Literature DB >> 10683162

Differential branchial and renal handling of urea, acetamide and thiourea in the gulf toadfish Opsanus beta: evidence for two transporters.

M D McDonald1, C M Wood, Y Wang, P J Walsh.   

Abstract

The possible presence of a urea transporter in the kidney of the gulf toadfish (Opsanus beta) and further characterization of the pulsatile facilitated transporter previously identified in its gills were investigated by comparing the extra-renal and renal handling of two urea analogues with the handling of urea. Toadfish were fitted with caudal artery and indwelling urinary ureteral catheters and injected with an iso-osmotic dose of (14)C-labelled urea analogue (acetamide or thiourea) calculated to bring plasma analogue concentrations close to plasma urea concentrations. Branchial permeabilities to urea, acetamide and thiourea were similar during non-pulsing periods and all increased during pulse events, although urea permeability was greater than analogue permeability during pulses. The incidence and magnitude of acetamide and urea pulses at the gills were significantly correlated, acetamide pulses being 35-50 % of the size of urea pulses. However, the thiourea and urea pulses at the gills were only weakly correlated, thiourea pulses being less than 16 % of the size of urea pulses. Thiourea inhibited branchial urea excretion by reducing the pulse frequency. The renal handling of thiourea and urea were similar in that both substances were more concentrated in the urine than in the plasma, whereas acetamide was found in equal concentrations in the urine and plasma. Urea and thiourea were secreted 2-3 times more effectively than Cl(-) and water, whereas acetamide was secreted at a similar relative rate. The differential handling of the urea analogues by the gills and kidney indicates the presence of a different, possibly unique, transporter in the kidney. The movement of thiourea and urea into the renal tubule against an apparent concentration gradient suggests the presence of an active transport mechanism.

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Year:  2000        PMID: 10683162     DOI: 10.1242/jeb.203.6.1027

Source DB:  PubMed          Journal:  J Exp Biol        ISSN: 0022-0949            Impact factor:   3.312


  7 in total

Review 1.  The physiology and evolution of urea transport in fishes.

Authors:  M D McDonald; C P Smith; P J Walsh
Journal:  J Membr Biol       Date:  2007-01-30       Impact factor: 1.843

2.  Embryonic development and metabolic costs in Gulf killifish Fundulus grandis exposed to varying environmental salinities.

Authors:  Charles A Brown; Fernando Galvez; Christopher C Green
Journal:  Fish Physiol Biochem       Date:  2012-01-18       Impact factor: 2.794

3.  Glucocorticoid receptors are involved in the regulation of pulsatile urea excretion in toadfish.

Authors:  M D McDonald; C M Wood; M Grosell; P J Walsh
Journal:  J Comp Physiol B       Date:  2004-10-28       Impact factor: 2.200

4.  Olfactory sensitivity of the gilthead seabream (Sparus auratus L) to conspecific body fluids.

Authors:  P C Hubbard; E N Barata; A V M Canário
Journal:  J Chem Ecol       Date:  2003-11       Impact factor: 2.626

5.  Crowding stress inhibits serotonin 1A receptor-mediated increases in corticotropin-releasing factor mRNA expression and adrenocorticotropin hormone secretion in the Gulf toadfish.

Authors:  Lea R Medeiros; Maria C Cartolano; M Danielle McDonald
Journal:  J Comp Physiol B       Date:  2013-12-21       Impact factor: 2.200

6.  A perfusion study of the handling of urea and urea analogues by the gills of the dogfish shark (Squalus acanthias).

Authors:  Chris M Wood; Hon Jung Liew; Gudrun De Boeck; Patrick J Walsh
Journal:  PeerJ       Date:  2013-02-12       Impact factor: 2.984

7.  Treatment with the selective serotonin reuptake inhibitor, fluoxetine, attenuates the fish hypoxia response.

Authors:  Jennifer M Panlilio; Sara Marin; Marissa B Lobl; M Danielle McDonald
Journal:  Sci Rep       Date:  2016-08-08       Impact factor: 4.379

  7 in total

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