Abstract
The ion permeability of the membrane junctions between Chironomus salivary gland cells is strongly depressed by treatments that are generally known to inhibit energy metabolism. These treatments include prolonged cooling at 6 degrees -8 degrees C, and exposure to dinitrophenol, cyanide, oligomycin, and N-ethylmaleimide. Intracellular injection of ATP appears to prevent depression of junctional permeability by dinitrophenol or to reverse it. Ouabain, azide, p-chloromercuriphenylsulfonic acid, reserpine, and acetazolamide fail to depress junctional permeability. Thus the ion permeability of the junctional membranes appears to depend on energy provided by oxidative phosphorylation. Possible energy-linked processes for maintaining junctional permeability are discussed, including processes involving transport of permeability-modifying species such as Ca(++).
MeSH Terms
Adenosine Triphosphate/pharmacology
Animals
Calcium/metabolism
Cell Membrane/metabolism
Cell Membrane Permeability/drug effects
Dinitrophenols/pharmacology
Diptera
Electrophysiology
Ethylmaleimide/pharmacology
Iontophoresis
Methods
Oligomycins/pharmacology
Ouabain/pharmacology
Reserpine/pharmacology
Salivary Glands/metabolism
Temperature
Chemicals
Dinitrophenols
Oligomycins
Ouabain
Reserpine
Adenosine Triphosphate
Ethylmaleimide
Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Politoff A L
Socolar S J
Loewenstein W R
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23 references, click to expand
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