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      Phospholipids and sports performance

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          Abstract

          Phospholipids are essential components of all biological membranes. Phosphatidylcholine (PC) and Phosphatidylserine (PS) are Phosphatidyl-phospholipids that are required for normal cellular structure and function. The participation in physical activity often challenges a variety of physiological systems; consequently, the ability to maintain normal cellular function during activity can determine sporting performance. The participation in prolonged intense exercise has been shown to reduce circulatory choline concentrations in some individuals. As choline is a pre-cursor to the neurotransmitter Acetylcholine, this finding has encouraged researchers to investigate the hypothesis that supplementation with PC (or choline salts) could enhance sporting performance. Although the available data that evaluates the effects of PC supplementation on performance are equivocal, acute oral supplementation with PC (~0.2 g PC per kg body mass) has been demonstrated to improve performance in a variety of sporting activities where exercise has depleted circulatory choline concentrations. Short term oral supplementation with soy-derived PS (S-PS) has been reported to attenuate circulating cortisol concentrations, improve perceived well-being, and reduce perceived muscle soreness after exercise. More recently, short term oral supplementation (750 mg per day of S-PS for 10 days) has been demonstrated to improve exercise capacity during high intensity cycling and tended to increase performance during intermittent running. Although more research is warranted to determine minimum dietary Phospholipid requirements for optimal sporting performance, these findings suggest that some participants might benefit from dietary interventions that increase the intakes of PC and PS.

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          Most cited references48

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          Human serial learning: enhancement with arecholine and choline impairment with scopolamine.

          Arecholine (4 milligrams), a cholinergic agonist, and choline (10 grams), a precursor of acetylcholine, significantly enhanced serial learning in normal human subjects. The subjects received methscopolamine prior to both arecholine and placebo injections. Conversely, scopolamine (0.5 milligram), a cholinergic antagonist, impaired learning and this impairment was reversed by arecholine and choline and the impairment after scopolamine were inversely proportional to the subject's performance on placebo; that is, "poor" performers were more vulnerable to both the enhancing effect of cholinergic agonist and precursor and the impairment after cholinergic antagonist than "good" performers.
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            Heart rate and performance parameters in elite cyclists: a longitudinal study.

            This study was designed to evaluate the stability of target heart rate (HR) values corresponding to performance markers such as lactate threshold (LT) and the first and second ventilatory thresholds (VT1, VT2) in a group of 13 professional road cyclists (VO2max, approximately 75.0 mL x kg(-1) x min(-1)) during the course of a complete sports season. Each subject performed a progressive exercise test on a bicycle ergometer (ramp protocol with workload increases of 25 W x min(-1)) three times during the season corresponding to the "active" rest (fall: November), precompetition (winter: January), and competition periods (spring: May) to determine HR values at LT, VT1 and VT2. Despite a significant improvement in performance throughout the training season (i.e., increases in the power output eliciting LT, VT1, or VT2), target HR values were overall stable (HR at LT: 154 +/- 3, 152 +/- 3, and 154 +/- 2 beats x min(-1); HR at VT1: 155 +/- 3, 156 +/- 3, and 159 +/- 3 beats x min(-1); and at VT2: 178 +/- 2, 173 +/- 3, and 176 +/- 2 beats x min(-1) during rest, precompetition, and competition periods, respectively). A single laboratory testing session at the beginning of the season might be sufficient to adequately prescribe training loads based on HR data in elite endurance athletes such as professional cyclists. This would simplify the testing schedule generally used for this type of athlete.
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              Effects of soy lecithin phosphatidic acid and phosphatidylserine complex (PAS) on the endocrine and psychological responses to mental stress.

              Phosphatidylserine, derived from cow brains, has been shown previously to dampen the ACTH and cortisol response to physical stress. Further research investigated the influence of soy lecithin phosphatidylserine supplementation on mood and heart rate when faced with an acute stressor. In this study, we investigated the effects of soy lecithin phosphatidic acid and phosphatidylserine complex (PAS) supplementation on pituitary adrenal reactivity (ACTH, cortisol) and on the psychological response (Spielberger State Anxiety Inventory stress subscale) to a mental and emotional stressor. Four groups of 20 subjects were treated for three weeks with daily dosages of either 400 mg PAS, 600 mg PAS, 800 mg PAS, or placebo before exposure to the Trier Social Stress Test (TSST). Treatment with 400 mg PAS resulted in a pronounced blunting of both serum ACTH and cortisol, and salivary cortisol responses to the TSST, but did not affect heart rate. The effect was not seen with larger doses of PAS. With regard to the psychological response, 400 mg PAS seemed to exert a specific positive effect on emotional responses to the TSST. While the placebo group showed the expected increase in distress after the test, the group treated with 400 mg PAS showed decreased distress. These data provide initial evidence for a selective stress dampening effect of PAS on the pituitary-adrenal axis, suggesting the potential of PAS in the treatment of stress related disorders.
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                Author and article information

                Journal
                J Int Soc Sports Nutr
                Journal of the International Society of Sports Nutrition
                BioMed Central (London )
                1550-2783
                2007
                25 July 2007
                : 4
                : 5
                Affiliations
                [1 ]Increnovo LLC, 2138 E Lafayette Pl, Milwaukee, WI 53202, USA
                [2 ]Department of Sports Science, University of Wales Swansea, Singleton Park, Swansea, SA2 8PP, UK
                Article
                1550-2783-4-5
                10.1186/1550-2783-4-5
                1997116
                17908342
                f6660e86-e585-4d22-af45-e432ad6fdd10
                Copyright © 2007 Jäger et al; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 30 May 2007
                : 25 July 2007
                Categories
                Review

                Sports medicine
                Sports medicine

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