Evidence map›Paper›PMID 17387459›Full record

ArticlePsychopharmacology2007

Differential effects of the D- and L- isomers of amphetamine on pharmacological MRI BOLD contrast in the rat.

Neil Easton, Fiona Marshall, Kevin C F Fone, Charles A Marsden

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Article in Psychopharmacology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Chronic exposure to manganese alters brain responses to amphetamine: a pharmacological magnetic resonance imaging study.Toxicological sciences : an official journal of the Society of Toxicology · 2010
    Article
  6. Article
  7. Article
  8. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Neil EastonSchool of Biomedical Sciences, Medical School, Institute of Neuroscience, University of Nottingham, Queens Medical Centre, Nottingham, NG7 2UH, UK.
Fiona Marshall
Kevin C F Fone
Charles A Marsden

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleThe D - and L-amphetamine sulphate isomers are used in the formulation of Adderall XR(R), which is effective in the treatment of attention-deficit hyperactivity disorder (ADHD). The effects of these isomers on brain activity has not been examined using neuroimaging.

objectivesThis study determines the pharmacological magnetic resonance imaging blood-oxygenation-level-dependent (BOLD) response in rat brain regions after administration of each isomer. MATERIALS AND

methodsRats were individually placed into a 2.35 T Bruker magnet for 60 min to achieve basal recording of variation in signal intensity. Either saline (n = 9), D-amphetamine sulphate (2 mg/kg, i.p.; n = 9) or L: -amphetamine sulphate (4 mg/kg, i.p.; n = 9) were administered, and recording continued for a further 90 min. Data were analysed for BOLD effects using statistical parametric maps. Blood pressure, blood gases and respiratory rate were monitored during scanning.

resultsThe isomers show overlapping effects on the BOLD responses in areas including nucleus accumbens, medial entorhinal cortex, colliculi, field CA1 of hippocampus and thalamic nuclei. The L-isomer produced greater global changes in the positive BOLD response than the D-isomer, including the somatosensory and motor cortices and frontal brain regions such as the orbitofrontal cortices, prelimbic and infralimbic cortex which were not observed with the D-isomer.

conclusionsThe amphetamine isomers produce different BOLD responses in brain areas related to cognition, pleasure, pain processing and motor control probably because of variations on brain amine systems such as dopamine and noradrenaline. The isomers may, therefore, have distinct actions on brain regions affected in ADHD patients.

Indexed as

AmphetamineAnimalsBlood PressureBrainBrain MappingCentral Nervous System StimulantsDextroamphetamineInjections, IntraperitonealMagnetic Resonance ImagingMaleRatsRats, Sprague-DawleyStereoisomerismStructure-Activity RelationshipAmphetamineCentral Nervous System StimulantsDextroamphetamine

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.