Posts Tagged ‘insulin’

Insulin stimulates Mg2+ uptake in mouse distal convoluted tubule cells

Monday, September 14th, 2009

Dai LJ, Bapty BW, Ritchie G, Kerstan D, and Quamme GA: Insulin stimulates Mg2+ uptake in  mouse distal convoluted tubule cells. American Journal of Physiology 277:F907-F913, 1999.

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Abstract Insulin has been shown to be a magnesium-conserving hormone acting, in part, through stimulation of magnesium absorption within the thick ascending limb. Although the distal convoluted tubule possesses the most insulin receptors, it is unclear what, if any, actions insulin has in the distal tubule. The effects of insulin were studied on immortalized mouse distal convoluted tubule (MDCT) cells by measuring cellular cAMP formation with radioimmunoassays and Mg21 uptake with fluorescence techniques using mag-fura 2. To assess Mg21 uptake, MDCT cells were first Mg21 depleted to 0.22 6 0.01 mM by culturing in Mg21-free media for 16 h and then placed in 1.5 mM MgCl2, and the changes in intracellular Mg21 concentration ([Mg21]i) were measured with microfluorescence. [Mg21]i returned to basal levels, 0.53 6 0.02 mM, with a mean refill rate, d([Mg21]i)/dt, of 164 6 5 nM/s. Insulin stimulated Mg21 entry in a concentration-dependent manner with maximal response of 214 6 12 nM/s, which represented a 30 6 5% increase in the mean uptake rate above control values. This was associated with a 2.5-fold increase in insulin-mediated cAMP generation (52 6 3 pmol·mg protein21 ·5 min21). Genistein, a tyrosine kinase inhibitor, diminished insulin-stimulated Mg21 uptake (169 6 11 nM/s), but did not change insulin-mediated cAMP formation (47 6 5 pmol·mg protein21 ·5 min21). PTH stimulates Mg21 entry, in part, through increases in cAMP formation. Insulin and PTH increase Mg21 uptake in an additive fashion. In conclusion, insulin mediates Mg21 entry, in part, by a genistein-sensitive mechanism and by modifying hormone-responsive transport. These studies demonstrate that insulin stimulates Mg21 uptake in MDCT cells and suggest that insulin acts in concert with other peptide and steroid hormones to control magnesium conservation in the distal convoluted tubule.

Insulin
has been shown to be a magnesium-conserving hormone
acting, in part, through stimulation of magnesium absorption
within the thick ascending limb. Although the distal convoluted
tubule possesses the most insulin receptors, it is
unclear what, if any, actions insulin has in the distal tubule.
The effects of insulin were studied on immortalized mouse
distal convoluted tubule (MDCT) cells by measuring cellular
cAMP formation with radioimmunoassays and Mg21 uptake
with fluorescence techniques using mag-fura 2. To assess
Mg21 uptake, MDCT cells were first Mg21 depleted to 0.22 6
0.01 mM by culturing in Mg21-free media for 16 h and then
placed in 1.5 mM MgCl2, and the changes in intracellular
Mg21 concentration ([Mg21]i) were measured with microfluorescence.
[Mg21]i returned to basal levels, 0.53 6 0.02 mM,
with a mean refill rate, d([Mg21]i)/dt, of 164 6 5 nM/s. Insulin
stimulated Mg21 entry in a concentration-dependent manner
with maximal response of 214 6 12 nM/s, which represented
a 30 6 5% increase in the mean uptake rate above control
values. This was associated with a 2.5-fold increase in
insulin-mediated cAMP generation (52 6 3 pmol·mg protein21
·5 min21). Genistein, a tyrosine kinase inhibitor, diminished
insulin-stimulated Mg21 uptake (169 6 11 nM/s), but
did not change insulin-mediated cAMP formation (47 6 5
pmol·mg protein21 ·5 min21). PTH stimulates Mg21 entry, in
part, through increases in cAMP formation. Insulin and PTH
increase Mg21 uptake in an additive fashion. In conclusion,
insulin mediates Mg21 entry, in part, by a genistein-sensitive
mechanism and by modifying hormone-responsive transport.
These studies demonstrate that insulin stimulates Mg21
uptake in MDCT cells and suggest that insulin acts in concert
with other peptide and steroid hormones to control magnesium
conservation in the distal convoluted tubule.