Investigations into Annona fruit consumption as a potential source of dietary higenamine intake in the context of sports drug testing

Author:

Rubio Ana1,Thomas Andreas2ORCID,Euler Luisa2,Geyer Hans23,Krug Oliver23,Reis Gabriel4,Padilha Monica Costa4,Pereira Henrique Marcelo Gualberto4ORCID,Muniz‐Santos Renan5,Cameron Luiz Claudio5,Stojanovic Biljana6,Kuehne Dirk7,Lagojda Andreas7,McLeod Malcolm Donald8ORCID,Thevis Mario23ORCID

Affiliation:

1. Laboratory Medicine Department Hospital Universitario Son Espases Palma Spain

2. Center for Preventive Doping Research ‐ Institute of Biochemistry German Sport University Cologne Cologne Germany

3. European Monitoring Center for Emerging Doping Agents (EuMoCEDA) Cologne/Bonn Germany

4. Brazilian Doping Control Laboratory (LBCD ‐ LADETEC/IQ ‐ UFRJ) ‐ Chemistry Institute Rio de Janeiro Brazil

5. Laboratory of Protein Biochemistry The Federal University of State of Rio de Janeiro Rio de Janeiro Brazil

6. Seibersdorf Labor GmbH Seibersdorf Austria

7. Crop Science Division Bayer AG Monheim Germany

8. Research School of Chemistry Australian National University Canberra Australian Capital Territory Australia

Abstract

AbstractHigenamine is prohibited in sports as a β2‐agonist by the World Anti‐Doping Agency. As a key component of a great variety of plants, including the Annonaceae family, one aim of this research project was to evaluate whether the ingestion of Annona fruit could lead to higenamine adverse analytical findings. Single‐dose administration studies including three Annona species (i.e., Annona muricata, Annona cherimola, and Annona squamosa) were conducted, leading to higenamine findings below the established minimum reporting level (MRL) of 10 ng/mL in urine. In consideration of cmax values (7.8 ng/mL) observed for higenamine up to 24 h, a multidose administration study was also conducted, indicating cumulative effects, which can increase the risk of exceeding the applicable MRL doping after Annona fruit ingestion. In this study, however, the MRL was not exceeded at any time point. Further, the major urinary excretion of higenamine in its sulfo‐conjugated form was corroborated, its stability in urine was assessed, and in the absence of reference material, higenamine sulfo‐conjugates were synthesized and comprehensively characterized, suggesting the predominant presence of higenamine 7‐sulfate. In addition, the option to include complementary biomarkers of diet‐related higenamine intake into routine doping controls was investigated. A characteristic urinary pattern attributed to isococlaurine, reticuline, and a yet not fully characterized bismethylated higenamine glucuronide was observed after Annona ingestion but not after supplement use, providing a promising dataset of urinary biomarkers, which supports the discrimination between different sources of urinary higenamine detected in sports drug testing programs.

Funder

World Anti-Doping Agency

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Financiadora de Estudos e Projetos

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro

Universidade Federal do Estado do Rio de Janeiro

Waters Corporation

Publisher

Wiley

Subject

Spectroscopy,Pharmaceutical Science,Environmental Chemistry,Analytical Chemistry

Reference31 articles.

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