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Localization of barriers to water flow in toad urinary bladder
1Department of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461.
Biology of the Cell
|January 1, 1989
Summary
Vasopressin (ADH) affects water permeability in toad bladders. Only reduced bladder volume, not CO2 or ADH stimulation, altered postluminal water flow, indicating a specific regulatory site.
Area of Science:
- Cell biology
- Renal physiology
- Membrane transport
Background:
- Vasopressin (ADH) is known to increase water permeability in toad bladder granular cells.
- Recent studies suggest a
- postluminal
- regulatory site in addition to the luminal membrane.
- Freeze-fracture electron microscopy shows particle aggregates on the luminal membrane, believed to mediate water transport.
Purpose of the Study:
- To differentiate between changes in luminal membrane aggregate permeability and a postluminal barrier.
- To investigate the effect of specific experimental protocols on water permeability regulation in toad bladders.
Main Methods:
- Paired toad bladders were used to study three protocols altering vasopressin-stimulated water flow.
- Amphotericin B was used to create water-permeant channels in the luminal membrane to estimate postluminal barrier permeability.
- Protocols included diminishing bladder filling volume, increasing PCO2, and repeated vasopressin stimulation.
Main Results:
- Diminishing bladder filling volume decreased water flow elicited by amphotericin B, indicating reduced postluminal barrier permeability.
- Increasing PCO2 and repeated vasopressin stimulation did not alter amphotericin B-elicited flow, suggesting no change in postluminal barriers.
- These results dissociate aggregate frequency from changes in water permeability.
Conclusions:
- Reduced bladder filling volume specifically impacts a postluminal water barrier in toad bladder granular cells.
- Increased PCO2 and repeated vasopressin stimulation do not alter this postluminal barrier.
- Water permeability regulation in toad bladders involves distinct luminal and postluminal components.