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Neonatal administration with dexmedetomidine does not impair the rat hippocampal synaptic plasticity later in adulthood
Author(s) -
Tachibana Kaori,
Hashimoto Toshikazu,
Kato Rui,
Uchida Yosuke,
Ito Ryoko,
Takita Koichi,
Morimoto Yuji
Publication year - 2012
Publication title -
pediatric anesthesia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.704
H-Index - 82
eISSN - 1460-9592
pISSN - 1155-5645
DOI - 10.1111/j.1460-9592.2012.03810.x
Subject(s) - medicine , hippocampal formation , long term potentiation , dexmedetomidine , hippocampus , anesthesia , population , sedative , population spike , synaptic plasticity , neuroscience , sedation , dentate gyrus , receptor , biology , environmental health
Summary Background and objective: The use of dexmedetomidine (DEX), a selective alpha‐2 agonist, in pediatric practice is expanding as a result of its desirable properties. To clarify the long‐term neurological consequences of neonatal administration of DEX, we investigated the long‐term effects of neonatal administration of DEX on hippocampal synaptic activity. Methods: The rat pups received a bolus intraperitoneal injection of either 5 or 10 μg·kg −1 DEX, or an equivalent volume of vehicle on postnatal day 7 (P7). Nine weeks after administration, evoked potentials (population spike, PS) and long‐term potentiation (LTP) in the hippocampal CA1 region of rats were studied in vivo. Results: Dexmedetomidine had a considerable sedative effect at these doses with little respiratory depression on P7. Nine weeks after administration of DEX, the amplitude of PS in the two treated groups was similar to that in the control group. DEX‐treated rats showed no impairment in the induction of LTP. Furthermore, the response in PS to the paired stimuli was not impaired by neonatal administration of DEX. Conclusion: These findings demonstrate that a single administration of DEX to rats on P7 preserves hippocampal synaptic plasticity as well as synaptic transmission later in life. In view of the some evidence that have demonstrated the permanent detrimental impact of commonly used anesthetics on neurological outcomes after neonatal exposure, our findings may suggest the relative safety of DEX administered as a sedative agent to neonatal animals with regard to the development of hippocampal synaptic functions.