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

---

Query: EC:3.2.1.31 (beta-glucuronidase)
7,680 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

An inhibitor of lysosomal acid cholesteryl ester hydrolase (Acid CEH), (EC 3.1.1.13) was found in the cytosolic fraction of rat liver and various other tissues. The extent of the inhibitory effect was dependent on the concentration of the cytosolic protein. The Acid CEH inhibitor was heat-labile, non-dialyzable, and its inhibitory activity significantly decreased by trypsin or chymotrypsin digestion, but not by lipase digestion. The inhibitor had no effect on the activity of cathepsin D, beta-glucuronidase and acid phosphatase, which are other enzymes found in lysosomes. The present findings suggest that the inhibitor may be involved in the regulation of the hydrolysis of cholesteryl esters in lipoproteins that have been transferred into the liver.
...
PMID:Characterization of a cytosolic protein inhibiting lysosomal acid cholesteryl ester hydrolase. 650 18

During gel filtration on Sephadex G-200 human cancerocerebral antigen (CCA) was eluted as two protein fractions with molecular mass of 135,000 and 270.000 daltons. Only one band of protein with molecular mass of about 15,000 daltons was noted after electrophoresis in 10% polyacrylamide gel containing SDS. As characteristic properties of CCA were recognized an electrophoretic polymorphism and a distinct trend to polymerization and isomeria. The antigen was not stained with dyes designed for staining base proteins, lipo-,glyco- and ferroproteins; CCA was thermostable (5 min at 80 degrees), it was inactivated by trypsin and protease but was resistant to pronase, hexokinase, alpha-amylase and beta-glucuronidase. A procedure was developed for isolation of CCA from brain, including fractionation with ammonium sulfate, ion exchange chromatography on DEAE-Sephadex A-50. The procedure enabled to obtain the CCA preparations suitable for radioimmunological, immunobiological assays and amino acid analyses.
...
PMID:[Isolation and physico-chemical characteristics of human cancerocerebral antigen]. 671 Sep 41

In 15 mongrel dogs acute experimental pancreatitis (AEP) was induced by injection of bile and trypsin into the pancreatic duct. After 12 hrs in lysosomal enriched subfraction of the liver in untreated group (N = 5) relative free activity of cathepsins (Cs), acid phosphatase (AP) and beta-glucuronidase (beta G) increased to 50,62, and 53% respectively in comparison to the healthy dogs (N = 6) : 19,43 and 20%. In dogs with AEP treated with prostacyclin (PGI2) in the dose of 20 ng/kg X min for 12 hrs these activities of Cs, AP and beta G were lowered to 30,55 and 41% in comparison with the untreated group. In dogs with AEP (N = 5) additionally pretreated during 1 hr before the induction of AEP with the same rate of PGI2 i.v. infusion, the relative free activity of enzymes was similar to the treated group. After two hrs incubation of lysosomal enriched subfraction in acidic medium (pH = 5,0), the highest values of relative free activity were observed in untreated group, the difference being more pronounced in comparison with control group than before incubation. In those animals treated and pretreated with PGI2, postincubation activities were much lower than in untreated dogs. These results suggest the stabilising effect of PGI2 on hepatic lysosomes, damaged during the course of AEP in dogs.
...
PMID:Prostacyclin (PGI2) stabilises hepatic lysosomes during acute experimental pancreatitis in dogs. 675 74

Enzymatic characterization of 48 Aeromonas hydrophila complex isolates from various sources was determined with the API ZYM system (Analytab Products, Plainview, N.Y.). All isolates lacked valine and cystine aminopeptidases, chymotrypsin, alpha-mannosidase, alpha-fucosidase, alpha-galactosidase, and beta-glucuronidase but possessed caprylate esterase-lipase, leucine aminopeptidase, acid phosphatase, phosphoamidase, and N-acetyl-beta-glucosidase. Variability was found in the presence of alkaline phosphatase, butyrate esterase, myristate lipase, trypsin, beta-galactosidase, alpha-glucosidase, and beta-glucosidase. No significant differences were evident among the enzymatic profiles of isolates from various sources.
...
PMID:Enzymatic characterization of Aeromonas hydrophila complex by the API ZYM system. 681 46

beta-Hexosaminidase, beta-glucuronidase, arylsulfatase, and tryptase were each released along with histamine from dispersed purified human lung mast cells of 40 to 80% purity by rabbit IgG anti-human IgE. The net per cent release ratio of each enzyme to histamine was determined over all doses of antibody employed to activate the mast cells and over all time points after activation, and indicated the per cent of each enzyme stored in secretory granules along with histamine. By multiplying the net per cent release ratio of each enzyme to histamine by total enzyme content in a preparation of 10(6) mast cells, values for secretory granule content per 10(6) mast cells were found to be 3.8 U for beta-hexosaminidase, 0.03 U for beta-glucuronidase, 0.03 U for arylsulfatase, and 0.9 U for tryptase. Subtype analysis of beta-hexosaminidase by diethylaminoethyl- (DEAE) cellulose chromatography revealed that the B isomer predominates in human mast cell secretory granules, whereas the A isomer predominates in secretory granules of the rat mast cell. Tryptase, the predominant neutral protease of the human mast cell secretory granule, has a m.w. of 130,000 by gel filtration chromatography, whereas the major neutral protease of the rat mast cell is chymotryptic and of 25,000 m.w. The presence of acid hydrolases, a tryptase, and histamine in human mast cell secretory granules suggests that the activated mast cell plays a direct role in the production of acute and subacute inflammation.
...
PMID:Acid hydrolases and tryptase from secretory granules of dispersed human lung mast cells. 700 36

Human blood-group A, B and O erythrocytes did not possess receptor sites for either crude or ether-ethanol extracted chlamydial soluble hemagglutinin. Sensitive chicken erythrocytes were agglutinated to higher titres by ether-ethanol extracted than by crude chlamydial hemagglutinin. Studies indicated that trypsin-, chymotrypsin-, neuramanidase-sensitive receptor sites were not essential for binding of ether-ethanol extracted chlamydial hemagglutinin; neither were beta-glucuronidase- nor periodate-sensitive receptor sites essential. Since soluble chlamydial hemagglutinin consists of components of host cells and that of chlamydiae purification of hemagglutinin from chlamydiae is required in future studies.
...
PMID:C. psittaci 6 BC soluble hemagglutinin: factors influencing the red cell receptor sites. 702 29

Samples of blood, liver and brain taken from 13 cases of fatal poisoning with barbiturates, antidepressants, phenothiazines and anticonvulsants were digested with trypsin and beta-glucuronidase. The concentrations of drugs were higher in hydrolyzed livers in barbiturate and phenothiazine poisonings. In the case of diazepam, phenytoin, carbamazepine, amitriptyline, imipramine and chloroprothixene poisonings the results obtained after enzymic hydrolysis were the same or worse than in controls. The blood levels of drugs in non-fatal poisonings with diazepam, doxepin and chlorpromazine were similar in samples digested with trypsin and in controls. All samples were extracted with Amberlite XAD-2 resin by XAD-2 Bag technique.
...
PMID:Enzymic hydrolysis of tissues before XAD-2 extraction in poisoning cases. 709 74

Rat embryo fibroblast suspensions were prepared from 19-day-old wistar rat fetuses by trypsin digestion of the minced fetal tissue. Drug-metabolizing capability of isolated viable rat embryo cells on 7-ethoxycoumarin and 1,3-cyclohexadiene has been investigated. The biotransformation of 7-ethoxycoumarin represents a suitable experimental tool to measure the level and significance of the Phase I and Phase II metabolism systems. We estimated the mixed-function oxidation by the fluorimetric measurement of "unconjugated" 7-hydroxycoumarin in the incubation medium while the conjugates formation was determined by subsequent hydrolysis with beta-glucuronidase and aryl sulphatase. 1,3-Cyclohexadiene was selected as a substrate for mixed-function oxidation for a useful comparison of drug-metabolizing capability in isolated viable rat embryo cells with rat hepatocytes. When 1,3-cyclohexadiene was incubated with rat embryo fibroblasts for different times, cyclohexene-1,2-diol resulted to be the main metabolite. Cyclohexene-1,4-diol was detected only in traces. Therefore the metabolic pathway of 1,3-cyclohexadiene with rat embryo cells, as well as isolated hepatocytes, involves the intermediate formation of the 3,4-epoxycyclohexene, that is rapidly hydrolyzed to diols by a non enzymatic process.
...
PMID:[Determination of metabolizing activities of xenobiotic tissue in rat embryo fibroblasts]. 713 88

Thirty strains of Propionibacterium acnes were grown in basal salt medium containing lecithin as a lipid substrate and in other media. The cultures were assayed for production of lipase (measured as fatty acid esterase) and other exoenzymes. Lipase was assayed spectrophotometrically; other enzymes were assayed using the API ZYM system (Analytab Products Inc., Plainview, NY). Substance for lipase were alpha- and beta-naphthol esters of propionic, butyric, valeric, caprylic, lauric, myristic, and oleic acids. All strains showed fatty acid esterase activity. Using the API ZYM system 19 enzymes were detected, 8 of which were found frequently and had high activity in most strains. Acid and alkaline phosphatases, phosphoamidase, ester lipase, trypsin-chymotrypsin-like proteases, beta-glucuronidase (80%), beta-galactosidase (80%), and N-acetyl-beta-glucosaminidase were found. Many enzymes of P. acnes appear to be adaptive, dependent on the culture substrate.
...
PMID:Exoenzymes of Propionibacterium acnes. 717 37

The features and function of IgM-FcR of rat peritoneal macrophages were studied. Macrophages specifically bind and phagocytose ox red blood cells coated with rat IgM (EA-IgM) through a specific receptor. This receptor is trypsin sensitive and its activity requires Ca++ ions. Both sodium azide and low temperature (4 degrees) inhibit the bindings as well as ingestion of EA-IgM by macrophages, suggesting the metabolically dependent character of the interaction between EA-IgM and macrophages. Colchicine inhibits the binding of EA-IgM by macrophages. Similarly, the ingestion of EA-IgM was also inhibited when peritoneal exudate cells (PEC) were pre-treated with colchicine or vinblastine or cytochalasin B. It is suggested that cytoskeletal elements of macrophages play an important role both in the binding of EA-IgM to their receptors and in the subsequent internalization of the receptor-ligand complexes. Ingestion of soluble IgM antibodies containing immune complexes (IC) resulted in a release of beta-glucuronidase from macrophages.
...
PMID:IgM-Fc receptor-mediated phagocytosis of rat macrophages. 720 29


<< Previous 1 2 3 4 5 6 7 Next >>

---