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Biomedical subjects

F H Güldner

Publications and source records attributed to F H Güldner.

At least 37 records · Page 2Linked to original sources
PubMed1979

Plasticity in synaptic appositions of optic nerve afferents under different lighting conditions.

The influence of constant light and darkness (14 days) on the ultrastructure of synaptic appositions of optic nerve afferents has been studied in the suprachiasmatic nucleus (SCN) of hooded rats. Light exposure causes a general loss of postsynaptic density (PD) material, whereas after constant darkness the postsynaptic densities are thicker and the number of subjunctional bodies is higher. Accordingly, there are changes in the relative number of 'asymmetrical' (excitatory?) and 'symmetrical' (inhibitory?) synaptic appositions in optic and non-optic synapses. This phenomenon seems to reflect an adaptive response of the postsynaptic neurons to a long-term change of input activity.

Afferent Pathways↗
PubMed1978

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.

Animals↗
PubMed1978

Synapses of optic nerve afferents in the rat suprachiasmatic nucleus. II. Structural variability as revealed by morphometric examination.

The identification of optic synapses in the rat suprachiasmatic nucleus (Güldner, 1978) has made it possible to study them morphometrically. The measurements followed the check-list introduced by Palay and Chan-Palay (1976). There are several items which could usefully be added to this list. The structure of essential synaptic components varies considerably in what is apparently one synaptic population based on morphological criteria. The possible reasons for the variable sizes of the optic boutons containing different amounts of clear and dense core vesicles are discussed in terms of different activities or metabolic states of the individual boutons and/or different metabolic states of neuronal and glial elements in their vicinity. The active zones of optic synapses are also extremely variable. One optic bouton can form several active zones of very different sizes, or form Gray-type-I ("asymmetric"), Gray-type-II ("symmetric") and intermediate contacts at the same time. The function and/or functional efficiency of a single optic bouton therefore could then be quite different with respect to its various postsynaptic elements. The different appearance of the active zones is discussed mainly in terms of possible regulative influences from neighboring synapses via the postsynaptic neuron.

Animals↗
PubMed1978

Self-innervation of dendrites in the rat suprachiasmatic nucleus.

Golgi-Cox impregnantions of the rat suprachiasmatic nucleus show small dendritic side branches which appear to contact their neurons of origin. Electronmicroscopically a dendrite has been found forming a Gray-type-II synapse with one of its own branches. The arrangement is discussed as a general phenomenon of a feedback connection for temporal limitation of local excitation.

Animals↗
PubMed1978

Retinal afferents form Gray-type-I and type-II synapses in the suprachiasmatic nucleus (rat).

The synapses of optic nerve afferents in the suprachiasmatic nucleus (SCN) usually form Gray type I (asymmetrical) synapses, but about 13% show clear-cut Gray type II ( symmetrical) active zones. Some presynaptic elements form a Gray type I--active zone with one dendrite and a Gray type II-active zone with another postsynaptic element at the same time. It is discussed whether this variabilility is related to a simultaneous excitatory and inhibitory action, to a variable activity or efficiency of the synapses or to various stages of maturation.

Animals↗
PubMed1976

Synaptology of the rat suprachiasmatic nucleus.

Within the suprachiasmatic nucleus (SCN) of the rat the fine structure of the synapses and some features of their topological arrangement were studied. Five types of synapses could be distinguished with certainty: A. Two types of Gray-type-I (GTI) or asymmetrical synapses (approximately 33%). The presynaptic elements contain strikingly different types of mitochondria. Size of clear vesicles: approximately 450 A. Synapses with subjunctional bodies often occur, among these also "crest synapses". Localization: dendritic shafts and spines, rarely somata. B. Three types of Gray-type-2 (GTII) or symmetrical synapses (approximately 66%):1) Axo-dendritic and -somatic (=AD) synapses. Size of clear vesicles: approximately 500 A. 2) Invaginated axo-dendritic and -somatic (=IAD) synapses with club-like postsynaptic protrusions within the presynaptic elements (PreE1). Size of clear vesicles is very variable: approximately 400-1,000 A. 3) Dendro-dendritic, -somatic and somato-dendritic (=DD) synapses occurring at least partly in reciprocal arrangements. They represent an intrinsic system. Shape of clear vesicles: often oval; sucrose treatment partly produces flattening. Dense core-vesicles (dcv) are found in all GTII- and most of the GTI-synapses after three-dimensional reconstruction. All types of synapses (mostly GTII-synapses) can be enclosed by multilamellar astroglial formations. The synapses often occur in complex synaptic arrangements. Dendrites and somata of females show significantly more multivesiculated bodies than those of males. Further pecularities of presynaptic (PreELs) and postsynaptic elements (PostELs) within the SCN are described and discussed.

Animals↗