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1.
Exp Clin Psychopharmacol ; 26(3): 302-309, 2018 06.
Article in English | MEDLINE | ID: mdl-29863386

ABSTRACT

Glucose intake has been found to improve some aspects of cognitive performance; however, results are often inconsistent. This inconsistency may be related to expectations surrounding glucose, which can have strong effects on performance outcomes. The present study evaluated the independent and interactive effects of acute sugar intake, in the form of high-fructose corn syrup (HFCS), and sugar expectancies on cognitive performance and mood. One hundred five healthy young adults were randomized according to sugar intake and expectation: consumed-sugar/told-sugar, consumed-sugar/told-no-sugar, consumed-no-sugar/told-sugar, and consumed-no-sugar/told-no-sugar. Thirty minutes after sugar or no-sugar intake, participants completed the Profile of Mood States and a battery of cognitive tests, including immediate and delayed recall, the Stroop test, n-back task, and continuous performance task. Tension increased following the expectation of consuming sugar, regardless of sugar consumption (p < .05). On the continuous performance task, accuracy and sensitivity were higher (ps < .05) and false alarm rate was lower (p < .05) following sugar than no sugar intake. No effects of sugar intake or expectation were found for any other mood or cognitive measure (ps > .05). The findings suggest that sugar intake in the form of HFCS may benefit certain cognitive processes, such as those that require sustained attention, but that the expectation of sugar intake is not sufficient to produce such benefits. (PsycINFO Database Record


Subject(s)
Affect/drug effects , Cognition/drug effects , High Fructose Corn Syrup/administration & dosage , Motivation/drug effects , Adolescent , Adult , Affect/physiology , Blood Glucose/drug effects , Blood Glucose/metabolism , Carbonated Beverages , Cognition/physiology , Double-Blind Method , Female , Humans , Male , Motivation/physiology , Psychomotor Performance/drug effects , Psychomotor Performance/physiology , Surveys and Questionnaires , Young Adult
2.
Environ Health Perspect ; 113(6): 700-7, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15929892

ABSTRACT

In this study we examined the effects of exposure to the antiandrogenic fungicide vinclozolin (Vz) on the development of two sex-differentiated behaviors that are organized by the perinatal actions of androgens. Pregnant Long-Evans rats were administered a daily oral dose of 0, 1.5, 3, 6, or 12 mg/kg Vz from the 14th day of gestation through postnatal day (PND)3. The social play behavior of juvenile offspring was examined on PND22 and again on PND34 during play sessions with a same-sex littermate. After they reached adulthood, the male offspring were examined with the ex copula penile reflex procedure to assess erectile function. Vz did not produce any gross maternal or neonatal toxicity, nor did it reduce the anogenital distance in male pups. We observed no effects of Vz on play behavior on PND22. However, the 12-mg/kg Vz dose significantly increased play behavior in the male offspring on PND34 compared with controls. The most dramatic increases were seen with the nape contact and pounce behavior components of play. The Vz effect was more pronounced in male than in female offspring. As adults, male offspring showed a significant reduction of erections at all dose levels during the ex copula penile reflex tests. The 12-mg/kg dose was also associated with an increase in seminal emissions. These effects demonstrate that perinatal Vz disrupts the development of androgen-mediated behavioral functions at exposure levels that do not produce obvious structural changes or weight reductions in androgen-sensitive reproductive organs.


Subject(s)
Androgen Antagonists/toxicity , Behavior, Animal/drug effects , Fungicides, Industrial/toxicity , Oxazoles/toxicity , Penile Erection/drug effects , Animals , Female , Male , Maternal Exposure , Pregnancy , Prenatal Exposure Delayed Effects , Rats , Rats, Long-Evans , Sex Differentiation , Sexual Behavior, Animal/drug effects
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