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1.
Psicol Reflex Crit ; 31(1): 28, 2018 Oct 19.
Article in English | MEDLINE | ID: mdl-32026138

ABSTRACT

OBJECTIVE: The aim of this study was to investigate the effects of adverse childhood experiences and life events on the inhibitory control ability, cognitive flexibility, and working memory of college students. METHODS: The study involved testing the participants using the Adverse Childhood Experiences (ACEs) Questionnaire, the Adolescent Life Events Scale (Adolescent Self-rating Life Events Checklist, ASLEC), and the program of executive functions designed by E-prime software. RESULTS: The incidence rate of ACEs was 44.8%. ACEs, life events, and inhibition ability were found to have a significant correlation (r1 = 0.50, r1 = 0.47, p < 0.01). In the switching task, the reaction time of the ACEs group was longer than the reaction time of the non-ACEs group (t = - 2.55, p < 0.05). Low scorers in the ASLEC exhibited lesser reaction times than their high-scoring counterparts in the tasks related to inhibition, switching, and working memory experiments. The regression analysis results showed that ACEs and life events had a possibility rate of 56% in predicting inhibition ability. CONCLUSIONS: The incidence of ACEs was found to be high, and cognitive flexibility is significantly influenced by ACEs. Life events have a significant impact on inhibition ability, cognitive flexibility, and working memory. ACEs and life events were found to be reliable predictors of inhibition ability.

2.
Psicol. reflex. crit ; 31: 28, 2018. tab
Article in English | LILACS, Index Psychology - journals | ID: biblio-976640

ABSTRACT

Abstract Objective: The aim of this study was to investigate the effects of adverse childhood experiences and life events on the inhibitory control ability, cognitive flexibility, and working memory of college students. Methods: The study involved testing the participants using the Adverse Childhood Experiences (ACEs) Questionnaire, the Adolescent Life Events Scale (Adolescent Self-rating Life Events Checklist, ASLEC), and the program of executive functions designed by E-prime software. Results: The incidence rate of ACEs was 44.8%. ACEs, life events, and inhibition ability were found to have a significant correlation (r1 = 0.50, r1 = 0.47, p < 0.01). In the switching task, the reaction time of the ACEs group was longer than the reaction time of the non-ACEs group (t = ­ 2.55, p < 0.05). Low scorers in the ASLEC exhibited lesser reaction times than their high-scoring counterparts in the tasks related to inhibition, switching, and working memory experiments. The regression analysis results showed that ACEs and life events had a possibility rate of 56% in predicting inhibition ability. Conclusions: The incidence of ACEs was found to be high, and cognitive flexibility is significantly influenced by ACEs. Life events have a significant impact on inhibition ability, cognitive flexibility, and working memory. ACEs and life events were found to be reliable predictors of inhibition ability.


Subject(s)
Humans , Male , Female , Adolescent , Adult , Executive Function , Psychological Trauma/psychology , Life Change Events , Students , China , Universities
3.
Biomed Res Int ; 2015: 651218, 2015.
Article in English | MEDLINE | ID: mdl-25883968

ABSTRACT

The present study was designed to investigate the effect of Agaricus brasiliensis extract (ABE) on phenylhydrazine-induced neonatal jaundice in rats. Administration of ABE dose-dependently reduced the elevated bilirubin level induced by phenylhydrazine. It can be somewhat supported from the results of in vitro bilirubin degradation experiment. ABE treatment also reduced the total antioxidant status (TAOS), cascade O2(-)/SOD, level of NF-κB protein, and adrenomedullin (AM). Overall, the results of this study demonstrated that Agaricus brasiliensis extract may be beneficial to reducing bilirubin level without causing hepatotoxicity in neonatal jaundice.


Subject(s)
Complex Mixtures/pharmacology , Jaundice, Neonatal , Phenylhydrazines/toxicity , Adrenomedullin/metabolism , Agaricus , Animals , Antioxidants/metabolism , Complex Mixtures/chemistry , Disease Models, Animal , Jaundice, Neonatal/chemically induced , Jaundice, Neonatal/drug therapy , Jaundice, Neonatal/metabolism , NF-kappa B/metabolism , Rats , Rats, Wistar , Superoxide Dismutase/metabolism , Superoxides/metabolism
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