Effects of Niacin on Intramyocellular Fatty Acid Trafficking in Upper Body Obesity and Type 2 Diabetes Mellitus
Status:
Recruiting
Trial end date:
2021-12-31
Target enrollment:
Participant gender:
Summary
Muscle insulin resistance is a hallmark of upper body obesity (UBO) and Type 2 diabetes
(T2DM). It is unknown whether muscle free fatty acid (FFA) availability or intramyocellular
fatty acid trafficking is responsible for the abnormal response to insulin. Likewise, the
investigators do not understand to what extent the incorporation of FFA into ceramides or
diacylglycerols (DG) affect insulin signaling and muscle glucose uptake. The investigators
will measure muscle FFA storage into intramyocellular triglyceride, intramyocellular fatty
acid trafficking, activation of the insulin signaling pathway and glucose disposal rates
under both saline control (high overnight FFA) and after an overnight infusion of intravenous
niacin (lower/normal FFA) to provide the first integrated examination of the interaction
between FFA and muscle insulin action from the whole body to the cellular/molecular level. By
identifying which steps in the insulin signaling pathway are most affected, the investigators
will determine the site-specific effect of ceramides and/or DG on different degrees of
insulin resistance.
Hypothesis 1: Greater trafficking of plasma FFA into intramyocellular DG will impair proximal
insulin signaling and reduce muscle glucose uptake.
Hypothesis 2: Lowering FFA in UBO and T2DM by using an intravenous infusion of niacin will
alter trafficking of plasma FFA into intramyocellular ceramides in a way that will improve
insulin signaling and increase muscle glucose uptake.
Hypothesis 3: Lowering FFA in UBO and T2DM by using an intravenous infusion of niacin will
alter trafficking of plasma FFA into intramyocellular DG in a way that will improve insulin
signaling and increase muscle glucose uptake.
Phase:
Early Phase 1
Details
Lead Sponsor:
Mayo Clinic
Collaborator:
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)