Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0027819 (neuroblastoma)
 27,800 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A method using electronically excited oxygen for destruction of organic matter and atomic absorption spectrophotometry for the determination of beryllium, cadmium and tellurium in animal tissues is presented. Samples are solubilized in dilute aqua regia after being subjected to an oxygen plasma, low-temperature (less than 190 degrees C) ashing system for 20 to 30 hours. Recovery data from spiked NBS freeze-dried bovine liver indicate a quantitative determination for the three elements. Limits of detection in micrograms of element per milliliter of solubilized sample solution are: beryllium, 0.05; cadmium 0.05; and tellurium, 0.50. Beryllium, cadmium, and tellurium assay data are reported for the fresh tissues of albino rats exposed to inorganic chemicals by oral or intraperitoneal routes. The tissues analyzed include: adrenal, brain, femur, heart, kidney, liver, lung, mesenteric lymph node, pancreas, prostate, seminal vesicle, spleen, testicle, and tracheal-bronchial lymph node.
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PMID:Determination of beryllium, cadmium, and tellurium in animal tissues using electronically excited oxygen and atomic absorption spectrophotometry. 111 Dec 68

A semiautomated method consisting of digestion of animal feeds in a block digestor and determination of ammonia by ammonia-salicylate reaction has been studied collaboratively, along with the official final action Kjeldahl method, sec. 7.016. Each collaborator analyzed 16 feed samples, tryptophan, ammonium dihydrogen phosphate NBS standard, and ammonium sulfate primary standard. Statistical analysis showed that the 2 methods agreed. The semiautomated method has been adopted as official first action.
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PMID:Collaborative study of a semiautomated method for the determination of crude protein in animal feeds. 124 27

An automated macro Kjeldahl instrument determines per cent protein at the rate of 20 samples/hr. The methodology involved is similar to the present official final action Kjeldahl method, sec. 7.016. The 2 methods were compared in a collaborative study. Sixteen animal feeds, 4 meats, tryptophan, ammonium dihydrogen phosphate NBS standard, and ammonium sulfate primary standard were analyzed by the participating laboratories. The data were agreement between the 2 methods. The automated method has been adopted as official first action for the determination of crude protein in feeds, plants, and cereal foods.
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PMID:Collaborative study of an automated method for the determination of crude protein in animal feeds. 124 29

In order to investigate a possible role of lectin activity of ricin in its absorption from the small intestine, we prepared two ricin derivatives. BMH-ricin, prepared by crosslinking A and B chains of ricin with 1,6-bismaleimidohexane, was nearly non-toxic but the lectin activity was unaltered. And, NBS-ricin, prepared by the oxidation of tryptophanyl residues of ricin with N-bromosuccinimide, was not only non-toxic but also non-lectinic. After the oral administration of ricin derivatives to rats, their interaction with the digestive tract and absorption into the circulatory systems have been compared with those of ricin, immunochemically and histologically. It was shown by immunostaining that ricin and BMH-ricin could bind to the intestinal mucosa, whereas NBS-ricin could not. No appreciable damage in the small intestine from rats treated with either BMH-ricin or NBS-ricin has been observed, in contrast to ricin treatment where severe impairment of the small intestinal tissues resulted after 5 h. Immunoreactive ricin in the liver has been determined with the ricin enzyme immunoassay (EIA). When compared at 48 h after oral administration, NBS-ricin was not detected, whereas BMH-ricin was found to be 38 micrograms/liver and ricin 100 micrograms/liver. From these results, it was inferred that the lectin activity of ricin plays an important role in the absorption of ricin from the small intestine and that the absorption of ricin protein was enhanced by its high toxicity.
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PMID:Biochemical studies on oral toxicity of ricin. V. The role of lectin activity in the intestinal absorption of ricin. 139 37

Acquired resistance to doxorubicin and other anti-cancer drugs is generally dependent on gene amplification of a specific nucleotide sequence, the MDR1 gene. Verapamil, cyclosporin and other drugs have been used to circumvent the resistance in experimental models in vitro and/or in vivo. We have attempted to reverse the MDR phenotype by treating human adenocarcinoma resistant cells with 20 mers of synthetic unmodified oligodeoxynucleotide MDR1 antisenses. Five ODNs towards different mRNA regions and three different schedules of ODN antisense administration were tested. We found that FCS concentration greatly influenced the stability of ODN, whereas heat-inactivated FCS had no effect. The kinetics of ODN cellular uptake suggest the presence of a saturable receptor. Among the five antisense ODNs used, the most efficient was the oligomer (ODN-1) complementary to 20 bases upstream of the AUG initiation codon. No effect was observed with antisense complementary to the nucleotide binding sites. Administration of ODN-1 every 12 hr for 72 hr partially reversed the MDR phenotype. Approximately 60% of the cells lost their resistance to doxorubicin and did not form colonies in the presence of the drug. The MDR1 mRNA was transiently down-regulated so that the level of gp170 was slightly reduced. The incomplete switch off of MDR1 gene expression may be ascribed to the large abundance and great stability of MDR1 messenger RNA. Moreover, the inactivity of the two ODNs complementary to the NBS protein domains suggests that translation inhibition is ineffective. It is likely that ODN-4 and ODN-5 complement a large number of mRNAs competing for duplex formation, because these sequences are highly conserved among many proteins.
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PMID:An oligomer complementary to the 5' end region of MDR1 gene decreases resistance to doxorubicin of human adenocarcinoma-resistant cells. 144 3

The concentrations of cocaine and benzoylecgonine (BE) in Standard Reference Material (SRM) 1508, cocaine and metabolites in freeze-dried human urine, were determined at the National Institute of Standards and Technology (NIST, formerly NBS) by two independent methods. For cocaine, one method was based on gas chromatography/mass spectrometry (GC/MS); the other was based on high-performance liquid chromatography (HPLC). For BE, one method was based on GC/MS; the other was based on flow injection analysis/thermospray mass spectrometry (FIA/MS). The results for each pair of methods were statistically evaluated. Concentrations were determined in the SRM for three levels of cocaine and three levels of benzoylecgonine. Methylecgonine, although present in the material, was not determined. For cocaine, the concentrations were 90, 263, and 429 ng/mL of human urine. For BE, the concentrations were 103, 259, and 510 ng/mL of human urine.
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PMID:The certification of cocaine and benzoylecgonine in a human urine standard reference material. 152 7

The purpose of this study was to obtain normal hearing thresholds for an ER-3A insert earphone as a contribution for future standardization and for comparison with previous studies and interim ANSI and ISO insert earphone reference equivalent threshold sound pressure levels (RETSPLs). Hearing thresholds were obtained on each ear of 48 normal-hearing subjects from 125 to 8000 Hz using ER-3A and TDH-49P earphones referenced to a Bruel and Kjaer DB-0138 HA-2 and NBS-9A acoustic coupler, respectively. The mean unadjusted and adjusted ER-3A thresholds were in very good agreement with the mean thresholds averaged over eight other studies. Further, the mean adjusted ER-3A thresholds were in very good agreement with the interim ANSI RETSPLs while the mean unadjusted ER-3A thresholds were slightly higher than the ISO RETSPLs. Also, mean ER-3A thresholds averaged over a nine study data base were in closer agreement with the interim ANSI than the ISO RETSPLS. Overall, the interim ANSI insert earphone RETSPLs were recommended for clinical use.
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PMID:Reference threshold levels for an ER-3A insert earphone. 157 87

A total of 645 cotton mill operatives were administered a respiratory questionnaire. Of these, 85 (13.2%) complained of one or more work-related respiratory symptoms: 23 (3.6%) had byssinosis and the remaining 62 had symptoms not conforming to byssinosis (nonbyssinotic symptomatics, NBS). All byssinotic, 56 NBS, and 84 matched asymptomatic operatives underwent pulmonary function testing (FEV1 and FVC), skin testing to common allergens, and histamine bronchial challenge. Work area and personal breathing zone cotton dust concentrations were assessed, and a cumulative cotton dust exposure index was calculated for each individual. Byssinotic, NBS, and asymptomatic operatives all had reduced FEV1; observed mean liters (95% CI); predicted mean: byssinosis, 2.36 (2.09 to 2.63), 3.02; NBS, 2.94 (2.71 to 3.17), 3.29; and asymptomatic, 3.12 (2.95 to 3.29), 3.31. Only byssinotic subjects had evidence of impaired FVC: 3.31 (2.97 to 3.65), 3.69. The majority of byssinotic operatives (18 of 23) had bronchial hyperreactivity (BHR) in comparison with 21 of 56 NBS and 14 of 84 asymptomatic operatives. Mean log PD20 (95% CI) values were significantly lower in the byssinotic group -0.72 (-1.42, -0.02) than in NBS 0.57 (0.08, 1.06) and asymptomatic subjects 0.57 (-0.26, 1.39). The distribution of atopy did not differ significantly between groups, and lung function did not differ significantly between atopic and nonatopic subjects. The cumulative cotton dust exposure index was the only dust parameter to be significantly greater in those with BHR (mean mg-yr/m3 [95% CI] 14.13 [13.1 to 15.1]) than those with normal reactivity [5.35 (3.9 to 6.8)].
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PMID:Lung function, bronchial reactivity, atopic status, and dust exposure in Lancashire cotton mill operatives. 158 54

Although beta-D-fucosidase (beta-D-fucoside fucohydrolase, EC 3.2.1.38) has been isolated from various sources, the identity of this enzyme is still not settled. We have purified a specific beta-D-fucosidase in electrophoretically homogeneous form crude extracts of Aspergillus phoenicis by polyethyleneglycol 6000-phosphate buffer aqueous two-phase separation, and successive chromatography on DEAE-Sephadex A-50, hydroxyapatite and Sephadex G-100 columns. The molecular weight of the enzyme was estimated to be 57000 by SDS-polyacrylamide gel electrophoresis and 50000 to 60000 by gel filtration on Sephadex G-100. The enzyme showed optimum coside were 2.4mmol/L, and 1.28 mumol min-1 the pH range 5.5-6.5 and below 35 degrees C. The Km and the Vmax values for pNP-beta-D-fucoside were 2.4mmol/L, and 1.28 mumol.min-1.mg-1 respectively. The enzyme was strongly inhibited by sulfhydryl group reagents, PCMB-NEM and iodoacetate. It was also inhibited by EDC, DEP and NBS. Thus, -SH, -COOH groups, histidyl and tryptophyl residues were essential for enzyme activity. The purified beta-D-fucosidase showed high specificity toward p-nitrophenyl beta-D-fucoside. The enzyme was inhibited by D-fucose and D-fucono-gamma-lactone, but not by D-galactose, D-galactono-gamma-lactone, D-glucose or D-glucono-gamma-lactone; the latter compounds are specific inhibitors of beta-D-galactosidase and beta-D-glucosidase respectively. Thus, this enzyme is the most strictly specific beta-D-fucosidase when compared with those previously reported.
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PMID:[Studies on the beta-D-fucosidase from Aspergillus phoenicis]. 159 57

The ko-standardization method used in instrumental neutron activation analysis (INAA) was applied to the determination of some elements in geological and biological reference materials. We analyzed NBS SRM 1572 Citrus Leaves and SRM 1645 River Sediment and the CRM materials, IAEA Soil-7, SL-1, and MA-A-2. Comparison is made with reference values whenever available. Good agreement is found. The potential of the ko-standardization method in reactor INAA is discussed.
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PMID:Instrumental neutron activation analysis of geological and biological reference materials using the ko-standardization method. 170 19


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