Remote ischemic conditioning: A potential therapeutic strategy of type 2 diabetes

Jie Liu1, Xin Sun2, Hang Jin2

  • 1Stroke Center & Clinical Trial and Research Center for Stroke, Department of Neurology, the First Hospital of Jilin University, No. 1 Xinmin Street, Changchun 130021, China; China National Comprehensive Stroke Center, No. 1 Xinmin Street, Changchun 130021, China; Jilin Provincial Key Laboratory of Cerebrovascular Disease, No. 1 Xinmin Street, Changchun 130021, China.

Medical Hypotheses
|December 5, 2020
PubMed

Insights

Remote ischemic conditioning (RIC) may protect against type 2 diabetes (T2D) by targeting inflammation and oxidative stress. Higher intensity RIC may restore protective effects diminished by T2D, offering a novel therapeutic approach.

Area of Science:

  • Cardiovascular Medicine
  • Endocrinology
  • Physiology

Background:

  • Type 2 diabetes (T2D) involves insulin resistance and beta-cell failure, with inflammation and oxidative stress playing key roles.
  • Remote ischemic conditioning (RIC) is a non-invasive intervention known for protecting against ischemia-reperfusion (I/R) injuries.
  • T2D may impair RIC's protective effects due to heightened inflammation and oxidative stress.

Purpose of the Study:

  • To hypothesize that RIC could offer therapeutic benefits for T2D.
  • To explore the potential of RIC in targeting T2D-related signaling pathways.

Main Methods:

  • Review of existing literature on RIC and T2D mechanisms.
  • Hypothesis generation based on overlapping pathways.

Main Results:

  • RIC activates neural, humoral, and immune pathways, modulating inflammation and oxidative stress.
  • T2D can attenuate RIC's benefits, potentially reversed by higher conditioning intensity.
  • Overlapping mechanisms suggest RIC's applicability to T2D.

Conclusions:

  • RIC holds potential as a therapeutic strategy for T2D.
  • Targeting inflammation, oxidative stress, and immune dysregulation via RIC may be beneficial.
  • Further research is warranted to validate RIC's efficacy in T2D treatment.

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