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Activation of the Sodium Pump Blocks the Growth Hormone-Induced Increase in Cytosolic Free Calcium in Rat Adipocytes1
Author(s) -
Shikha Gaur,
Hiroshi Yamaguchi,
H. M. Goodman
Publication year - 2000
Publication title -
endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.674
H-Index - 257
eISSN - 1945-7170
pISSN - 0013-7227
DOI - 10.1210/endo.141.2.7310
Subject(s) - endocrinology , medicine , ouabain , calcium , calcium pump , insulin , sodium , chemistry , stimulation , hyperpolarization (physics) , cytosol , symporter , diaphragm pump , adipocyte , atpase , biology , biochemistry , adipose tissue , enzyme , organic chemistry , transporter , nuclear magnetic resonance spectroscopy , gene , materials science , micropump , nanotechnology
GH promptly increases cytosolic free calcium ([Ca2+]i) in freshly isolated rat adipocytes. Adipocytes deprived of GH for 3 h or longer are incapable of increasing [Ca2+]i in response to GH, but instead respond in an insulin-like manner. Insulin blocks the GH-induced increase in [Ca2+]i in GH-replete cells and stimulates the sodium pump (i.e. Na+/K+-ATPase), thereby hyperpolarizing the cell membrane. Blockade of the Na+/K+-ATPase with 100 microM ouabain reversed these effects of insulin and enabled GH to increase [Ca2+]i in GH-deprived adipocytes. Both insulin and GH activated the sodium pump in GH-deprived adipocytes, as indicated by increased uptake of 86Rb+. Decreasing availability of intracellular Na+ by blockade of Na+/K+/ 2Cl- symporters or Na+/H+ antiporters abolished the effects of both hormones on 86Rb+ uptake and enabled both GH and insulin to increase [Ca2+]i in GH-deprived adipocytes. The data suggest that hormonal stimulation of Na+/K+-ATPase activity interferes with activation of voltage-sensitive calcium channels by either membrane hyperpolarization or some unknown interaction between the sodium pump and calcium channels.

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