Chloride cotransport in the membrane of earthworm body wall muscles
Language English Country Czech Republic Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
14535834
Knihovny.cz E-resources
- MeSH
- Chlorides metabolism pharmacology MeSH
- Potassium pharmacology MeSH
- Electrophysiology MeSH
- Furosemide pharmacology MeSH
- Sodium Potassium Chloride Symporter Inhibitors MeSH
- Ion Transport physiology MeSH
- Hydrogen-Ion Concentration MeSH
- Muscle Fibers, Skeletal drug effects physiology MeSH
- Membrane Potentials drug effects physiology MeSH
- Oligochaeta physiology MeSH
- Osmolar Concentration MeSH
- Ouabain pharmacology MeSH
- Sodium-Potassium-Chloride Symporters physiology MeSH
- Sodium pharmacology MeSH
- Sodium-Potassium-Exchanging ATPase antagonists & inhibitors MeSH
- Muscles physiology MeSH
- In Vitro Techniques MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Chlorides MeSH
- Potassium MeSH
- Furosemide MeSH
- Sodium Potassium Chloride Symporter Inhibitors MeSH
- Ouabain MeSH
- Sodium-Potassium-Chloride Symporters MeSH
- Sodium MeSH
- Sodium-Potassium-Exchanging ATPase MeSH
The resting membrane potential (V(m)) of isolated somatic longitudinal muscles of the earthworm Lumbricus terrestris was studied by glass microelectrodes. The inhibition of chloride permeability by low pH did not affect V(m) of the muscle fibers in isolated somatic longitudinal muscles of the earthworm Lumbricus terrestris which was -48.7 mV (inside negative) at pH 7.3 and -49.1 at pH 5.6. On the other hand, bathing the muscles in Cl(-) and Na(+)-free solutions, or application of the chloride transporter inhibitor furosemide and Na(+)-K(+)-ATPase inhibitor ouabain depolarized the V(m) by 3-5 mV. The effects of a Cl(-) -free solution and ouabain were not additive. This demonstrates relatively small contribution of equilibrium potential for Cl(-) to the resting membrane potential and electrogenic effect of Na(+)K(+)-ATPase which is dependent on the supply of Na(+)(i) ions by furosemide-sensitive and Cl(-)(e)- and Na(+)(e)-dependent electroneutral transport (most probably Na(+)K(+)Cl(-) cotransport).
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