Demonstration of a 2d LH-RH neurosecretory system in the duck hypothalamus]

Using immunocytochemical techniques with an anti-LH-RH immuneserum, evidence of two neuronal systems secreting LH-RH has been shown in the Duck hypothalamus. In addition to the previously described system, located in the preoptic nucleus, a second system could be demonstrated in the infundibular nucleus. The perikarya of the infundibular LH-RH producing neurons were significantly smaller than those of the preoptic neurons. On the other hand, under the experimental conditions used, the infundibular system had approximately five times less LH-RH secreting neurons than the preoptic system, and its perikarya appeared less heavily loaded in IR LH-RH. The LH-RH containing axons from both neuronal populations ran down to the external layer of the median eminence, where they ended in close contact with the capillaries of the hypophysial portal system.     

Presence of neurons synthesizing LH-RH in the anterior hypothalamus of the duck (Anas platyrhynchos)]

Using histochemical techniques with LH-RH anti-serum, a large number of LH-RH producing neurons were identified in the Duck hypothalamus, under different physiological conditions. The LH-RH pericaryas were localized in a well delimited area of the anterior hypothalamus, including the dorsal part of the periventricular preoptic nucleus. The LH-RH containing axons were directed downwards towards the infundibulum, and terminated within the external layer of the rostral and caudal median eminence, in close vicinity to the capillaries of the pituitary portal system.     

Immunohistochemical identification, in an anuran amphibian (Xenopus laevis Daud.) of infundibular neurons reacting with antigastrin serum]

Neurons containing peptides immunocytologically related to gastrin have been revealed by immuno-cytology in the post-chiasmatic hypothalamus of Xenopus laevis. Their pericarya are localized in the postero-dorsal zone of the pars ventralis of the tuber cinereum; their axons end on the capillaries of the external zone of the median eminence.     

Description of neurons immunoreactive to anti-beta-endorphin immune serum present in the infundibular nucleus in man]

Neurons containing peptide (s) immunologically related to beta-endorphin have been detected by immunochemistry in human adult and fetal hypothalami. Their perikarya are located in the infundibular nucleus. Some fibres terminate close to vessels in the median eminence, others form pericellular baskets around perikarya of non-immunoreactive neurons of the infundibular nucleus. These results suggest that the central nervous system elaborates beta-endorphin or immunologically related peptides.     

Differential displacement of cells from the median eminence into the arcuate nucleus during puberty. Effects of melatonin administration

A displacement of catecholaminergic-positive and catalase-containing cells from the median eminence into the arcuate nucleus at puberty has been described previously. This study reports on the displacement phenomena after postnatal administration of melatonin. Catalase-positive cells undergo a delayed displacement from the median eminence into the arcuate nucleus. However, part of this cell population lags behind within the median eminence. This differential reaction of cell displacement by catalase-positive cells is considered as a special reaction of these cells to melatonin administration.     

Differential displacement of cells from the median eminence into the arcuate nucleus during puberty. Effects of melatonin administration

Summary A displacement of catecholaminergic-positive and catalase-containing cells from the median eminence into the arcuate nucleus at puberty has been described previously. This study reports on the displacement phenomena after postnatal administration of melatonin. Catalase-positive cells undergo a delayed displacement from the median eminence into the arcuate nucleus. However, part of this cell population lags behind within the median eminence. This differential reaction of cell displacement by catalase-positive cells is considered as a special reaction of these cells to melatonin administration.     

Immunohistochemical demonstration of an SRIF-like system in the brain of the reptile: Lacerta muralis Laur

Summary The distribution of an SRIF-like substance in the brain of normal lizards (Lacerta muralis Laur.) has been determined. SRIF is shown to be present in neural cell bodies in the hypothalamic paraventricular nucleus, the hypothalamo-hypophysial tractus and the median eminence.Contrat INSERM, No. 74.1.444.35.     

Immunohistochemical localization by electron microscopy of GnRH in the median eminence of Xenopus laevis daud]

Using antibodies against mammalian LHRH with the unlabeled antibody enzyme method immunoreactive nerve fibres were localized in the median eminence of Xenopus laevis at the electron microscopic level. These fibres contain irregularly shaped neurosecretory granules with an average diameter of 890 A.     

Metallothionein promotes regenerative axonal sprouting of dorsal root ganglion neurons after physical axotomy

Prior studies have reported that metallothionein I/II (MT) promote regenerative axonal sprouting and neurite elongation of a variety of central nervous system neurons after injury. In this study, we evaluated whether MT is capable of modulating regenerative axon outgrowth of neurons from the peripheral nervous system. The effect of MT was firstly investigated in dorsal root ganglion (DRG) explants, where axons were scratch-injured in the presence or absence of exogenous MT. The application of MT led to a significant increase in regenerative sprouting of neurons 16 h after injury. We show that the pro-regenerative effect of MT involves an interaction with the low-density lipoprotein receptor megalin, which could be blocked using the competitive antagonist RAP. Pre-treatment with the mitogen-activated protein kinase (MAPK) inhibitor PD98059 also completely abrogated the effect of exogenous MT in promoting axonal outgrowth. Interestingly, we only observed megalin expression in neuronal soma and not axons in the DRG explants. To investigate this matter, an in vitro injury model was established using Campenot chambers, which allowed the application of MT selectively into either the axonal or cell body compartments after scratch injury was performed to axons. At 16 h after injury, regenerating axons were significantly longer only when exogenous MT was applied solely to the soma compartment, in accordance with the localized expression of megalin in neuronal cell bodies. This study provides a clear indication that MT promotes axonal regeneration of DRG neurons, via a megalin- and MAPK-dependent mechanism.     

«LH-Releasing-Factor» beim Menschen

Summary There is evidence for LH-releasing-factor (LH-RF) in 18 crude acid extracts of human median eminence preparation following the procedure described byRamirez andMcCann.     

Neuronal growth cone migration

The neuronal growth cone is a semi-autonomous portion of the developing neuron that is highly specialized for motile activity. Migrating neurons may share some features with neuronal growth cones. I review some of what has been learned about growth cone initiation, the differentiation of axons and dendrites, the role of the cytoskeleton in motility, the movements of membrane vesicles, the factors regulating the rate and direction of growth cone movement, and the further differentiation of growth cones as they enter the target area and initiate synaptogenesis. Where appropriate, I draw comparisons to what is known about the migration of neurons.     

Electrophysiologic and anatomic demonstration of inhibitory commisural vestibular neurons in the tench (Tinca tinca)]

Horseradish peroxydase was injected intracellularly in some of the medullary neurons which, in Fish, exhibit a passive hyperpolarizing potential after spinal cord stimulation (this indicates that such neurons both electrical and chemical inhibitions of the Mauthner cells). With positive staining, commissural vestibular neurons were identified; their axons cross the midline and they establish connexions with the Mauthner cell and with vestibular neurons of both sides. Thus the existence of a crossed vestibular inhibitory pathway, previously suggested by electrophysiological studies in lower Vertebrates as well as in Mammals, is now correlated with histological evidence.     

Neuronal growth cone migration

Summary The neuronal growth cone is a semi-autonomous portion of the developing neuron that is highly specialized for motile activity. Migrating neurons may share some features with neuronal growth cones. I review some of what has been learned about growth cone initiation, the differentiation of axons and dendrites, the role of the cytoskeleton in motility, the movements of membrane vesicles, the factors regulating the rate and direction of growth cone movement, and the further differentiation of growth cones as they enter the target area and initiate synaptogenesis. Where appropriate, I draw comparisons to what is known about the migration of neurons.     

Targeting of olfactory neurons

Olfactory sensory neurons detect an enormous variety of small volatile molecules with extremely high sensitivity and specificity. The actual recognition and discrimination of odorous compounds is accomplished by specific receptor proteins located in the ciliary membrane of the sensory neurons. Axonal connections into the olfactory bulb, the first relay station for odor processing in the brain, are organized such that all neurons expressing the same odorant receptor converge their axons onto common glomeruli which are located at similar positions in all individuals from one species. For the establishment of this precise targeting of olfactory axons to their appropriate glomeruli, combinatorial functions of axon-associated cell adhesion molecules and odorant receptor proteins appear to be required. Odorants that stimulate distinct receptor cell populations will thereby activate a specific combination of glomeruli in the bulb; this characteristic activity pattern may be used by the system to encode the quality of a particular odorant.     

Transport and diffusion of Tau protein in neurons

In highly polarized and elongated cells such as neurons, Tau protein must enter and move down the axon to fulfill its biological task of stabilizing axonal microtubules. Therefore, cellular systems for distributing Tau molecules are needed. This review discusses different mechanisms that have been proposed to contribute to the dispersion of Tau molecules in neurons. They include (1) directed transport along microtubules as cargo of tubulin complexes and/or motor proteins, (2) diffusion, either through the cytosolic space or along microtubules, and (3) mRNA-based mechanisms such as transport of Tau mRNA into axons and local translation. Diffusion along the microtubule lattice or through the cytosol appear to be the major mechanisms for axonal distribution of Tau protein in the short-to-intermediate range over distances of up to a millimetre. The high diffusion coefficients ensure that Tau can distribute evenly throughout the axonal volume as well as along microtubules. Motor protein-dependent transport of Tau dominates over longer distances and time scales. At low near-physiological levels, Tau is co-transported along with short microtubules from cell bodies into axons by cytoplasmic dynein and kinesin family members at rates of slow axonal transport.     

Stimulation of olfactory ensheathing cell motility enhances olfactory axon growth

Axons of primary olfactory neurons are intimately associated with olfactory ensheathing cells (OECs) from the olfactory epithelium until the final targeting of axons within the olfactory bulb. However, little is understood about the nature and role of interactions between OECs and axons during development of the olfactory nerve pathway. We have used high resolution time-lapse microscopy to examine the growth and interactions of olfactory axons and OECs in vitro. Transgenic mice expressing fluorescent reporters in primary olfactory axons (OMP-ZsGreen) and ensheathing cells (S100ß-DsRed) enabled us to selectively analyse these cell types in explants of olfactory epithelium. We reveal here that rather than providing only a permissive substrate for axon growth, OECs play an active role in modulating the growth of pioneer olfactory axons. We show that the interactions between OECs and axons were dependent on lamellipodial waves on the shaft of OEC processes. The motility of OECs was mediated by GDNF, which stimulated cell migration and increased the apparent motility of the axons, whereas loss of OECs via laser ablation of the cells inhibited olfactory axon outgrowth. These results demonstrate that the migration of OECs strongly regulates the motility of axons and that stimulation of OEC motility enhances axon extension and growth cone activity.     

Intrinsic and extrinsic neural and neurohumoral control of the decapod heart

The intra-cardiac nervous system of the decapod heart is composed of large and small ganglionic cells (LGCs and SGCs) and axons of extrinsic cardio-acceleratory and-inhibitory neurons (CAs and CIs). Candidate neurotransmitters for the neurons have been determined by pharmacological, cytochemical and immunocytochemical tests. SGCs may be cholinergic, LGCs and CAs are probably dopaminergic, and CIs are GABAergic. Serotonin and octopamine were cardio-excitatory neuromodulators of the heart. Proctolin, crustacean cardio-active peptide (CCAP), red pigment concentrating hormone (RPCH), and FMRFamide also had modulatory actions on the heart. Proctolin was the most potent peptide, which acted primary on the cardiac ganglion. Insect adipokinetic hormones had little effect on the heart.     

Axon guidance at the central nervous system midline

A key feature of the central nervous system of most higher organisms is their bilateral symmetry about the midline. The specialised cells that lie at the midline have an essential role in regulating the axon guidance decisions of both neurons that project axons across the midline and those that project on one side. The midline cells produce both attractive and repellent short- and long-range signals to guide axonal growth. The axons themselves express specific receptors that can be dynamically regulated in response to midline-derived signals. In this way, axons extend toward or away from the midline and those that do cross change their behaviour to respond to longitudinal signals on the contralateral side.     

Inhibitor interneurons of horizontal ocular saccades studied in the alert cat with the aid of intra-axonal injections of peroxidase

A simultaneous study of the functional and morphological characteristics of burst inhibitory neurons (B.I.N.) has been performed in the alert cat. For the first time, in the central nervous system of mammal, extra- and intracellular records have been coupled with intra-axonal injection of H.R.P. in the alert animal. The B.I.N. discharge during saccades and the quick phase of vestibular and optokinetic nystagmus oriented toward the ipsilateral side of recording. The frequency of discharges is proportional to the eye angular velocity. The axons end on the abducens motoneuron. Collaterals reach the controlateral prepositus hypoglossi nucleus, medial vestibular nucleus and reticular nuclei.     

Antigenic determinants of beta-LPH, beta-MSH, alpha-endorphin, ACTH and alpha-MSH revealed by anti-beta-endorphin in neurons of the human infundibular nucleus]

Comparison of adjacent serial sections of the tubero-infundibular region of Human adult hypothalamus demonstrates that the same perikarya, axons and terminals are stained both with anti-beta-endorphin and anti 17-39 ACTH antisera. The most immunoreactive of these neurons are also revealed with anti alpha-endorphin, anti alpha and beta-MSH, anti-1-24 ACTH and anti beta-LPH. These results suggest that neurons of the infundibular nucleus can store and probably secrete peptide similar to propiocortin or fragment(s) of this molecule.