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[Morphometric investigation on the changes of the paramembranous structures of the CA 1 hippocampal synapses of trained rats, with special reference to the morphological plasticity of the synapses].

Albino rats aged 13 weeks experienced a single training for bright-dark discrimination in a Y-chamber. 24 hours later after a successful training the paramembranaceous structures of the synapses contrasted by phosphotungstic acid were morphometrically analysed. As a result of this investigation a signifikant reduction of the height and the width of the dense projections was to be stated compared to untrained rats. Likewise the length and the width of the postsynaptic ribbon were reduced in trained rats. But this alteration proved not to be significant.

Animals↗

Synapse disassembly and formation of new synapses in postnatal muscle upon conditional inactivation of MuSK.

The muscle-specific-kinase MuSK is required for the formation of acetylcholine receptor clusters during embryonic development, but its physiological role in adult muscle is not known. We used the loxP/Cre system in mice to conditionally inactivate MuSK whereby expression of Cre recombinase increases during postnatal development. The MuSK-inactivated mice develop myasthenic symptoms and die prematurely due to severe muscle weakness. The postnatal inactivation of MuSK causes loss of acetylcholine receptors and disassembly of the postsynaptic organization and innervating axons retract but start to grow and branch extensively. Due to the mosaic expression of Cre recombinase, MuSK is not globally inactivated and new synapses are formed aberrantly patterned across the diaphragm. Our findings demonstrate that MuSK kinase activity is required throughout postnatal development to hold up MuSK and AChR levels at endplates. Thus, MuSK and AChR together maintain the functional and structural integrity of the postsynaptic architecture and prevent axon growth.

Acetylcholine↗

The human posterior tibial somatosensory evoked potential: synapse dependent and synapse independent spinal components.

Evidence has been obtained for the existence of two separate events occurring in the human spinal cord following posterior tibial nerve (PTN) stimulation. These events can be recorded on the surface in unanesthetized individuals. The first is an ascending wave which is conducted up to the cord at constant velocity and has a relatively short refractory period consistent with a compound nerve action potential. This represents the afferent volley traversing the lumbosacral plexus and the ascending dorsal columns. A second event, the N22/P22 complex, is surface negative on the back and surface positive anteriorly; its amplitude is maximal 5-15 cm above the level of the L4 spine and its peak latency remains constant at all levels. This activity has a relatively long refractory period. These characteristics of N22/P22 indicate that it is a localized synaptically dependent event conforming to a transverse dipole with dorsal negativity and a simultaneous anterior positivity. The N22/P22 is probably generated in the dorsal grey at the root entry zone. The N22/P22 is analogous to the stationary N13/P13 recorded over the neck following median nerve stimulation.

Adult↗

Control of number and distribution of synapses during ectopic synapse formation in adult rat soleus muscles.

Changes in the number and distribution of synaptic inputs and acetylcholine receptor clusters were studied during the formation of ectopic nerve-muscle junctions between the transplanted fibular nerve and the denervated soleus muscle of adult rats. The tibial nerve was cut 3 weeks after implanting the fibular nerve. New sites of transmission were first detected 3 days after the cut. These sites were located electrophysiologically, marked by dye and found to coincide with clusters of acetylcholine receptors. There were no ectopic clusters away from fibular nerve sprouts and no clusters on muscles which had not been denervated. Three days after cutting the tibial nerve, the acetylcholine receptor clusters, and probably also the sites of transmission, were randomly distributed along individual muscle fibres. Six days after the cut, the clusters continued to be randomly distributed whereas the synaptic inputs were either close together (within 300 microns) or more than 600 microns apart. Two weeks later the spatial distributions of both clusters and inputs were similar with peaks around 100-300 microns, 1200-1400 microns and 2000-2600 microns. No ectopic clusters were closer than 0.5 mm to the original endplate. We conclude that nerve-muscle contacts and associated acetylcholine receptor clusters initially form at random. One or a few of these contacts develop further and, as a result, the surrounding regions undergo changes that prevent the contacts initially formed there from being maintained. Apparently, in this preparation, approximately 1.5 mm length of fibre is needed to support the maturation and maintenance of each ectopic endplate (mean length 111 micron).

Animals↗

Synaptic membrane morphology in the rat cerebral cortex during development: image analysis of freeze-etching replicas of isolated synapses and synapses in situ.

Both synaptic sites in situ from rat cerebral cortex and isolated ones in synaptosomal and growth cone fractions derived from it were studied during postnatal development. Freeze-etching technique and image analysis were used to determine the size of the intramembranous particles in the pre- and postsynaptic sites. At each age investigated, the greatest mean particle size was established on the E-face of the postsynaptic sites and ranges from 6.2 nm (day 0) to nearly 10 nm (day 90). The continuous mean particle size increase from birth to maturity shows the same rate but a different rhythm for the two synaptic sites. The results indicate that fractionation do not disturb the correlation between the particle size and age thus outlining the stability of the developing synaptic membrane morphology to physical treatments.

Animals↗