Related Experiment Videos
Organic cation secretion by Cancer borealis urinary bladder
The American Journal of Physiology
|January 1, 1987
Summary
Crabs possess a potent renal excretory system for organic cations like tetraethylammonium (TEA). Their urinary bladders actively secrete TEA via a carrier-mediated transcellular pathway.
Area of Science:
- Marine biology
- Comparative physiology
- Renal physiology
Background:
- The model organic cation tetraethylammonium (TEA) serves as a probe for studying renal transport mechanisms.
- Previous studies indicated a potent renal excretory system in the crab Cancer borealis.
Purpose of the Study:
- To investigate the mechanisms of tetraethylammonium (TEA) transport in the urinary bladder of Cancer borealis.
- To characterize the cellular and molecular pathways involved in TEA secretion and reabsorption.
Main Methods:
- Clearance studies were performed to measure TEA excretion rates.
- Uptake studies using urinary bladder slices assessed TEA transport kinetics.
- Flux measurements in mounted bladders quantified secretory and reabsorptive fluxes.
- Inhibitor studies with quinine and N1-methylnicotinamide chloride were conducted.
Main Results:
- Cancer borealis demonstrated a potent renal excretory system for TEA, with clearance significantly exceeding polyethylene glycol clearance.
- Urinary bladder uptake of TEA was concentrative, saturable, and dependent on glycolysis.
- Bladders exhibited a large net secretory flux for TEA, with a high secretory to reabsorptive flux ratio.
- Secretory transport was concentrative and sensitive to quinine, while reabsorptive transport was not.
Conclusions:
- The urinary bladder of Cancer borealis employs a transcellular pathway for TEA transport, mediated by carriers at both serosal and luminal membranes.
- This study elucidates the complex transport mechanisms of organic cations in marine invertebrates, providing insights into renal function.
- Similar TEA secretion mechanisms were observed in Cancer irroratus and Homarus americanus, suggesting conserved pathways in crustaceans.