DiabetesPhysiologyPeer-reviewed journal article
Morning Engagement of Hepatic Insulin Receptors Improves Afternoon Hepatic Glucose Disposal and Storage
Hannah L. WatermaniD, Mary Courtney MooreiD, Marta S. Smith, Ben FarmeriD, Kalisha C Yankey, Melanie F. Scott, Dale S. EdgertoniD, Alan D. CherringtoniD
Abstract
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 insulins delivery route affects the second meal response. To determine whether morning peripheral insulin delivery (as occurs clinically (subcutaneous)) can enhance afternoon HGU, conscious dogs were treated in the morning with insulin delivered 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 when insulin was delivered peripherally. 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. Article HighlightsO_LIMorning insulin delivery primes the liver for increased hepatic glucose uptake (HGU) later in the day, but the mechanism (direct hepatic and/or indirect insulin action) remains unclear. C_LIO_LIThis study compared insulin infusion via physiologic (hepatic portal vein) and clinical (peripheral) routes to assess their impact on afternoon hepatic glucose disposal. C_LIO_LIMorning peripheral insulin delivery failed to induce a significant enhancing effect on afternoon HGU and glycogen storage, unlike morning hepatic portal vein insulin delivery, which did. C_LIO_LIThese findings highlight the importance of achieving appropriate hepatic insulin exposure in the morning to effectively prime the liver for efficient glucose disposal. C_LI
- Citations
- 3
- FWCI
- 0.87
- Field percentile
- top 24%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Morning Elevation in Insulin Enhances Afternoon Hepatic Glucose Disposal in Dogs by Increasing Both Insulin Signaling and Glucose Action
Hannah L. Waterman, Marta S. Smith, … Dale S. Edgerton·DiabetesPeer-reviewed·May 18, 2026
- Duration of Morning Hyperinsulinemia Determines Hepatic Glucose Uptake and Glycogen Storage Later in the Day
Hannah L. Waterman, Mary Courtney Moore, … Alan D. Cherrington·American Journal of Physiology-Endocrinology and MetabolismPeer-reviewed·Sep 11, 2024
- Morning Glucagon Disrupts Insulin Induced Hepatic Metabolic Memory and Subsequent Afternoon Glucose Metabolism in Canines
Hannah L. Waterman, Marta S. Smith, … Dale S. Edgerton·Frontiers in EndocrinologyPeer-reviewed·Apr 29, 2026
- A novel subset of hepatocytes is simultaneously gluconeogenic and de novo lipogenic in the fed state and is naturally insulin resistant
Junichi Okada, Austin Landgraf, … Jeffrey E. Pessin·bioRxiv·Mar 16, 2026
- IPMK modulates insulin-mediated suppression of hepatic glucose production
Ik‐Rak Jung, Frederick Anokye‐Danso, … Sangwon F. Kim·bioRxiv·Mar 10, 2022
- AKT signaling in hepatocytes rapidly increases glucose phosphorylation and contribution to glycogen without affecting metabolite pool sizes or glycogen breakdown
Megan L. Stefkovich, Won Dong Lee, … Paul M. Titchenell·bioRxiv·Dec 3, 2025