Human pharmacology of a performance-enhancing dietary supplement under resting and exercise conditions.

Christine A Haller, Minjing Duan, Peyton Jacob, Neal Benowitz
Author Information
  1. Christine A Haller: Department of Medicine, Division of Clinical Pharmacology, University of California, San Francisco, San Francisco General Hospital, San Francisco, CA, USA. challer@amgen.com

Abstract

WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT: Performance-enhancing dietary supplements have not been clinically tested for safety or efficacy. In clinical trials performed under resting conditions, performance-enhancing supplements raise blood pressure and affect glucose homeostasis. The effect of exercise on the pharmacokinetics and pharmacodynamics of stimulant herbals is unknown.
WHAT THIS STUDY ADDS: Supplement-induced effects on blood pressure and glucose levels are not ameliorated by exercise. Exercise does not affect the kinetics of stimulant ingredients, caffeine and synephrine. Performance-enhancing supplement use modestly improves exercise tolerance. AIMS Dietary supplements (DS) promoted to enhance athletic performance often contain herbal sympathomimetics such as Citrus aurantium (synephrine) and caffeine. We aimed to characterize the pharmacology of a performance-enhancing DS in the setting of exercise.
METHODS: Ten healthy adults (three women) aged 20-31 years participated in a three-arm, double-blind, placebo-controlled, crossover study. Subjects ingested one dose of DS (Ripped Fuel Extreme Cut(R) with 21 mg synephrine and 304 mg caffeine by analysis) under resting conditions and 1 h prior to moderately intense exercise (30 min on cycle ergometer at 75-80% HR(max)), with a placebo (PLC)/exercise control. Plasma synephrine and caffeine concentrations were measured over 12 h, and vital signs, serum electrolytes, oxygen consumption and perceived exercise exertion were monitored.
RESULTS: No significant adverse events occurred. Synephrine and caffeine pharmacokinetics were unaffected by exercise. Post-exercise diastolic blood pressure was higher after DS (peak mean 71.7 +/- 8.7 mmHg) than PLC (63.0 +/- 4.9 mmHg) (p = 0.007). There were no substantial treatment-related differences in post-exercise HR, systolic blood pressure, or temperature. Postprandial plasma glucose increased to 121.0 +/- 31.6 mg dl(-1) with DS and exercise vs. 103.7 +/- 25.5 mg dl(-1) with PLC and exercise (P = 0.004). No treatment differences in exercise-related oxygen consumption, serum lactate, or insulin were observed. Exercise was rated less difficult with DS than PLC (P = 0.001).
CONCLUSIONS: Blood pressure and plasma glucose increased post-exercise with DS use, which could be detrimental in some people. Exercise was perceived as less strenuous after DS, presumably due to the stimulant effects of caffeine.

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Grants

  1. DA12393/NIDA NIH HHS
  2. K23 AT000069/NCCIH NIH HHS
  3. P30 DA012393/NIDA NIH HHS
  4. M01 RR000083/NCRR NIH HHS
  5. K23AT00069-04/NCCIH NIH HHS
  6. M01RR00083-41/NCRR NIH HHS

MeSH Term

Adult
Blood Glucose
Caffeine
Central Nervous System Stimulants
Dietary Supplements
Double-Blind Method
Energy Metabolism
Exercise
Female
Humans
Male
Statistics as Topic
Synephrine

Chemicals

Blood Glucose
Central Nervous System Stimulants
Caffeine
Synephrine

Word Cloud

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