The effects of magnesium upon adenosine triphosphate‐sensitive potassium channels in a rat insulin‐secreting cell line.
- 1 October 1987
- journal article
- research article
- Published by Wiley in The Journal of Physiology
- Vol. 391 (1) , 611-629
- https://doi.org/10.1113/jphysiol.1987.sp016759
Abstract
1. The patch-clamp method of single-channel recording was applied to K+ channels which are inhibited by intracellular adenosine 5''-triphosphate (ATP: K+-ATP channels) in membrane patches obtained from the insulin-secreting cloned cell line RINm5F. 2. The magnitude of K+ currents flowing outwards through these K+-ATP channels was reduced by internal Mg2+ ions in a dose-dependent manner. Currents flowing inwards through the channels were not affected by Mg2+. Internal Na+ ions had similar effects. 3. Divalent cations (Mg2+, Sr2+ and Ca2+) applied to the internal surface of the patch membrane inhibited the opening of K+-ATP channels in a dose-dependent manner. Internal Na+ ions had no effect. 4. K+-ATP channel activity was stimulated by adenosine 5''-diphosphate (ADP), guanosine 5''-triphosphate (GTP), guanosine 5''-diphosphate (GDP), guanosine 5''-o-(3-thiotriphosphate) (GTP.gamma.S) and guanosine 5''-o-(2-thiodiphosphate) (GDP.beta.S) when millimolar Mg2+ bathed the internal surface of the patch membrane. In the virtual absence of internal Mg2+ ions ADIP, GTP, and GPT.gamma.S inhibited K+-ATP channels and GDP and GDP.beta.S were without effect. Adenosine 5''-o-(2-thiodiphosphate) (ADP.beta.S) inhibited K+-ATP channel activity in the presence and absence of Mg2+. 5. K+-ATP channel openings could be evoked by either ADP or GDP in the presence of an inhibitory concentration of ATP. These openings were abolished in the absence of internal Mg2+. 6. Run-down K+-ATP channels could be reactivated by ATP in the presence of internal Mg2+, but not in its absence. Analogues of ATP were unable to reactivate K+-ATP channels even in the presence of Mg2+. 7. It is concluded that internal Mg2+ ions (i) cause the rectification of the K+-ATP channels current-voltage relationship, (ii) are required for K+-ATP channels activity to be maintained by a phosphorylation process and (iii) are required for K+-ATP channel activity evoked by ADP, GTP and GDP.This publication has 41 references indexed in Scilit:
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