𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The energetics of osmotic regulation in ureotelic and hypoosmotic fishes

✍ Scribed by Kirschner, Leonard B.


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
898 KB
Volume
267
Category
Article
ISSN
0022-104X

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The major mechanisms of urea turnover and of active ion transport in osmoregula‐ tory organs are reviewed. Using published values for the molecular flow through these systems it is possible to estimate the energetic cost of osmotic regulation in hyporegulating marine teleosts and in ureotelic elasmobranchs. Oxygen consumption dedicated to osmotic regulation in the flounder (Platichthys flesus) is about 7 ml kg^βˆ’1^ hr^βˆ’1^ and in the rainbow trout (Salmo gairdneri) 6 ml kg^βˆ’1^ hr^βˆ’1^ For a dogfish (Scyliorhynus canicular) it was 5 ml kg^βˆ’1^ hr^βˆ’1^ and for the skate (Raja erinacea) 5 or 11 ml kg^βˆ’1^ hr^βˆ’1^ based on two values for urea loss by the fish. Both groups of fish used 10–15% of their standard metabolism for osmotic regulation. There are a number of uncertainties that may require modification of these values. It is not known whether TMAO lost by ureotelic regulators is replaced by ingestion or by synthesis. If by synthesis, the cost of regulation would be higher than calculated. Even more serious is the uncertainty regarding the use of organic osmolytes to maintain equilibrium between cells and blood. This strategy almost certainly requires some energy input, but there is insufficient information to permit its quantitative estimation, so the factor was omitted from the calculation. Among hyporegulators the sole unknown is whether the esophagus may absorb some of the ingested salt by diffusion. If so, it would decrease the energy expended in the intestinal tract and lower the total cost of regulation. The conclusion, based on known factors for the species examined, is that both modes are about equally efficient. If it becomes possible to factor in the unknowns it may be that hyporegulation is slightly more economical than ureosmotic. Β© 1993 Wiley‐Liss, Inc.


πŸ“œ SIMILAR VOLUMES


Osmotic regulation of the heat shock res
✍ Anna Kordelia Kurz; Freimut Schliess; Prof. Dr. Dieter HΓ€ussinger πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 363 KB

The influence of cell hydration and taurine on the heat shock response was studied in primary rat hepatocytes. Heat-induced accumulation of inducible heat shock protein 70 (HSP70) mRNA and protein was increased under hypoosmotic conditions. In contrast, hyper-osmotic exposure blocked the HSP70 respo

Regulation of proline synthesis during o
✍ Burton, Ronald S. πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 727 KB

## Abstract The marine copepod __Tigriopus californicus__ shows rapid adjustment of intracellular proline and alanine pools in response to salinity stress. Small increases in salinity (on the order of 2 ppt or 50 mOsmoles) are sufficient to elicit proline synthesis in animals acclimated to 50% seaw

Energetics of osmoregulation: II. water
✍ Kidder, George W. ;Petersen, Christopher W. ;Preston, Robert L. πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 256 KB

## Abstract Teleost fish experience passive osmotic water influx in fresh water (FW) and water outflux in salt water, which is normally compensated by water flow driven by active ion transport mechanisms. Euryhaline fish may also minimize osmotic energy demand by β€œbehavioral osmoregulation”, seekin

Channels, pumps, and exchangers in the g
✍ PERRY, S.F. ;Shahsavarani, A. ;Georgalis, T. ;Bayaa, M. ;Furimsky, M. ;Thomas, S πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 170 KB

## Abstract In freshwater fishes, the gill and kidney are intricately involved in ionic and acid‐base regulation owing to the presence of numerous ion channels, pumps, or exchangers. This review summarizes recent developments in branchial and renal ion transport physiology and presents several mode