MedPath

Translational Study Using Human Abdominal Adipose Tissue Biopsies to Investigate the Role of Cannabinoid Receptor 1 (CB1) in Controlling Endocannabinoid and Adipokine Secretion

Not Applicable
Recruiting
Conditions
Abdominal Obesity
Diabete Type 2
Interventions
Procedure: Sampling of adipose tissue
Registration Number
NCT04940962
Lead Sponsor
Centre Hospitalier Universitaire Dijon
Brief Summary

Abdominal obesity and type 2 diabetes are associated with the hyperactivation of the endocannabinoid system. Several animal and human studies indicate that circulating endocannabinoid (EC) levels are correlated with body fat. Thus, adipose tissue, which possesses the enzymatic machinery for the synthesis of ECs, could be the main producer of plasma ECs.

Today, it is clearly established that stimulation of the endocannabinoid system, via activation of cannabinoid receptor 1 (CB1s) located in the brain, leads to increased food intake and weight gain. Moreover, peripheral CB1s present in organs such as the liver, muscles and adipose tissue are involved in the establishment of metabolic deregulations linked to obesity (steatosis, insulin resistance, dyslipidemia).

Thus, ECs produced by adipose tissue could play a key role in the regulation of carbohydrate-lipid homeostasis through their autocrine or paracrine actions by activating central and peripheral CB1s. Therefore, the objective of this study is to:

1. clarify whether obesity, associated or not with diabetes, leads to an overproduction of ECs (specifying which ones) by visceral or subcutaneous adipose tissue

2. to determine whether blocking CB1s with new peripherally acting antagonists can lead to a reduction in the production of ECs by adipose tissue.

This study will also provide an opportunity to evaluate the production of adipokines and cytokines involved in the control of energy homeostasis under the different experimental conditions.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
Male
Target Recruitment
45
Inclusion Criteria
  • Controls:
  • men or post-menopausal women aged between 18 and 80
  • gave oral consent
  • to undergo visceral surgery

Non-diabetic obese subjects:

  • men or post-menopausal women aged between 18 and 80
  • BMI > 30
  • gave oral consent
  • to undergo visceral surgery

Obese diabetic subjects:

  • men or post-menopausal women aged between 18 and 80
  • type 2 diabetic not treated with Insulin or GLP-1 agonist
  • BMI > 30
  • gave oral consent
  • to undergo visceral surgery
Exclusion Criteria
  • Controls:
  • Person not covered by national health insurance.
  • BMI > 30
  • diabetes
  • chronic inflammatory disease
  • cancer undergoing chemotherapy or chemotherapy less than a year old
  • digestive cancer with recent weight loss (≥10%) and/or malnutrition
  • known metastatic cancer
  • cancer undergoing long-term hormonal treatment
  • protected adult

Non-diabetic obese subjects:

  • Person not covered by national health insurance
  • diabetes
  • chronic inflammatory disease
  • cancer undergoing chemotherapy or chemotherapy less than a year old
  • digestive cancer with recent weight loss (≥10%) and/or malnutrition
  • known metastatic cancer
  • cancer undergoing long-term hormonal treatment
  • protected adult

Obese diabetic subjects:

  • Person not covered by national health insurance
  • chronic inflammatory disease
  • cancer undergoing chemotherapy or chemotherapy less than a year old
  • digestive cancer with recent weight loss (≥10%) and/or malnutrition
  • known metastatic cancer
  • cancer undergoing long-term hormonal treatment
  • type 1 diabetes
  • secondary diabetes
  • protected adult

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Non-diabetic obeseSampling of adipose tissue-
Diabetic obeseSampling of adipose tissue-
WitnessesSampling of adipose tissue-
Primary Outcome Measures
NameTimeMethod
Kinetics of the appearance of endocannabinoids produced by visceral adipose tissue explants in culture medium estimated by the area under the curve in obese subjects and in controls.12 hours

The assay will be performed using a technique of liquide chromatography coupled to a mass spectrometer.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Chu Dijon Bourgogne

🇫🇷

Dijon, France

© Copyright 2025. All Rights Reserved by MedPath