Saccades and Prefrontal Hemodynamics in Basketball Players

Abstract

We investigated saccade performance and prefrontal hemodynamics in basketball players with different skill levels. Subjects were 27 undergraduate basketball players and 13 non-athlete undergraduates (control group: CON). The players were divided into two groups: those who had played in the National Athletic Meet during high school or played regularly (n=13, elite group: ELI) and those who were bench warmers (n=14, skilled group: SKI). Horizontal eye movement and oxy-, deoxy-, and total-hemoglobin (Hb) concentration in the prefrontal cortex during pro- and anti-saccade were measured using electro-oculography and near-infrared spectroscopy, respectively. Only error rate in anti-saccade was less in ELI (4.8±4.0%) than SKI (13.7±12.6%) and CON (13.9±8.3%) (p<0.05). In ELI alone, oxy- (−0.15±0.18 mmol*mm) and total-Hb (−0.12±0.15 mmol*mm) during anti-saccade decreased significantly compared with that during rest (p<0.05), while those in CON significantly increased (oxy-Hb: 0.17±0.15 mmol*mm, total-Hb: 0.14±0.14 mmol*mm) (p<0.05). These results suggest that inhibition of eye movement to a visual target changes from voluntary to automatic through the motor learning of basketball.

Anti-saccade - prefrontal hemodynamics - basketball - motor skill - near-infrared spectroscopy

References

• 1 Brown MR, Goltz HC, Vilis T, Ford KA, Everling S. Inhibition and generation of saccades: rapid event-related fMRI of prosaccades, antisaccades, and nogo trials.  Neuroimage. 2006;  33 644-659
• 2 Clementz BA, McDowell JE, Stewart SE. Timing and magnitude of frontal activity differentiates refixation and anti-saccade performance.  Neuroreport. 2001;  12 1863-1868
• 3 Deiber MP, Wise SP, Honda M, Catalan MJ, Grafman J, Hallett M. Frontal and parietal networks for conditional motor learning: a positron emission tomography study.  J Neurophysiol. 1997;  78 977-991
• 4 Di Russo F, Pitzalis S, Spinelli D. Fixation stability and saccadic latency in élite shooters.  Vision Res. 2003;  43 1837-1845
• 5 Ericsson KA, Krampe RT, Tesch-Römer C. The role of deliberate practice in the acquisition of expert performance.  Psychol Rev. 1993;  100 363-406
• 6 Evdokimidis I, Smyrnis N, Constantinidis TS, Stefanis NC, Avramopoulos D, Paximadis C, Theleritis C, Efstratiadis C, Kastrinakis G, Stefanis CN. The antisaccade task in a sample of 2,006 young men. I. Normal population characteristics.  Exp Brain Res. 2002;  147 45-52
• 7 Everling S, Fischer B. The antisaccade: a review of basic research and clinical studies.  Neuropsychologia. 1998;  36 885-899
• 8 Ford KA, Goltz HC, Brown MR, Everling S. Neural processes associated with antisaccade task performance investigated with event-related FMRI.  J Neurophysiol. 2005;  94 429-440
• 9 Fujiwara K, Kunita K, Toyama H. Changes in saccadic reaction time while maintaining neck flexion in men and women.  Eur J Appl Physiol. 2000;  81 317-324
• 10 Fujiwara K, Kunita K, Watanabe H. Sports exercise effect on shortening of saccadic reaction time associated with neck extensor muscle activity.  Int J Sports Med. 2006;  27 792-797
• 11 Gais S, Köster S, Sprenger A, Bethke J, Heide W, Kimmig H. Sleep is required for improving reaction times after training on a procedural visuo-motor task.  Neurobiol Learn Mem. 2008;  90 610-615
• 12 Gusnard DA, Raichle ME. Searching for a baseline: functional imaging and the resting human brain.  Nat Rev Neurosci. 2001;  2 685-694
• 13 Hermann MJ, Plichta MM, Ehlis AC, Fallgatter AJ. Optical topography during a Go-NoGo task assessed with multi-channel near-infrared spectroscopy.  Behav Brain Res. 2005;  160 135-140
• 14 Homan RW, Herman J, Purdy P. Cerebral location of international 10–20 system electrode placement.  Electroencephalogr Clin Neurophysiol. 1987;  66 376-382
• 15 Hoshi Y. Functional near-infrared optical imaging: utility and limitations in human brain mapping.  Psychophysiology. 2003;  40 511-520
• 16 Jasper HH. The ten twenty electrode system of the international federation.  Electroencephalogr Clin Neurophysiol. 1958;  10 371-375
• 17 Jueptner M, Stephan KM, Frith CD, Brooks DJ, Frackowiak RS, Passingham RE. Anatomy of motor learning. I. Frontal cortex and attention to action.  J Neurophysiol. 1997;  77 1313-1324
• 18 Kalesnykas RP, Hallett PE. Retinal eccentricity and the latency of eye saccades.  Vision Res. 1993;  34 517-531
• 19 Kassubek J, Shmidtke K, Kimming H, Lucking CH, Greenlee MW. Changes in cortical activation during mirror reading before and after training: an fMRI study of procedural learning.  Brain Res Cogn Brain Res. 2001;  10 207-217
• 20 Krause J. Coaching basketball: the complete coaching guide of the National Association of Basketball Coaches. Indianapolis: Masters Press 1994
• 21 Land MF, McLeod P. From eye movements to actions: how batsmen hit the ball.  Nat Neurosci. 2000;  3 1340-1345
• 22 Leff DR, Elwell CE, Orihuela-Espina F, Atallah L, Delpy DT, Darzi AW, Yang GZ. Changes in prefrontal cortical behaviour depend upon familiarity on a bimanual co-ordination task: an fNIRS study.  Neuroimage. 2008;  39 805-813
• 23 Leigh RJ, Kennard C. Using saccades as a research tool in the clinical neurosciences.  Brain. 2004;  127 460-477
• 24 Lenoir M, Crevits L, Goethals M, Wildenbeest J, Musch E. Are better eye movements an advantage in ball games? A study of prosaccadic and antisaccadic eye movements.  Percept Mot Skills. 2000;  91 546-552
• 25 Mihara M, Miyai I, Hatakenaka M, Kubota K, Sakoda S. Sustained prefrontal activation during ataxic gait: a compensatory mechanism for ataxic stroke?.  Neuroimage. 2007;  37 1338-1345
• 26 Miyai I, Tanabe HC, Sase I, Eda H, Oda I, Konishi I, Tsunazawa Y, Suzuki T, Yanagida T, Kubota K. Cortical mapping of gait in humans: a near-infrared spectroscopic topography study.  Neuroimage. 2001;  14 1186-1192
• 27 Morrillo M, Di Russo F, Pitzalis S, Spinelli D. Latency of prosaccades and antisaccades in professional shooters.  Med Sci Sports Exerc. 2006;  38 388-394
• 28 Pierrot-Deseilligny C, Müri RM, Ploner CJ, Gaymard B, Demeret S, Rivaud-Pechoux S. Decisional role of the dorsolateral prefrontal cortex in ocular motor behaviour.  Brain. 2003;  126 1460-1473
• 29 Ploner CJ, Gaymard BM, Rivaud-Péchoux S, Pierrot-Deseilligny C. The prefrontal substrate of reflexive saccade inhibition in humans.  Biol Psychiatry. 2005;  57 1159-1165
• 30 Sakai K, Hikosaka O, Miyauchi S, Takino R, Sasaki Y, Putz B. Transition of brain activation from frontal to parietal areas in visuomotor sequence learning.  J Neurosci. 1998;  18 1827-1840
• 31 Shibukawa K. Undo rikigaku (Motion dynamics) [in Japanese]. Tokyo: Taishukan publishing 1969
• 32 Stine CD, Arterburn MR, Stern NS. Vision and sports: a review of the literature.  J Am Optom Assoc. 1982;  53 627-633
• 33 Strangman G, Culver JP, Thompson JH, Boas DA. A quantitative comparison of simultaneous BOLD fMRI and NIRS recordings during functional brain activation.  Neuroimage. 2002;  17 719-731
• 34 Suzuki M, Miyai I, Ono T, Oda I, Konishi I, Kochiyama T, Kubota K. Prefrontal and premotor cortices are involved in adapting walking and running speed on the treadmill: an optical imaging study.  Neuroimage. 2004;  23 1020-1026
• 35 Wade AR. The negative BOLD signal unmasked.  Neuron. 2002;  36 993-995
• 36 Wolf M, Wolf U, Toronov V, Michalos A, Choi JH, Gratton E. Different time evolution of oxyhemoglobin and deoxyhemoglobin concentration changes in the visual and motor cortices during functional stimulation: a near-infrared spectroscopy study.  Neuroimage. 2002;  16 704-712

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