It is an important and exciting first step in understanding how much pancreatic insulin can be produced and secreted in the clinical setting.

TOP INSIGHT
The fact that not all islets are created equal may provide some hope in the future of activating these backup islets to fight diabetes.
Researchers were then able to see, in real time, when the mouse was releasing its insulin by giving the mouse sugar water (glucose). After the glucose entered the stomach and blood sugar began to rise, insulin was released in response and fluorescence was released from some of the islets.
When isolated pancreatic beta cells were stimulated the same way, individual fluorescent flashes indicating secretion of small packets of insulin from the cells could be observed. Each flash is thought to release between 100,000 and 1 million insulin molecules. When the beta cells were not stimulated, insulin release was very low and no flashes were seen, indicating the amount of fluorescence released from beta cells was proportional to the amount of insulin released.
"We could see responses in specific pancreatic islets that were releasing insulin into the bloodstream," Arvan says. "Amazingly, only a small fraction of the pancreatic islets showed a major response to glucose, while the rest of the islets appeared to remain mostly inactive."
This surprising result implies that some islets represent the body's first line of defense against high blood sugar -- an observation that before this study has never been made. "Perhaps only after we have lost our first responder islets do we recruit backup islets to provide insulin," Arvan says.
"It has been a holy grail to try to look inside a living person's pancreas and see how much insulin that person has stored away," Arvan adds. "This study is an important and exciting first step in understanding how much pancreatic insulin can be produced and secreted in the clinical setting."
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