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James B. Koprich

3 papers in the library · 83 citations · publishing 2006-2012

Papers

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Prenatal exposure to MDMA alters noradrenergic neurodevelopment in the rat.

Neurotoxicology and Teratology 2012 Valerie B Thompson, James B. Koprich, E Y Chen et al.

3,4-methylenedioxymethamphetamine (MDMA; ecstasy) binds with high affinity to the norepinephrine transporter (NET), making the noradrenergic system a potential target during fetal exposure. Recent data indicate that adult rats that had been prenatally exposed to MDMA display persistent deficits in working memory and attention; behaviors consistent with abnormal noradrenergic signaling in the...

Characterization of 3,4-Methylenedioxymethamphetamine (MDMA) EnantiomersIn Vitroand in the MPTP-Lesioned Primate:R-MDMA Reduces Severity of Dyskinesia, WhereasS-MDMA Extends Duration of ON-Time

Journal of Neuroscience May 11, 2011 Philippe Huot, Tom H. Johnston, Katie D. Lewis et al. 83 citations

l -3,4-Dihydroxyphenylalanine ( l -DOPA) is the most effective treatment for Parkinson's disease, but long-term l -DOPA administration is marred by the emergence of motor complications, namely, dyskinesia and a shortening of antiparkinsonian benefit (wearing-OFF). 3,4-Methylenedioxymethamphetamine (MDMA) is unique in that it exerts antidyskinetic effects and may enhance antiparkinsonian actions...

MDMA administration to pregnant Sprague-Dawley rats results in its passage to the fetal compartment.

Neurotoxicology and Teratology 2006 Nicholas G Campbell, James B. Koprich, Nicholas M Kanaan et al.

Recent investigations have demonstrated that prenatal 3,4-methylenedeoxymethamphetamine (MDMA; ecstasy) exposure in rats results in significant and persistent changes in the developing brain. However, no published pharmacokinetic studies exist demonstrating that MDMA administered during pregnancy passes to the fetal compartment. This leaves open the question whether MDMA is directly acting on...