Abstract
Caffeine is a well-described ergogenic aid used to enhance athletic performance. Using animal models can greatly increase our understanding of caffeine's mechanisms in performance. Here, we adapted an animal weight-lifting exercise model to demonstrate caffeine's ergogenic effect in rats. Male Wistar rats (315 ± 35 g) were randomly divided into two groups: one group received 5 mg·kg-1 of caffeine (0.5 mL; CEx; n = 5) and the other 0.9% NaCl (0.5 mL; PEx; n = 4) through an orogastric probe (gavage) one hour before exercise. Weight-lifting exercise sessions were performed over three subsequent days, and the number of complete squats performed was counted. Analyses of the area under the curve in all three experiments showed that the CEx group responded more to stimuli, performing more squats (1.7-, 2.0-, and 1.6-fold; p < 0.05) than the control group did. These three days' data were analyzed to better understand the cumulative effect of this exercise, and a hyperbolic curve was fitted to these data. Data fitting from the caffeine-supplemented group, CEx, also showed larger Smax and Kd (2.3-fold and 1.6-fold, respectively) than the PEx group did. Our study demonstrated an acute ergogenic effect of caffeine in an animal weight-lifting exercise model for the first time, suggesting potential avenues for future research.
Keywords:
animal; caffeine; exercise; weight lifting.
MeSH terms
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Animals
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Caffeine* / administration & dosage
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Caffeine* / pharmacology
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Male
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Performance-Enhancing Substances / administration & dosage
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Performance-Enhancing Substances / pharmacology
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Physical Conditioning, Animal / physiology
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Pilot Projects
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Rats
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Rats, Wistar*
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Weight Lifting* / physiology
Substances
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Caffeine
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Performance-Enhancing Substances
Grants and funding
This study was funded by the Brazil Olympic Committee (BOC); Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq); Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES); Financiadora de Estudos e Projetos (FINEP); Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ); INCT-TeraNano (CNPq #403193/2022-2, -FAPEMIG CBB # APQ-03613-17). Merck-Sigma-Aldrich; SISCAPA; Universidade Federal do Estado do Rio de Janeiro (UNIRIO); and the Waters Corporation. Also, it was supported in part by funding from the Natural Sciences Research Council (NSERC #203475), the Canada Foundation for Innovation (CFI #225404, #30865), the Ontario Research Fund (RDI #34876, RE010-020), IBM, and the Ian Lawson van Toch Fund. V.C. is supported by a Clinician Scientist Salary Support Award from the Department of Medicine, University of Toronto, Toronto, Canada. The funders had no role in this study’s design, data collection, analysis, publication decisions, or manuscript preparation.