Literature DB >> 1640263

The splanchnic organs, liver and kidney have unique roles in the metabolism of sulfur amino acids and their metabolites in rats.

R A Garcia1, M H Stipanuk.   

Abstract

The arterial-venous differences for methionine and cysteine and their metabolites, glutathione, taurine and sulfate, were measured across the splanchnic organs, the liver, the kidney and the hindlimb of fed rats. Methionine and cysteine were released into the blood by the splanchnic organs and removed by the liver. These results indicate that more than half of the sulfur amino acids taken up by the liver were used for synthesis of glutathione for export into the plasma. The kidney removed about half of the glutathione exported by the liver, presumably due to action of gamma-glutamyl transpeptidase and dipeptidase, and released to the circulation a comparable amount of cysteine. Taurine, presumably from deconjugation of bile acids, was released into the plasma by the splanchnic organs; taurine was also released by the liver. The hepatosplanchnic release of taurine into the plasma indicates that the liver is the major site of taurine biosynthesis; taurine was removed by the kidney for excretion in the urine. A small amount of methionine was removed by the kidney, and the hindlimb released a small amount of glutathione and methionine into the plasma. The splanchnic organs seemed to remove substantial sulfate from the plasma in addition to that provided by the diet, and a net release of sulfate from the liver was observed. The relative roles of the various tissues in sulfate production and removal was not clear from these studies, due to the large variability in the arterial-venous differences observed.

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Year:  1992        PMID: 1640263     DOI: 10.1093/jn/122.8.1693

Source DB:  PubMed          Journal:  J Nutr        ISSN: 0022-3166            Impact factor:   4.798


  14 in total

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Review 2.  Redox Regulation via Glutaredoxin-1 and Protein S-Glutathionylation.

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3.  Extrahepatic tissues compensate for loss of hepatic taurine synthesis in mice with liver-specific knockout of cysteine dioxygenase.

Authors:  Iori Ueki; Heather B Roman; Lawrence L Hirschberger; Carolyn Junior; Martha H Stipanuk
Journal:  Am J Physiol Endocrinol Metab       Date:  2012-03-13       Impact factor: 4.310

Review 4.  Colonic sulfide in pathogenesis and treatment of ulcerative colitis.

Authors:  W E Roediger; J Moore; W Babidge
Journal:  Dig Dis Sci       Date:  1997-08       Impact factor: 3.199

5.  Regulation of cysteine dioxygenase degradation is mediated by intracellular cysteine levels and the ubiquitin-26 S proteasome system in the living rat.

Authors:  John E Dominy; Lawrence L Hirschberger; Relicardo M Coloso; Martha H Stipanuk
Journal:  Biochem J       Date:  2006-02-15       Impact factor: 3.857

Review 6.  Dealing with methionine/homocysteine sulfur: cysteine metabolism to taurine and inorganic sulfur.

Authors:  Martha H Stipanuk; Iori Ueki
Journal:  J Inherit Metab Dis       Date:  2010-02-17       Impact factor: 4.982

Review 7.  Role of the liver in regulation of body cysteine and taurine levels: a brief review.

Authors:  Martha H Stipanuk
Journal:  Neurochem Res       Date:  2004-01       Impact factor: 3.996

8.  Iodothyronine deiodinase activity in methionine-deficient rats fed selenium-deficient or selenium-sufficient diets.

Authors:  Z Zhu; M Kimura; Y Itokawa
Journal:  Biol Trace Elem Res       Date:  1995-05       Impact factor: 3.738

9.  Sulfur Metabolism Under Stress.

Authors:  Colin G Miller; Edward E Schmidt
Journal:  Antioxid Redox Signal       Date:  2020-08-14       Impact factor: 8.401

10.  Enzymes of the taurine biosynthetic pathway are expressed in rat mammary gland.

Authors:  Iori Ueki; Martha H Stipanuk
Journal:  J Nutr       Date:  2007-08       Impact factor: 4.798

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