Type 2 Diabetes Is Associated with Altered NF-κB DNA Binding Activity, JNK Phosphorylation, and AMPK Phosphorylation in Skeletal Muscle after LPS
2011

Type 2 Diabetes and Inflammation Response in Muscle

Sample size: 20 publication 10 minutes Evidence: moderate

Author Information

Author(s): Andreasen Anne Sofie, Kelly Meghan, Berg Ronan Martin Griffin, Møller Kirsten, Pedersen Bente Klarlund

Primary Institution: University Hospital Rigshospitalet, Copenhagen, Denmark

Hypothesis

The inflammatory stimulus, an intravenous bolus injection of Escherichia coli LPS, would increase the activity of intermediates associated with insulin resistance more profoundly in patients with type 2 diabetes.

Conclusion

Patients with type 2 diabetes exhibit a different inflammatory response in skeletal muscle compared to those with normal glucose tolerance, which may contribute to insulin resistance.

Supporting Evidence

  • Patients with type 2 diabetes showed increased NF-κB binding activity after LPS.
  • JNK phosphorylation was more pronounced in diabetic patients compared to those with normal glucose tolerance.
  • AMPK phosphorylation increased in volunteers with normal glucose tolerance but not in those with diabetes.

Takeaway

This study looked at how inflammation affects muscle in people with type 2 diabetes. It found that their muscles react differently to inflammation than those of people without diabetes.

Methodology

The study involved 10 patients with type 2 diabetes and 10 participants with normal glucose tolerance who received an intravenous bolus of E. coli lipopolysaccharide (LPS) and had muscle biopsies taken at various time points.

Potential Biases

Potential variability in human responses and small sample sizes may introduce bias.

Limitations

The study had a small sample size and did not investigate other important signaling pathways that may affect insulin sensitivity.

Participant Demographics

10 patients with type 2 diabetes and 10 age-matched participants with normal glucose tolerance.

Statistical Information

P-Value

p<0.05

Confidence Interval

95% CI

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pone.0023999

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication