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      Evaluation of the effects of two doses of alpha glycerylphosphorylcholine on physical and psychomotor performance

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          Abstract

          Background

          Recent studies have suggested that alpha glycerylphosphorylcholine (A-GPC) may be an effective ergogenic aid. The present study was designed to assess the efficacy of two doses of A-GPC in comparison to placebo and caffeine for increasing countermovement jump performance, isometric strength, and psychomotor function.

          Methods

          Forty-eight healthy, college aged males volunteered for the present study and underwent baseline assessment of countermovement jump (CMJ), isometric mid thigh pull (IMTP), upper body isometric strength test (UBIST), and psychomotor vigilance (PVT). Following this assessment participants were randomly assigned to groups consisting of 500 mg A-GPC, 250 mg A-GPC, 200 mg Caffeine or Placebo taken daily. Blood samples were collected 1 h and 2 h post initial dose to quantify serum free choline and thyroid stimulating hormone then subjects returned after 7 days of supplementation to repeat CMJ, IMTP, UBIST and PVT.

          Results

          No differences were noted between groups for IMTP, UBIST or PVT performance. Serum free choline was found to be elevated in the two A-GPC groups as compared to placebo (132% and 59% respectively). Serum TSH was found to be significantly depressed in the 500 mg A-GPC group compared to other treatments ( p < 0.04). Group differences were noted for maximum velocity and maximum mechanical power on the CMJ ( p < 0.05) with the 250 mg A-GPC group demonstrating the greatest improvements in result.

          Conclusions

          Based upon this evidence, and previous evidence regarding A-GPC, it should be considered as an emerging ergogenic supplement.

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          Most cited references21

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          The Walter Reed palm-held psychomotor vigilance test.

          This field-portable reaction time test and analysis software run on devices using the Palm operating system. It is designed to emulate a test and commercial device widely used in sleep deprivation, shift work, fatigue, and stimulant drug research but provides additional capabilities. Experimental comparisons with the standard commercial device in a 40-hour total sleep deprivation study show it to be comparably sensitive to selected experimental variables. A Pocket PC-compatible version is under developement.
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            Cholinergic precursors in the treatment of cognitive impairment of vascular origin: ineffective approaches or need for re-evaluation?

            Inhibition of endogenous acetylcholine degradation through cholinesterase inhibitors represents a milestone in symptomatic treatment of cognitive symptoms in mild to moderate stages of Alzheimer's disease. Cholinesterase inhibitors are also under investigation for treating cognitive dysfunction of cerebrovascular origin, but to date they do not have specific indication for vascular dementia or vascular cognitive impairment. This paper reviews the main clinical studies assessing the activity of cholinergic precursors in the treatment of adult-onset dementia disorders of vascular origin. The first cholinergic precursor used phosphatidylcholine (lecithin) did not show any clear clinical benefit on symptoms of dementia disorders. The same is not true for other phospholipids involved in choline biosynthetic pathways such as cytidine 5'-diphosphocholine (CDP-choline) and choline alphoscerate for which a modest improvement of cognitive dysfunction in dementia of neurodegenerative and vascular origin is documented. Positive results obtained with selected cholinergic precursors cannot be generalized due to the small numbers of patients studied in appropriate clinical trials. However, they probably would justify reconsideration of the most promising molecules in larger carefully controlled studies.
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              Choline: an important micronutrient for maximal endurance-exercise performance?

              Choline plays a central role in many physiological pathways, including neurotransmitter synthesis (acetylcholine), cell-membrane signaling (phospholipids), lipid transport (lipoproteins), and methyl-group metabolism (homocysteine reduction). Endurance exercise might stress several of these pathways, increasing the demand for choline as a metabolic substrate. This review examines the current literature linking endurance exercise and choline demand in the human body. Also reviewed are the mechanisms by which exercise might affect blood choline levels, and the links between methyl metabolism and the availability of free choline are highlighted. Finally, the ability of oral choline supplements to augment endurance performance is assessed. Most individuals consume adequate amounts of choline, although there is evidence that current recommendations might be insufficient for some adult men. Only strenuous and prolonged physical activity appears sufficient to significantly decrease circulating choline stores. Moreover, oral choline supplementation might only increase endurance performance in activities that reduce circulating choline levels below normal.
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                Author and article information

                Contributors
                kinesiology@louisina.edu
                Jason.Soileau@pbrc.edu
                lwjudge@bsu.edu
                (337) 482-6615 , dbellar@louisiana.edu
                Journal
                J Int Soc Sports Nutr
                J Int Soc Sports Nutr
                Journal of the International Society of Sports Nutrition
                BioMed Central (London )
                1550-2783
                5 October 2017
                5 October 2017
                2017
                : 14
                : 39
                Affiliations
                [1 ]ISNI 0000 0000 9831 5270, GRID grid.266621.7, School of Kinesiology, , University of Louisiana at Lafayette, ; Lafayette, LA 70503 USA
                [2 ]ISNI 0000 0001 0662 7451, GRID grid.64337.35, Pennington Biomedical Research Center, , Louisiana State University, ; Baton Rouge, LA 70808 USA
                [3 ]ISNI 0000 0001 2111 9017, GRID grid.252754.3, School of Kinesiology, , Ball State University, ; Muncie, IN 47306 USA
                [4 ]ISNI 0000 0000 9831 5270, GRID grid.266621.7, School of Kinesiology, , University of Louisiana at Lafayette, ; 225 Cajundome Blvd, Lafayette, LA 70506 USA
                Author information
                http://orcid.org/0000-0001-8273-1373
                Article
                196
                10.1186/s12970-017-0196-5
                5629791
                29042830
                573de64b-6383-4885-a9f9-3238a05bca0d
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 31 March 2017
                : 28 September 2017
                Funding
                Funded by: ChemiNutra
                Award ID: R4475
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2017

                Sports medicine
                power,strength,reaction time
                Sports medicine
                power, strength, reaction time

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