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Forschungsdatenbank PMU-SQQUID

Activation of cell membrane potassium conductance by mercury in cultured renal epithelioid (MDCK) cells.
Jungwirth, A; Ritter, M; Paulmichl, M; Lang, F;
J Cell Physiol. 1991; 146(1): 25-33.
Originalarbeiten (Zeitschrift)

PMU-Autor/inn/en

Paulmichl Markus
Ritter Markus

Abstract

To elucidate mechanisms of mercury toxicity, the cell membrane potential has been determined continuously in cultured kidney (MDCK)-cells during reversible application of mercury ions to extracellular perfusate. Exposure of the cells to 1 microM mercury ions is followed by rapid, sustained, and slowly reversible hyperpolarization of the cell membrane, increase of cell membrane potassium selectivity, and decrease of cell membrane resistance. Thus, mercury ions enhance the potassium conductance of the cell membrane. Half maximal hyperpolarizing effect is elicited by approximately 0.2 microM. Higher concentrations of mercury ions (greater than 10 microM) eventually depolarize the cell membrane. At extracellular calcium activity reduced to less than 0.1 microM, 1 microM mercury ions still leads to a sustained hyperpolarization and increase of potassium selectivity of the cell membrane. As evident from fluorescence measurements, 10 microM, but not 1 microM mercury ions leads to a rapid increase of intracellular calcium activity. Pretreatment of the cells with either pertussis toxin or cholera toxin does not blunt the hyperpolarizing effect of mercury ions. In conclusion, mercury ions activate the potassium conductance by a mechanism independent of increase of intracellular calcium activity and of cholera toxin- or pertussis toxin-sensitive G-proteins. This activation of potassium conductance may account for early effects of mercury intoxication, such as kaliuresis.


Useful keywords (using NLM MeSH Indexing)

Animals

Barium/pharmacology

Calcium/physiology

Cell Division

Cell Line

Cholera Toxin/pharmacology

Dogs

Epithelium/drug effects

Kidney/drug effects*

Membrane Potentials/drug effects

Mercury/toxicity*

Microelectrodes

Pertussis Toxin

Potassium Channels/drug effects*

Quinidine/pharmacology

Signal Transduction/drug effects

Virulence Factors, Bordetella/pharmacology