“Dark” (compacted) neurons may not die through the necrotic pathway

Dark neurons were produced in the cortex of the rat brain by hypoglycemic convulsions. In the somatodendritic domain of each affected neuron, the ultrastructural elements, except for disturbed mitochondria, were remarkably preserved during the acute stage, but the distances between them were reduced dramatically (ultrastructural compaction). Following a 1-min convulsion period, only a few neurons were involved and their environment appeared undamaged. In contrast, 1-h convulsions affected many neurons and caused swelling of astrocytic processes and neuronal dendrites (excitotoxic neuropil). A proportion of dark neurons recovered the normal structure in 2 days. The non-recovering dark neurons were removed from the brain cortex through two entirely different pathways. In the case of 1-h convulsions, their organelles swelled, then disintegrated and finally dispersed into the neuropil through large gaps in the plasma membrane (necrotic-like removal). Following a 1-min convulsion period, the non-recovering dark neurons fell apart into membrane-bound fragments that retained the compacted interior even after being engulfed by astrocytes or microglial cells (apoptotic-like removal). Consequently, in contrast to what is generally accepted, the dark neurons produced by 1-min hypoglycemic convulsions do not die as a consequence of necrosis. As regards the case of 1-h convulsions, it is assumed that a necrotic-like removal process is imposed, by an excitotoxic environment, on dark neurons that previously died through a non-necrotic pathway. Apoptotic neurons were produced in the hippocampal dentate gyrus by intraventricularly administered colchicine. After the biochemical processes had been completed and the chromatin condensation in the nucleus had reached an advanced phase, the ultrastructural elements in the somatodendritic cytoplasm of the affected cells became compacted. If present in an apparently undamaged environment such apoptotic neurons were removed from the dentate gyrus through the apoptotic sequence of morphological changes, whereas those present in an impaired environment were removed through a necrotic-like sequence of morphological changes. This suggests that the removal pathway may depend on the environment and not on the death pathway, as also assumed in the case of the dark neurons produced by hypoglycemic convulsions.     

Participation of Ia reciprocal inhibitory neurons in the spinal circuitry of the tonic neck reflex

Summary As part of our studies of the spinal circuitry of the tonic neck reflex, we have recorded extracellularly from Ia reciprocal inhibitory neurons of the decerebrate, labyrinthectomized cat. The activity of a majority of neurons driven by stimulation of the quadriceps nerve was modulated by sinusoidal rotation of the neck; such modulation was much less frequent in the case of neurons driven by stimulation of nerves to more distal muscles. The results suggest that some of the inhibition which is part of the tonic neck reflex is mediated by Ia reciprocal inhibitory neurons, but that other pathways must also play an important role.     

Developing neuronal populations of the cat retinal ganglion cell layer

An improved flat-mount procedure demonstrates that the developing ganglion cell layer of the cat retina contains two morphologically distinct populations of presumed neurons at all ages between embryonic day 36 (E36) and adulthood. One population resembles the adult "classical neurons" composing the ganglion cells and bar-cells of Hughes, while the remaining cells, which are smaller and possess much less Nissl substance, presumably correspond to precursors of the adult microneurons. Although the total neuron population of the retinal ganglion cell layer remains quite constant at all studied ages, its component subpopulations alter significantly during prenatal development; some 50% of classical neurons disappear before birth and the microneuron population doubles during the same period. An obvious centroperipheral gradient exists for classical neurons by stage E47, but the microneuron density gradient only becomes apparent at birth. A 2:1 centroperipheral ratio for the total neuron population is also apparent at E47. Centroperipheral neuronal density gradients continue to increase during postnatal growth. Loss of classical neurons during prenatal life as a result of cell death or transformation into microneurons, has been postulated as a mechanism for determining neuron density gradients. Cell death does occur in the ganglion cell population but it is not yet established whether microneurons of the ganglion cell layer originate from ganglion cell transformation or migrate as a differentiated class from the ventricular layer. However, it can be concluded that not all microneurons originate from ganglion cell transformation, because the total loss of classical neurons is less than the increase in microneuron numbers during development. The population magnitudes of both neuronal classes in the ganglion cell layer stabilise after birth. However, it is during the postnatal period that the adult cruciate density topography is achieved by both populations. It is concluded that differential areal growth is the prime mechanism for postnatal cell redistribution.     

Histological characterization of neurones innervating functionally different muscles of Locusta

The innervation of four functionally different muscles (subalar, remotor 1, remotor 2, pleuroalar), all served by the same nerve branch, was studied in both winged segments of the locust, Locusta migratoria. Several anatomical techniques were applied: With the cobalt backfill and silver intensification technique four cell types (motoneurone, dorsal unpaired median neurone, common inhibitory neurone, and small median neurone) were demonstrated. Serial sections enabled the morphology of the motoneurones to be described in more detail and in respect to a possible functional organization of the arborizations. A differential staining technique allowed us to stain various neurones in different colours in the same preparation. With this technique the anatomy of both the "rostral" and the "caudal" subalar motoneurones could be described in parallel, thus avoiding errors in comparison due to possible individual variations from preparation to preparation. Axon counts in the peripheral nerve branch enabled us to compile a list of the total innervation for each muscle. Results from other orthopterans are integrated and whether differences in the dendritic fields might be of functional significance is discussed.     

Endogenous dopamine release from tuberoinfundibular neurons: Does calmodulin play any role?

Summary The possible involvement of calmodulin in the process of endogenous dopamine (DA) release from arcuateperiventricular nuclei-median eminence fragments, containing tuberoinfundibular dopaminergic (TIDA) neurons, has been investigated in an in vitro incubation system. For this purpose the basal and K⁺-stimulated DA release was examined in the presence and in the absence of the different putative calmodulin antagonists, pimozide, trifluoperazine, penfluridol and N-(6-aminohexyl)-5-chloro-1-naphthalene-sulfonamide (W-7).Trifluoperazine and pimozide in concentrations up to 100 M were both uneffective in blocking K⁺-evoked DA release. Penfluridol in doses of 5 and 10 M, did not prevent 35 mM K⁺-induced endogenous DA release. It was able to reduce K⁺-stimulated DA release only at the very large concentration of 100 M.W-7 added in vitro to the hypothalamic fragments, prevented endogenous DA release evoked by 35 mM K⁺ in a dose-dependent manner. W-5, a chlorine deficient analogue of W-7, that interacts only weakly with calmodulin, failed to modify K⁺-stimulated endogenous DA release in doses up to 200 M.All the putative calmodulin antagonists used in the present study did not induce any change of basal DA release.IN conclusion the fact that most of the agents, except W-7, known to antagonize calmodulin-dependent processes in many biological systems failed to interfere with the release of endogenous DA from TIDA neurons seems to suggest that calmodulin does not play a crucial role in the process of DA release and that the inhibitory effect of W-7 on endogenous DA release may be better attributed to other mechanisms different from its anticalmodulin action.     

Sizes, laminar and topographic origins of cortical projections to the major divisions of the red nucleus in the monkey

The retrograde transport of horseradish peroxidase was used to study the topographic and laminar origins of the cortical projections to the parvocellular and the magnocellular divisions of the red nucleus in Macaca mulatta and Macaca fascicularis. Approximately 90% of the corticorubral projection is directed to the parvocellular division of the nucleus. Corticoparvocellular (CRp) neurons are pyramidally shaped, are smaller in size than corticospinal neurons, and are more numerous. They are found principally in sublamina Va of cytoarchitectonic areas 4 and 6, and in moderate quantities in sublamina Vb of posterior area 8 and area 5. In areas 4 and 6, the cells are grouped in clusters of three to 15 neurons each and are arranged in cellular bands of varying rostrocaudal thickness which course mediolaterally. With respect to functionally defined zones, CRp neurons are found throughout the supplementary motor area and the precentral motor cortex. In addition, they are found in parts of areas 5, 6, and 24 that project to these cortical motor areas, and that are thought to have "premotor" or movement-programming functions. The corticomagnocellular (CRm) projection arises principally from cells in sublamina Vb of the precentral arm and leg areas (area 4), and from adjacent parts of posterior area 6, CRm cells are pyramidally shaped, and their size distribution is bimodal, with peaks that correspond, respectively, to the modal diameters of CRp and of corticospinal neurons. These results and those of previous studies suggest that CRm neurons are involved principally in the control of hand and foot movements, with little effect on more proximal musculature. The massive CRp projection, however, is clearly part of a large cerebrocerebellar communication system, with motor and/or movement programming functions that have yet to be clearly defined.     

Neuronale reaktionen im tectum opticum der katze auf bewegte und stationäre lichtreize

Zusammenfassung Es wurden 80 Einheiten des Tectum opticum der Katze abgeleitet und ihre Reaktionen auf stationäre und bewegte optische Reize geprüft.Neben den Neuronen, die in ihrer Reaktionsweise retinalen Einheiten vergleichbar waren, fanden sich überwiegend (89%) Neurone, die auf bewegte optische Reize reagierten. Unter den letzteren zeigte die Mehrheit (70%) richtungsspezifisches Verhalten. Bei einigen Neuronen war in einem beschränkten Bereich von 1–7.5/sec die Reaktion gesetzmäßig abhängig von der Winkelgeschwindigkeit des Bewegungsreizes (Potenzfunktion mit dem Exponenten 0.67). Die rezeptiven Felder waren meist rund mit einem durchschnittlichen Durchmesser von 8.1 (3–22). 68% der Einheiten reagierten nicht auf diffusen Lichtreiz. Die Reaktionen auf nicht bewegte Punktlichtreize waren rasch adaptierend und inkonstant in ihrer Art und Stärke. In kurzen Abständen mehrfach wiederholte Bewegungsreize bewirkten bei einem Teil der Bewegungsneurone rasche Adaptation.Zwei kurz aufeinander folgende Punktlichtreize ergaben eine Reaktion, die niedriger als die Summe der Erregungen der jeweils einzeln gegebenen Lichtreize war, wenn die zeitliche Folge der beiden Reize der Vorzugsrichtung des Neurons entgegengesetzt war. Bei Reizfolgen entsprechend der Vorzugsrichtung entsprach die Gesamtreaktion der Summe der Einzelreizantworten. Dies läßt vermuten, daß die Richtungsspezifität durch unilaterale Hemmung bedingt ist.

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Summary Recordings were made from 80 single units in cat's Tectum opticum during visual stimulation with moving and stationary optic stimuli. The majority of units (89%) showed movement specific reactions, the rest behaved functionally similar to retinal or geniculate neurons. 70% of the movement specific units showed directional selective reactions. The receptive fields, as determined with stationary and moving stimuli were mostly circular with an average diameter of 8.1° (range 3–22°). Stimuli passing through the periphery of the field led to less pronounced reactions than those going through the center. In 10 out of 30 units, the relation between discharge rate and angular velocity in a restricted range from 1°–7.5°/sec could be approximated by a power function with an exponent of 0.67. Above 10°/sec irregular and unsystematic alterations of reactivity were observed. 68% of the tectal units recorded did not respond to diffuse light stimuli. The reactions to localized intermittent stationary light stimuli were mostly off (42%) or on-off-responses (19%) and were characterized by fast adaptation, change of reaction type during successive intermittent stimulation and by the absence of an antagonistic field-structure. Stimulation of adjacent points in a temporal sequence corresponding to movement opposite to the most sensitive direction of a directional specific neuron led to a reaction which was below the sum of the reaction of the two stimuli given alone. At a temporal sequence of the two stimuli such as to simulate the most sensitive direction, the resulting reaction corresponded to the sum of the reactions of both stimuli given alone. This suggests a mechanism of unilateral inhibition to be responsible for directional selectivity.

Wir danken Priv.-Dozent Dr. O.D. Creutzfeldt für Beratung und Diskussion bei Durchführung der Experimente und Abfassung des Manuskriptes, Herrn Wickelmaier für seine tatkräftige Hilfe bei technischen Problemen der Versuchsanordnung.     

Acetylcholinesterase activity in senile plaques of aged macaques

A modified acetylcholinesterase (AChE)-histochemical technique, which demonstrates axonal morphology to a high degree, was used to examine the neocortices of aged monkeys. This approach disclosed slender linear axonal profiles in young animals. In older monkeys, there was a variety of abnormalities of AChE-containing fibers, including multifocal distentions of individual fibers and aggregations of neuritesized, AChE-rich swellings. Combined with thioflavin-T staining to visualize amyloid, this histochemical technique showed that some of these AChE-containing fibers were present in proximity to deposits of amyloid. This association suggests that abnormal AChE-rich axons participate in the formation of some senile plaques in the neocortices of aged nonhuman primates. While it is probable that many of these AChE-rich fibers are axons of cholinergic neurons residing in the basal forebrain, it is also likely that some of these fibers are derived from noncholinergic neuronal populations known to synthesize AChE. Immunocytochemical strategies can be used to assess the involvement of other systems, including cholinergic, noradrenergic, dopaminergic, somatostatinergic, and serotonergic neurons in the formation of senile plaques in the brains of aged nonhuman primates.     

Golgi-like demonstration of “dark” neurons with an argyrophil III method for experimental neuropathology

Summary A silver method is proposed for the selective, well-contrasted and reproducible demonstration of dark neurons in frozen, vibratome and paraffin sections cut at a thickness of 5 to 200 m from aldehyde-fixed brains. The Golgi-like staining of the dendrites enables asorting of dark neurons according to characteristic neuron classifications. The staining procedure includes an esterification with 1-propanol, a treatment with diluted acetic acid and development. The esterification strongly increases the argyrophilia of both dark neurons and mitochondria. Unwanted co-staining of mitochondria is suppressed by the acetic acid treatment, while a special developer is used to render the staining controllable. The applicability of the method to experimental neuropathology is demonstrated by Golgi-like staining of dark neurons in rat brains exposed, before transcardial perfusion-fixation and delayed autopsy, to various pathological conditions including ischemia, hypoglycemia, trauma, status epilepticus, deafferentation and poisoning with kainic acid, colchicine and sodium azide, respectively.     

Enflurane reduces the excitation and inhibition of dorsal horn WDR neuronal activity induced by BK injection in spinal cats

The effects of enflurane (0.5%, 1.5% and 2.5%) on the excitation and inhibition of dorsal horn wide dynamic range (WDR) neuronal activity induced by bradykinin (BK) injection was studied in spinal cats. Extracellular activity was recorded in the dorsal horn from single WDR neurons responding to noxious and non-noxious stimuli applied to the cutaneous receptive fields on the left hind paw foot pads of decerebrate, spinal cord transected (L_1–2) cats. When 10µg of BK was injected into the femoral artery ipsilateral to the recording site as the noxious test stimulus, 24 of 26 WDR neurons (92%) gave excitatory responses and 2 (8%) gave inhibitory resposes. On the other hand, when the injection of 10µg of BK into the femoral artery contralateral to the recording site was used as the noxious test stimulus, 7 of 12 WDR neurons (58%) gave inhibitory responses, 3 (25%) gave excitatory responses, and 2 (17%) showed no response. The excitatory neuronal activity in WDR neurons was not depressed by 0.5% or 1.5% enflurane but was depressed significantly by 2.5%. However, the inhibitory neuronal activity in WDR neurons was significantly depressed by 0.5%, 1.5% and 2.5% enflurane. We have found that enflurane reduces the excitation as well as the inhibition of dorsal horn WDR neuronal activity induced by BK injection. These results suggest that the reduction of excitatory and inhibitory responses produced by noxious stimulation is likely to be the fundamental basis of the enflurane-induced anesthetic state in terms of WDR neurons.(Nagasaka H, Nakajima T, Takano Y et al.: Enflurane reduces the excitation and inhibition of dosal horn WDR neuronal activity induced by BK injection in spinal cats. J Anesth 4: 102–109, 1990)