered for zinc.
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PMID:Diagnosis of trace metal deficiency--with emphasis on copper and zinc. 678 53

The activities of several enzymes - hydrolases, oxidoreductases and carbonic anhydrase - were demonstrated histochemically in the epithelial parenchyma of the human juxtaoral organ. Two characteristics enzyme-activity-patterns provided morphological distinction between two different forms of the juxtaoral organ, independently of the sex or age of the patient. Provisionally we have called them type I and type II. Type I showed a strong activity of alkaline phosphatase and carbonic anhydrase and low activity of non-specific esterases, whereas type II showed just the contrary. The enzyme activities in the epithelial parenchyma displayed obvious similarities to those of the duct cells of salivary glands but they were different from those of the oral mucosa studied. Only alkaline phosphatase of the enzymes demonstrated, showed activity in the epithelia of the juxtaoral organ but none in the oral mucosa or salivary glands. On account of the multiple nerve endings present, a receptor function is presumed for these, whereas the function of the epithelial parenchyma is still unknown.
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PMID:Enzyme-histochemistry of the juxtaoral organ in man ("organ of Chievitz"). 678 2

Clinical and experimental studies were performed on the mechanisms of metabolic acidosis observed in the children with epilepsy who had long been treated with anticonvulsants such as phenobarbital (PB) or diphenylhydantoin (DPH). The effect of the anticonvulsants was studied on the erythrocyte carbonic anhydrase isozymes (CA-B and CA-C) and on the calcium ion metabolism. The results obtained were as follows: (1) Ten cases with metabolic acidosis were found in 37 cases of epilepsy (27%). Hypocalcemia and high alkaline phosphatase activity in the serum were observed in the acidotic cases. The specific activity of erythrocyte CA-B isozyme was significantly lower in the acidotic cases as compared to those in nonacidotic cases or normal individuals, suggesting that the metabolic acidosis may bring about an inhibition of this enzyme. (2) In vitro experiments were performed to further study the effect of DPH on the erythrocyte CA-B and CA-C. Incubation of the enzymes with DPH resulted in an inhibition of their activities. Affinity binding of DPH to the enzymes was studied using a gel filtration method. The binding of DPH was not replaced by the presence of salicylate, indicating that the binding is non-specific. The addition of ethylenediamine tetraacetic acid did not show any influence on the binding, suggesting that the binding is not chelate-bound with zinc ion which locates at the active center of the enzyme. The binding of DPH was not competitive with respect to acetazolamide which is known to have an affinity for the active center of the enzyme. These results suggest that the binding site of DPH for the enzyme is in the vicinity of its active center, however definitely different from those of acetazolamide. PB was supposed to behave in the same manner as DPH for carbonic anhydrases. (3) This study lead to the conclusion that a long term treatment with PB or DPH specifically inhibits the activity of carbonic anhydrases in erythrocytes. The inhibition of the enzyme activity may result in the metabolic acidosis. Imbalanced calcium ion metabolism was supposed to be induced by the acidosis. The considerable care is requisite for a long-term treatment of anticonvulsants.
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PMID:[Studies on the mechanism of metabolic acidosis observed in the children treated with anticonvulsants]. 682 Jul 90

In this paper clinical similarities between sickle cell anemia patients and zinc deficient subjects, the latter as reported from the Middle East have been presented. Zinc levels in plasma, red cells, hair and neutrophils were decreased in our adult patients with SCA. The activities of certain zinc dependent enzymes such as plasma RNase, red cell carbonic anhydrase, leucocyte alkaline phosphatase, and deoxythymidine kinase activity in freshly synthesized collagen connective tissue were consistent with the concept that indeed zinc deficiency occurred in SCA patients. Zinc supplementation under controlled conditions showed that the SCA patients gained weight, their serum testosterone level increased and plasma ammonia level decreased. Finally, we also observed abnormal dark adaptation in some SCA patients which improved following zinc supplementation. Inasmuch as we have previously reported that the number of irreversible sickle cells decrease following zinc supplementation, we would like to suggest that zinc supplementation at earlier age may be benefical in preventing organ damage. In conclusion, zinc supplementation should be prescribed for patients with SCA, particularly if they show evidences for zinc deficiency.
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PMID:Zinc deficiency and effects of zinc supplementation on sickle cell anemia subjects. 729 Dec 6

Immortalized rat proximal tubule cell (IRPTC) lines should be useful for investigation of proximal tubule (PT) regulation and function but previously have been unavailable. We now report the establishment and characterization of an immortalized transformed, temperature-sensitive IRPTC cell line containing renin-angiotensin system (RAS) components. Primary PT cells prepared from male Wistar rats (4-5 wk old) after collagenase digestion, sieving, and Percoll gradient were cultured on collagen-coated T-75 flasks in Dulbecco's modified Eagle's medium containing 5% fetal calf serum. Subconfluent PT cells were transfected with the temperature-sensitive SV40 mutant viruses (tsA SV40) by direct exposure. After 7-8 wk, several clones were obtained, from which one has been characterized and designated as line 3-2. This cell line appears stable up to 45 passages. Clonal cells transformed with this virus exhibit a transformed phenotype at a permissive temperature of 34 degrees C and grow in multiple layers. When the cells are subsequently placed at a nonpermissive temperature of 41 degrees C, they return to morphology similar to that of untransformed cells of the same lineage. At either 34 degrees C or 41 degrees C, this cell line expresses a variety of PT markers including alkaline phosphatase, cytokeratin, carbonic anhydrase, and glucose transporter isoform 2 (GLUT2), while not expressing factor VIII. Uniquely, these cells also appear to express PT proteins gp330 and CHIP28, markers which are usually lost in cultured cells. Furthermore, the cell line expresses protein and mRNA components of RAS, including angiotensinogen, angiotensin converting enzyme, and renin. The IRPTC cell line expresses few angiotensin II (ANG II) receptors at 34 degrees C, the permissive temperature. However, at the nonpermissive temperature, 41 degrees C, IRPTC expresses ANG II receptor (dissociation constant of 0.7 nM; maximum binding capacity of 265 fmol/mg protein). ANG II (10(-8) M) induced a transient rise in cytoplasmic Ca2+ concentration, which was nearly abolished with losartan but not PD-123319, suggesting this finding is AT1 receptor mediated. This cell line should provide an excellent model of PT and should make it possible to study the cell and molecular biology of the RAS, as well as other regulatory systems of the PT.
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PMID:Temperature-sensitive SV40 immortalized rat proximal tubule cell line has functional renin-angiotensin system. 790 Aug 43


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