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Sara Garcia-Ratés

3 papers in the library · 4 citations · publishing 2007-2014

Papers

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Molecular basis of the selective binding of MDMA enantiomers to the alpha4beta2 nicotinic receptor subtype: synthesis, pharmacological evaluation and mechanistic studies.

European journal of medicinal chemistry June 23, 2014 Salomé Llabrés, Sara Garcia-Ratés, Edgar Cristóbal-Lecina et al.

The α4β2 nicotinic acetylcholine receptor (nAChR) is a molecular target of 3,4-methylenedioxymethamphetamine (MDMA), a synthetic drug also known as ecstasy, and it modulates the MDMA-mediated reinforcing properties. However, the enantioselective preference of the α4β2 nAChR subtype still remains unknown. Since the two enantiomers exhibit different pharmacological profiles and stereoselective...

DOI: 10.1016/j.ejmech.2014.04.044 (opens in new tab) Full text (opens in new tab) MDMA Alpha4beta2 nicotinic receptor Enantioselective binding Molecular modelling +2

Neuronal Nicotinic Receptors as New Targets for Amphetamine-Induced Oxidative Damage and Neurotoxicity

Pharmaceuticals June 15, 2011 Elena Escubedo, Sara Garcia-Ratés, Jordi Camarasa et al. 4 citations

Amphetamine derivatives such as methamphetamine (METH) and 3,4-methylenedioxymethamphetamine (MDMA, “ecstasy”) are widely abused drugs in a recreational context. This has led to concern because of the evidence that they are neurotoxic in animal models and cognitive impairments have been described in heavy abusers. The main targets of these drugs are plasmalemmal and vesicular monoamine...

DOI: 10.3390/ph4060822 (opens in new tab) Full text (opens in new tab) MDMA Methamphetamine Nicotinic Neuroprotection +1

Methamphetamine and 3,4-methylenedioxymethamphetamine interact with central nicotinic receptors and induce their up-regulation.

Toxicology and Applied Pharmacology September 15, 2007 Sara Garcia-Ratés, Jordi Camarasa, Elena Escubedo et al.

Previous work from our group indicated that alpha7 nicotinic acetylcholine receptors (alpha7 nAChR) potentially play a role in methamphetamine (METH) and 3,4-methylenedioxymethamphetamine (MDMA) neurotoxicity. The aims of the present study were two-fold: (1) to demonstrate the interaction of METH and MDMA with homomeric alpha7 nAChR ([(3)H]methyllycaconitine binding) and other heteromeric...