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European Journal of Pharmacology
Volume 509, Issues 2-3, 21 February 2005, Pages 155-159
 
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doi:10.1016/j.ejphar.2005.01.001    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2005 Elsevier B.V. All rights reserved.

Short communication

Maternal caffeine intake impairs MK-801-induced hyperlocomotion in young rats

Rosane Souza da Silvaa, b, Corresponding Author Contact Information, E-mail The Corresponding Author, Anselmo Hoffmanc, Diogo Onofre de Souzac, Diogo R. Larac and Carla Denise Bonana

aLaboratório de Pesquisa Bioquímica, Departamento de Ciências Fisiológicas, Faculdade de Biociências, Pontifícia Universidade Católica do Rio Grande do Sul, Avenida Ipiranga, 6681, 90619-900, Porto Alegre, RS, Brazil bLaboratório de Enzimologia, Departamento de Bioquímica, Universidade Federal do Rio Grande do Sul, Avenida Ramiro Barcelos, 2600-Anexo, Porto Alegre, RS, Brazil cLaboratório de Neurobiologia Experimental, Departamento de Bioquímica, Universidade Federal do Rio Grande do Sul, Avenida Ramiro Barcelos, 2600-Anexo, Porto Alegre, RS, Brazil

Received 22 September 2004; 
revised 5 January 2005; 
accepted 7 January 2005. 
Available online 5 February 2005.

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Abstract

Here we have investigated the effects of maternal caffeine intake (1 g/l) on MK-801-induced hyperlocomotion in rat pups. Animals submitted to caffeine treatment during the gestational and lactational period were separated in two groups: caffeine-treated group (up to 21 days old) and washout group (caffeine treatment up to 7 days old). MK-801 (0.25 mg/kg, i.p.) promoted hyperlocomotion in control rats, but this stimulatory effect was significantly decreased in caffeine-treated and washout groups. The permanent effect after caffeine withdrawal suggests durable or adaptive changes during neurodevelopment, mainly on adenosine receptors or neurotransmitter systems modulated by adenosine, such as the glutamatergic system.

Keywords: Adenosine; Caffeine; Neurodevelopment; Maternal intake; Glutamate; Locomotor activity

Article Outline

1. Introduction
2. Material and methods
2.1. Caffeine treatment
2.2. Locomotor activity assessment
2.3. Statistical analysis
3. Results
4. Discussion
Acknowledgements
References


 
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