sodium-nitrite and sodium-sulfite

sodium-nitrite has been researched along with sodium-sulfite* in 2 studies

Other Studies

2 other study(ies) available for sodium-nitrite and sodium-sulfite

ArticleYear
Analysis of 6R- and 6S-tetrahydrobiopterin and other pterins by reversed-phase ion-pair liquid-chromatography with fluorimetric detection by post-column sodium nitrite oxidation.
    Journal of chromatography, 1993, Aug-11, Volume: 617, Issue:2

    A rapid and sensitive reversed-phase ion-pair liquid chromatographic system with fluorimetric detection by post-column sodium nitrite oxidation was established for measuring six pterin compounds (6R-5,6,7,8-tetrahydrobiopterin, 6S,5,6,7,8-tetrahydrobiopterin, 7,8-dihydrobiopterin, biopterin, pterin and D-neopterin). The coefficients of variation for these pterins were 0.705-3.714%, and the minimum detectable amount was ca. 10-20 pg at a signal-to-noise ratio of 3. A linear detector response was also verified. The concentrations of the pterin compounds in rat tissues were measured by the described method. Furthermore, by means of brain microdialysis, the output of pterin compounds from rat striatum was detected. Therefore, these results demonstrate that this system can be applied to analyses not only of various rat tissues but also of dialysates collected in vivo.

    Topics: Animals; Biopterins; Brain Chemistry; Chromatography, High Pressure Liquid; Corpus Striatum; Ions; Liver; Male; Microdialysis; Oxidation-Reduction; Pterins; Rats; Rats, Inbred F344; Reproducibility of Results; Sodium Nitrite; Spectrometry, Fluorescence; Sulfites; Temperature

1993
Selective reduction of fatty acid oxidation in colonocytes: correlation with ulcerative colitis.
    Lipids, 1990, Volume: 25, Issue:10

    Attempts were made to define which fatty acid (2:0 to 18:1) was optimally oxidized by isolated colonocytes (colonic epithelial cells) and to select inhibitors of fatty acid oxidation which would be analogous in their action to the inhibition of fatty acid oxidation observed in colonocytes involved with ulcerative colitis. Isolated colonic epithelial cells of Sprague-Dawley rats were used with 2-mercaptoacetate, dichloroacetate, 3-mercaptopropionate, 4-mercaptobutyrate, 4-sulfatebutyrate, 2-bromobutyrate, sulfite ions and nitrite ions. n-Butyrate (4:0) was maximally oxidized to CO2 and ketone bodies (mean value 5.46 mumols/min/g dry wt). Oxidation of butyrate to CO2 was diminished by 2-bromobutyrate, sulfite ions and all mercapto fatty acids. Both fatty acid oxidation and glucose oxidation were significantly inhibited by 2-bromobutyrate, while mercapto fatty acids and sulfite inhibited fatty acid oxidation (p less than 0.01) without significantly changing glucose oxidation. Observation with 2-mercaptoacetate and sulfite correlate with early changes of fatty acid oxidation observed in cases of ulcerative colitis, and warrant further study with isolated colonocytes of man.

    Topics: 3-Mercaptopropionic Acid; Animals; Butyrates; Butyric Acid; Carbon Dioxide; Colitis, Ulcerative; Colon; Epithelium; Fatty Acids; Glucose; Ketone Bodies; Oxidation-Reduction; Rats; Rats, Inbred Strains; Sodium Nitrite; Sulfites; Thioglycolates

1990