Effects of inhibiting neonatal methamphetamine‐induced corticosterone release in rats by adrenal autotransplantation on later learning, memory, and plasma corticosterone levels
Autor: | Devon L. Graham, Matthew R. Skelton, Michael T. Williams, Charles V. Vorhees, Curtis E. Grace, Tori L. Schaefer |
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Rok vydání: | 2010 |
Předmět: |
Male
medicine.medical_specialty medicine.medical_treatment Spatial Behavior Morris water navigation task Motor Activity Article Methamphetamine Rats Sprague-Dawley chemistry.chemical_compound Developmental Neuroscience Memory Corticosterone Internal medicine Adrenal Glands medicine Animals Maze Learning 5-HT receptor Analysis of Variance business.industry Adrenalectomy Brain Recognition Psychology Autotransplantation Rats Endocrinology Animals Newborn chemistry Exploratory Behavior Female Serotonin Analysis of variance business Developmental Biology medicine.drug |
Zdroj: | International Journal of Developmental Neuroscience. 28:331-342 |
ISSN: | 1873-474X 0736-5748 |
Popis: | Neonatal rat methamphetamine (MA) exposure has been shown to cause long-term behavioral impairments similar to some of those observed following neonatal stress. The mechanism by which MA induces impairments is unknown but may be related to early increases in corticosterone release. We previously developed a method to attenuate MA-induced corticosterone release using adrenal autotransplantation (ADXA) in neonatal rats. This exposure period corresponds to the second-half of human pregnancy.To determine whether inhibition of neonatal MA-induced increases in corticosterone attenuates the long-term behavioral deficits associated with early MA treatment.ADXA successfully attenuated MA-induced plasma corticosterone increases by approximately 50% during treatment (P11-20) but did not attenuate the long-term behavioral effects of MA treatment. MA-treated rats, regardless of surgery, showed increased errors and latencies in the Cincinnati water maze test of egocentric learning and increased latency, path length, and cumulative distance in three phases of Morris water maze spatial learning and reference memory. MA-treated offspring were hypoactive, had subtle reductions in anxiety in the elevated zero maze but not in the light-dark test. ADXA had no effect on MA-induced long-term 5-HT reductions in the neostriatum or entorhinal cortex or on 5-HIAA reductions in the hippocampus.Fifty percent attenuation of neonatal MA-induced elevations in corticosterone does not alter the long-term egocentric or allocentric learning deficits or other behavioral effects of neonatal MA exposure. Because the ADXA effect was partial, the data cannot rule out the possibility that a more complete block of MA-induced corticosterone release might not prevent later cognitive deficits. |
Databáze: | OpenAIRE |
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