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Insulin is produced in the pancreas within the islets of Langerhans by β-cells and is secreted in response to rising blood glucose levels and neurohormonal signaling. When functioning normally, β-cells help maintain euglycemia via endogenous release of insulin to cover basal and prandial needs. In normal physiology, “basal insulin secretion” describes the low rate of insulin release between meals that is sufficient to inhibit overproduction of glucose and ketone bodies by the liver in the fasting state. Additional bursts of insulin are released to prevent hyperglycemia in the prandial state and promote conversion of nutrients to energy for short- and long-term use and storage (see Figure 1). Although Figure 1 provides generalized statements related to physiologic insulin secretion during a given day, individual responses will vary.

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