Copyright is owned by the Author of the thesis. Permission is given for a copy to be downloaded by an individual for the purpose of research and private study only. The thesis may not be reproduced elsewhere without the permission of the Author. EFFECT OF CAFFEINE SUPPLEMENTATION ON METABOLISM AND PHYSICAL AND COGNITIVE FUNCTION IN FEMALE INTERMITTENT GAMES PLAYERS By Jemma May O?Donnell A thesis presented in partial fulfilment for the requirements of a Master of Science in Human Nutrition at Massey University, Auckland, New Zealand March 2012 ii ACKNOWLEDGMENTS The first thank you must of course go to the girls who volunteered their time to be participants for this demanding research. Without them none of this would have been possible! Acknowledgements must also go to my supervisors Dr. Ajmol Ali, Dr. Andrew Foskett, and Dr. Pam von Hurst. Their assistance and advice has helped me turn an idea into a fully- fledged Masters project, and their continued time and efforts have helped me successfully complete my MSc. Huge thanks must also go to Mr. Simon Bennett who?s technical and practical contributions have been absolutely invaluable! To the third year students who assisted me on this project, Mr. David Wolf, Miss Rebecca Watkin, and Mr. Naser Naser, thank you for providing that often essential second pair of hands. I hope that in taking on a research assistant role, this has furthered your own understanding and knowledge, possibly even tempted you onto the postgraduate pathway. iii ABSTRACT Purpose: To investigate the effects of caffeine ingestion on metabolism and physical and cognitive performance in female team-sport players taking a monophasic oral contraceptive. Method: In a randomized, double-blind, placebo-controlled crossover design, 10 participants (age 23.6 ? 4.1 y; height 1.62 ? 0.06 m; body mass 59. O2 max 50.0 ? 5.3 ml?kg-1?min-1) completed a 90 min intermittent treadmill-running protocol twice, during days 5-8 and 18-22 of their pill cycle. All participants were taking a monophasic oral contraceptive of the same hormonal composition (Levlen ED, Nordette, Monofeme, or Microgynon). During the familiarisation session participants completed a maximal oxygen uptake test, practiced the cognitive, strength, power testing, and underwent 30 min of the running protocol. Upon arrival at the laboratory for the main trials, hydration status was measured via urine specific gravity (USG) using a handheld refractometer and a heart rate (HR) monitor fitted. A capsule containing 6 mg?kg-1 body mass (BM) of anhydrous caffeine or placebo (Maltodextrin, 1.62 kJ?g-1) was administered 45 min before commencing exercise with a 500 ml bolus of water. Further 3 ml?kg-1 BM boluses of water were provided every 15 min during exercise. Before, during and after the exercise protocol, venous blood samples were taken and cognitive (Choice Reaction Time, CRT; Digit Vigilance, DV; Stroop test), perceptual (Ratings of Perceived Exertion, RPE; Feeling Scale, FS; Felt Arousal Scale, FAS; Profile of Mood States, POMS), and physical tests (countermovement jump, CMJ; strength testing on the isokinetic dynamometer) were administered. These tests were then all performed again at a follow-up 12 h post session in the morning, including a venipuncture blood sample, and the addition of sleep quality assessment using the Leeds Sleep Evaluation Questionnaire (LSEQ). Results: There were no significant effects of caffeine supplementation on HR, USG, CMJ, isometric strength, RPE, cognitive performance or glucose and insulin concentrations. Caffeine supplementation improved levels of pleasure, activation and vigour compared to iv placebo, and reduced levels of fatigue (P < 0.05). Caffeine supplementation also improved average power in eccentric contractions of the knee extensors and flexors, and peak torque in the eccentric contractions of the knee flexors (P < 0.05). Getting to sleep and subsequent quality of sleep was impaired following caffeine supplementation (P < 0.05). Free fatty acid (FFA) concentration increased over the duration of exercise (P < 0.05), and increased at a greater rate on the caffeine trial (P < 0.05). Conclusions: This is the first controlled study to examine caffeine supplementation in female games players who are taking a low-dose monophasic oral contraceptive, using an intermittent based running protocol. These athletes experienced an improved performance in various strength and power aspects, but no improvement in cognitive performance. Perceptual and mood responses were also improved as a result of caffeine supplementation. Metabolically, caffeine had an effect on markers of fat metabolism but not on carbohydrate metabolism. Keywords: caffeine, female, metabolism, performance, intermittent exercise v Table of contents Page Acknowledgments ii Abstract iii Table of contents v List of figures viii List of tables xi 1.0 INTRODUCTION 1 1.1 Overview of thesis 7 2.0 LITERATURE REVIEW 8 2.1 Caffeine as an intervention to overcome fatigue and improve performance 8 2.1.1 Absorption, metabolism, elimination 8 2.2 Caffeine and peripheral mechanisms of action 10 2.2.1 Fat oxidation and glycogen sparing 10 2.2.2 Blood glucose 12 2.2.3 Lactate 14 2.2.4 Catecholamines 15 2.2.5 Ionic balance 16 2.3 Central Mechanisms of action ? adenosine antagonism 18 2.3.1 Pain perception 19 2.3.2 Ratings of Perceived Exertion (RPE) 21 2.3.3 ?-endorphins 22 2.4 The role of genetics and caffeine 23 2.5 Caffeine and cognition, mood and perception 24 2.5.1 Cognition 24 2.5.2 Mood (POMS) 26 2.5.3 Perception 27 2.6 Caffeine, strength and power 29 2.7 Caffeine and sleep quality 31 2.8 The effect of caffeine on performance in team sports players 33 vi 2.9 Caffeine and women/sex effects 36 2.9.1 Effect of menstrual cycle on caffeine metabolism 36 2.9.2 OCS use and the effect on caffeine metabolism 37 2.9.3 OCS use and intermittent exercise 38 2.9.4 Performance in female athletes with caffeine supplementation 40 2.10 Summary 42 3.0 METHODOLOGY 43 3.1 Participants 43 3.2 Subject control 3.2.1 Dietary control 43 3.2.2 Oral contraceptive use and cycle control 44 3.3 Description of physiological tests and measures 44 3.3.1 Height and mass measurements 44 3.3.2 Heart rate measurements 45 3.3.3 Urine analysis 45 3.3.4 Expired air collection 45 3.3.5 Strength and power testing 45 3.3.5.1 Isokinetic dynamometer 45 3.3.5.2 Countermovement jump (CMJ) 47 3.3.6 Blood sampling and analysis 47 3.3.6.1 Sample collection 47 3.3.6.2 Treatment, storage, and analysis of blood samples 47 3.3.7 Maximal oxygen uptake test ( O2max) 48 3.4 Description of cognitive measures 49 3.4.1 Cognitive testing 49 3.4.1.1 Choice Reaction time test (CRT) 50 3.4.1.2 Stroop test 50 3.4.2 Profile of Mood States questionnaire (POMS) 50 3.5 Description of perceptual scales 51 3.5.1 Ratings of Perceived Exertion (RPE) 51 3.5.2 Feeling Scale (FS) 51 3.5.3 Felt arousal scale (FAS) 51 3.6 Description of sleep quality measures 52 3.6.1 Leeds Sleep Evaluation questionnaire (LSEQ) 52 3.7 Description of intermittent treadmill running protocol 52 3.8 Preliminary familiarisation testing 53 3.9 Study design 54 3.10 Statistical analysis 57 vii 4.0 RESULTS 58 4.1 Strength and power data 58 4.2 Cognitive data 60 4.3 Perceptual data 61 4.4 Mood data 65 4.5 Blood analysis 66 4.6 Sleep quality 69 4.7 Other data 72 5.0 DISCUSSION 73 5.1 Conclusions 83 5.2 Limitations 83 5.3 Future directions 84 6.0 REFERENCES 85 7.0 APPENDICES 102 viii LIST OF FIGURES Figure 2.1 ? A visual depiction of the circumplex model used for plotting the perceptual responses to exercise. Figure 3.1 ? Isokinetic dynamometer (Biodex) setup. Figure 3.2 ? COMPASS software for administering cognitive tests. Figure 3.3 ? Intermittent treadmill running protocol based on each participants O2 max (Atkinson, et al., 2005). Figure 3.4 ? Detailed schematic of main trials. Figure 4.1 ? Mean power output during eccentric contractions of knee extensors in caffeine and placebo trials. Values are mean ? SD. The ?pre? time point represents before caffeine/placebo administration; ?mid? is after block 3 during the 15 min break; and post following the final block of exercise. Figure 4.2 ? Mean power output during eccentric contractions of the knee extensors in caffeine and placebo trials. Values are mean ? SD. The ?pre? time point represents before caffeine/placebo administration; ?mid? is after block 3 during the 15 min break; and post following the final block of exercise. ix Figure 4.3 ? Mean RPE scores for all participants in caffeine and placebo trials. Each block was 15 min long, and blocks 1, 2, 4, and 5 were separated by a 4 min break; after block 3 there was a 15 min break. Figure 4.4 ? Mean FS scores for all participants in caffeine and placebo trials. Each block was 15 min long, and blocks 1, 2, 4, and 5 were separated by a 4 min break; after block 3 there was a 15 min break. Figure 4.5 ? Mean FAS scores for all participants in caffeine and placebo trials. Each block was 15 min long, and blocks 1, 2, 4, and 5 were separated by a 4 min break; after block 3 there was a 15 min break. Figure 4.6 ? Mean FS and FAS values plotted as Cartesian coordinates in a circumplex model. 4.6A represents caffeine values and 4.6B is placebo values. Figure 4.7 ? Figure 4.7A depicts the fatigue scores in the POMS, and 4.7B depicts the vigour score. POMS ? Profile of Mood States questionnaire. Figure 4.8 ? Mean ? SD values of plasma caffeine concentration over duration of study. Time values on the horizontal axis indicate total time since 45 min prior to caffeine ingestion, which is represented as time 0 min. * significant difference between trials, P<0.05. Figure 4.9 ? Individual values for plasma caffeine concentration over duration of caffeine trial. Time values on the horizontal axis indicate total time since 45 min prior to caffeine ingestion, which is represented as time 0 min. x Figure 4.10 ? Mean ? SD plasma glucose concentrations. Time values on the horizontal axis indicate total time since 45 min prior to caffeine ingestion, which is represented as time 0 min. Figure 4.11 ? Mean ? SD plasma insulin concentrations. Time values on the horizontal axis indicate total time since 45 min prior to caffeine ingestion, which is represented as time 0 min. Figure 4.12 ? Mean ? SD plasma FFA concentrations. Time values on the horizontal axis indicate total time since 45 min prior to caffeine ingestion, which is represented as time 0 min. * significant difference between trials, P<0.05. xi LIST OF TABLES Table 2.1 ? Summary of literature pertaining to caffeine supplementation and team sports. Table 2.2 ? Summary of literature pertaining to caffeine supplementation and exercise performance in women. Table 4.1 ? Data from the Leeds Sleep Evaluation Questionnaire. Table 4.2 ? Nutritional composition of diet from 48 h food diaries.