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Urea transport in toad skin (Bufo marinus)
G Dytko1, P L Smith, L B Kinter
1Department of Pharmacology, SmithKline Beecham Pharmaceuticals, King of Prussia, Pennsylvania.
The Journal of Pharmacology and Experimental Therapeutics
|October 1, 1993
Summary
Toad skin actively transports urea via a carrier-mediated mechanism, especially when adapted to high salt conditions. This urea transport is distinct from sodium transport and is not significantly affected by common pharmacological agents.
Area of Science:
- Physiology
- Comparative Physiology
- Membrane Transport
Background:
- Urea transport across biological membranes is crucial for osmoregulation and waste excretion.
- The skin of the toad Bufo marinus serves as a model for studying epithelial transport processes.
Purpose of the Study:
- To investigate the characteristics of urea transport across the skin of the toad Bufo marinus.
- To determine if urea transport is carrier-mediated and how it is affected by adaptation to hypertonic conditions and various pharmacological agents.
Main Methods:
- Short-circuit current (SCC) measurements were used to assess transepithelial transport.
- Urea transport (Jm-->s(urea)) was quantified in toads adapted to hypertonic NaCl.
- The effects of amiloride, phloretin, ouabain, NaCN, vasopressin, and 2-pyrazinoylguanidine on urea and sodium transport were evaluated.
Main Results:
- Transepithelial urea transport (Jm-->s(urea)) was enhanced and showed saturation kinetics in toads adapted to 150 mM NaCl, indicating carrier-mediated transport.
- Amiloride inhibited Jm-->s(urea) in a dose-dependent manner, but with significantly lower potency than its effect on SCC.
- Phloretin, ouabain, NaCN, vasopressin, and 2-pyrazinoylguanidine did not significantly affect Jm-->s(urea), suggesting a distinct transport mechanism from active sodium transport.
Conclusions:
- The skin of Bufo marinus possesses a carrier-mediated system for urea transport from mucosa to serosa.
- This urea transport system is upregulated in hypertonic conditions and operates independently of active sodium transport pathways.
- Pharmacological agents known to affect urea transport in other tissues or sodium transport in toad skin had minimal impact on Jm-->s(urea).