| Title | Methamphetamine mimics the neurochemical profile of aging in rats and impairs recognition memory |
| Publication Type | Journal Article |
| 2012 |
| Authors | Melo, P, Magalhães, A, Alves, CJ, Tavares, MA, De Sousa, L, Summavielle, T, Moradas-Ferreira, P |
| Journal | NeuroToxicologyNeuroToxicology |
| Volume | 33 |
| Issue | 3 |
| Pagination | 491 - 499 |
| Date Published | 2012/// |
| 0161813X (ISSN) |
| Accelerated aging, Age Factors, aging, animal behavior, animal experiment, animal model, animal tissue, Animalia, Animals, anxiety, article, behavior change, Behavior, Animal, Brain, Brain Chemistry, controlled study, corpus striatum, dopamine, Exploratory Behavior, hippocampus, Hydroxyindoleacetic Acid, long term exposure, male, Memory Disorders, mental performance, Methamphetamine, Neurochemistry, neurotransmission, nonhuman, perinatal drug exposure, prefrontal cortex, priority journal, rat, Rats, Rats, Wistar, Rattus, recognition, Recognition (Psychology), Recognition memory, serotonin, sodium chloride, Time Factors |
| Brain neurochemistry and cognition performance are thought to decline with age. Accumulating data indicate that similar events occur after prolonged methamphetamine (MA) exposure. Using the rat as a model, the present study was designed to uncover common alteration patterns in brain neurochemistry and memory performance between aging and prolonged MA exposure. To this end, animals were treated with a chronic binge MA administration paradigm (20. mg/kg/day from postnatal day 91 to 100). Three-age control groups received isovolumetric saline treatment and were tested at the MA age-matched period, and at 12 and 20 months. We observed that both MA and aged animals presented a long, but not short, time impairment in novelty preference and an increased anxiety-like behavior. Neurochemical analysis indicated similar MA- and age-related impairments in dopamine, serotonin and metabolites in the striatum, prefrontal cortex and hippocampus. Thus, the present data illustrate that MA may be used to mimic age-related effects on neurotransmitter systems and advocate MA treatment as a feasible animal model to study neuronal processes associated with aging. © 2012 Elsevier Inc. |
| http://www.scopus.com/inward/record.url?eid=2-s2.0-84861188767&partnerID=40&md5=9c50ef658007fb37150c8b2d6d235d29 |
