Optic Synapses Research Articles

Structural plasticity of optic synapses in the rat suprachiasmatic nucleus: adaptation to long-term influence of light and darkness.

Synapses of optic afferents (optic synapses) in the suprachiasmatic nucleus of hooded rats were morphometrically evaluated after exposing the animals to 12 h, 14 days, 2 months, and 8 months of constant light (light rats) and darkness (dark rats). Compared with dark rats, optic synapses from light rats have larger boutons with larger mitochondria, more clear vesicles, fewer dense-core vesicles and front-line vesicles, smaller presynaptic dense projections, a smaller amount of postsynaptic density material, a smaller relative number of Gray-type I (asymmetric) junctions, a greater relative number of Gray-type II (symmetric) junctions, as well as more and larger mitochondria in the postsynaptic dendrites. Junctions of optic synapses are mostly straight, but the small number of positively curved contacts are more flattened in light rats than in dark rats. An age-related increase in the size of presynaptic dense projections was also observed. There are no changes in the sizes of clear and dense-core vesicles, in the size of synaptic junctions and their numerical density in area, and in the unspecific contact area between pre- and postsynaptic elements. The changes in optic boutons are characteristic for activated and relatively disused synapses with a slow, tonic firing rate. It appears that (1) the amount of postsynaptic density material is proportional to the strength of Gray-type I synapses, and that (2) some excitatory optic synapses become inhibitory after long-term activity, whereas some inhibitory synapses turn into excitatory contacts after long-term disuse.

Structural differences between optic synapses in the suprachiasmatic nucleus of hooded and albino rats

Synapses of retinal afferents (optic synapses) in the suprachiasmatic nucleus (SCN) were morphometrically compared between hooded and albino rats. Optic synapses from albino rats show larger boutons with larger mitochondria, synaptic appositions with less postsynaptic density material, relatively more symmetric (presumably inhibitory) contacts, and relatively less asymmetric (presumably excitatory) contacts, compared with hooded rats. There are no differences in the numbers of clear and dense core vesicles, the size of synaptic appositions, and their numerical density in area of micrograph. Possible differences in activity and/or metabolism between optic synapses from hooded and albino rats are discussed.

Optic synapses are found in diencephalic neuropils before development of the tectum in Xenopus.

The position of the earliest optic synapses in Xenopus and the stage at which they developed were studied with the electron microscope after labelling of optic axons with horseradish peroxidase. In addition, tritiated thymidine autoradiography and bromodeoxyuridine immunohistology were used to identify the birth dates of cells in the regions where the synapses had been found. The earliest mature optic synapses were found in the mid-diencephalic region, where the major diencephalic optic neuropils were beginning to develop. These synapses were seen at stage 35/36, before cells in the tectal precursor region had become postmitotic. In other animals labelling with tritiated thymidine or bromodeoxyuridine showed that cells in the diencephalon, close to where the synapses had been seen, were becoming postmitotic at the time the earliest optic axons arrived. The first optic synapses to form in the developing Xenopus visual system thus appeared to do so in the neuropil of Bellonci and the rostral visual nucleus.

Retinotopically inappropriate synapses of subnormal density formed by surgically misdirected optic fibers in goldfish tectum

Selected optic fibers were surgically deflected from one tectum onto the opposite host tectum which was denervated by eye enucleation. At 6–8 months, deflected fibers were labeled with horseradish peroxidase and the retinotopically inappropriate part of tectum was examined using electron microscopy. Numerous (labeled) optic synapses were found in the primary optic innervation layer of the ‘wrong’ part of tectum but they were about half the normal density. The number and density of non-optic synapses was not found to be affected. These findins indicate optic fibers compete with each other but not with non-optic fibers for synaptic sites in tectum.

Synapses of optic nerve afferents in the rat suprachiasmatic nucleus. I. Identification, qualitative description, development and distribution.

Synapses of optic nerve afferents (optic synapses) in the rat suprachiasmatic nucleus (SCN) have been identified ultrastructurally. They are easily distinguished from other types of synapses. The optic boutons are characterized by the presence of large mitochondria with a swollen electron lucent matrix and an interconnected tubular system formed by their inner membrane. Other, more variable features include: 1) a scattered pattern of synaptic vesicles which are found throughout the entire presynaptic element with relatively little accumulation near the active zones; 2) the occurrence of dense core vesicles and glycogen granules; 3) the active zones, the majority of which is Gray-type I, but a minority can obviously be classified as Gray's type II; 4) the innervation of smaller peripheral dendrites and dendritic spines. Boutons of this kind are exclusively filled with anterogradely transported horseradish peroxidase injected into both eyes. Very few neuronal elements containing the typical mitochondria have been observed in the SCN on the 6th day post partum, increasingly more on the 9th and 12th day, but considerably higher numbers after opening of the eyes on the 17th and the following days. The location of normal and degenerating optic boutons was examined light- and electron microscopically. In the rostral third of the SCN there are relatively few optic synapses which are found close to the optic chiasma. In the middle portion of the SCN optic synapses increase in number; they are found not only in the ventral part of the nucleus but also in lateral regions. This becomes particularly obvious in the caudal third of the SCN.