TY - JOUR
T1 - Detection of multiple patterns of oscillatory oxygen consumption in single mouse islets of Langerhans
AU - Jung, Sung Kwon
AU - Aspinwall, Craig A.
AU - Kennedy, Robert T.
N1 - Funding Information:
This work was supported by NIH Grant DK46960. R.T.K. received support as a Presidential Faculty Fellow. C.A.A. received support as an ACS Division Analytical Chemistry Fellow (Eastman Chemical Co.).
PY - 1999/6/7
Y1 - 1999/6/7
N2 - A novel oxygen microsensor was used to measure oxygen levels in single mouse islets as a function of glucose concentration. Oxygen consumption of individual islets was 5.99 ± 1.17, 9.21 ± 2.15, and 12.22 ± 2.16 pmol/min at 3, 10, and 20 mM glucose, respectively (mean ± SEM, n = 10). Consumption of oxygen was islet-size dependent as larger islets consumed more oxygen than smaller islets but smaller islets consumed more oxygen per unit volume than larger islets. Elevating glucose levels from 3 to 10 mM induced pronounced fast oscillations in oxygen level (period of 12.1 ± 1.7 s, n = 6) superimposed on top of large slow oscillations (period of 3.3 ± 0.6 min, n = 6). The fast oscillations could be completely abolished by treatment with the L-type Ca2+-channel blocker nifedipine (40 μM) with a lesser effect on slow oscillations. Slow oscillations were almost completely dependent upon extracellular Ca2+. The oxygen patterns closely mimic those that have previously been reported for intracellular Ca2+ levels and are suggestive of an important role for Ca2+ in amplifying metabolic oscillations.
AB - A novel oxygen microsensor was used to measure oxygen levels in single mouse islets as a function of glucose concentration. Oxygen consumption of individual islets was 5.99 ± 1.17, 9.21 ± 2.15, and 12.22 ± 2.16 pmol/min at 3, 10, and 20 mM glucose, respectively (mean ± SEM, n = 10). Consumption of oxygen was islet-size dependent as larger islets consumed more oxygen than smaller islets but smaller islets consumed more oxygen per unit volume than larger islets. Elevating glucose levels from 3 to 10 mM induced pronounced fast oscillations in oxygen level (period of 12.1 ± 1.7 s, n = 6) superimposed on top of large slow oscillations (period of 3.3 ± 0.6 min, n = 6). The fast oscillations could be completely abolished by treatment with the L-type Ca2+-channel blocker nifedipine (40 μM) with a lesser effect on slow oscillations. Slow oscillations were almost completely dependent upon extracellular Ca2+. The oxygen patterns closely mimic those that have previously been reported for intracellular Ca2+ levels and are suggestive of an important role for Ca2+ in amplifying metabolic oscillations.
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U2 - 10.1006/bbrc.1999.0784
DO - 10.1006/bbrc.1999.0784
M3 - Article
C2 - 10362508
AN - SCOPUS:0033532591
SN - 0006-291X
VL - 259
SP - 331
EP - 335
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -