Protein Ingestion Induces Muscle Insulin Resistance Independent of Leucine-Mediated mTOR Activation

Diabetes. 2015 May;64(5):1555-63. doi: 10.2337/db14-1279. Epub 2014 Dec 4.

Abstract

Increased plasma branched-chain amino acid concentrations are associated with insulin resistance, and intravenous amino acid infusion blunts insulin-mediated glucose disposal. We tested the hypothesis that protein ingestion impairs insulin-mediated glucose disposal by leucine-mediated mTOR signaling, which can inhibit AKT. We measured glucose disposal and muscle p-mTOR(Ser2448), p-AKT(Ser473), and p-AKT(Thr308) in 22 women during a hyperinsulinemic-euglycemic clamp procedure with and without concomitant ingestion of whey protein (0.6 g/kg fat-free mass; n = 11) or leucine that matched the amount given with whey protein (n = 11). Both whey protein and leucine ingestion raised plasma leucine concentration by approximately twofold and muscle p-mTOR(Ser2448) by ∼30% above the values observed in the control (no amino acid ingestion) studies; p-AKT(Ser473) and p-AKT(Thr308) were not affected by whey protein or leucine ingestion. Whey protein ingestion decreased insulin-mediated glucose disposal (median 38.8 [quartiles 30.8, 61.8] vs. 51.9 [41.0, 77.3] µmol glucose/µU insulin · mL(-1) · min(-1); P < 0.01), whereas ingestion of leucine did not (52.3 [43.3, 65.4] vs. 52.3 [43.9, 73.2]). These results indicate that 1) protein ingestion causes insulin resistance and could be an important regulator of postprandial glucose homeostasis and 2) the insulin-desensitizing effect of protein ingestion is not due to inhibition of AKT by leucine-mediated mTOR signaling.

Trial registration: ClinicalTrials.gov NCT01538836 NCT01757340.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Amino Acids / blood
  • Amino Acids / metabolism
  • Blood Glucose
  • Dietary Proteins / administration & dosage
  • Dietary Proteins / pharmacology*
  • Female
  • Glucose Clamp Technique
  • Humans
  • Insulin / blood
  • Insulin / metabolism
  • Insulin Resistance / physiology*
  • Leucine / metabolism*
  • Middle Aged
  • Milk Proteins / pharmacology*
  • Muscle, Skeletal / physiology*
  • Signal Transduction
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism*
  • Whey Proteins

Substances

  • Amino Acids
  • Blood Glucose
  • Dietary Proteins
  • Insulin
  • Milk Proteins
  • Whey Proteins
  • MTOR protein, human
  • TOR Serine-Threonine Kinases
  • Leucine

Associated data

  • ClinicalTrials.gov/NCT01538836
  • ClinicalTrials.gov/NCT01757340