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Effects of Cannabidiol on Exercise Physiology and Bioenergetics: A Randomised Controlled Pilot Trial
BACKGROUND: Cannabidiol (CBD) has demonstrated anti-inflammatory, analgesic, anxiolytic and neuroprotective effects that have the potential to benefit athletes. This pilot study investigated the effects of acute, oral CBD treatment on physiological and psychological responses to aerobic exercise to...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891421/ https://www.ncbi.nlm.nih.gov/pubmed/35235092 http://dx.doi.org/10.1186/s40798-022-00417-y |
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author | Sahinovic, Ayshe Irwin, Christopher Doohan, Peter T. Kevin, Richard C. Cox, Amanda J. Lau, Namson S. Desbrow, Ben Johnson, Nathan A. Sabag, Angelo Hislop, Matthew Haber, Paul S. McGregor, Iain S. McCartney, Danielle |
author_facet | Sahinovic, Ayshe Irwin, Christopher Doohan, Peter T. Kevin, Richard C. Cox, Amanda J. Lau, Namson S. Desbrow, Ben Johnson, Nathan A. Sabag, Angelo Hislop, Matthew Haber, Paul S. McGregor, Iain S. McCartney, Danielle |
author_sort | Sahinovic, Ayshe |
collection | PubMed |
description | BACKGROUND: Cannabidiol (CBD) has demonstrated anti-inflammatory, analgesic, anxiolytic and neuroprotective effects that have the potential to benefit athletes. This pilot study investigated the effects of acute, oral CBD treatment on physiological and psychological responses to aerobic exercise to determine its practical utility within the sporting context. METHODS: On two occasions, nine endurance-trained males (mean ± SD V̇O(2max): 57.4 ± 4.0 mL·min(−1)·kg(−1)) ran for 60 min at a fixed intensity (70% V̇O(2max)) (RUN 1) before completing an incremental run to exhaustion (RUN 2). Participants received CBD (300 mg; oral) or placebo 1.5 h before exercise in a randomised, double-blind design. Respiratory gases (V̇O(2)), respiratory exchange ratio (RER), heart rate (HR), blood glucose (BG) and lactate (BL) concentrations, and ratings of perceived exertion (RPE) and pleasure–displeasure were measured at three timepoints (T1–3) during RUN 1. V̇O(2max), RER(max), HR(max) and time to exhaustion (TTE) were recorded during RUN 2. Venous blood was drawn at Baseline, Pre- and Post-RUN 1, Post-RUN 2 and 1 h Post-RUN 2. Data were synthesised using Cohen’s d(z) effect sizes and 85% confidence intervals (CIs). Effects were considered worthy of further investigation if the 85% CI included ± 0.5 but not zero. RESULTS: CBD appeared to increase V̇O(2) (T2: + 38 ± 48 mL·min(−1), d(z): 0.25–1.35), ratings of pleasure (T1: + 0.7 ± 0.9, d(z): 0.22–1.32; T2: + 0.8 ± 1.1, d(z): 0.17–1.25) and BL (T2: + 3.3 ± 6.4 mmol·L(−1), d(z): > 0.00–1.03) during RUN 1 compared to placebo. No differences in HR, RPE, BG or RER were observed between treatments. CBD appeared to increase V̇O(2max) (+ 119 ± 206 mL·min(−1), d(z): 0.06–1.10) and RER(max) (+ 0.04 ± 0.05 d(z): 0.24–1.34) during RUN 2 compared to placebo. No differences in TTE or HR(max) were observed between treatments. Exercise increased serum interleukin (IL)-6, IL-1β, tumour necrosis factor-α, lipopolysaccharide and myoglobin concentrations (i.e. Baseline vs. Post-RUN 1, Post-RUN 2 and/or 1-h Post-RUN 2, p’s < 0.05). However, the changes were small, making it difficult to reliably evaluate the effect of CBD, where an effect appeared to be present. Plasma concentrations of the endogenous cannabinoid, anandamide (AEA), increased Post-RUN 1 and Post-RUN 2, relative to Baseline and Pre-RUN 1 (p’s < 0.05). CBD appeared to reduce AEA concentrations Post-RUN 2, compared to placebo (− 0.95 ± 0.64 pmol·mL(−1), d(z): − 2.19, − 0.79). CONCLUSION: CBD appears to alter some key physiological and psychological responses to aerobic exercise without impairing performance. Larger studies are required to confirm and better understand these preliminary findings. Trial Registration This investigation was approved by the Sydney Local Health District’s Human Research Ethics Committee (2020/ETH00226) and registered with the Australia and New Zealand Clinical Trials Registry (ACTRN12620000941965). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40798-022-00417-y. |
format | Online Article Text |
id | pubmed-8891421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-88914212022-03-08 Effects of Cannabidiol on Exercise Physiology and Bioenergetics: A Randomised Controlled Pilot Trial Sahinovic, Ayshe Irwin, Christopher Doohan, Peter T. Kevin, Richard C. Cox, Amanda J. Lau, Namson S. Desbrow, Ben Johnson, Nathan A. Sabag, Angelo Hislop, Matthew Haber, Paul S. McGregor, Iain S. McCartney, Danielle Sports Med Open Original Research Article BACKGROUND: Cannabidiol (CBD) has demonstrated anti-inflammatory, analgesic, anxiolytic and neuroprotective effects that have the potential to benefit athletes. This pilot study investigated the effects of acute, oral CBD treatment on physiological and psychological responses to aerobic exercise to determine its practical utility within the sporting context. METHODS: On two occasions, nine endurance-trained males (mean ± SD V̇O(2max): 57.4 ± 4.0 mL·min(−1)·kg(−1)) ran for 60 min at a fixed intensity (70% V̇O(2max)) (RUN 1) before completing an incremental run to exhaustion (RUN 2). Participants received CBD (300 mg; oral) or placebo 1.5 h before exercise in a randomised, double-blind design. Respiratory gases (V̇O(2)), respiratory exchange ratio (RER), heart rate (HR), blood glucose (BG) and lactate (BL) concentrations, and ratings of perceived exertion (RPE) and pleasure–displeasure were measured at three timepoints (T1–3) during RUN 1. V̇O(2max), RER(max), HR(max) and time to exhaustion (TTE) were recorded during RUN 2. Venous blood was drawn at Baseline, Pre- and Post-RUN 1, Post-RUN 2 and 1 h Post-RUN 2. Data were synthesised using Cohen’s d(z) effect sizes and 85% confidence intervals (CIs). Effects were considered worthy of further investigation if the 85% CI included ± 0.5 but not zero. RESULTS: CBD appeared to increase V̇O(2) (T2: + 38 ± 48 mL·min(−1), d(z): 0.25–1.35), ratings of pleasure (T1: + 0.7 ± 0.9, d(z): 0.22–1.32; T2: + 0.8 ± 1.1, d(z): 0.17–1.25) and BL (T2: + 3.3 ± 6.4 mmol·L(−1), d(z): > 0.00–1.03) during RUN 1 compared to placebo. No differences in HR, RPE, BG or RER were observed between treatments. CBD appeared to increase V̇O(2max) (+ 119 ± 206 mL·min(−1), d(z): 0.06–1.10) and RER(max) (+ 0.04 ± 0.05 d(z): 0.24–1.34) during RUN 2 compared to placebo. No differences in TTE or HR(max) were observed between treatments. Exercise increased serum interleukin (IL)-6, IL-1β, tumour necrosis factor-α, lipopolysaccharide and myoglobin concentrations (i.e. Baseline vs. Post-RUN 1, Post-RUN 2 and/or 1-h Post-RUN 2, p’s < 0.05). However, the changes were small, making it difficult to reliably evaluate the effect of CBD, where an effect appeared to be present. Plasma concentrations of the endogenous cannabinoid, anandamide (AEA), increased Post-RUN 1 and Post-RUN 2, relative to Baseline and Pre-RUN 1 (p’s < 0.05). CBD appeared to reduce AEA concentrations Post-RUN 2, compared to placebo (− 0.95 ± 0.64 pmol·mL(−1), d(z): − 2.19, − 0.79). CONCLUSION: CBD appears to alter some key physiological and psychological responses to aerobic exercise without impairing performance. Larger studies are required to confirm and better understand these preliminary findings. Trial Registration This investigation was approved by the Sydney Local Health District’s Human Research Ethics Committee (2020/ETH00226) and registered with the Australia and New Zealand Clinical Trials Registry (ACTRN12620000941965). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40798-022-00417-y. Springer International Publishing 2022-03-02 /pmc/articles/PMC8891421/ /pubmed/35235092 http://dx.doi.org/10.1186/s40798-022-00417-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Research Article Sahinovic, Ayshe Irwin, Christopher Doohan, Peter T. Kevin, Richard C. Cox, Amanda J. Lau, Namson S. Desbrow, Ben Johnson, Nathan A. Sabag, Angelo Hislop, Matthew Haber, Paul S. McGregor, Iain S. McCartney, Danielle Effects of Cannabidiol on Exercise Physiology and Bioenergetics: A Randomised Controlled Pilot Trial |
title | Effects of Cannabidiol on Exercise Physiology and Bioenergetics: A Randomised Controlled Pilot Trial |
title_full | Effects of Cannabidiol on Exercise Physiology and Bioenergetics: A Randomised Controlled Pilot Trial |
title_fullStr | Effects of Cannabidiol on Exercise Physiology and Bioenergetics: A Randomised Controlled Pilot Trial |
title_full_unstemmed | Effects of Cannabidiol on Exercise Physiology and Bioenergetics: A Randomised Controlled Pilot Trial |
title_short | Effects of Cannabidiol on Exercise Physiology and Bioenergetics: A Randomised Controlled Pilot Trial |
title_sort | effects of cannabidiol on exercise physiology and bioenergetics: a randomised controlled pilot trial |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891421/ https://www.ncbi.nlm.nih.gov/pubmed/35235092 http://dx.doi.org/10.1186/s40798-022-00417-y |
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