In situ metabolomic changes in rat hippocampus after acute cocaine administration

• Published in: International journal of mass spectrometry 2019-03, Vol.437, p.87-91
• Main Authors: Joye, Timothée, Bararpour, Nasim, Augsburger, Marc, Boutrel, Benjamin, Thomas, Aurélien
• Format: Article
• Language: English
• Subjects: Cocaine; Hippocampus; Imaging mass spectrometry; Metabolomics; Toxicodynamics
• ISSN: 1387-3806; 1873-2798
• DOI: 10.1016/j.ijms.2017.12.001

[Display omitted] •MSI is a promising approach for toxicodynamic studies in rodent brain models.•In situ metabolomics reveal metabolite changes in hippocampus after acute cocaine administration.•MSI may increase our understanding of molecular mechanisms associated to reward-related processes. Addiction is a complex brain disease, whose molecular and cellular underpinnings remain largely unknown. Repeated drug use induces long-term plasticity in various brain areas that is considered to potentially trigger further compulsive use. Converging evidence has revealed that memory and addiction share both neural circuitry and molecular mechanisms. While many studies investigated the mesocorticolimbic system, the hippocampus has become a region of interest. Matrix assisted laser desorption and ionization mass spectrometry imaging (MALDI-MSI) presents a unique ability to map the toxicodynamic changes associated to drugs of abuse. In this study, the acute effect of cocaine in rat brain was investigated with or without co-administration of alcohol. Brain tissue sections for each condition were analyzed using a MALDI-MSI in negative polarity after 9-aminoacridine (9-AA) deposition on the tissue surface. Multivariate analysis including principal component analysis (PCA) and spatial shrunken centroids have been performed to differentiate the metabolic profiles in hippocampus according to the type of administration. This study offers promising results showing the potential of MSI for investigating the metabolomic changes in the brain associated with drug consumption. It may bring new insights into the study of toxicodynamic responses of cocaine consumption in reward-learning related regions.