Citation
Vorhees, Charles V., et al. "(+/-)3,4-Methylenedioxymethamphetamine (MDMA) Dose-dependently Impairs Spatial Learning in the Morris Water Maze After Exposure of Rats to Different Five-day Intervals From Birth to Postnatal Day Twenty." Developmental Neuroscience, vol. 31, no. 1-2, 2009, pp. 107-20.
Vorhees CV, Schaefer TL, Skelton MR, et al. (+/-)3,4-Methylenedioxymethamphetamine (MDMA) dose-dependently impairs spatial learning in the morris water maze after exposure of rats to different five-day intervals from birth to postnatal day twenty. Dev Neurosci. 2009;31(1-2):107-20.
Vorhees, C. V., Schaefer, T. L., Skelton, M. R., Grace, C. E., Herring, N. R., & Williams, M. T. (2009). (+/-)3,4-Methylenedioxymethamphetamine (MDMA) dose-dependently impairs spatial learning in the morris water maze after exposure of rats to different five-day intervals from birth to postnatal day twenty. Developmental Neuroscience, 31(1-2), 107-20. https://doi.org/10.1159/000207499
Vorhees CV, et al. (+/-)3,4-Methylenedioxymethamphetamine (MDMA) Dose-dependently Impairs Spatial Learning in the Morris Water Maze After Exposure of Rats to Different Five-day Intervals From Birth to Postnatal Day Twenty. Dev Neurosci. 2009;31(1-2):107-20. PubMed PMID: 19372692.
TY - JOUR
T1 - (+/-)3,4-Methylenedioxymethamphetamine (MDMA) dose-dependently impairs spatial learning in the morris water maze after exposure of rats to different five-day intervals from birth to postnatal day twenty.
AU - Vorhees,Charles V,
AU - Schaefer,Tori L,
AU - Skelton,Matthew R,
AU - Grace,Curtis E,
AU - Herring,Nicole R,
AU - Williams,Michael T,
Y1 - 2009/04/17/
PY - 2008/03/25/received
PY - 2008/08/07/accepted
PY - 2009/4/18/entrez
PY - 2009/4/18/pubmed
PY - 2009/6/17/medline
SP - 107
EP - 20
JF - Developmental neuroscience
JO - Dev Neurosci
VL - 31
IS - 1-2
N2 - During postnatal days (PD) 11-20, (+/-)3,4-methylenedioxymethamphetamine (MDMA) treatment impairs egocentric and allocentric learning, and reduces spontaneous locomotor activity; however, it does not have these effects during PD 1-10. How the learning impairments relate to the stress hyporesponsive period (SHRP) is unknown. To test this association, the preweaning period was subdivided into 5-day periods from PD 1-20. Separate pups within each litter were injected subcutaneously with 0, 10, 15, 20, or 25 mg/kg MDMA x4/day on PD 1-5, 6-10, 11-15, or 16-20, and tested as adults. The 3 highest MDMA dose groups showed reduced locomotor activity during the first 10 min (of 60 min), especially in the PD 1-5 and 6-10 dosing regimens. MDMA groups in all dosing regimens showed impaired allocentric learning in the Morris water maze (on acquisition and reversal, all MDMA groups were affected; on the small platform phase, the 2 high-dose groups were affected). No effects of MDMA were found on anxiety (elevated zero maze), novel object recognition, or egocentric learning (although a nonsignificant trend was observed). The Morris maze results did not support the idea that the SHRP is critical to the effects of MDMA on allocentric learning. However, since no effects on egocentric learning were found, but were apparent after PD 11-20 treatment, the results show that these 2 forms of learning have different exposure-duration sensitivities.
SN - 1421-9859
UR - https://www.unboundmedicine.com/medline/citation/19372692/_+/__34_Methylenedioxymethamphetamine__MDMA__dose_dependently_impairs_spatial_learning_in_the_morris_water_maze_after_exposure_of_rats_to_different_five_day_intervals_from_birth_to_postnatal_day_twenty_
L2 - https://www.karger.com?DOI=10.1159/000207499
DB - PRIME
DP - Unbound Medicine
ER -