Details

Autor(en) / Beteiligte

• Ardais, Ana Paula
• Rocha, Andréia S.
• Borges, Maurício Felisberto
• Fioreze, Gabriela T.
• Sallaberry, Cássia
• Mioranzza, Sabrina
• Nunes, Fernanda
• Pagnussat, Natália
• Botton, Paulo Henrique S.
• Cunha, Rodrigo A.
• Porciúncula, Lisiane de Oliveira

Titel

Caffeine exposure during rat brain development causes memory impairment in a sex selective manner that is offset by caffeine consumption throughout life

Ist Teil von

• Behavioural brain research, 2016-04, Vol.303, p.76-84

Ort / Verlag

Netherlands: Elsevier B.V

Erscheinungsjahr

2016

Quelle

MEDLINE

Beschreibungen/Notizen

• •Behavior and synaptic proteins were modified by caffeine throughout life and during development.•Adult female rats receiving caffeine during development displayed impaired recognition memory.•Caffeine at highest dose throughout life attenuates anxiety-related behavior in both sexes.•Caffeine treatments modified locomotion in a different manner according to sexes.•Caffeine treatments change BDNF and related proteins in the hippocampus from both sexes. Caffeine is the psychostimulant most consumed worldwide. In moderate doses, it affords a beneficial effect in adults and upon aging, but has a deleterious effect during brain development. We now tested if caffeine consumption by rats (0.1, 0.3, 1.0g/L in the drinking water, only during active cycle and weekdays) during adulthood could revert the potentially negative effects of caffeine during early life. Thus, we compared caffeine intake starting 15 days before mating and lasting either up to weaning (development) or up to adulthood, on behavior and synaptic proteins in male and female rats. Recognition memory was impaired only in female rats receiving caffeine (0.3 and 1.0g/L) during development, coincident with increased proBDNF and unchanged BDNF levels in the hippocampus. Caffeine in both treatment regimens caused hyperlocomotion only in male rats, whereas anxiety-related behavior was attenuated in both sexes by caffeine (1.0g/L) throughout life. Both caffeine treatment regimens decreased GFAP (as an astrocyte marker) and SNAP-25 (as a nerve terminals marker) in the hippocampus from male rats. TrkB receptor was decreased in the hippocampus from both sexes and treatment regimens. These findings revealed that caffeine intake during a specific time window of brain development promotes sex-dependent behavioral outcomes related to modification in BDNF signaling. Furthermore, caffeine throughout life can overcome the deleterious effects of caffeine on recognition memory during brain development in female rats.