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Improved Afternoon Hepatic Glucose Disposal and Storage Requires Morning Engagement of Hepatic Insulin Receptors

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posted on 2024-11-27, 18:25 authored by Hannah L. Waterman, Mary Courtney Moore, Marta S. Smith, Ben Farmer, Kalisha Yankey, Melanie Scott, Dale S. Edgerton, Alan D. Cherrington

Glucose tolerance improves significantly upon consuming a second, identical meal later in the day (second meal phenomenon). We previously established that morning hyperinsulinemia primes the liver for increased afternoon hepatic glucose uptake (HGU). Although the route of insulin delivery is an important determinant of the mechanisms by which insulin regulates liver glucose metabolism (direct hepatic vs indirect insulin action), it is not known if insulin’s delivery route affects the second meal response. To determine whether morning peripheral insulin delivery (as occurs clinically, i.e. subcutaneous) can enhance afternoon HGU, conscious dogs were treated in the morning with insulin delivered either via the portal vein or peripherally (leg vein), while glucose was infused to maintain euglycemia. Consequently, arterial insulin levels increased similarly in both groups, but relative hepatic insulin deficiency occurred with peripheral insulin delivery. In the afternoon, all animals were challenged with the same hyperinsulinemic-hyperglycemic clamp to simulate identical postprandial-like conditions. The substantial enhancement of HGU in the afternoon caused by morning portal vein insulin delivery was lost when insulin was delivered peripherally. This indicates that morning insulin does not cause the second meal phenomenon via its indirect actions on the liver, but rather through direct activation of hepatic insulin signaling.

Funding

This work was supported by National Institutes of Health (NIH) Grant R01DK131082. H.W. was supported in part by the Vanderbilt University Training Program in Molecular Endocrinology NIH grant 5T32DK007563. Hormone analysis was completed by Vanderbilt’s Hormone Assay and Analytical Services Core, supported by NIH grants DK020593 and DK059637. Vanderbilt’s Large Animal Core provided surgical expertise, supported by the NIH Grant DK020593.

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