Metformin's Effect on Glucagon-induced Glucose Production and Protein Metabolism.

Metformin's Effect on Glucagon-induced Endogenous Glucose Production, Protein Metabolism and Resting Energy Expenditure in Insulin Resistant Individuals.

This study is being done to understand metformin's mechanisms of action regarding glucose production, protein metabolism, and mitochondrial function.

Study Overview

• Status: Completed
• Conditions: Insulin Resistance; Prediabetic State
• Intervention / Treatment: Drug: Metformin; Drug: Placebo

Detailed Description

It is believed that Metformin antagonizes the action of glucagon through different pathways. In mice, Metformin leads to inhibition of adenylate cyclase, reduction of levels of cyclic AMP and protein kinase A (PKA) activity, therefore blocking glucagon-dependent glucose output form hepatocytes. Glucagon plays an important role in the increased catabolic state seen in insulin deficiency. Hyperglucagonaemia states have been shown to accelerate proteolysis and leucine oxidation in insulin-deficient humans. Patients with insulin resistance and increased levels of glucagon have an increased in energy expenditure which may contribute to the catabolic state associated with this condition. We hypothesized that treatment with Metformin for 2 weeks will significantly inhibit glucagon-induced endogenous glucose production in insulin resistant individuals. We also hypothesized that glucagon-induced alterations in whole body protein metabolism and the increases in O2 consumption associated with hyperglucagonaemia states will be significantly inhibited by Metformin in these individuals. This would open the door for the development of other antidiabetic drugs with antagonism of glucagon as their principal mechanism of action.

• Study Type: Interventional
• Enrollment (Actual): 12
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • Minnesota
    • Rochester, Minnesota, United States, 55905
      • Mayo Clinic in Rochester

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 35 years to 65 years (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• 35-65 years of age
• Fasting blood glucose >100 mg/dl
• BMI 27-36 kg/m2
• Waist Circumference: Men ≥ 104 cm; women ≥ 88 cm
• If previously on anti-diabetic medication, should be off for at least 1 month

Exclusion Criteria:

• Active use of hypoglycemic agents (< 1 month)
• Renal failure, creatinine ≥ 1.5 mg/dL in men or ≥ 1.4 mg/dL in women
• Alanine aminotransferase levels exceed 135 IU/L or aspartate aminotransferase levels exceed 129 IU/L (3 x the upper limit of normal)
• Congestive Heart Failure (EF < 40 %)
• Active coronary artery disease
• Recent (less than 6 weeks) or planned imaging study requiring IV contrast
• Participation in structured exercise (> 2 hr per week)
• Recent change in dietary habits or weight
• Tobacco use
• Use of systemic glucocorticoids
• Anti-coagulant therapy (warfarin/heparin)
• Pregnancy or breastfeeding
• Alcohol consumption greater than 2 drinks/day
• Uncontrolled Hypothyroidism, abnormal thyroid stimulating hormone levels
• Metformin Allergy

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Basic Science
• Allocation: Randomized
• Interventional Model: Crossover Assignment
• Masking: Double

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Metformin; 2 weeks of Metformin use. First week 1000mg/day, Second week Max dose of 2000 mg/day.	Drug: Metformin; Metformin 1000mg daily for one week, then 2000 mg daily for the second week. 4 week washout period, then crossover to placebo.; Other Names: Glucophage
Placebo Comparator: Placebo; 2 weeks of Placebo (lactulose pills)	Drug: Placebo; Placebo tablets for 2 weeks, then 4 weeks of washout period, then crossover to metformin.; Other Names: Lactulose

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in Glucagon-induced endogenous glucose production.	To assess the effect of Metformin on glucose metabolism, at baseline and during a period of hyperglucagonemia, endogenous glucose production will be measured using a stable isotope tracer during the application of a somatostatin-based pancreatic clamp. Participants will be assessed before and following two weeks of consuming either metformin or placebo.	Measured at week 0, 2, 4, 6 and 8

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in glucagon-induced alterations in whole body protein metabolism and resting energy expenditure.	Alterations in whole body protein metabolism will be measured by using leucine as a tracer that measures leucine flux, and leucine transamination and oxidation as measures of leucine catabolism. Whole body oxygen consumption will be assessed by open circuit indirect calorimetry with a ventilated hood system. Skeletal muscle biopsies will be obtained at baseline and four hours after a high fat, high glycemic meal. Mitochondria will be isolated from the muscle samples to assess mitochondrial oxygen consumption and hydrogen peroxide emissions using high-resolution respirometry and spectrofluorometry, respectively. In addition, we will measure skeletal muscle intracellular AMP-activated protein kinase activity.	Measured at week 0, 2, 4, 6 and 8

Collaborators and Investigators

• Sponsor: Mayo Clinic
• Investigators: Principal Investigator: K Nair, MD, PhD, Mayo Clinic

Study record dates

Study Major Dates

• Study Start: October 1, 2013
• Primary Completion (Actual): March 1, 2016
• Study Completion (Actual): March 1, 2016

Study Registration Dates

• First Submitted: September 23, 2013
• First Submitted That Met QC Criteria: October 7, 2013
• First Posted (Estimate): October 8, 2013

Study Record Updates

• Last Update Posted (Actual): September 1, 2017
• Last Update Submitted That Met QC Criteria: August 31, 2017
• Last Verified: August 1, 2017

More Information

Terms related to this study

• Keywords: Insulin Resistance; Metformin; Prediabetic State
• Additional Relevant MeSH Terms: Glucose Metabolism Disorders; Metabolic Diseases; Endocrine System Diseases; Diabetes Mellitus; Hyperinsulinism; Prediabetic State; Insulin Resistance; Hypoglycemic Agents; Physiological Effects of Drugs; Gastrointestinal Agents; Lactulose; Metformin
• Other Study ID Numbers: 13-004966