Cu2+ reveals amiloride-induced activation and blocking of non-selective cation channel in larval bullfrog skin

Pflugers Archiv European Journal of Physiology

Volumn 442, Issue 4, 2001, Pages 534-536

  Takada, Makoto ^a   Kasai, Miyoko ^a   Shiibashi, Michio ^a  

^a SAITAMA MEDICAL UNIVERSITY   (Japan)

Author keywords

Amiloride; Cu2+; Frog skin; Non selective cation channel

Indexed keywords

ACETYLCHOLINE; AMILORIDE; CATION CHANNEL; COPPER ION; COPPER; DIURETIC AGENT; ION CHANNEL; VASODILATOR AGENT;

ANIMAL TISSUE; ARTICLE; BINDING SITE; BULLFROG; DRUG EFFECT; LARVA; NONHUMAN; PRIORITY JOURNAL; SHORT CIRCUIT CURRENT; SKIN; ANIMAL; CELL MEMBRANE POTENTIAL; CHANNEL GATING; CHEMISTRY; FROG; METABOLISM;

ACETYLCHOLINE; AMILORIDE; ANIMALS; BINDING SITES; COPPER; DIURETICS; ION CHANNEL GATING; ION CHANNELS; LARVA; MEMBRANE POTENTIALS; RANA CATESBEIANA; SKIN; VASODILATOR AGENTS;

EID: 0034924605     PISSN: 00316768     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004240100580     Document Type: Article

References (7)

1. Calcium channel blockers inhibit amiloride-stimulated short-circuit current in frog tadpole skin
2. Low-affinity mixed acetylcholine-responsive receptors at the apical membrane of frog tadpole skin
3. Amiloride analog stimulation of short-circuit current in larval frog skin epithelium
4. 2+ reveals different binding sites of amiloride and CDPC on the apical Na channel of frog skin
5. Effect of amiloride on the poorly selective cation channel of larval bullfrog skin
6. Poorly selective cation channels in the skin of the larval frog (stage ≤ XXI)
7. + channels in the skin