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3.
Int J Clin Exp Hypn ; 66(1): 83-105, 2018.
Article in English | MEDLINE | ID: mdl-29319456

ABSTRACT

We investigated the association between hypnotizability, COMT polymorphism, P50 suppression ratio, and prepulse inhibition of acoustic startle response (ASR) in 21 high (HH) and 19 low (LH) hypnotizable subjects. The frequency of Met/Met carriers of COMT polymorphysm was higher in HH than in LH group (33.3% versus 10.6%, p = .049). Increased ASR amplitude and latency and decreased prepulse inhibition at 120 ms lead interval were found in the HH compared to the LH group. The effect of COMT genotype on prepulse inhibition was observed in LH group only. No between-group differences in P50 measures were found. The obtained results suppose the participation of dopamine system in mechanisms of hypnotizability and different allocation of attentional resources in HH and LH subjects.


Subject(s)
Catechol O-Methyltransferase/genetics , Hypnosis , Sensory Gating/genetics , Adult , Catechol O-Methyltransferase/physiology , Electromyography , Electrooculography , Female , Genotype , Humans , Male , Middle Aged , Polymorphism, Genetic , Young Adult
4.
Phytomedicine ; 19(14): 1250-5, 2012 Nov 15.
Article in English | MEDLINE | ID: mdl-23079230

ABSTRACT

The objective of this study was to evaluate the feeding behavior and weight gain in rats with high-calorie diet-induced obesity that are treated with Bergenia crassifolia black and fermented leaves extracts. The daily dietary intake of all treated animals was reduced to 40% compared with the control group on day 22 of the experiment. A significant improvement in glucose tolerance was noted after 7 days of treatment with the Bergenia extracts. In rats treated with an extract of black leaves for 7 days, a significant reduction in the serum triglyceride level, 45% (p<0.05), compared with the control group was observed. However, the treatment did not affect the cholesterol level. Our results provide evidence for the potential use of B. crassifolia as an appetite and energy intake suppressant.


Subject(s)
Energy Intake/drug effects , Feeding Behavior/drug effects , Obesity/drug therapy , Phytotherapy , Plant Extracts/therapeutic use , Saxifragaceae , Weight Gain/drug effects , Animals , Appetite/drug effects , Blood Glucose/metabolism , Cholesterol/blood , Diet/adverse effects , Female , Fermentation , Glucose Intolerance/blood , Glucose Intolerance/drug therapy , Glucose Intolerance/etiology , Obesity/blood , Obesity/etiology , Plant Extracts/pharmacology , Rats , Rats, Wistar , Triglycerides/blood
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