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1.
Pharmacol Biochem Behav ; 96(1): 67-74, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20417659

ABSTRACT

OBJECTIVE: Cannabis intake has been reported to affect cognitive functions such as selective attention. This study addressed the effects of exposure to cannabis with up to 69.4mg Delta(9)-tetrahydrocannabinol (THC) on Event-Related Potentials (ERPs) recorded during a visual selective attention task. METHODS: Twenty-four participants smoked cannabis cigarettes with four doses of THC on four test days in a randomized, double blind, placebo-controlled, crossover study. Two hours after THC exposure the participants performed a visual selective attention task and concomitant ERPs were recorded. RESULTS: Accuracy decreased linearly and reaction times increased linearly with THC dose. However, performance measures and most of the ERP components related specifically to selective attention did not show significant dose effects. Only in relatively light cannabis users the Occipital Selection Negativity decreased linearly with dose. Furthermore, ERP components reflecting perceptual processing, as well as the P300 component, decreased in amplitude after THC exposure. Only the former effect showed a linear dose-response relation. CONCLUSIONS: The decrements in performance and ERP amplitudes induced by exposure to cannabis with high THC content resulted from a non-selective decrease in attentional or processing resources. SIGNIFICANCE: Performance requiring attentional resources, such as vehicle control, may be compromised several hours after smoking cannabis cigarettes containing high doses of THC, as presently available in Europe and Northern America.


Subject(s)
Attention/drug effects , Dronabinol/chemistry , Evoked Potentials, Visual/drug effects , Marijuana Smoking/adverse effects , Psychomotor Performance/drug effects , Visual Perception/drug effects , Adolescent , Adult , Attention/physiology , Cannabis/chemistry , Cross-Over Studies , Double-Blind Method , Dronabinol/administration & dosage , Evoked Potentials, Visual/physiology , Humans , Male , Marijuana Smoking/physiopathology , Photic Stimulation/methods , Psychomotor Performance/physiology , Reaction Time/drug effects , Reaction Time/physiology , Time Factors , Visual Perception/physiology , Young Adult
2.
Parasite Immunol ; 24(4): 189-201, 2002 Apr.
Article in English | MEDLINE | ID: mdl-12010484

ABSTRACT

The efficacy of two recombinant proteins of Haemonchus contortus was studied in both adult sheep and young lambs. These 15 and 24 kDa excretory/secretory proteins were given combined, either supplemented or not with a glycan-rich insect cell extract. In 9-month-old sheep (trial 1), faecal egg output and worm burden were reduced by 49% and 55%, respectively, after vaccination with rec15/24, and by 46% and 65% after vaccination with rec15/24 and glycan extract. No reduction in egg output or number of worms was found in young lambs using the above recombinant proteins plus glycan-rich extract (trial 2). When trial 1 was repeated (trial 3), the protection could not be reproduced, possibly due to differences in batches of recombinant proteins. In all sheep, independent of their age, rec15/24-specific immunoglobulin (Ig)G1 and IgA titres were present, but 9-month-old protected sheep had significantly higher IgA titres than the lambs. Addition of glycans resulted in lower rec15/24-specific IgG1 and IgA in 9-month-old sheep after challenge. This did not affect the level of protection. A significant negative correlation was found between IgA and worm numbers in protected sheep immunized with rec15/24 supplemented with glycans. Total IgE and rec15/24 specific IgE titres were low. The number of eosinophils, mast cells, sheep mast cell protease (SMCP)+ cells and IgA+ cells did not differ between the protected and unprotected sheep, but the lambs had significantly fewer mast cells independent of their immunization.


Subject(s)
Antigens, Helminth/immunology , Haemonchus/immunology , Sheep Diseases/prevention & control , Animals , Haemonchus/chemistry , Immunoglobulin A/analysis , Immunoglobulin E/analysis , Immunoglobulin G/analysis , Immunohistochemistry , Lymphocyte Activation/immunology , Recombinant Proteins/immunology , Sheep , Sheep Diseases/parasitology , Vaccination/veterinary
3.
Environ Health Perspect ; 109(7): 731-7, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11485873

ABSTRACT

Children may ingest contaminated soil from hand to mouth. To assess this exposure route, we need to know the oral bioavailability of the contaminants. Two determining steps in bioavailability of soil-borne contaminants are mobilization from soil during digestion, which is followed by intestinal absorption. The first step has been investigated in previous studies that showed that a substantial fraction of PCBs and lindane is mobilized from soil during artificial digestion. Furthermore, almost all contaminants are sorbed to constituents of artificial human small intestinal fluid (i.e., chyme), whereas only a small fraction is freely dissolved. In this study, we examine the second step using intestinal epithelial Caco-2 cells. The composition of the apical exposure medium was varied by addition of artificial chyme, bile, or oleic acid at similar or increasing total contaminant concentrations. The uptake curves were described by rate constants. The uptake flux seemed to be dose-dependent. Furthermore, different exposure media with similar total contaminant concentrations resulted in various uptake rates. This can be attributed to different freely dissolved concentrations and carrier effects. In addition, the large fractions of contaminants in the cells indicate that PCBs and lindane sorbed to bile, oleic acid, and digestive proteins contributed to the uptake flux toward the cells. These results can be extrapolated qualitatively to in vivo conditions. Because the sorbed contaminants should be considered available for absorption, the first step of mobilization from soil is the most important step for oral bioavailability of the presently investigated soil-borne contaminants.


Subject(s)
Environmental Pollutants/pharmacokinetics , Hexachlorocyclohexane/pharmacokinetics , Insecticides/pharmacokinetics , Polychlorinated Biphenyls/pharmacokinetics , Soil Pollutants/pharmacokinetics , Administration, Oral , Biological Availability , Caco-2 Cells/drug effects , Caco-2 Cells/physiology , Environmental Exposure , Fatty Acids/metabolism , Humans , Intestinal Absorption , Kinetics , Solubility
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