Adenosine and A2A Receptors in Human Brown Adipose Tissue
NCT ID: NCT03327168
Last Updated: 2017-11-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
11 participants
INTERVENTIONAL
2015-11-01
2016-06-30
Brief Summary
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Understanding the mechanisms of BAT activation and the role of endocannabinoids in humans is important and beneficial in fighting against the epidemic of obesity and diabetes.
Detailed Description
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In this study the investigators use the PET radiotracer \[15O\]-H2O to quantify perfusion of BAT, white adipose tissue (WAT) and muscle in three conditions: room temperature, cold exposure and intravenous infusion of adenosine. Another PET radiotracer \[11C\]TMSX is used to quantify adenosine A2A receptor density of BAT, WAT and muscle in room temperature and during cold exposure.
Conditions
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Keywords
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Study Design
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NON_RANDOMIZED
CROSSOVER
BASIC_SCIENCE
NONE
Study Groups
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Adenosine
Perfusion is measured using PET/CT during intravenous infusion (0.14 mg/kg/min) of adenosine.
Adenosine
Intravenous infusion of adenosine (0.14 mg/kg) is administered for 5 minutes during PET/CT scan.
Room temperature
Perfusion and A2A receptor density is measured using PET/CT in resting room temperature conditions.
No interventions assigned to this group
Cold exposure
Perfusion and A2A receptor density is measured using PET/CT during controlled cold exposure.
Cold exposure
Controlled cold exposure is performed before and during PET/CT scan.
Interventions
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Adenosine
Intravenous infusion of adenosine (0.14 mg/kg) is administered for 5 minutes during PET/CT scan.
Cold exposure
Controlled cold exposure is performed before and during PET/CT scan.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. BMI 20 - 28 kg/m2
3. Age: 18- 40 years
4. Normal OGTT
5. Healthy, no regular medication
Exclusion Criteria
2. Low or high blood pressure
3. Asthma or other obstructive lung disease
4. Sick sinus syndrome, prolonged QT-interval, or any heart disease
5. Any chronic disease that could affect the study outcome, including diabetes
6. Mental disorder or poor compliance
7. Eating disorder or excessive use of alcohol, tobacco smoking or drug use
8. Past dose of radiation
9. Any other condition that in the opinion of the investigator could create a hazard to the subject safety, endanger the study procedures or interfere with the interpretation of study results
18 Years
40 Years
MALE
Yes
Sponsors
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University of Bonn
OTHER
Turku University Hospital
OTHER_GOV
Responsible Party
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Kirsi Virtanen
Adjunct Professor
Principal Investigators
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Kirsi A Virtanen, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Turku University Hospital
Other Identifiers
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T201/2015
Identifier Type: -
Identifier Source: org_study_id