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Analytical strategy for the detection of ecdysterone and its metabolites in vivo in uPA(+/+)‐SCID mice with humanized liver, human urine samples, and estimation of prevalence of its use in anti‐doping samples
Ecdysteroids are of interest as potential sport performance enhancers, due to their anabolic effects. The current study aimed to analyze levels of the most abundant ecdysteroid, ecdysterone (20‐hydroxyecdysone, 20‐OHE) in easily available dietary supplements, and, outline an analytical strategy for...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291035/ https://www.ncbi.nlm.nih.gov/pubmed/33759363 http://dx.doi.org/10.1002/dta.3032 |
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author | Kraiem, Souhail Al‐Jaber, Maneera Y. Al‐Mohammed, Hana Al‐Menhali, Afnan S. Al‐Thani, Noora Helaleh, Murad Samsam, Waseem Touil, Soufiane Beotra, Alka Georgakopoulas, Costas Bouabdallah, Sondes Mohamed‐Ali, Vidya Al Maadheed, Mohammed |
author_facet | Kraiem, Souhail Al‐Jaber, Maneera Y. Al‐Mohammed, Hana Al‐Menhali, Afnan S. Al‐Thani, Noora Helaleh, Murad Samsam, Waseem Touil, Soufiane Beotra, Alka Georgakopoulas, Costas Bouabdallah, Sondes Mohamed‐Ali, Vidya Al Maadheed, Mohammed |
author_sort | Kraiem, Souhail |
collection | PubMed |
description | Ecdysteroids are of interest as potential sport performance enhancers, due to their anabolic effects. The current study aimed to analyze levels of the most abundant ecdysteroid, ecdysterone (20‐hydroxyecdysone, 20‐OHE) in easily available dietary supplements, and, outline an analytical strategy for its detection, and that, of its metabolites, (1) following administration of pure 20‐OHE to uPA(+/+)‐SCID mice with humanized liver, (2) in a human volunteer after ingestion of two supplements, one with a relatively low, and the other a high, concentration of 20‐OHE, and, (3) to estimate the prevalence of use of 20‐OHE in elite athletes (n = 1000). Of the 16 supplements tested, only five showed detectable levels of 20‐OHE, with concentrations ranging from undetectable up to 2.3 mg per capsule. Urine of uPA(+/+)‐SCID urine showed the presence of 20‐OHE and its metabolite, 14 deoxy ecdysterone, within 24 hours (hr) of ingestion. In humans, both the parent and the metabolite were detectable within 2 to 5 hr of ingestion, with the metabolite being detectable for longer than the parent. After ingestion of a low dose supplement, the parent and metabolite were detectable for 70 and 48 hr, while following the higher dose it was 96 and 48 hr, respectively. Analysis of urines from athletes (n = 1000) confirmed four positives for 20‐OHE, suggesting a prevalence of use of 0.4%. Prevalence of its use by elite athletes was relatively low, however, this needs to be confirmed in other populations, and with other related ecdysteroids. |
format | Online Article Text |
id | pubmed-9291035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92910352022-07-20 Analytical strategy for the detection of ecdysterone and its metabolites in vivo in uPA(+/+)‐SCID mice with humanized liver, human urine samples, and estimation of prevalence of its use in anti‐doping samples Kraiem, Souhail Al‐Jaber, Maneera Y. Al‐Mohammed, Hana Al‐Menhali, Afnan S. Al‐Thani, Noora Helaleh, Murad Samsam, Waseem Touil, Soufiane Beotra, Alka Georgakopoulas, Costas Bouabdallah, Sondes Mohamed‐Ali, Vidya Al Maadheed, Mohammed Drug Test Anal Research Articles Ecdysteroids are of interest as potential sport performance enhancers, due to their anabolic effects. The current study aimed to analyze levels of the most abundant ecdysteroid, ecdysterone (20‐hydroxyecdysone, 20‐OHE) in easily available dietary supplements, and, outline an analytical strategy for its detection, and that, of its metabolites, (1) following administration of pure 20‐OHE to uPA(+/+)‐SCID mice with humanized liver, (2) in a human volunteer after ingestion of two supplements, one with a relatively low, and the other a high, concentration of 20‐OHE, and, (3) to estimate the prevalence of use of 20‐OHE in elite athletes (n = 1000). Of the 16 supplements tested, only five showed detectable levels of 20‐OHE, with concentrations ranging from undetectable up to 2.3 mg per capsule. Urine of uPA(+/+)‐SCID urine showed the presence of 20‐OHE and its metabolite, 14 deoxy ecdysterone, within 24 hours (hr) of ingestion. In humans, both the parent and the metabolite were detectable within 2 to 5 hr of ingestion, with the metabolite being detectable for longer than the parent. After ingestion of a low dose supplement, the parent and metabolite were detectable for 70 and 48 hr, while following the higher dose it was 96 and 48 hr, respectively. Analysis of urines from athletes (n = 1000) confirmed four positives for 20‐OHE, suggesting a prevalence of use of 0.4%. Prevalence of its use by elite athletes was relatively low, however, this needs to be confirmed in other populations, and with other related ecdysteroids. John Wiley and Sons Inc. 2021-05-04 2021-07 /pmc/articles/PMC9291035/ /pubmed/33759363 http://dx.doi.org/10.1002/dta.3032 Text en © 2021 The Authors. Drug Testing and Analysis published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Kraiem, Souhail Al‐Jaber, Maneera Y. Al‐Mohammed, Hana Al‐Menhali, Afnan S. Al‐Thani, Noora Helaleh, Murad Samsam, Waseem Touil, Soufiane Beotra, Alka Georgakopoulas, Costas Bouabdallah, Sondes Mohamed‐Ali, Vidya Al Maadheed, Mohammed Analytical strategy for the detection of ecdysterone and its metabolites in vivo in uPA(+/+)‐SCID mice with humanized liver, human urine samples, and estimation of prevalence of its use in anti‐doping samples |
title | Analytical strategy for the detection of ecdysterone and its metabolites in vivo in uPA(+/+)‐SCID mice with humanized liver, human urine samples, and estimation of prevalence of its use in anti‐doping samples |
title_full | Analytical strategy for the detection of ecdysterone and its metabolites in vivo in uPA(+/+)‐SCID mice with humanized liver, human urine samples, and estimation of prevalence of its use in anti‐doping samples |
title_fullStr | Analytical strategy for the detection of ecdysterone and its metabolites in vivo in uPA(+/+)‐SCID mice with humanized liver, human urine samples, and estimation of prevalence of its use in anti‐doping samples |
title_full_unstemmed | Analytical strategy for the detection of ecdysterone and its metabolites in vivo in uPA(+/+)‐SCID mice with humanized liver, human urine samples, and estimation of prevalence of its use in anti‐doping samples |
title_short | Analytical strategy for the detection of ecdysterone and its metabolites in vivo in uPA(+/+)‐SCID mice with humanized liver, human urine samples, and estimation of prevalence of its use in anti‐doping samples |
title_sort | analytical strategy for the detection of ecdysterone and its metabolites in vivo in upa(+/+)‐scid mice with humanized liver, human urine samples, and estimation of prevalence of its use in anti‐doping samples |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291035/ https://www.ncbi.nlm.nih.gov/pubmed/33759363 http://dx.doi.org/10.1002/dta.3032 |
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