The Role of Glucagon Like Peptide-1 in the Protective Effect of Remote Ischemic Conditioning During Ischemia-reperfusion

The mechanism behind the cardioprotective effect of remote preconditioning is incompletely understood. Data from experimental studies suggest that a combination of humoral and neurogenic factors mediate the transition of protective signals from peripheral tissues to the myocardium. A major break-through in the understanding of the signaling was the observation that vagal nerve activation is involved. Key signaling pathways in the target organ are likely to be mediated via the vascular endothelium which is known to play an important role during the early reperfusion period. Thus, animal studies have demonstrated that RIPC stimulates endothelial nitric oxide production secondary to down-regulation of arginase. It remains unclear, however, whether RIPC via activation of endothelial nitric oxide preserves endothelial function in humans. Additional data indicate strongly that glucagon-like peptide-1 (GLP-1) provides protection against ischemia-reperfusion injury in experimental animals models as well as in clinical studies. The role of GLP-1 in the protective effect of RIPC has previously not been investigated, however. The present study was therefore designed to determine the involvement of GLP-1 in the protection induced by RIPC via endothelial activation in humans. To this end we use a model of reversible ischemia-reperfusion injury in the forearm, and the GLP-1 antagonist exendin 9-39 (Ex 9-39).

Objective To test the hypothesis that GLP-1 is a mediator of protection of endothelial function induced by RIPC in ischemia-reperfusion.

Endpoints Primary: Change in endothelium dependent vasodilatation induced by RIPC Secondary: Change in plasma GLP-1

Study subjects The study is performed on healthy volunteers 18-60 years of age. All subjects will undergo a screening including medical history and routine clinical examination, and should be free of medication. A screening blood sample includes hemoglobin, leukocyte and platelet count, fasting blood glucose, HbA1c, total cholesterol, LDL cholesterol, HDL cholesterol, triglycerides.

Methods Endothelial function is determined in the brachial artery by flow-mediated dilation (FMD). Briefly, non-invasive examination of the radial artery of the non-dominant arm is performed with a 11 MHz (output 12 MHz) linear-array transducer connected to a Vivid E9. The transducer is connected to a flexible tripod to prevent movement of the probe. Images are recorded and saved every third second at end-diastole. Baseline radial artery diameter is recorded for one minute and defined as a mean from 20 images. A blood pressure cuff is placed around the upper part of the forearm, which is inflated to 30 mmHg above systolic pressure or 200 mmHg for 5 min. The diameter of the radial artery is continuously recorded for 3 min during hyperemia following deflation of the cuff. The three frames displaying maximum dilatation at end-diastole (triggered from the ECG) are used to calculate a mean diameter. All images are analyzed with Brachial analyzer (Medical Imaging Applications, Iowa City, IA, USA). FMD is calculated as a percentage increase in diameter from baseline diameter according to the following formula: diameter following cuff deflation-baseline diameter/baseline diameter x 100. All evaluations are performed blinded. A decrease in endothelial function is an established outcome of reperfusion injury.