Hyperglycemia Clinical Trial
Official title:
Ischemia/Reperfusion Injury of Human Endothelium: Role of Glucose and Statins
Anesthetic preconditioning (APC, a brief exposure to an anesthetic gas) has become an area of intense research interest because of its ability to protect tissue and organs from injury resulting from a cessation of blood flow and then a re-establishment of flow. The blood vessel lining plays a key role in this injury. This research will examine, in human volunteers, several important modifiers of APC in human blood vessels: high blood sugar, vitamin C, and statin drugs. Thus, the proposed studies will advance the investigators' understanding of mechanisms of this injury in humans and explore important modifiers of APC protection from injury.
Injury to vital organs and tissue can occur when blood flow is stopped and then
re-established. This happens in a variety of clinical situations and contributes to poor
outcomes. A newer concept of protection from this injury by an anesthetic drug might occur
because of the effect of the volatile anesthetics on the tissue that lines blood vessels.
Thus, a brief exposure to a volatile anesthetic before a cessation of blood flow, called
anesthetic preconditioning (APC), can substantially reduce the resulting injury to the
lining of the blood vessels. In animal models, high levels of blood sugar block this
protection, while cholesterol lowering drugs (statins) restore the protection and may
independently protect blood vessel lining from injury. The interactions of high blood sugar
and statin drugs on the blood vessel reaction to APC and a subsequent 20-min cessation of
blood flow to the forearm will be studied in humans. In addition, the involvement of
reactive oxygen species (ROS) in the harmful effects of high blood sugar and the beneficial
effects of statins will be explored. The following four hypotheses will be studied: 1) high
blood sugar blocks the anesthetic protection of blood vessels from injury in a dose and time
dependent manner; 2) reactive oxygen species are involved in the inhibition of APC by high
blood sugar; 3) statins modulate injury in a dose related manner; and 4) statins reduce high
blood sugar inhibition of APC.
A standard model to evaluate forearm blood vessel function will be used. Thin
rubber-band-like strain gauges will be strapped around each forearm and the change in their
stretch during a variety of interventions on the experimental arm (the other arm will not
receive any interventions and will be the control arm) will be measured. These interventions
will allow the investigator to determine whether the hypotheses listed above are true.
During all studies, there will be a 20-min arrest of the forearm circulation. Additional
effects of injury, APC, high blood sugar, and statins will be determined by evaluating blood
vessel inflammatory responses from "markers" in blood samples taken before and after I/R
injury. Several studies will involve varying the forearm blood glucose concentration for
brief (30 min) to longer (2 hours) periods prior to APC and injury. The ROS scavenger
vitamin C will be used to evaluate the role of ROS in adverse effects of high blood sugar.
There are several other studies that will continue to seek the mechanism of action of this
effect via the use of other drug interactions.
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Allocation: Non-Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science
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