Complex neuronal circuitries such as those present in the mammalian
cerebral cortex have evolved as balanced networks of excitatory and inhibitory
neurons. Although the establishment of appropriate numbers for these cells is
essential for brain function and behaviour, our understanding of this
fundamental process is very fragmentary. Here we show that interneuron cell
survival in mice depends on the activity of pyramidal cells during a critical
window of postnatal development, in which excitatory synaptic input to
individual interneurons predicts their outcome. Pyramidal cells regulate
interneuron survival through the negative modulation of PTEN signalling, which
effectively drives interneuron cell death during this period. Taken together,
our findings indicate that activity-dependent mechanisms dynamically adjust the
number of inhibitory cells in nascent local cortical circuits, ultimately
establishing the appropriate proportions of excitatory and inhibitory neurons in
the cerebral cortex.
Psychophysiological studies of infants have found a relation between behavioral reactivity and indices of autonomic state. The relation between behavioral reactivity, assessed via maternal report, and autonomic state, assessed via cardiac vagal tone in 9-month-old infants was examined. Cardiac vagal tone was quantified by measuring the amplitude of respiratory sinus arrhythmia. High cardiac vagal tone was associated with greater behavioral reactivity, resulting in maternal reports of more difficult temperament. Stability of the two measures, cardiac vagal tone and difficult temperament, from 9 months to 3 years of age was demonstrated. In addition, 9-month cardiac vagal tone, independent of 9-month temperament, was related to 3-year difficultness with higher 9-month cardiac vagal tone being related to less-difficult 3-year behavior.
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