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Study of In Vivo Glucose Metabolism in High-fat Diet-fed Mice Using Oral Glucose Tolerance Test (OGTT) and Insulin Tolerance Test (ITT)
Published on: January 7, 2018
Insulin induced hypoglycaemia: comparison of glucose and glycerol concentrations in plasma and microdialysate from
Insights
Interstitial glucose levels in children lag behind plasma glucose during hypoglycemia recovery. This delay impacts how the body responds to low blood sugar and insulin.
Area of Science:
- Pediatric Endocrinology
- Metabolic Dynamics
- Glucose Homeostasis
Background:
- Understanding glucose dynamics in children is crucial for managing metabolic disorders.
- Hypoglycemia poses significant risks in pediatric populations.
- Interstitial glucose monitoring offers insights into tissue-level metabolic changes.
Purpose of the Study:
- To investigate the relationship between plasma and interstitial glucose during induced hypoglycemia in children.
- To examine the dynamics of glucose and glycerol in plasma and subcutaneous adipose tissue.
- To assess the counterregulatory hormone response during hypoglycemia.
Main Methods:
- Studied six prepubertal/early pubertal children undergoing an arginine-insulin tolerance test.
- Utilized multiple blood sampling and microdialysis of subcutaneous adipose tissue.
- Measured glucose and glycerol (lipolysis index) in plasma and dialysate, alongside hormone levels.
Main Results:
- Plasma and dialysate glucose mirrored each other at baseline and after arginine infusion.
- Glucose levels decreased in parallel in both compartments after insulin administration.
- Interstitial glucose rebound was delayed by 16 minutes post-hypoglycemia compared to plasma.
- Lipolysis, indicated by glycerol, was suppressed by insulin but reactivated during hypoglycemia despite hyperinsulinemia.
Conclusions:
- Interstitial glucose concentration recovery is significantly delayed after induced hypoglycemia in children.
- The body's counterregulatory response to hypoglycemia can override the antilipolytic effects of insulin.
- These findings highlight differences in glucose kinetics between plasma and interstitial fluid during metabolic stress.
Aims:
To investigate the dynamics between plasma and dialysate glucose during hypoglycaemia in children.
Study Design:
Six children in prepuberty or early puberty were investigated by multiple blood sampling and microdialysis of subcutaneous adipose tissue during a standard arginine-insulin tolerance test. Glucose and glycerol, as an index of lipolysis, were measured in samples from both compartments. Plasma concentrations of insulin and the main counterregulatory hormones were also measured.
Results:
Plasma and dialysate glucose concentrations were very similar at baseline and increased in concert after infusion of arginine, probably in response to glucagon release. After insulin injection, glucose in both plasma and dialysate fell in parallel. The subsequent hypoglycaemic stress response induced a rapid rebound in the plasma concentration with a mean (SD) delay in the dialysate of 16 (3) minutes. Plasma glycerol was approximately fivefold lower than in the dialysate and did not fluctuate significantly. Dialysate glycerol decreased with arginine infusion and reached a nadir immediately following insulin administration. Subsequently, the antilipolytic effect of insulin was overcome by the hypoglycaemic stress response, and lipolysis prevailed in spite of hyperinsulinaemia.
Conclusion:
After rapidly induced hypoglycaemia, rebound of interstitial glucose concentrations is significantly delayed compared with plasma concentrations, and the antilipolytic effect of hyperinsulinaemia is opposed possibly by the hypoglycaemic stress response.
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