During development, neuronal connectivity has a remarkable plasticity. Synaptic refinement in the spinal autonomic nucleus might be involved in the elimination of primitive segmental reflexes and the emergence of mature spinobulbospinal reflexes, which occurs a few weeks after birth. To address this possibility, we examined the postnatal changes of segmental excitatory synaptic transmission by applying the whole-cell recording technique to parasympathetic preganglionic neurons in slice preparations of the rat lumbosacral spinal cord. The mean magnitude of unitary excitatory synaptic currents evoked in preganglionic neurons by stimulation of single interneurons remained unchanged during the first two postnatal weeks but was reduced by 50% during the third postnatal week. This reduction in synaptic efficacy was associated with a decrease in the amount of transmitter release from interneurons. Moreover, this developmental depression of segmental synaptic transmission was prevented by spinal cord transection at the thoracic level on postnatal day 14. Thus, developmental modification of excitatory synapses on preganglionic neurons appears to be attributable to competition between segmental interneuronal and descending bulbospinal inputs, which results in the developmental reorganization of parasympathetic excretory reflex pathways.
Key words: synaptic plasticity; developmental synaptic depression; glutamatergic excitatory synaptic currents; spinal autonomic nucleus; parasympathetic preganglionic neurons; micturition reflex; chronic spinal transection; quantal analysisDuring early postnatal life, synaptic refinements are well known to occur in the central (Hubel and Wiesel, 1965;Mendell, 1984;Fregnac et al., 1988;Reiter and Stryker, 1988;Constantine-Paton et al., 1990) and peripheral (Redfern, 1970;Ridge and Betz, 1984;Dan and Poo, 1992;Balice-Gorden and Lichtman, 1994;Colman et al., 1997) nervous systems. This synaptic remodeling serves to refine initial coarse-grained and exuberant neuronal connections and results in formation of highly tuned neural circuits (Purves and Lichtman, 1985;Goodman and Shatz, 1993). In spinal autonomic reflex pathways, synaptic refinement could be involved in the elimination of primitive segmental reflexes and the emergence of mature reflex patterns. In neonates of many species, excretory f unctions (micturition and defecation) are mediated exclusively by the segmental parasympathetic reflex pathway, which is activated when the mother licks the perineum of the neonate (Beach, 1966;de Groat et al., 1975;Thor et al., 1989). A few weeks after birth, this segmental reflex begins to disappear and is replaced by the newly developed spinobulbospinal reflex as the principal mechanism for excretion (de Groat, 1975;Fukuda et al., 1981;Kruse and de Groat, 1990;de Groat et al., 1993). This is also a critical period for the establishment of synaptic refinements (Purves and Lichtman, 1985) as well as for the functional maturation of descending pathways to the spinal cord (Gilbert and Stelzner, 1979;Men...