Insulin Sensitivity Determines Effects of Insulin and Meal Ingestion on Systemic Vascular Resistance in Healthy Subjects

Jorn Woerdeman, Rick I Meijer, Etto C Eringa, T. Hoekstra, Yvo M Smulders, Erik H Serné

Research output: Contribution to journalArticleAcademicpeer-review

6 Citations (Scopus)

Abstract

OBJECTIVE: In addition to insulin's metabolic actions, insulin can dilate arterioles which increase blood flow to metabolically active tissues. This effect is blunted in insulin-resistant subjects. Insulin's effect on SVR, determined by resistance arterioles, has, however, rarely been examined directly. We determined the effects of both hyperinsulinemia and a mixed meal on SVR and its relationship with insulin sensitivity.

METHODS: Thirty-seven lean and obese women underwent a hyperinsulinemic-euglycemic clamp, and 24 obese volunteers underwent a mixed-meal test. SVR was assessed using CPP before and during hyperinsulinemia as well as before and 60 and 120 minutes after a meal.

RESULTS: SVR decreased significantly during hyperinsulinemia (-13%; p < 0.001) and after the meal (-11%; p < 0.001). Insulin decreased SVR more strongly in insulin-sensitive individuals (standardized β: -0.44; p = 0.01). In addition, SVR at 60 minutes after meal ingestion was inversely related to the Matsuda index (β: -0.39; p = 0.04) and the change in postprandial SVR was directly related to postprandial glycemia (β: 0.53; p < 0.01).

CONCLUSIONS: Hyperinsulinemia and meal ingestion decrease SVR, which is directly associated with metabolic insulin resistance. This suggests that resistance to insulin-induced vasodilatation contributes to regulation of vascular resistance.

Original languageEnglish
Pages (from-to)62-8
Number of pages7
JournalMicrocirculation
Volume23
Issue number1
DOIs
Publication statusPublished - Jan 2016

Keywords

  • Adolescent
  • Adult
  • Blood Flow Velocity
  • Clinical Trial
  • Eating
  • Female
  • Glucose Clamp Technique
  • Humans
  • Hyperinsulinism
  • Insulin
  • Insulin Resistance
  • Journal Article
  • Male
  • Middle Aged
  • Postprandial Period
  • Research Support, Non-U.S. Gov't
  • Vascular Resistance
  • Vasodilation
  • hypertension

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