RECRUITING

Menthol Stimulation of Brown Adipose Tissue in Humans: Aim 1

Description

Brown adipose tissue becomes activated during cold conditions to increase thermogenesis (i.e., energy expenditure). Topical menthol application increases resting energy expenditure but it is unclear whether brown adipose tissue activation contributes to this rise in the energy expenditure. The overall goal with this project is to determine whether topical menthol application stimulates brown adipose tissue.

Study Overview

Study Details

Study overview

Brown adipose tissue becomes activated during cold conditions to increase thermogenesis (i.e., energy expenditure). Topical menthol application increases resting energy expenditure but it is unclear whether brown adipose tissue activation contributes to this rise in the energy expenditure. The overall goal with this project is to determine whether topical menthol application stimulates brown adipose tissue.

Targeted TRPM8 Stimulation and Brown Adipose Tissue Activation in Humans

Menthol Stimulation of Brown Adipose Tissue in Humans: Aim 1

Condition
Regulation of Energy Expenditure
Intervention / Treatment

-

Contacts and Locations

Bloomington

Indiana University, Bloomington, Indiana, United States, 47405

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Fluency in English
  • * Participate in 150 minutes or more of at least moderate intensity exercise per week during the previous year. Assessment of moderate intensity physical activity will be determined via the International Physical Activity Questionnaire (i.e., IPAQ) (described in detail in Section 7.0). This questionnaire defines moderate intensity exercise as "activities that take moderate physical effort and make you breathe somewhat harder than normal".
  • * Body fat ≤ 30% as determined by DEXA scan
  • * Be cleared for physical activity according to the 2020 Physical Activity Readiness Questionnnaire (PAR-Q+).
  • * Any autonomic cardiovascular, metabolic, neurologic, endocrine, or respiratory disease, that, in the opinion of the investigator, would exclude them from participation.
  • * Previously diagnosed liver and/or kidney dysfunction, including, but not limited to, acute and/or chronic kidney disease, cirrhosis, hepatitis, and fatty liver disease.
  • * Women who are pregnant or breastfeeding.
  • * Current use of tobacco or electronic cigarette, or regular (i.e., more than twice a week) use within the last 1 year.
  • * History of peripheral cold injury, skin disorder (eczema, psoriasis), or excessive tattooing.
  • * Known chronic (i.e., cancer, surgery) or acute conditions (i.e., diarrhea, constipation) of the rectum.
  • * Menthol allergy (described in detail in Section 7.0 and 9.0). Menthol can cause skin irritation when applied topically, especially for people with sensitive skin or allergies. For this reason, recruited participants will be screened for a menthol allergy during the informed consent/screening visit. We will apply a small quantity of the cream (\~2ml) to an isolated body area to limit skin exposure. In the case a rash develops during the application of the cream, research staff will irrigate the area to remove the substance and limit further exposure. A 24-hour follow-up phone call initiated by research staff will be implemented to follow-up on all adverse reactions. Detectable BAT activation during a localized cold stress test (i.e., face cooling test) (procedure described in detail in Section 7.0).
  • * Using medications with direct effects on the cardiovascular system including, but not limited to:
  • * Anticoagulants.
  • * Antiplatelet agents.
  • * ACE Inhibitors.
  • * Angiotensin II receptor blockers.
  • * Angiotensin-receptor neprilysin inhibitors.
  • * Beta blockers.
  • * Calcium, potassium, or sodium channel blockers.
  • * Cholesterol lowering medications.
  • * Digitalis preparations.
  • * Diuretics.
  • * Vasodilators.
  • * Anticholinergics.

Ages Eligible for Study

18 Years to 40 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Indiana University,

Blair D Johnson, PhD, PRINCIPAL_INVESTIGATOR, Indiana University

Study Record Dates

2026-09