scholarly journals Electrical Bursting, Calcium Oscillations, and Synchronization of Pancreatic Islets

Author(s):  
Richard Bertram ◽  
Arthur Sherman ◽  
Leslie S. Satin
Cell Calcium ◽  
2005 ◽  
Vol 38 (2) ◽  
pp. 131-139 ◽  
Author(s):  
Carlos Villalobos ◽  
Angel Nadal ◽  
Lucía Núñez ◽  
Iván Quesada ◽  
Pablo Chamero ◽  
...  

2008 ◽  
Vol 95 (10) ◽  
pp. 4676-4688 ◽  
Author(s):  
Min Zhang ◽  
Bernard Fendler ◽  
Bradford Peercy ◽  
Pranay Goel ◽  
Richard Bertram ◽  
...  

Cell Calcium ◽  
2008 ◽  
Vol 43 (1) ◽  
pp. 39-47 ◽  
Author(s):  
Ivan Quesada ◽  
Carlos Villalobos ◽  
Lucía Núñez ◽  
Pablo Chamero ◽  
María Teresa Alonso ◽  
...  

Cell Calcium ◽  
2019 ◽  
Vol 83 ◽  
pp. 102081 ◽  
Author(s):  
Rachel T. Scarl ◽  
Kathryn L. Corbin ◽  
Nicholas W. Vann ◽  
Hallie M. Smith ◽  
Leslie S. Satin ◽  
...  

Endocrinology ◽  
2009 ◽  
Vol 150 (2) ◽  
pp. 607-615 ◽  
Author(s):  
Pooya Jahanshahi ◽  
Runpei Wu ◽  
Jeffrey D. Carter ◽  
Craig S. Nunemaker

Pulsatility is a fundamental feature of pancreatic islets and a hallmark of hormone secretion. Isolated pancreatic islets endogenously generate rhythms in secretion, metabolic activity, and intracellular calcium ([Ca2+]i) that are important to normal physiological function. Few studies have directly compared oscillatory and nonoscillatory islets to identify possible differences in function. We investigated the hypothesis that the loss of these oscillations is a leading indicator of islet dysfunction by comparing oscillatory and nonoscillatory mouse islets for multiple parameters of function. Nonoscillatory islets displayed elevated basal [Ca2+]i and diminished [Ca2+]i response and insulin secretory response to 3–28 mm glucose stimulation compared with oscillatory islets, suggesting diminished glucose sensitivity. We investigated several possible mechanisms to explain these differences. No differences were observed in mitochondrial membrane potential, estimated ATP-sensitive potassium channel and L-type calcium channel activity, or cell death rates. Nonoscillatory islets, however, showed a reduced response to the sarco(endo)plasmic reticulum calcium ATPase inhibitor thapsigargin, suggesting a disruption in calcium homeostasis in the endoplasmic reticulum (ER) compared with oscillatory islets. The diminished ER calcium homeostasis among nonoscillatory islets was also consistent with the higher cytosolic calcium levels observed in 3 mm glucose. Inducing mild damage with low-dose proinflammatory cytokines reduced islet oscillatory capacity and produced similar effects on glucose-stimulated [Ca2+]i, basal [Ca2+]i, and thapsigargin response observed among untreated nonoscillatory islets. Our data suggest the loss of oscillatory capacity may be an early indicator of diminished islet glucose sensitivity and ER dysfunction, suggesting targets to improve islet assessment. The loss of islet calcium oscillations correlates with impaired calcium regulation and reduced insulin secretion, suggesting oscillatory capacity is important to islet health and function.


2013 ◽  
Vol 305 (7) ◽  
pp. E805-E817 ◽  
Author(s):  
Jianhua Ren ◽  
Arthur Sherman ◽  
Richard Bertram ◽  
Paulette B. Goforth ◽  
Craig S. Nunemaker ◽  
...  

We used the patch clamp technique in situ to test the hypothesis that slow oscillations in metabolism mediate slow electrical oscillations in mouse pancreatic islets by causing oscillations in KATP channel activity. Total conductance was measured over the course of slow bursting oscillations in surface β-cells of islets exposed to 11.1 mM glucose by either switching from current clamp to voltage clamp at different phases of the bursting cycle or by clamping the cells to −60 mV and running two-second voltage ramps from −120 to −50 mV every 20 s. The membrane conductance, calculated from the slopes of the ramp current-voltage curves, oscillated and was larger during the silent phase than during the active phase of the burst. The ramp conductance was sensitive to diazoxide, and the oscillatory component was reduced by sulfonylureas or by lowering extracellular glucose to 2.8 mM, suggesting that the oscillatory total conductance is due to oscillatory KATP channel conductance. We demonstrate that these results are consistent with the Dual Oscillator model, in which glycolytic oscillations drive slow electrical bursting, but not with other models in which metabolic oscillations are secondary to calcium oscillations. The simulations also confirm that oscillations in membrane conductance can be well estimated from measurements of slope conductance and distinguished from gap junction conductance. Furthermore, the oscillatory conductance was blocked by tolbutamide in isolated β-cells. The data, combined with insights from mathematical models, support a mechanism of slow (∼5 min) bursting driven by oscillations in metabolism, rather than by oscillations in the intracellular free calcium concentration.


Author(s):  
F. B. P. Wooding ◽  
K. Pedley ◽  
N. Freinkel ◽  
R. M. C. Dawson

Freinkel et al (1974) demonstrated that isolated perifused rat pancreatic islets reproduceably release up to 50% of their total inorganic phosphate when the concentration of glucose in the perifusion medium is raised.Using a slight modification of the Libanati and Tandler (1969) method for localising inorganic phosphate by fixation-precipitation with glutaraldehyde-lead acetate we can demonstrate there is a significant deposition of lead phosphate (identified by energy dispersive electron microscope microanalysis) at or on the plasmalemma of the B cell of the islets (Fig 1, 3). Islets after incubation in high glucose show very little precipitate at this or any other site (Fig 2). At higher magnification the precipitate seems to be intracellular (Fig 4) but since any use of osmium or uranyl acetate to increase membrane contrast removes the precipitate of lead phosphate it has not been possible to verify this as yet.


2007 ◽  
Vol 74 (1) ◽  
pp. 1 ◽  
Author(s):  
Michael J. Berridge

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