Influence of the paraventricular nucleus and oxytocin on the retrograde stain of pubococcygeus muscle motoneurons in male rats.

Lumbosacral cord motoneurons innervating the pubococcygeus muscle (Pcm) at the pelvic floor of male rats were analyzed. We showed previously that these motoneurons participate in sexual functions and are sensitive to fluctuations of systemic androgen and estrogen. Though estrogen receptors have not been identified in Lamina IX at these spinal areas, the release of oxytocin from the paraventricular nucleus of the hypothalamus (PvN) has been found to control pelvic sexual physiology. We therefore worked on the hypothesis that steroid hormones in the PvN induce the release of oxytocin at the lumbosacral level to modulate the function of Pcm motoneurons. Four experiments were developed, and results were observed with the retrograde staining of motoneurons with horseradish peroxidase. Data indicated that morphometric parameters of Pcm motoneurons were significantly reduced after castration or blocking of the steroids at the PvN site, or following complete transection of the spinal cord at the T8 level. In each case, the reduction of the stain was recovered after intrathecal treatment with oxytocin. Thus, present results show that Pcm motoneurons respond to spinal oxytocin. The conclusive model that we propose is that steroids stimulate the PvN, causing the nucleus to release oxytocin at the level of the lumbosacral spinal cord, and the release of the peptide regulates the spread of the stain of Pcm motoneurons. This work also shows that motoneurons distal to a transected area in the spinal cord could respond to exogenous oxytocin, an important finding for the research of spinal cord lesioned subjects.

Synaptic plasticity in the oedematous human cerebral cortex.

Synaptic plastic changes are fundamental events which occur spontaneously during development, maturity and aging processes or can be induced by injury or trauma. To examine lesion-induced synaptic plasticity, cortical biopsies were taken from the frontal, parietal, temporal and occipital cortex of living patients during neurosurgical treatment of brain trauma, brain tumours and vascular malformations, and processed for transmission electron microscopy. Enlargement of both pre- and postsynaptic endings, irregularly shaped, lobulated, stellate and bifurcated presynaptic endings and conformational changes of dendritic spines were observed. Numerous flat, curved and invaginated axodendritic and axospinous asymmetric synapses were distinguished and a smaller proportion of axodendritic and axosomatic symmetric synapses. Activated or sensitized synapses showed numerous frontline spheroid synaptic vesicles, prominent dense presynaptic dense projections and increased length of synaptic membrane complex. Perforated synapses, multiple synapses and serial synapses were also found evincing synaptic splitting and formation of new synaptic connections. The overall images suggest increased number of excitatory circuits, which were correlated with the tonico-clonic convulsion or post-traumatic seizures observed in some patients. Numerous coated vesicles were observed in pre- and postsynaptic structures. Increased number of polyribosomes were found in the dendritic shafts. The dilated spine apparatus, the coated vesicles and the increased number of polyribosomes seem to represent a system for synthesis, transport and storage of synaptic proteins for the formation of new synapses. Coexisting synaptic plasticity and synaptic degeneration were observed in the patients under study. Dendritic and astrocyte synapse-like junctions were also characterized.

Time course of the effects of prenatal gamma irradiation on the dorsal lateral geniculate nucleus of Swiss mice.

A previous study reported that adult mice irradiated at the 16th embryonic day present a severe neuronal number reduction in the dorsal lateral geniculate thalamic nucleus. In the present study, we investigated the time course of the effects of prenatal irradiation on this thalamic nucleus. One day after irradiation, a great number of pyknotic figures were seen mainly in the cerebral proliferative zones. In the geniculate nucleus, only scattered pyknotic figures were identified. On the first week after birth, the geniculate nucleus presented frequent pyknotic figures. From five days after birth onwards, a severe shrinkage of the occipital cortex and a great reduction in the geniculate nucleus neuronal number were found. On the second week after birth this neuronal number reduction reached as high as 75%. At each postnatal analyzed age, severe volumetric geniculate nucleus shrinkage was combined to non-significant neuronal density variations. The presence of few pyknotic figures in the geniculate nucleus one day after irradiation and its delayed neuronal loss indicate an indirect effect of irradiation. We suggest that the effect upon the geniculate nucleus is secondary to the damage of the occipital cortex. A possible interpretation for thalamic neuronal loss is that geniculate neurons fail to establish cortical arbors after major target loss. In this case, the loss of trophic support should also be considered.

Expression of neuronal isoform of nitric oxide synthase in spinal neurons of neonatal rats after sciatic nerve transection.

Motoneuron death induced by sciatic nerve transection in neonatal rats has been related to induction of the neuronal isoform of nitric oxide synthase (nNOS), a diaphorase of which one of the cofactors is nicotinamide adenine dinucleotide phosphate (NADPH). We transected the sciatic nerve of neonatal rats (P2) and examined nNOS expression by immunostaining in neurons of the sciatic pool and of other spinal levels on the 5th day after surgery. No correspondence was observed between the surviving motoneurons and nNOS positive cells. The appearance and distribution of nNOS positive neurons at all spinal levels and laminae were similar to those of adult animals. These results are at variance with previous studies which showed correlation between motoneuron loss after axotomy and number of NADPH-diaphorase positive motoneurons after sciatic transection.