1988
DOI: 10.1093/clinchem/34.1.91
|View full text |Cite
|
Sign up to set email alerts
|

Liquid-chromatographic profiling of solutes in serum of uremic patients undergoing hemodialysis and chronic ambulatory peritoneal dialysis (CAPD); high concentrations of pseudouridine in CAPD patients.

Abstract: Using "high performance" liquid chromatography, we studied non-protein-bound fractions and total concentrations of 18 solutes accumulating in sera from a group of 12 patients who were undergoing chronic ambulatory peritoneal dialysis (CAPD) and in predialysis sera from a group of 15 hemodialysis (HD) patients. We monitored longitudinal changes in solute concentrations for two patients with respect to change of therapy between HD and CAPD. The concentrations of pseudouridine (P less than 0.001), uric acid (P le… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

1
8
0

Year Published

1988
1988
2004
2004

Publication Types

Select...
7
1

Relationship

2
6

Authors

Journals

citations
Cited by 22 publications
(9 citation statements)
references
References 3 publications
1
8
0
Order By: Relevance
“…Pseudouridine (⌿), 1-methyladenosine (m 1 A), 1-methylinosine (m 1 I), 1-methylguanosine (m 1 G), N 4 -acetylcytidine (ac 4 C), N 2methylguanosine (m 2 G), adenosine (A), N 6 -methyladenosine (m 6 A), allopurinol ribonucleoside (APR), 3-methyluridine (m 3 U) and 5-bromouridine (br 5 U) were obtained from Sigma Chemical Co. (St. Louis, MO, USA). Uridine (U), guanosine (G) and cytidine (C) were obtained from Kohjin Co. (Tokyo, Japan), and xanthosine (X) from Nakarai Chemical Co. (Kyoto, Japan).…”
Section: Chemicalsmentioning
confidence: 99%
See 1 more Smart Citation
“…Pseudouridine (⌿), 1-methyladenosine (m 1 A), 1-methylinosine (m 1 I), 1-methylguanosine (m 1 G), N 4 -acetylcytidine (ac 4 C), N 2methylguanosine (m 2 G), adenosine (A), N 6 -methyladenosine (m 6 A), allopurinol ribonucleoside (APR), 3-methyluridine (m 3 U) and 5-bromouridine (br 5 U) were obtained from Sigma Chemical Co. (St. Louis, MO, USA). Uridine (U), guanosine (G) and cytidine (C) were obtained from Kohjin Co. (Tokyo, Japan), and xanthosine (X) from Nakarai Chemical Co. (Kyoto, Japan).…”
Section: Chemicalsmentioning
confidence: 99%
“…Pseudouridine derived predominantly from tRNA is not catabolized but excreted in urine as the intact molecule. The serum level of pseudouridine has been reported to be increased in uremic patients [3][4][5][6], especially when they are undergoing continuous ambulatory peritoneal dialysis (CAPD) [4]. Further analytical study on the metabolism of modified ribonucleosides in uremic patients is required to shed light on their possible roles as uremic toxins.…”
mentioning
confidence: 99%
“…HPLC. This was performed as described previously (10,11). A column of "Ultrasphere Octyl" (C8-modifled silica), 4.6 mm (i.d.)…”
Section: Methodsmentioning
confidence: 99%
“…Twentytwo characteristic uremic solutes in sera of dialyzed and non-dialyzed uremic patients were subjected to principal component analysis, in order to explore interdependencies between these concentrations and their distribution in different patients. These ultraviolet-absorbing and (or) fluorescent solutes were analyzed by gradient-elution high-performance liquid chromatography (HPLC) as described previously (10,11).…”
mentioning
confidence: 99%
“…Organic acids in uremic serum can be analyzed, as a group, by use of temperature-programmed gas chromatography (17,18) or "high-performance" liquid chromatography (HPLC) with gradient-elution (9,(19)(20)(21), both of which are relatively time-consuming procedures. Specific analysis for HA has also been done colorimetrically (22) in the injected calibration solutions of 0, 12.5, 25, 50, and 125 p.moIJL for CZE analysis and 0, 25, 50, 100, and 250 p.moliL for HPLC analysis.…”
Section: Renal Function Tubular Secretion Anion Gap Uremic Toxins Hplc Compared Solvent Effectmentioning
confidence: 99%