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Muscle Reflex Inhibition in Hypoxic Exercise

Primary Purpose

Dyspnea, Muscle Strain

Status
Not yet recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Fentanyl
Saline
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Dyspnea focused on measuring Dyspnea, Exercise, Muscle reflex, Type III/IV afferents

Eligibility Criteria

19 Years - 40 Years (Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • University of British Columbia - Okanagan Campus

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Experimental

Placebo Comparator

Experimental

Arm Label

Sea level control

Sea level experimental (muscle reflex suppression)

High altitude control

High altitude experimental (muscle reflex suppression)

Arm Description

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

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

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

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

Outcomes

Primary Outcome Measures

Ventilation
Ventilation, in liters per minute.

Secondary Outcome Measures

Mean arterial blood pressure (entire pressure wave)
Blood pressure, in millimeters of mercury

Full Information

First Posted
November 9, 2022
Last Updated
November 19, 2022
Sponsor
University of British Columbia
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1. Study Identification

Unique Protocol Identification Number
NCT05619887
Brief Title
Muscle Reflex Inhibition in Hypoxic Exercise
Official Title
Effect of Muscle Reflex Inhibition on Cardiorespiratory Responses to Exercise in Hypoxia
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
June 2023 (Anticipated)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
June 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of British Columbia

4. Oversight

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
Data Monitoring Committee
No

5. 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).
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dyspnea, Muscle Strain
Keywords
Dyspnea, Exercise, Muscle reflex, Type III/IV afferents

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Participants will complete all interventions (control and experimental) following drug washout.
Masking
ParticipantInvestigator
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.
Allocation
Randomized
Enrollment
14 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sea level control
Arm Type
Placebo Comparator
Arm Description
Sea level exercise will be completed after the administration of 1 mL of isotonic saline into the intrathecal (spinal) space between L3-L4.
Arm Title
Sea level experimental (muscle reflex suppression)
Arm Type
Experimental
Arm Description
Sea level exercise will be completed after the administration of 0.25 mL of fentanyl into the intrathecal (spinal) space between L3-L4.
Arm Title
High altitude control
Arm Type
Placebo Comparator
Arm Description
High altitude exercise will be completed after the administration of 1 mL of isotonic saline into the intrathecal (spinal) space between L3-L4.
Arm Title
High altitude experimental (muscle reflex suppression)
Arm Type
Experimental
Arm Description
High altitude exercise will be completed after the administration of 0.25 mL of fentanyl into the intrathecal (spinal) space between L3-L4.
Intervention Type
Drug
Intervention Name(s)
Fentanyl
Other Intervention Name(s)
fentaNYL Citrate
Intervention Description
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.
Intervention Type
Other
Intervention Name(s)
Saline
Intervention Description
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.
Primary Outcome Measure Information:
Title
Ventilation
Description
Ventilation, in liters per minute.
Time Frame
Data collected during steady-state breathing in the last minute of exercise
Secondary Outcome Measure Information:
Title
Mean arterial blood pressure (entire pressure wave)
Description
Blood pressure, in millimeters of mercury
Time Frame
Data collected during steady-state breathing in the last minute of exercise
Other Pre-specified Outcome Measures:
Title
Exercise performance
Description
Time, in seconds, to complete 7 kilometers of cycling, i.e. a time-trial
Time Frame
The duration, i.e., however long it takes to complete the exercise; this is typically 7-14 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Travis D Gibbons, PhD
Phone
778.583.6976
Email
travis.gibbons@ubc.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Philip N Ainslie, PhD
Phone
250.807.8089
Email
philip.ainlie@ubc.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Philip N Ainslie, PhD
Organizational Affiliation
University of British Columbia- Okanagan
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of British Columbia - Okanagan Campus
City
Kelowna
State/Province
British Columbia
ZIP/Postal Code
V1V1V7
Country
Canada
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Philip N Ainslie, PhD
Phone
250.807.8089
Email
philip.ainslie@ubc.ca
First Name & Middle Initial & Last Name & Degree
Neil Eves, PhD
Phone
250.807.9676
Email
neil.eves@ubc.ca

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No personal data will be made available publicly or to other researchers.
Citations:
PubMed Identifier
19015193
Citation
Amann M, Proctor LT, Sebranek JJ, Pegelow DF, Dempsey JA. Opioid-mediated muscle afferents inhibit central motor drive and limit peripheral muscle fatigue development in humans. J Physiol. 2009 Jan 15;587(1):271-83. doi: 10.1113/jphysiol.2008.163303. Epub 2008 Nov 17.
Results Reference
result
PubMed Identifier
32816637
Citation
Wan HY, Weavil JC, Thurston TS, Georgescu VP, Bledsoe AD, Jessop JE, Buys MJ, Richardson RS, Amann M. The muscle reflex and chemoreflex interaction: ventilatory implications for the exercising human. J Appl Physiol (1985). 2020 Oct 1;129(4):691-700. doi: 10.1152/japplphysiol.00449.2020. Epub 2020 Aug 20.
Results Reference
result

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Muscle Reflex Inhibition in Hypoxic Exercise

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