6 research outputs found
Anthropometric data of included volunteers and MDMA doses according to gender and genotypes (mean ± SD [min, max]).
<p>MDMA, ±3,4-methylenedioxymethamphetamine; CYP2D6, cytochrome P450 2D6; FA: functional alleles COMT, catechol-O-methyltransferase; 5-HTTLPR, gene-linked polymorphic region. BMI: body mass index; <i>p.o: per os. *p</i><0.05<i>; **p</i><0.01.</p
Influence of gender and genetics (<i>COMT, 5-HTTLPR</i>) on the temporal course of systolic blood pressure (upper-left panel), heart rate (lower-left panel), and oral temperature (right-end panel) (mean ± SEM); women n = 12 <i>vs.</i> men n = 15; COMT, <i>val/val</i> n = 8 <i>vs. met/*</i> n = 18; 5-HTTLPR, <i>l/*</i> n = 18 <i>vs. s/s</i> n = 9).
<p>*<i>p</i><0.05, **<i>p</i><0.01. Graph A corresponds to gender differences in OT, graph B corresponds to differences in OT as a function of 5-HTTLPR polymorphisms (<i>l/l</i> n = 11 <i>vs. s/s</i> n = 9). Subjects <i>l/s</i> (n = 7) are not represented for graph clarity, but data almost fully overlaps with the <i>s/s</i> trace.</p
Gender differences in physiological and subjective effects after MDMA administration (mean ± SD; women n = 12 <i>vs.</i> men n = 15) (only significant effects included).
<p>AUC: area under the effect-time curve; Emax: peak effect; Tmax: time of peak effect. VAS: visual analogue scale. ARCI: Addiction Research Center Inventory, PCAG: pentobarbital-chlorpromazine-alcohol group. VESSPA: Evaluation of the Subjective Effects of Substances with Abuse Potential.</p>*<p>p<0.05,</p>**<p>p<0.01.</p
Gender differences in pharmacokinetic parameters of MDMA and its metabolites (mean ± SD; for MDMA and HMMA: women n = 11 <i>vs.</i> men n = 15; for MDA and HMA: women n = 11 <i>vs.</i> men n = 12).
<p>MDMA, ±3,4-methylenedioxymethamphetamine; MDA, 3,4-methylenedioxyamphetamine; HMA, 3-methoxy-4-hydroxyamphetamine; HMMA, 3-methoxy-4-hydroxymethamphetamine; AUC: area under the concentration-time curve, C<sub>max</sub>: peak plasma concentration; T<sub>max</sub>: time with peak plasma; T<sub>1/2</sub>: half-life of elimination; K<sub>e</sub>: elimination constant; K<sub>a</sub>: absorption constant; Vd: apparent volume of distribution; Cl: clearance; n.d: not determined, due to high variability (a).</p>**<p><i>p</i><0.01.</p
Genetic differences in physiological and subjective effects after MDMA administration (mean ± SD; women n = 12 vs. men n = 15) (only significant effects included).
<p>AUC: area under the effect-time curve; Emax: peak effect; COMT, catechol-O-methyltransferase; SBP: systolic blood pressure; DBP: diastolic blood pressure. 5-HTTLPR, gene-linked polymorphic region VESSPA: Evaluation of the Subjective Effects of Substances with Abuse Potential.</p>*<p>p<0.05;</p>**<p>p<0.01. N = [COMT, valval n = 8 vs. met/* n = 18; 5-HTTLPR, l/* n = 18 vs. s/s n = 9.</p
Plasma Concentrations of MDMA, HMMA, MDA, and HMA in both genders (mean ± standard error of the mean, SEM; for MDMA and HMMA: women n = 11 <i>vs.</i> men n = 15; for MDA and HMA: women n = 11 <i>vs.</i> men n = 12).
<p>Influence of <i>CYP2D6</i> genotype in plasma concentrations of HMMA (mean ± SEM; subjects with 2 FA n = 18 <i>vs.</i> with 1 FA n = 8. *<i>p</i><0.05, **<i>p</i><0.01.</p