Literature DB >> 9080382

Renal handling of guanidino compounds in rat and rabbit.

O Levillain1, B Marescau, P P De Deyn.   

Abstract

1. Guanidino compounds (GCs) have been quantified in different mammalian tissues such as brain, liver, muscle and kidney. The high anatomical heterogeneity of the kidney suggests that GCs could be unevenly distributed along the corticopapillary axis of the kidney in different species. 2. This study was designed to quantify twelve GCs in the different zones of rat and rabbit kidney. The kidneys were sliced and pieces of seven definite zones were weighed and homogenized for further GC extraction. GCs were determined by liquid chromatography. 3. The results indicate that: (1) GCs were unevenly distributed along rat and rabbit kidney; (2) qualitative and quantitative studies proved that each GC shows a particular distribution pattern along the corticopapillary axis for a given species; (3) in rats, alpha-keto-delta-guanidinovaleric acid, guanidinosuccinic acid, creatinine (CTN), methylguanidine and to a lesser extent gamma-guanidinobutyric acid increased steeply along the inner medulla in parallel to urea, whereas in rabbits, most of the GCs reached a plateau in the inner medulla and remained constant at this level; (4) gamma-guanidinobutyric acid was specifically found in the rat kidney; (5) argininic acid was higher in rabbit compared with rat kidney; (6) significantly higher levels of homoarginine were found in all zones of the rat kidney compared with the rabbit kidney. 4. The results suggest that: (1) GCs are mostly localized within the nephron segments; (2) an accumulation of GCs in the inner medulla might be explained either by a recycling process or by an intracellular storage as has been reported for urea, amino acids and organic osmolytes; (3) some GCs might be synthesized in nephron segments as reported for arginine (Arg) and guanidinoacetic acid (GAA); (4) several metabolic pathways of the GCs seemed to differ between rat and rabbit; (5) except for creatine, CTN, Arg and GAA, it seems unlikely that GCs might significantly increase the intracellular osmolality.

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Year:  1997        PMID: 9080382      PMCID: PMC1159327          DOI: 10.1113/jphysiol.1997.sp021949

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  33 in total

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Journal:  Biol Chem Hoppe Seyler       Date:  1996-02

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Authors:  S Natelson; J E Sherwin
Journal:  Clin Chem       Date:  1979-07       Impact factor: 8.327

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Journal:  Am J Med       Date:  1968-07       Impact factor: 4.965

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Journal:  Clin Chem       Date:  1971-05       Impact factor: 8.327

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Authors:  K Takemura; S Nagase; K Aoyagi; M Gotoh; A Koyama; M Narita
Journal:  Nephron       Date:  1994       Impact factor: 2.847

9.  N-methyl-D-aspartate receptor activation by guanidinosuccinate but not by methylguanidine: behavioural and electrophysiological evidence.

Authors:  R D'Hooge; A Raes; P Lebrun; M Diltoer; P P Van Bogaert; J Manil; F Colin; P P De Deyn
Journal:  Neuropharmacology       Date:  1996-04       Impact factor: 5.250

10.  Guanidino compound metabolism in rats subjected to 20% to 90% nephrectomy.

Authors:  O Levillain; B Marescau; P P de Deyn
Journal:  Kidney Int       Date:  1995-02       Impact factor: 10.612

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