The Role of Histamine in Muscle Protein Synthesis Following Resistance Training

December 6, 2023 updated by: University Ghent

The Role of Histamine in Muscle Protein Synthesis Following Chronic Resistance Training

Blocking histamine H1/H2 receptors blunts chronic endurance training adaptations. The current study addresses the following research question: "What is the influence of histamine H1 signaling on training adaptations following ten weeks of resistance training in human skeletal muscle." Results from this study will yield more insights into the molecular mechanisms of adaptations to exercise training.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

50

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Oost-Vlaanderen
      • Ghent, Oost-Vlaanderen, Belgium, 9000
        • Recruiting
        • Department of movement and sports sciences, Ghent University, Belgium
        • Contact:

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.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Male
  • 18-45 years
  • Not to medium physically active

Exclusion Criteria:

  • Smoking
  • Chronic disease
  • High blood pressure
  • Supplement or medication intake
  • Seasonal allergies
  • Vegetarian / vegan
  • Resistance trained

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Placebo Comparator: 1: Placebo
Lactose
Oral placebo
Resistance training: lower body exercise
Experimental: H1 blockade: Telfast (180mg Fexofenadine)
H1: Telfast (180mg Fexofenadine)
Resistance training: lower body exercise
H1 blockade: oral blockade with 180mg Fexofenadine

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscle volume
Time Frame: Before and after the 10 weeks of resistance training
Change in muscle volume
Before and after the 10 weeks of resistance training
Maximal dynamic strength of leg press, bench press, bicep curl and leg curl
Time Frame: Before and after the 10 weeks of resistance training
Change in maximal dynamic strength of leg press, bench press, bicep curl and leg curl
Before and after the 10 weeks of resistance training
Muscle fiber hypertrophy in muscle biopsies
Time Frame: Before and after the 10 weeks of resistance training
Change in muscle fiber hypertrophy in muscle biopsies
Before and after the 10 weeks of resistance training
Vascular function measured with a single passive leg movement (sPLM: change in femoral blood flow measured with Doppler ultrasound before and after one passive flexion/extension of the leg)
Time Frame: Before and after the 10 weeks of resistance training
Change in vascular function with a single passive leg movement (sPLM: change in femoral blood flow measured with Doppler ultrasound before and after one passive flexion/extension of the leg)
Before and after the 10 weeks of resistance training
Matsuda index, to estimate whole body glucose metabolism, will be calculated using an oral glucose tolerance test (OGTT: concentration of glucose and insulin in the blood will be measured before and after drinking 75g glucose)
Time Frame: Before and after the 10 weeks of resistance training
Change in Matsuda index, to estimate whole body glucose metabolism, will be calculated using an oral glucose tolerance test (OGTT: concentration of glucose and insulin in the blood will be measured before and after drinking 75g glucose)
Before and after the 10 weeks of resistance training

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Blood pressure (systolic and diastolic)
Time Frame: Before and after the 10 weeks of resistance training
Chance in Blood pressure (systolic and diastolic)
Before and after the 10 weeks of resistance training
Resting heart rate
Time Frame: Before and after the 10 weeks of resistance training
Chance in Resting heart rate
Before and after the 10 weeks of resistance training

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Wim Derave, Professor, University Ghent

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2023

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

December 20, 2022

First Submitted That Met QC Criteria

November 29, 2023

First Posted (Actual)

November 30, 2023

Study Record Updates

Last Update Posted (Estimated)

December 13, 2023

Last Update Submitted That Met QC Criteria

December 6, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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