Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07106450

Training Induced Muscle-Adipose EV Communication

This study examines how muscle cells communicate with fat cells through tiny packages called extracellular vesicles (EV) during exercise. These vesicles carry important molecules that may affect how the body processes sugar and fat. The research team observed significant variability in the adipose response to exercise, and used this variability to gain further insight into the mechanism through which mature microRNA-1 (miR-1) changes in adipose tissue. The investigators selected six subjects with the highest increase in miR-1 abundance in adipose tissue after exercise and compared them with the six subjects that had the most dramatic decrease in miR-1 abundance after exercise. The research team observed that participants intrinsically vary in their ability to endocytose EV into adipose tissue. It is unclear whether this variance in receptivity is a cause or consequence of the significant difference in EV-delivery of miR-1 to adipose tissue.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

30 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Kentucky

Lexington, Kentucky, 40506, United States

About this study

This study investigates muscle-derived extracellular vesicle (EV) communication with adipose tissue and how this pathway is altered in pre-diabetes. The investigators will recruit 40 participants (20 euglycemic controls, 20 pre-diabetic) aged 30-55 years, equally distributed by sex. Pre-diabetes will be defined as impaired fasting glucose (100-125 mg/dL), impaired glucose tolerance (2-hour oral glucose tolerance test (OGTT) 140-199 mg/dL), or HbA1C 5.7-6.4%.

Following informed consent and medical screening at the Center for Clinical and Translational Sciences, participants will undergo baseline blood draw and tissue biopsies (subcutaneous adipose and vastus lateralis muscle) one hour prior to exercise. The resistance exercise protocol consists of whole-body resistance training at 80% 1RM (repetition maximum) intensity including bench press, leg press, and pull-downs. Blood samples will be collected immediately post-exercise and at 30, 60, and 90 minutes. Post-exercise biopsies will be obtained approximately 60 minutes after exercise cessation.

Laboratory analyses will include: (1) microRNA-1 (miR-1) quantification in adipose tissue by quantitative reverse transcription polymerase chain reaction (qRT-PCR) as the primary validated outcome of EV uptake; (2) fluorescently-labeled EV uptake assessment in cultured adipocytes using microscopy; (3) RNA sequencing (RNA-seq) of adipose tissue to identify transcriptomic signatures associated with EV uptake capacity; (4) primary cell culture studies using adult-derived human adipocyte stem cells (ADHASC); and (5) EV isolation and characterization using size exclusion chromatography and density gradient centrifugation.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 30-55 years
  • Sedentary lifestyle (exercise <1 day/week for at least 3 months prior to enrollment)
  • Able to provide informed consent
  • For Control Group: BMI < 27 kg/m², normal glucose tolerance, no more than 1 feature of metabolic syndrome
  • For Prediabetic Group: BMI > 30 kg/m², at least 3 features of metabolic syndrome including prediabetes (defined as fasting plasma glucose 100-125 mg/dL OR 2-hour post-load glucose on 75g OGTT 140-199 mg/dL OR HbA1C 5.7-6.4%)

Exclusion criteria

  • Pregnancy (confirmed by pregnancy test in women of childbearing potential)
  • Type 2 diabetes mellitus
  • Cardiovascular contraindications to resistance exercise
  • Medical conditions that would interfere with muscle or adipose tissue biopsy procedures
  • Use of medications that significantly affect glucose metabolism or exercise response
  • Active participation in structured exercise programs (>1 day/week) within 3 months of enrollment
  • Inability to safely participate in resistance exercise protocol

Treatment and study plan

Acute Resistance Exercise

Behavioral

Participants will perform three sets of eight repetitions, with a 90-120 second rest between sets, with a fourth set performed to failure. All resistance exercise will be performed on pneumatic resistance devices (Keiser Sports Health Equipment, Fresno, CA).

Other names: Strength Training

Primary outcomes

  1. miR-1 abundance in adipose tissue

    Time frame: 60 minutes post-exercise (single measurement)

    Quantification of mature microRNA-1 levels in subcutaneous adipose tissue biopsies using quantitative Real Time-PCR as validated biomarker of in vivo extracellular vesicle uptake

  2. Extracellular vesicle uptake capacity in primary adipocytes

    Time frame: 24-48 hours post-isolation (in vitro culture)

    Measurement of fluorescently-labeled extracellular vesicle internalization in cultured primary adipocytes using confocal microscopy to quantify uptake rates in units of vesicles per minute per cell.

Secondary outcomes

  1. Serum extracellular vesicle miR-1 content

    Time frame: Baseline, 0, 30, 60, and 90 minutes post-exercise

    Time-course analysis of microRNA-1 abundance in isolated serum extracellular vesicles using quantitative RT-PCR to track temporal dynamics of muscle-derived vesicle release

  2. Adipose tissue transcriptomic signatures

    Time frame: 60 minutes post-exercise (single measurement)

    RNA-sequencing analysis of subcutaneous adipose tissue to identify differential gene expression patterns associated with high versus low extracellular vesicle uptake capacity, focusing on endocytotic pathways

  3. Adrenergic receptor gene expression in adipose tissue

    Time frame: 60 minutes post-exercise (single measurement)

    Quantitative RT-PCR measurement of ADRβ1, ADRβ2, and ADRβ3 receptor mRNA levels in subcutaneous adipose tissue as downstream targets of miR-1 delivery

  4. Primary muscle miR-1 transcript levels

    Time frame: 60 minutes post-exercise (single measurement)

    Quantification of pri-miR-1a and pri-miR-1b primary transcript abundance in vastus lateralis muscle biopsies using quantitative RT-PCR to assess exercise-induced miR-1 biogenesis

Other outcomes

  1. Extracellular vesicle tetraspanin marker profiles using ExoView platform

    Time frame: Baseline and 90 minutes post-exercise

    Characterization of circulating extracellular vesicle subpopulations based on surface tetraspanin protein expression (CD63, CD81, CD9) using ExoView R100 platform immunofluorescence detection and high resolution imaging.

    Units of Measure: Percentage of total vesicles positive for each marker.

  2. Circulating extracellular vesicle count using ExoView single vesicle analysis platform

    Time frame: Baseline and 90 minutes post-exercise

    Total number of circulating extracellular vesicles quantified using the ExoView R100 platform single vesicle analysis technology with tetraspanin capture antibodies (CD63, CD81, CD9). Units of Measure: Particles per milliliter

  3. Extracellular vesicle size distribution using ExoView single vesicle analysis

    Time frame: Baseline and 90 minutes post-exercise

    Size characterization of individual circulating extracellular vesicles measured using ExoView R100 platform automated analysis. Units of Measure: Nanometers (diameter).

Study contacts

Contact information is provided by the study sponsor or research team.

Yuan Wen, MD/PhD

CONTACT

[email protected]

18592187185

Sponsors and collaborators

Lead sponsor

Yuan Wen

Other

Collaborators

  • National Institute of General Medical Sciences (NIGMS)

Registry information

Official study title

Muscle-derived Extracellular Vesicles and Their Interactions With Adipocytes in Human Metabolic Dysfunction

Acronym: TIMER2

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Aug 6, 2025
Registry last updated
Jun 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.