Does Pulsatile Urea Excretion Serve as a Social Signal in the Gulf Toadfish Opsanus beta?

2005 ◽  
Vol 78 (5) ◽  
pp. 724-735 ◽  
Author(s):  
Katherine A. Sloman ◽  
M. Danielle McDonald ◽  
John F. Barimo ◽  
Olivier Lepage ◽  
Svante Winberg ◽  
...  
2017 ◽  
Vol 171 ◽  
pp. 92-99 ◽  
Author(s):  
Jeremy Fulton ◽  
Christophe M.R. LeMoine ◽  
Carol Bucking ◽  
Kevin V. Brix ◽  
Patrick J. Walsh ◽  
...  

2000 ◽  
Vol 203 (15) ◽  
pp. 2357-2364 ◽  
Author(s):  
P.J. Walsh ◽  
M.J. Heitz ◽  
C.E. Campbell ◽  
G.J. Cooper ◽  
M. Medina ◽  
...  

Urea excretion by the gulf toadfish (Opsanus beta) has been shown in previous studies to be a highly pulsatile facilitated transport, with excretion probably occurring at the gill. The present study reports the isolation of an 1800 base pair (kb) cDNA from toadfish gill with one open reading frame putatively encoding a 475-residue protein, the toadfish urea transporter (tUT). tUT, the first teleostean urea transporter cloned, has high homology with UTs (facilitated urea transporters) cloned from mammals, an amphibian and a shark, and most closely resembles the UT-A subfamily. When expressed in Xenopus laevis oocytes, tUT increased urea permeability (as measured by [(14)C]urea uptake) five- to sevenfold, and this permeability increase was abolished by phloretin, a common inhibitor of other UTs. Northern analysis using the 1.8 kb clone was performed to determine the tissue distribution and dynamics of tUT mRNA expression. Of six tissues examined (gill, liver, red blood cells, kidney, skin and intestine), only gill showed expression of tUT mRNA, with a predominant band at 1.8 kb and a minor band at 3.5 kb. During several points in the urea pulse cycle of toadfish (0, 4, 6, 12 and 18 h post-pulse), measured by excretion of [(14)C]urea into the water, gill mRNA samples were obtained. Expression of tUT mRNA was found to be largely invariant relative to expression of beta-actin mRNA over the pulse cycle. These results further confirm the gill localization of urea transport in the toadfish and suggest that tUT regulation (and the regulation of pulsatile urea excretion) is probably not at the level of mRNA control. The results are discussed in the context of the mechanisms of vasopressin-regulated UT-A in mammalian kidney and morphological data for the toadfish gill.


Author(s):  
Maria C. Cartolano ◽  
Molly H.B. Amador ◽  
Velislava Tzaneva ◽  
William K. Milsom ◽  
M. Danielle McDonald

Author(s):  
Chris M. Wood ◽  
Justin M. Warne ◽  
Yuxiang Wang ◽  
M.Danielle McDonald ◽  
Richard J. Balment ◽  
...  

1995 ◽  
Vol 198 (7) ◽  
pp. 1559-1566 ◽  
Author(s):  
P Walsh ◽  
C Milligan

In order to elucidate further the cues for, and the biochemical mechanisms of, the transition to ureogenesis in the gulf toadfish Opsanus beta, experiments on the effects of feeding (i.e. nitrogen loading) were carried out. Baseline nitrogen excretion rates were first measured on solitary toadfish in large water volumes (i.e. unconfined conditions). These nitrogen excretion rates were higher, and had a higher proportion as ammonia (61 %), than previously published 'control' measurements. Feeding of unconfined toadfish elevated total nitrogen excretion approximately threefold, with little change in the proportion of urea versus ammonia. During the first 24 h of confinement of unfed toadfish, absolute levels of urea excretion remained constant while ammonia excretion rates fell to near zero, so that toadfish became 90 % ureotelic. When fed prior to confinement, urea excretion rates remained constant for the first 24 h, and the bulk of the nitrogen was excreted as ammonia (80 %); excretion of the excess dietary nitrogen took up to 48 h to complete. If pre-adapted to confinement and then fed, toadfish excreted only about 55 % of their nitrogenous waste as ammonia, and excretion of excess dietary nitrogen was completed by 24 h. Elevations of hepatic glutamine synthetase (GNS) activities accompanied confinement and were shown to be almost exclusively in the cytosolic compartment and to be correlated with a decrease in the ratio of hepatic levels of glutamate:glutamine. These GNS activity increases also appear to account in part for the decrease in the percentage of ammoniotely in toadfish under conditions of nitrogen loading after confinement. However, additional means of regulating total nitrogen excretion (e.g. changes in protein turnover rates) and the degree of ureogenesis versus ammoniogenesis (e.g. N-acetylglutamate stimulation of carbamoylphosphate synthetase) must be postulated to account fully for changes in nitrogen excretion rates and activation of ureogenesis under some circumstances.


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