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Modifications of inhibitory transmission onto pyramidal neurons by postnatal exposure to MK‐801: Effects of enriched environment
Author(s) -
Shojaei Amir,
Anaraki Afsaneh Kamali,
MirnajafiZadeh Javad,
Atapour Nafiseh
Publication year - 2017
Publication title -
international journal of developmental neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.761
H-Index - 88
eISSN - 1873-474X
pISSN - 0736-5748
DOI - 10.1016/j.ijdevneu.2017.01.006
Subject(s) - inhibitory postsynaptic potential , neurotransmission , gabaergic , prefrontal cortex , pyramidal cell , neuroscience , nmda receptor , antagonist , gabaa receptor , glutamate receptor , chemistry , medicine , biology , endocrinology , receptor , hippocampus , cognition , biochemistry
Early enriched environment (EE) prevents several deficits associated with postnatal MK‐801 [ N ‐Methyl‐ d ‐Aspartate (NMDA) receptor antagonist] treatment such as cognitive and locomotor deficits. We sought physiological correlates to such changes by looking at inhibitory synaptic inputs onto pyramidal cells in a prefrontal cortex slice preparation. Pharmacologically isolated γ‐amino‐butyric acid A (GABA A ) receptor‐mediated currents were measured using whole‐cell patch clamp recordings. Wistar rats were raised in standard or EE from birth up to the time of experiments and were injected with saline or MK‐801 (1 mg/ kg) on postnatal days (P) 6–10. We recorded miniature inhibitory post‐synaptic currents (mIPSCs) of pyramidal cells in layer II/III of prefrontal cortex and measured their frequency, amplitude and kinetics. In control animals, the amplitude and frequency of mIPSCs increased strikingly during development from P21 to P28. MK‐801 accelerated the development of mIPSCs frequency but caused a significant decrease in the amplitude of mIPSCs on P28 suggesting a significant reduction of inhibition onto pyramidal cells. EE per se led to a significant increase in both frequency and amplitude of mIPSCs, but its application to MK‐801‐treated rats resulted in moderate rescue of GABAergic transmission on P28. We conclude that postnatal MK‐801 leads to reduced inhibitory transmission onto pyramidal cells of prefrontal cortex at adolescence which may underlie behavioural and morphological differences detected in vivo in rats. EE presentation from birth rather prevents GABAergic alterations associated with postnatal MK‐801 treatment at adolescence.