CANBAT: CB1 Receptors in Human Brown Adipose Tissue

Sponsor
Turku University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT02941172
Collaborator
(none)
18
1
3
35.9
0.5

Study Details

Study Description

Brief Summary

This study investigates cannabinoid CB1 receptors in human brown adipose tissue (BAT) and other tissues using positron emission tomography (PET) imaging. Subjects will be scanned in room temperature conditions and during controlled cold exposure, and the density of CB1 receptors in BAT and other tissues will be quantified. The investigators hypothesize, that cannabinoid signaling is increased in cold conditions, when BAT is metabolically active.

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Cold exposure
  • Other: [18F]FMPEP-d2
  • Other: [18F]FDG
N/A

Detailed Description

Endocannabinoids have an important role in regulating energy balance and metabolism. Cannabinoid 1 receptors (CB1) are found in several tissues such as brown adipose tissue (BAT). Endocannabinoids and CB1 receptors participate in the control of lipid and glucose metabolism, and blockage of CB1 receptors has been found to improve metabolic factors linked to obesity and cardiovascular disease, making CB1 antagonists potential drugs against obesity and diabetes.

In this study the investigators use a PET radiotracer [18F]FMPEP-d2, which binds to CB1 receptors in vivo, to quantify the CB1 receptor density in BAT, white adipose tissue, muscle and the brain. This study is done once in warm conditions and once during controlled cold exposure. To verify whether the subject has metabolically active BAT, an additional PET scan with the radiotracer [18F]FDG is performed.

Study Design

Study Type:
Interventional
Actual Enrollment :
18 participants
Allocation:
Non-Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Cannabinoid CB1 Receptors in Human Brown Adipose Tissue
Study Start Date :
Jan 1, 2015
Actual Primary Completion Date :
Jul 30, 2017
Actual Study Completion Date :
Dec 30, 2017

Arms and Interventions

Arm Intervention/Treatment
Other: [18F]FMPEP-d2 in warm conditions

PET scan is performed using PET radiotracer [18F]FMPEP-d2 in standard room temperature conditions.

Other: [18F]FMPEP-d2
PET radiotracer used in imaging

Other: [18F]FMPEP-d2 in cold conditions

PET scan is performed using PET radiotracer [18F]FMPEP-d2 during controlled cold exposure.

Other: Cold exposure
Controlled cold exposure is performed before and during PET scan

Other: [18F]FMPEP-d2
PET radiotracer used in imaging

Other: [18F]FDG in cold conditions

PET scan is performed using PET radiotracer [18F]FDG during controlled cold exposure.

Other: Cold exposure
Controlled cold exposure is performed before and during PET scan

Other: [18F]FDG
PET radiotracer used in imaging

Outcome Measures

Primary Outcome Measures

  1. CB1 density of brown adipose tissue acquired with PET [within one study day]

    PET imaging is used to quantify CB1 receptors in tissues

Secondary Outcome Measures

  1. Glucose uptake of brown adipose tissue acquired with PET [within one study day]

    PET imaging is used to quantify glucose uptake in tissues

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 60 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Healthy volunteer

  • Group 1: BMI 20-26 kg/m2, Group2: BMI 27-40 kg/m2

Exclusion Criteria:
  • BMI < 20 kg/m2or BMI > 40 kg/m2

  • Any chronic disease that could affect the study outcome, including medicated type 2 diabetes

  • Mental disorder or poor compliance

  • Eating disorder or excessive use of alcohol, tobacco smoking or drug use

  • Past dose of radiation

  • Presence of any ferromagnetic objects that would make MR imaging contraindicated

  • 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Turku PET Centre (Turku University Hospital) Turku Finland 20521

Sponsors and Collaborators

  • Turku University Hospital

Investigators

  • Principal Investigator: Pirjo Nuutila, M.D., Ph.D., Turku PET Centre (Turku University Hospital)

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Pirjo Nuutila, Professor, Turku University Hospital
ClinicalTrials.gov Identifier:
NCT02941172
Other Study ID Numbers:
  • 42/2014
First Posted:
Oct 21, 2016
Last Update Posted:
Dec 20, 2018
Last Verified:
Dec 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Pirjo Nuutila, Professor, Turku University Hospital

Study Results

No Results Posted as of Dec 20, 2018