Postnatal development of membrane properties of layer I neurons in rat neocortex.
نویسندگان
چکیده
Using whole-cell patch-clamp techniques in brain slices, we studied the postnatal development of electrophysiological properties of rat neocortical layer I neurons during the first three weeks of postnatal life. Neurons, including Cajal-Retzius cells, were visualized under Nomarski optics before recording. In the first postnatal week, all layer I neurons, including Cajal-Retzius cells, had low resting membrane potentials (-40 to -55 mV), high input resistances (1-5 G omega), and long membrane time constants (80-130 msec). Action potentials (APs) of layer I neurons early in postnatal development were lower in amplitude and longer in duration. The threshold for APs also was more depolarized than in older neurons. A medium after-hyperpolarization already was present at postnatal day 0 (PN0), but fast afterhyperpolarizations were not seen until PN10. At all postnatal ages, layer I neurons were capable of repetitive firing, displayed little or no frequency adaptation, and did not display slow afterhyperpolarizations. Early in development, layer I neurons had a prominent hyperpolarization-activation depolarizing sag that decreased with age. These results suggest that the membrane properties of rat neocortical layer I neurons mature rapidly during the first two postnatal weeks. Cajal-Retzius cells had electrical properties similar to other layer I neurons and did not show an earlier maturation of membrane properties.
منابع مشابه
Two populations of layer v pyramidal cells of the mouse neocortex: development and sensitivity to anesthetics.
Previous studies have shown that layer V pyramidal neurons projecting either to subcortical structures or the contralateral cortex undergo different morphological and electrophysiological patterns of development during the first three postnatal weeks. To isolate the determinants of this differential maturation, we analyzed the gene expression and intrinsic membrane properties of layer V pyramid...
متن کاملLayer Specific Development of Neocortical Pyramidal to Fast Spiking Cell Synapses
All cortical neurons are engaged in inhibitory feedback loops which ensure excitation-inhibition balance and are key elements for the development of coherent network activity. The resulting network patterns are strongly dependent on the strength and dynamic properties of these excitatory-inhibitory loops which show pronounced regional and developmental diversity. Therefore we compared the prope...
متن کاملSpecificity of Synaptic Connectivity between Layer 1 Inhibitory Interneurons and Layer 2/3 Pyramidal Neurons in the Rat Neocortex
Understanding the structure and function of the neocortical microcircuit requires a description of the synaptic connectivity between identified neuronal populations. Here, we investigate the electrophysiological properties of layer 1 (L1) neurons of the rat somatosensory neocortex (postnatal day 24-36) and their synaptic connectivity with supragranular pyramidal neurons. The active and passive ...
متن کاملLoss of IA expression and increased excitability in postnatal rat Cajal-Retzius cells.
Although an important secretory function of Cajal-Retzius (CR) cells has been discovered recently, the precise electrical status of these cells among other layer I neurons in particular and in cortical function in general is still unclear. In this paper, early postnatal CR cells from rat neocortex were found to express an inactivating K current whose molecular substrate is likely to be the Kv1....
متن کاملDifferential distribution of group I metabotropic glutamate receptors during rat cortical development.
Neurons in the rat cerebral cortex are enriched in group I metabotropic glutamate receptor (mGluR) subtypes and respond to their activation during development. To understand better the mechanisms by which mGluR1 and mGluR5 mediate these effects, the goal of this study was to elucidate the expression pattern and to determine the cellular and the precise subcellular localization of these two rece...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Journal of neuroscience : the official journal of the Society for Neuroscience
دوره 16 3 شماره
صفحات -
تاریخ انتشار 1996