Muscle Reflex Inhibition in Hypoxic Exercise

Sponsor
University of British Columbia (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05619887
Collaborator
(none)
14
1
4
12
1.2

Study Details

Study Description

Brief Summary

The goal of this interventional study is to compare muscle reflex function under settings of normoxia (normal oxygen level), acute hypoxia (brief oxygen-lack) and chronic hypoxia (long-duration exposure to oxygen-lack).

The main question is: Does the muscle reflex adapt to chronic hypoxia?

Young, healthy participants will complete light-to-high intensity cycling exercise with and without suppression of the muscle reflex. Suppression of the muscle reflex will be via spinal administration of the opioid Fentanyl. In the control condition, saline will be administered into the spinal space. Participants will complete control (saline) and experimental (Fentanyl) exercise conditions at sea-level (Kelowna, BC, Canada) breathing room air and whilst breathing a lower fraction of oxygen (acute hypoxia). Thereafter, participants will complete the exercise test after living at high altitude (White Mountain, CA, USA) for 2 weeks whilst breathing room air (chronic hypoxia) and breathing a higher fraction of oxygen (restored normoxia).

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

Purpose:

To determine whether muscle reflex control of cardiorespiratory function is sensitized by chronic exposure to low oxygen environments. To do this, fentanyl will be administered into the lumbar spine to suppress nerve activity coming from the muscle during upright cycling exercise.

Hypothesis:

Cardiorespiratory responses (ventilation, blood pressure and heart rate) to cycling exercise will be suppressed when muscle reflex activity is partially blocked with fentanyl administration. This suppression will be augmented in a dose-dependent manner with the duration of hypoxic exposure.

Design:

This is a repeated measures cross-over design with participants completing control (saline) and experimental (fentanyl) conditions both low and high altitude; a total of six visits is required. Sea level testing sessions will involve a cycling exercise bout while breathing room air and a second exercise bout breathing a hypoxic gas mixture meant to simulate the altitude at White Mountain. High altitude testing sessions will involve the same cycling exercise bout while breathing room air and another exercise bout while breathing a hyperoxic gas mixture meant to simulate the altitude in Kelowna. Cardiorespiratory (ventilation, blood pressure and heart rate) will be measured throughout with (fentanyl) and without (saline) muscle reflex suppression. A 7-km time trial test will be performed during each visit to determine how the muscle reflex influences exercise performance.

Experimental procedures:

Participants will visit the lab on six occasions; 3 in both Kelowna and White Mountain. Participants will be requested to practice regular exercise and dietary habits that can be easily replicated in the 24 hours prior to every laboratory visit. Exercise and dietary patterns will be documented during the first visit and thereafter the participants will be reminded of these practices and instructed to match them as closely as possible in the 24 hours leading up to all subsequent visits. Participants will only be instructed to avoid heavy exercise in the 12 hours prior to testing sessions. On the first visit (Kelowna), participants will be introduced into the lab, where we will give oral and written instruction detailing the procedures and associated risks related to participating. Details of the experimental visits are outlined below:

Sea level:
  • Familiarization and fitness test (1 h) General introduction to the lab, testing equipment and measurements devices. Maximal aerobic power test on an upright cycle ergometer.

  • Main experimental visit #1, saline or fentanyl (2 h) Invasive cannulas will be inserted and drugs administered by an anesthetist. Complete four steady-state exercise bouts (3 min each) while breathing room air.

After a 2 min wash-in, complete four steady-state exercise bouts (3 min each) while breathing hypoxic gas (FiO2 = 0.15).

Complete a 7 km time trial test. - Main Experimental visit #2, Intrathecal (spinal) saline or fentanyl (2 h) Complete identical procedures as experimental visit #1, but the opposite condition.

High altitude:
  • High altitude fitness test #1 (30 min) Maximal aerobic power test on upright cycle ergometer.

  • Main experimental visit #3, saline or fentanyl (2 h) Invasive cannulas will be inserted and drugs administered by an anesthetist. Complete four steady-state exercise bouts (3 min each) while breathing room air.

After a 2 min wash-in, complete four steady-state exercise bouts (3 min each) while breathing hyperoxic gas (FiO2 = 0.30).

Complete a 7 km time trial test.

  • Main experimental visit #4, saline or fentanyl (2 h) Complete identical procedures as experimental visit #3, but the opposite condition.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
14 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
Participants will complete all interventions (control and experimental) following drug washout.Participants will complete all interventions (control and experimental) following drug washout.
Masking:
Double (Participant, Investigator)
Masking Description:
The participant will not know whether they are receiving placebo or fentanyl. The primary investigator will also no know if the participant is receiving placebo or fentanyl.
Primary Purpose:
Basic Science
Official Title:
Effect of Muscle Reflex Inhibition on Cardiorespiratory Responses to Exercise in Hypoxia
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Sea level control

Sea level exercise will be completed after the administration of 1 mL of isotonic saline into the intrathecal (spinal) space between L3-L4.

Other: Saline
An equal volume (as above) of saline will be administered into the intrathecal (spinal) space. This has no effect of cardiorespiratory responses at rest or during exercise; it is to control for the invasiveness of the procedure required to suppress muscle feedback in the experimental condition.

Experimental: Sea level experimental (muscle reflex suppression)

Sea level exercise will be completed after the administration of 0.25 mL of fentanyl into the intrathecal (spinal) space between L3-L4.

Drug: Fentanyl
Fentanyl, when administered into the intrathecal (spinal) space suppresses feedback from the muscles below the site of action, i.e., the legs. It does not affect resting cardiorespiratory responses. We are using this to test what role the muscle reflex plays during exercise.
Other Names:
  • fentaNYL Citrate
  • Placebo Comparator: High altitude control

    High altitude exercise will be completed after the administration of 1 mL of isotonic saline into the intrathecal (spinal) space between L3-L4.

    Other: Saline
    An equal volume (as above) of saline will be administered into the intrathecal (spinal) space. This has no effect of cardiorespiratory responses at rest or during exercise; it is to control for the invasiveness of the procedure required to suppress muscle feedback in the experimental condition.

    Experimental: High altitude experimental (muscle reflex suppression)

    High altitude exercise will be completed after the administration of 0.25 mL of fentanyl into the intrathecal (spinal) space between L3-L4.

    Drug: Fentanyl
    Fentanyl, when administered into the intrathecal (spinal) space suppresses feedback from the muscles below the site of action, i.e., the legs. It does not affect resting cardiorespiratory responses. We are using this to test what role the muscle reflex plays during exercise.
    Other Names:
  • fentaNYL Citrate
  • Outcome Measures

    Primary Outcome Measures

    1. Ventilation [Data collected during steady-state breathing in the last minute of exercise]

      Ventilation, in liters per minute.

    Secondary Outcome Measures

    1. Mean arterial blood pressure (entire pressure wave) [Data collected during steady-state breathing in the last minute of exercise]

      Blood pressure, in millimeters of mercury

    Other Outcome Measures

    1. Exercise performance [The duration, i.e., however long it takes to complete the exercise; this is typically 7-14 minutes]

      Time, in seconds, to complete 7 kilometers of cycling, i.e. a time-trial

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    19 Years to 40 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • aged 19 - 40 years old

    • not taking medications (exception oral contraception)

    • no history of cardiovascular, respiratory or neurological disease

    • members of the high altitude expedition to White Mountain in 2023

    Exclusion Criteria:
    • post-menopausal or pregnant

    • obese

    • current smokers

    • taking prescription medications that may affect responses to exercise

    All potential participants will be screened by a physician to identify co-morbidities

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of British Columbia - Okanagan Campus Kelowna British Columbia Canada V1V1V7

    Sponsors and Collaborators

    • University of British Columbia

    Investigators

    • Principal Investigator: Philip N Ainslie, PhD, University of British Columbia- Okanagan

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Phil Ainslie, Professor, University of British Columbia
    ClinicalTrials.gov Identifier:
    NCT05619887
    Other Study ID Numbers:
    • Muscle_reflex_hypoxia
    First Posted:
    Nov 17, 2022
    Last Update Posted:
    Nov 23, 2022
    Last Verified:
    Nov 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Phil Ainslie, Professor, University of British Columbia
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 23, 2022