Endogenous purine and pyrimidine derivative excretion in pregnant sows

The present experiment was camed out to study the endogenous losses of purine and pyrimidine derivatives from pregnant sows. Three pregnant and three non-pregnant Large White x Landrace sows were fed on a purine-free diet composed of starch, glucose, sucrose and vegetable oil, with casein as the pro...

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Detalles Bibliográficos
Autores: Martin-Orúe, S. M., Balcells Terés, Joaquim, Guada, J. A., Castrillo, C.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:1995
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10459.1/64892
Acceso en línea:https://doi.org/10.1079/BJN19950040
http://hdl.handle.net/10459.1/64892
Access Level:acceso abierto
Palabra clave:Purine derivatives
Pseudouridine
Pregnancy
Sow
Descripción
Sumario:The present experiment was camed out to study the endogenous losses of purine and pyrimidine derivatives from pregnant sows. Three pregnant and three non-pregnant Large White x Landrace sows were fed on a purine-free diet composed of starch, glucose, sucrose and vegetable oil, with casein as the protein source. The experiment began, for the six animals, after diagnosis of pregnancy and was divided into six 12 d periods. Urine was collected during the Arst 3 d of each experimental period by means of a urethral catheter for determination of allantoin, uric acid, xanthine, hypoxanthine and pseudouridine concentrations. In the absence of dietary nucleic acids (NA), allantoin and, as a consequence, excretion of total purine derivatives (PD) decreased significantly to a constant value (128.3 (SE 7.07) ,umol/kg metabolic live weight (W"75) per d), an amount assumed to represent endogenous excretion. Excretion of uric acid (38.7 (SE 2-15) mollkg W0'p7e5r d), hypoxanthine (21.0 (SE 2.58) ymollkg W'75 per d) and xanthine (11-2 (SE 0.83) pmol/kg W@" per d) were not affected by the experimental treatment, although there was a significant decrease in hypoxanthine excretion in pregnant sows (from 25.5 to 5.2 pnol/kg W@75 per d) compared with nowpregnant sows (from 26.7 to 44%/rmol/kg W@75p er d). Creatinine excretion was not affected by pregnancy and was used as an internal urinary marker. Purine excretion, either expressed as pmol/kg WoT5 per d or as the ratio PD:creatinine, was not affected by experimental treatment, although an apparent increase in pseudouridine excretion, a modified unsalvageable catabolite of RNA-pyrimidine, was found in late pregnancy (3.6 v. 5.2 mo1/100 mol creatinine in non-pregnant sows compared with pregnant sows at 102 d collection).