Acute Paraxanthine Ingestion Improves Cognition and Short-Term Memory and Helps Sustain Attention in a Double-Blind, Placebo-Controlled, Crossover Trial

This study examined the effects of acute paraxanthine (PXN) ingestion on markers of cognition, executive function, and psychomotor vigilance. In a randomized, double blind, placebo-controlled, crossover, and counterbalanced manner, 13 healthy male and female participants were randomly assigned to co...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Choongsung Yoo, Dante Xing, Drew Gonzalez, Victoria Jenkins, Kay Nottingham, Broderick Dickerson, Megan Leonard, Joungbo Ko, Mark Faries, Wesley Kephart, Martin Purpura, Ralf Jäger, Shawn D. Wells, Ryan Sowinski, Christopher J. Rasmussen, Richard B. Kreider
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
Materias:
Acceso en línea:https://doaj.org/article/97d8820a82244b568c0773caf7b327e9
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:97d8820a82244b568c0773caf7b327e9
record_format dspace
spelling oai:doaj.org-article:97d8820a82244b568c0773caf7b327e92021-11-25T18:35:46ZAcute Paraxanthine Ingestion Improves Cognition and Short-Term Memory and Helps Sustain Attention in a Double-Blind, Placebo-Controlled, Crossover Trial10.3390/nu131139802072-6643https://doaj.org/article/97d8820a82244b568c0773caf7b327e92021-11-01T00:00:00Zhttps://www.mdpi.com/2072-6643/13/11/3980https://doaj.org/toc/2072-6643This study examined the effects of acute paraxanthine (PXN) ingestion on markers of cognition, executive function, and psychomotor vigilance. In a randomized, double blind, placebo-controlled, crossover, and counterbalanced manner, 13 healthy male and female participants were randomly assigned to consume a placebo (PLA) or 200 mg of PXN (ENFINITY™, Ingenious Ingredients, L.P.). Participants completed stimulant sensitivity and side effect questionnaires and then performed the Berg Wisconsin Card Sorting Test (BCST), the Go/No-Go test (GNG), the Sternberg task test (STT), and the psychomotor vigilance task test (PVTT). Participants then ingested one capsule of PLA or PXN treatment. Participants completed side effect and cognitive function tests after 1, 2, 3, 4, 5, and 6 h after ingestion of the supplement. After 7 days, participants repeated the experiment while consuming the alternative treatment. Data were analyzed by general linear model (GLM) univariate analyses with repeated measures using body mass as a covariate, and by assessing mean and percent changes from baseline with 95% confidence intervals (CIs) expressed as means (LL, UL). PXN decreased BCST errors (PXN −4.7 [−0.2, −9.20], <i>p</i> = 0.04; PXN −17.5% [−36.1, 1.0], <i>p</i> = 0.06) and perseverative errors (PXN −2.2 [−4.2, −0.2], <i>p</i> = 0.03; PXN −32.8% [−64.4, 1.2], <i>p</i> = 0.04) at hour 6. GNG analysis revealed some evidence that PXN ingestion better maintained mean accuracy over time and Condition R Round 2 response time (e.g., PXN −25.1 [−52.2, 1.9] ms, <i>p</i> = 0.07 faster than PLA at 1 h), suggesting better sustained attention. PXN ingestion improved STT two-letter length absent and present reaction times over time as well as improving six-letter length absent reaction time after 2 h (PXN −86.5 ms [−165, −7.2], <i>p</i> = 0.03; PXN −9.0% [−18.1, 0.2], <i>p</i> = 0.05), suggesting that PXN enhanced the ability to store and retrieve random information of increasing complexity from short-term memory. A moderate treatment x time effect size (η<sub>p</sub><sup>2</sup> = 0.08) was observed in PVTT, where PXN sustained vigilance during Trial 2 after 2 h (PXN 840 ms [103, 1576], <i>p</i> = 0.03) and 4 h (PXN 1466 ms [579, 2353], <i>p</i> = 0.002) compared to PL. As testing progressed, the response time improved during the 20 trials and over the course of the 6 h experiment in the PXN treatment, whereas it significantly increased in the PL group. The results suggest that acute PXN ingestion (200 mg) may affect some measures of short-term memory, reasoning, and response time to cognitive challenges and help sustain attention.Choongsung YooDante XingDrew GonzalezVictoria JenkinsKay NottinghamBroderick DickersonMegan LeonardJoungbo KoMark FariesWesley KephartMartin PurpuraRalf JägerShawn D. WellsRyan SowinskiChristopher J. RasmussenRichard B. KreiderMDPI AGarticlemental performancenootropicsergogenic aidcaffeine alternativeNutrition. Foods and food supplyTX341-641ENNutrients, Vol 13, Iss 3980, p 3980 (2021)
institution DOAJ
collection DOAJ
language EN
topic mental performance
nootropics
ergogenic aid
caffeine alternative
Nutrition. Foods and food supply
TX341-641
spellingShingle mental performance
nootropics
ergogenic aid
caffeine alternative
Nutrition. Foods and food supply
TX341-641
Choongsung Yoo
Dante Xing
Drew Gonzalez
Victoria Jenkins
Kay Nottingham
Broderick Dickerson
Megan Leonard
Joungbo Ko
Mark Faries
Wesley Kephart
Martin Purpura
Ralf Jäger
Shawn D. Wells
Ryan Sowinski
Christopher J. Rasmussen
Richard B. Kreider
Acute Paraxanthine Ingestion Improves Cognition and Short-Term Memory and Helps Sustain Attention in a Double-Blind, Placebo-Controlled, Crossover Trial
description This study examined the effects of acute paraxanthine (PXN) ingestion on markers of cognition, executive function, and psychomotor vigilance. In a randomized, double blind, placebo-controlled, crossover, and counterbalanced manner, 13 healthy male and female participants were randomly assigned to consume a placebo (PLA) or 200 mg of PXN (ENFINITY™, Ingenious Ingredients, L.P.). Participants completed stimulant sensitivity and side effect questionnaires and then performed the Berg Wisconsin Card Sorting Test (BCST), the Go/No-Go test (GNG), the Sternberg task test (STT), and the psychomotor vigilance task test (PVTT). Participants then ingested one capsule of PLA or PXN treatment. Participants completed side effect and cognitive function tests after 1, 2, 3, 4, 5, and 6 h after ingestion of the supplement. After 7 days, participants repeated the experiment while consuming the alternative treatment. Data were analyzed by general linear model (GLM) univariate analyses with repeated measures using body mass as a covariate, and by assessing mean and percent changes from baseline with 95% confidence intervals (CIs) expressed as means (LL, UL). PXN decreased BCST errors (PXN −4.7 [−0.2, −9.20], <i>p</i> = 0.04; PXN −17.5% [−36.1, 1.0], <i>p</i> = 0.06) and perseverative errors (PXN −2.2 [−4.2, −0.2], <i>p</i> = 0.03; PXN −32.8% [−64.4, 1.2], <i>p</i> = 0.04) at hour 6. GNG analysis revealed some evidence that PXN ingestion better maintained mean accuracy over time and Condition R Round 2 response time (e.g., PXN −25.1 [−52.2, 1.9] ms, <i>p</i> = 0.07 faster than PLA at 1 h), suggesting better sustained attention. PXN ingestion improved STT two-letter length absent and present reaction times over time as well as improving six-letter length absent reaction time after 2 h (PXN −86.5 ms [−165, −7.2], <i>p</i> = 0.03; PXN −9.0% [−18.1, 0.2], <i>p</i> = 0.05), suggesting that PXN enhanced the ability to store and retrieve random information of increasing complexity from short-term memory. A moderate treatment x time effect size (η<sub>p</sub><sup>2</sup> = 0.08) was observed in PVTT, where PXN sustained vigilance during Trial 2 after 2 h (PXN 840 ms [103, 1576], <i>p</i> = 0.03) and 4 h (PXN 1466 ms [579, 2353], <i>p</i> = 0.002) compared to PL. As testing progressed, the response time improved during the 20 trials and over the course of the 6 h experiment in the PXN treatment, whereas it significantly increased in the PL group. The results suggest that acute PXN ingestion (200 mg) may affect some measures of short-term memory, reasoning, and response time to cognitive challenges and help sustain attention.
format article
author Choongsung Yoo
Dante Xing
Drew Gonzalez
Victoria Jenkins
Kay Nottingham
Broderick Dickerson
Megan Leonard
Joungbo Ko
Mark Faries
Wesley Kephart
Martin Purpura
Ralf Jäger
Shawn D. Wells
Ryan Sowinski
Christopher J. Rasmussen
Richard B. Kreider
author_facet Choongsung Yoo
Dante Xing
Drew Gonzalez
Victoria Jenkins
Kay Nottingham
Broderick Dickerson
Megan Leonard
Joungbo Ko
Mark Faries
Wesley Kephart
Martin Purpura
Ralf Jäger
Shawn D. Wells
Ryan Sowinski
Christopher J. Rasmussen
Richard B. Kreider
author_sort Choongsung Yoo
title Acute Paraxanthine Ingestion Improves Cognition and Short-Term Memory and Helps Sustain Attention in a Double-Blind, Placebo-Controlled, Crossover Trial
title_short Acute Paraxanthine Ingestion Improves Cognition and Short-Term Memory and Helps Sustain Attention in a Double-Blind, Placebo-Controlled, Crossover Trial
title_full Acute Paraxanthine Ingestion Improves Cognition and Short-Term Memory and Helps Sustain Attention in a Double-Blind, Placebo-Controlled, Crossover Trial
title_fullStr Acute Paraxanthine Ingestion Improves Cognition and Short-Term Memory and Helps Sustain Attention in a Double-Blind, Placebo-Controlled, Crossover Trial
title_full_unstemmed Acute Paraxanthine Ingestion Improves Cognition and Short-Term Memory and Helps Sustain Attention in a Double-Blind, Placebo-Controlled, Crossover Trial
title_sort acute paraxanthine ingestion improves cognition and short-term memory and helps sustain attention in a double-blind, placebo-controlled, crossover trial
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/97d8820a82244b568c0773caf7b327e9
work_keys_str_mv AT choongsungyoo acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT dantexing acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT drewgonzalez acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT victoriajenkins acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT kaynottingham acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT broderickdickerson acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT meganleonard acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT joungboko acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT markfaries acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT wesleykephart acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT martinpurpura acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT ralfjager acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT shawndwells acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT ryansowinski acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT christopherjrasmussen acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
AT richardbkreider acuteparaxanthineingestionimprovescognitionandshorttermmemoryandhelpssustainattentioninadoubleblindplacebocontrolledcrossovertrial
_version_ 1718410967207903232