PMID- 22216322 OWN - NLM STAT- MEDLINE DCOM- 20120521 LR - 20211021 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 6 IP - 12 DP - 2011 TI - Effects of 3,4-methylenedioxymethamphetamine administration on retinal physiology in the rat. PG - e29583 LID - 10.1371/journal.pone.0029583 [doi] LID - e29583 AB - 3,4-Methylenedioxymethamphetamine (MDMA; ecstasy) is known to produce euphoric states, but may also cause adverse consequences in humans, such as hyperthermia and neurocognitive deficits. Although MDMA consumption has been associated with visual problems, the effects of this recreational drug in retinal physiology have not been addressed hitherto. In this work, we evaluated the effect of a single MDMA administration in the rat electroretinogram (ERG). Wistar rats were administered MDMA (15 mg/kg) or saline and ERGs were recorded before (Baseline ERG), and 3 h, 24 h, and 7 days after treatment. A high temperature (HT) saline-treated control group was also included. Overall, significantly augmented and shorter latency ERG responses were found in MDMA and HT groups 3 h after treatment when compared to Baseline. Twenty-four hours after treatment some of the alterations found at 3 h, mainly characterized by shorter latency, tended to return to Baseline values. However, MDMA-treated animals still presented increased scotopic a-wave and b-wave amplitudes compared to Baseline ERGs, which were independent of temperature elevation though the latter might underlie the acute ERG alterations observed 3 h after MDMA administration. Seven days after MDMA administration recovery from these effects had occurred. The effects seem to stem from specific changes observed at the a-wave level, which indicates that MDMA affects subacutely (at 24 h) retinal physiology at the outer retinal (photoreceptor/bipolar) layers. In conclusion, we have found direct evidence that MDMA causes subacute enhancement of the outer retinal responses (most prominent in the a-wave), though ERG alterations resume within one week. These changes in photoreceptor/bipolar cell physiology may have implications for the understanding of the subacute visual manifestations induced by MDMA in humans. CI - (c) 2011 Martins et al. FAU - Martins, Joao AU - Martins J AD - Centre of Ophthalmology and Vision Sciences, IBILI, Faculty of Medicine, University of Coimbra, Coimbra, Portugal. FAU - Castelo-Branco, Miguel AU - Castelo-Branco M FAU - Batista, Ana AU - Batista A FAU - Oliveiros, Barbara AU - Oliveiros B FAU - Santiago, Ana Raquel AU - Santiago AR FAU - Galvao, Joana AU - Galvao J FAU - Fernandes, Eduarda AU - Fernandes E FAU - Carvalho, Felix AU - Carvalho F FAU - Cavadas, Claudia AU - Cavadas C FAU - Ambrosio, Antonio F AU - Ambrosio AF LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20111227 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - KE1SEN21RM (N-Methyl-3,4-methylenedioxyamphetamine) SB - IM MH - Animals MH - Electroretinography MH - Kidney/*drug effects/physiology MH - Male MH - N-Methyl-3,4-methylenedioxyamphetamine/*pharmacology MH - Rats MH - Rats, Wistar PMC - PMC3246479 COIS- Competing Interests: The authors have declared that no competing interests exist. EDAT- 2012/01/05 06:00 MHDA- 2012/05/23 06:00 PMCR- 2011/12/27 CRDT- 2012/01/05 06:00 PHST- 2011/05/25 00:00 [received] PHST- 2011/11/30 00:00 [accepted] PHST- 2012/01/05 06:00 [entrez] PHST- 2012/01/05 06:00 [pubmed] PHST- 2012/05/23 06:00 [medline] PHST- 2011/12/27 00:00 [pmc-release] AID - PONE-D-11-09482 [pii] AID - 10.1371/journal.pone.0029583 [doi] PST - ppublish SO - PLoS One. 2011;6(12):e29583. doi: 10.1371/journal.pone.0029583. Epub 2011 Dec 27.