Insulin sensitivity and glucose tolerance are altered by maintenance on a ketogenic diet

Endocrinology. 2010 Jul;151(7):3105-14. doi: 10.1210/en.2010-0175. Epub 2010 Apr 28.

Abstract

Low-carbohydrate, ketogenic diets (KD) are frequently implemented in efforts to reduce or maintain body weight, although the metabolic effects of long-term exposure to this type of diet remain controversial. This study assessed the responsivity to peripheral and central insulin, glucose tolerance, and meal-induced effects of consuming a KD in the rat. After 8 wk of consuming chow or KD, caloric intake after peripheral or central insulin and insulin and glucose levels after a glucose challenge were assessed. In a separate group of rats, glucose and insulin responses to either a low- or high-carbohydrate test meal were measured. Finally, rats maintained on KD were switched back to a chow diet, and insulin sensitivity and glucose tolerance were evaluated to determine whether the effects of KD were reversible. Maintenance on KD resulted in decreased sensitivity to peripheral insulin and impaired glucose tolerance. Furthermore, consumption of a high-carbohydrate meal in rats that habitually consumed KD induced significantly greater insulin and glucose levels for an extended period of time, as compared with chow-fed controls. Responsivity to central insulin was heightened in KD rats and associated with increased expression levels of insulin receptor mRNA. Finally, returning to a chow diet rapidly reversed the effects of KD on insulin sensitivity and glucose tolerance. These data suggest that maintenance on KD negatively affects glucose homeostasis, an effect that is rapidly reversed upon cessation of the diet.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Body Weight / drug effects
  • Diet, Ketogenic / methods*
  • Eating / drug effects
  • Energy Intake / drug effects
  • Glucose Intolerance / diet therapy*
  • Hypothalamus / drug effects
  • Hypothalamus / metabolism
  • Insulin / blood
  • Insulin / pharmacology
  • Insulin Resistance / physiology*
  • Male
  • Rats
  • Rats, Long-Evans
  • Receptor, Insulin / genetics

Substances

  • Blood Glucose
  • Insulin
  • Receptor, Insulin