Literature DB >> 426060

Kidney metabolite levels and ammonia production in acute acid-base alterations in the rat.

T A Boyd, L Goldstein.   

Abstract

Acute acid-base disturbances cause rapid changes in renal ammonia production in the rat. To investigate the regulation of ammonia production in acute acid-base stresses, we examined the effects of such conditions on tissue levels of metabolites such as alpha-ketoglutarate (KG), which inhibits kidney mitochondrial glutamine uptake and deamidation at physiological concentrations. In rats given low (5 mmol/kg) or high (20 mmol/kg) doses of NH4Cl by stomach tube or placed in a 10% CO2 atmosphere, kidney KG levels fell after 1-h by 44, 69, or 73%, respectively. NaHCO3 administration produced no change in KG levels. Renal glutamate and glutamine levels changed little, if at all, in any group, and renal phosphoenolpyruvate levels were not altered except for a decrease in the NH4HCO3 group. In livers of the same rats, treatments produced different patterns of metabolite changes; KG fell only in the NaHCO3 and NH4HCO3 groups. These results support the concept that KG is a specific regulator of renal ammonia production in acute acid-base stresses.

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Year:  1979        PMID: 426060     DOI: 10.1152/ajpendo.1979.236.3.E289

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  8 in total

1.  Transport and utilization of alpha-ketoglutarate by the rat kidney in vivo.

Authors:  M Martin; B Ferrier; G Baverel
Journal:  Pflugers Arch       Date:  1989-01       Impact factor: 3.657

2.  Ammonia metabolism during acid-base disturbance.

Authors:  D J O'Donovan
Journal:  Ir J Med Sci       Date:  1985-07       Impact factor: 1.568

3.  Properties of rat renal phosphate-dependent glutaminase coupled to Sepharose. Evidence that dimerization is essential for activation.

Authors:  R F Morehouse; N P Curthoys
Journal:  Biochem J       Date:  1981-03-01       Impact factor: 3.857

4.  Activation of oxoglutarate dehydrogenase in the kidney in response to acute acidosis.

Authors:  M Lowry; B D Ross
Journal:  Biochem J       Date:  1980-09-15       Impact factor: 3.857

5.  The effect of metabolic acidosis on the synthesis and turnover of rat renal phosphate-dependent glutaminase.

Authors:  J Tong; G Harrison; N P Curthoys
Journal:  Biochem J       Date:  1986-01-01       Impact factor: 3.857

6.  FNR regulates expression of important virulence factors contributing to pathogenicity of uropathogenic Escherichia coli.

Authors:  Nicolle L Barbieri; Bryon Nicholson; Ashraf Hussein; Wentong Cai; Yvonne M Wannemuehler; Giuseppe Dell'Anna; Catherine M Logue; Fabiana Horn; Lisa K Nolan; Ganwu Li
Journal:  Infect Immun       Date:  2014-09-22       Impact factor: 3.441

7.  A novel two-component signaling system facilitates uropathogenic Escherichia coli's ability to exploit abundant host metabolites.

Authors:  Wentong Cai; Yvonne Wannemuehler; Giuseppe Dell'anna; Bryon Nicholson; Nicolle L Barbieri; Subhashinie Kariyawasam; Yaping Feng; Catherine M Logue; Lisa K Nolan; Ganwu Li
Journal:  PLoS Pathog       Date:  2013-06-27       Impact factor: 6.823

8.  Transcriptional Control of Dual Transporters Involved in α-Ketoglutarate Utilization Reveals Their Distinct Roles in Uropathogenic Escherichia coli.

Authors:  Wentong Cai; Xuwang Cai; Yongwu Yang; Shigan Yan; Haibin Zhang
Journal:  Front Microbiol       Date:  2017-02-21       Impact factor: 5.640

  8 in total

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