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The effect of intrahippocampal injections of serotonin on bioelectrical activity of Gyrus cinguli and amygdaloid nucleus in the rabbit.

The effect of injection of serotonin (5-HT), dissolved in 2 mul of bidistilled water, into hippocampus was studied in rabbits with chronically implanted electrodes and cannulas. Bioelectric activity of gyrus cinguli, amygdaloid nucleus, and dorsal hippocampus was recorded. 5-HT (10--20 mug) inhibited the electrical activity of the structures investigated, and this inhibition was accompanied by a suppression of locomotor activity or sleep.

Amygdala

[Effect of sensory stimulation on the lamina V pyramidal neurons of the gyrus cinguli in the rat].

UNLABELLED: Three groups of Wistar-rats were exposed to permanent noise (80 db) during different periods in their postnatal life: the first group was exposed starting from birth for a period of four weeks, the second one from birth up to nine weeks of age and the third group from the fifth up to the ninth week postnatal. A fourth group (control animals) was reared under normal laboratory conditions. After the experiments the brains were exposed to a modified GOLGI-method. In lamina-V-pyramids of the gyrus cinguli lightmicroscopical results: length, number and distribution of spines on the main apical dendrites and on the apical dendritic branches where evaluated. MAIN RESULTS: 1. Permanent noise during the early postnatal development phase of the brain of rats (from birth up to the fourth week of age) causes a statistically significant increase of apical spines. The spines-values are 20% above those of the control animals. 2. Permanent noise from birth up to the ninth week of age or applied only during the later postnatal period (from the fifth week up to the ninth week of age) does not significantly alterate the spines-value. 3. The results are estimated as a consequence of extreme environmental factors causing effects, comparable with an universal stress reaction. Conclusions were discussed in comparison to the results of other authors.

Acoustic Stimulation

The histoenzymic activity of gyrus cinguli in the course of postnatal ontogeny of the rat.

Histochemical investigations concerning the activity of several dehydrogenases and hydrolases in the area cinguli during postnatal ontogenic development of the rat were performed. Brain sections corresponding to the region of area cinguli, obtained from rats aged 1, 3, 8, 17, 40 and 60 days postnatal, were subjected to histochemical assays for various dehydrogenases, phosphatases and esterases. The developmental changes concerning histoenzymic reactivity of the callosal gyrus with regard to several respiratory and hydrolytic enzymes were assessed and described. Considerable differences in enzymic reactivity, appertaining particularly to the phosphatases and esterases, between the anterior and posterior parts of the callosal gyrus were found. The unusual enzymic reactivity of glial cells in the individual regions of the area cinguli has been pointed out.

Animals

[Quantitative studies on the dendritic spine distribution on the lamina-5 pyramidal cells in the anterior gyrus cinguli of the rat].

At three months old male rats the spine-distribution of the main dendrite and of the apical and basal dendrites of 36 lamina V-pyramidal cells of the regio cingularis (anterior cingulate cortex) was analyzed (from every subregion -- neocortex, mesoneocortex, mesoarchicortex -- 12 neurons). 1. The limbic pyramidal neurons show the same spine-distribution at their main dendrite as neocortical neurons of other brain regions and other mammal-species do: after an initial segment with poor spines only there follows an rapid increase of the spine-values with an amount at a range of 150 mum from the perikaryon, thereafter spine-values decrease continuously and slowly up the branching into the terminal bundle. 2. Basal and apical lateral dendrites however show another spine-distribution: basally there is an increase of the spine-values from the 1st up to the 3rd order, followed by a decrease at subsequent orders. Apically spine-density decreases from the 1st up to the 4th order. 3. The spine-distribution at the parts of the dendritic tree is discussed as a general biological sign of pyramidal cells. 4. The total number of spines of lamina V-pyramidal cells in the regio cingularis (anterior cingulate cortex) is less than those in the sensomotoric cortex and in the hippocampus, which corresponds with the lower differentiation of the limbic cortex. 5. By means of a variance-analysis the pyramidal spine-values of the three subregions were compared: concerning the total number of spines of a pyramidal neuron there are significant differences between the three subregions; the values are in the ratio of 3 to 2 to 1 (Regio praecentralis agranularis, 2461; mesoneocortex, 1664; mesoarchicortex, 800). The significantly least spine-density of all parts of the dendritic tree you can find in lamina V-pyramidal cells of the mesoarchicortex. 6. The equality of the basal and apical spine-values in the mesoneocortex is due to less specialization of these neurons. 7. The spine-values for a single dendritic field (EDF) show the differences between the limbic subregions clearly: there are significant differences between the three subregions concerning not only the number of spines but also the spine-densities apically and basally.

Animals

Regional distribution of neuropeptide Y and its receptor in the porcine central nervous system.

The regional distribution of neuropeptide Y (NPY) immunoreactivity and receptor binding was studied in the porcine CNS. The highest amounts of immunoreactive NPY were found in the hypothalamus, septum pellucidum, gyrus cinguli, cortex frontalis, parietalis, and piriformis, corpus amygdaloideum, and bulbus olfactorius (200-1,000 pmol/g wet weight). In the cortex temporalis and occipitalis, striatum, hippocampus, tractus olfactorius, corpus mamillare, thalamus, and globus pallidus, the NPY content was 50-200 pmol/g wet weight, whereas the striatum, colliculi, substantia nigra, cerebellum, pons, medulla oblongata, and medulla spinalis contained less than 50 pmol/g wet weight. The receptor binding of NPY was highest in the hippocampus, corpus fornicis, corpus amygdaloideum, nucleus accumbens, and neurohypophysis, with a range of 1.0-5.87 pmol/mg of protein. Intermediate binding (0.5-1.0 pmol/mg of protein) was found in the septum pellucidum, columna fornicis, corpus mamillare, cortex piriformis, gyrus cinguli, striatum, substantia grisea centralis, substantia nigra, and cerebellum. In the corpus callosum, basal ganglia, corpus pineale, colliculi, corpus geniculatum mediale, nucleus ruber, pons, medulla oblongata, and medulla spinalis, receptor binding of NPY was detectable but less than 0.5 pmol/mg of protein. No binding was observed in the bulbus and tractus olfactorius and adenohypophysis. In conclusion, immunoreactive NPY and its receptors are widespread in the porcine CNS, with predominant location in the limbic system, olfactory system, hypothalamoneurohypophysial tract, corpus striatum, and cerebral cortex.

Animals

A primitive gigantopyramidal field buried in the depth of the cingulate sulcus of the human brain.

By stereomicroscopical examination of a complete series of pigment preparations up to 1000 mum thick, a gigantopyramidal area in the brain of man is described, which lies in front of the primary motor field on the medial surface of the hemisphere and is almost totally buried in the depth of the cingulate sulcus extending in both length and width over about 15 mm. Serial sections cut in the transverse plane display the field approximately within the limits of the commissura anterior on the one hand and the corpora mamillaria on the other, where it occupies large parts of the dorsal wall of the gyrus cinguli (lower bank of sulcus cinguli) and a small area of the adjacent superior frontal gyrus. The sharply outlined field does not fuse with the primary motor area and is evidently more primitively organized than the precentral motor field. Structural details betray an intimate relationship between this gigantopyramidal field and the archipallial proisocortex. We could clearly trace a gradation, that is, a stepwise change of architectonic features in constant orientation from the limbic proisocortex over a small paralimbic transition zone to the gigantopyramidal field, accounting for the numerous limbic traits recognizable within it, such as, for instance, an accentuated external granular layer, a dense and broad lamina pyramidalis, and a band-like appearance of Va.

Frontal Lobe

[Akinetic mutism and bicingular softening. 3 anatomo-clinical cases].

The authors describe three pathological cases of akinetic mutism with, as a common basic lesion, bilateral infarction of the cingulate gyrus secondary to aneurysm of the anterior communicating artery (case n degrees 1), to a huge olfactory meningioma (case n degrees 2), both operated on, and to atheromatous occlusion of the anterior cerebral arterial system (case n degrees 3). These three cases enable a variety of "anterior and waking" akinetic mutism to be described which is unusual enough to be compared with other mesencephalic and diencephalic aspects of this syndrome. It is in fact an akinetic mutism characterized by: a certain dissociation in its non-response to various stimuli, a particularly marked appearance of wakefulness when day-time alertness is considered, conservation of the waking-sleeping rhythm, perception and reaction unpredictable and paradoxical in both degree and quality, complete absence of any spontaneous verbal communication in contrast to relative break-down of solicited communication which is infrequent, uncertain and unresponsive to the usual methods of stimulation, without any possibility of a code. In addition, there is a remarkable mimic and segmental general akinesia, resistant to the usual nociceptive stimuli, but sensitive to slight excitation of the manual and oral zones. Besides this special akinetic mutism, there are variously systematised signs, mostly asymmetrical, indicating lesion of the cortico-sub-cortical frontal structures bordering on the gyrus cinguli. This unusual behaviour pattern corresponds in these three cases to extensive anterior bilateral ischemic lesions of the cingulate gyrus regularly associated with bilateral infarctions confined to the medial aspect of F1 in the superficial territory of the two anterior cerebral arteries, to possible neurosurgical changes (ablation of the right frontal pole) and to compressive or ischaemic lesions of the gyrus rectus. These exclusively cortico-sub-cortical associated lesions are in contrast with the remarkably intact caudate nuclei, the pallidal, thalamic, hypothalamic and septal formations and the anterior pillars of the fornix. These findings compared with the results of experimental research carried out by M. Kennard, help, if help is needed, to resolve the apparent contradictions between the effects of therapeutic cingulectomies or cingulotomies and the scanty pathological data already available in cerebral vascular pathology.

Adult

The pontine projection to the flocculonodular lobe and the paraflocculus studied by means of retrograde axonal transport of horseradish peroxidase in the rabbit.

The occurrence and distribution of labeled cells in the pontine nuclei were mapped following injections of small amounts of horseradish peroxidase (0.05-0.5 microliter, 50% suspension) in the flocculus, nodulus and the dorsal and ventral paraflocculus in adult albino rabbits. While no labeled cells were found in the pontine nuclei following injections in the nodulus, some were present following injections in the flocculus and a great number following injections in the paraflocculus. The projections onto the flocculus and paraflocculus are precisely organized. Following injections in the paraflocculus labeled neurons are arranged in four columns (E and G in the paramedian pontine nucleus, F in the peduncular and H in the dorsolateral nucleus). Following injections in the ventral paraflocculus labeled cells are present only in parts of column E and F, while columns G and H and parts of E and F project onto the dorsal paraflocculus. Following injections in the flocculus labeled cells occur in the rostral part of column E only. A comparison between the sites of termination of pontine afferents and the areas giving origin to floccular and parafloccular fibers shows that only few fibers mediating visual impulses end in these pontine areas, while they receive numerous fibers from gyrus cinguli and areas 18 and 19 of the cerebral cortex.

Animals

[Quantitative study of the apical dendritic spines in the cingulate lamina-V-pyramid neurons of the rat following oral application of alcohol].

The question answered in this paper is whether the apical dendritic spines-values of lamina-V-pyramidal cells of the gyrus cinguli of the rat are changed as a result of the oral application of ethanol. Alcohol-application causes a statistically significant increase of apical spines, especially at the main dendrite when given during the early postnatal development phase, where the brain is still impressible. The results are discussed as compensatory achievement of the not degeneratively changed neurons, while other pyramids show signs of degeneration. The conclusions were compared with the results of Kunz et al. (1976), who investigated the ethanol-effects on hippocampal pyramids.

Animals

[Effect of sensory deprivation on the lamina V pyramidal neurons in the rat cingulate gyrus].

Three groups of Wistar-rats were reared in the dark during different periods in their postnatal life: the first group was reared in the dark starting from birth for a period of four weeks, the second one from birth up to nine weeks of age and the third one from the fifth up to the ninth week postnatal. Two groups of control animals were reared under normal laboratory conditions from birth up to four or else up to nine weeks of age. The brains were processed according to a modified Golgi-Kopsch method. In lamina-V-pyramids of the gyrus cinguli there were evaluated lightmicroscopically for every group: length, number and distribution of spines on the main apical dendrites; on the apical oblique dendrites, too, these measures were made in the groups of four weeks of age (experimental and control animals). Main results are: 1. Rearing in the dark from birth up to the fourth week of age, i.e. during the early period of the postnatal brain development causes a growing-inhibition: the number of apical oblique dendrites (first order) was significantly decreased in comparison with the controls. The apical spines-values are not significantly altered. 2. Rearing in the dark from birth up to the ninth week of age as well as during the later postnatal development (from the fifth up to the ninth week) cause a statistically significant increase of spines values on the main apical dendrite. 3. These findings are discussed from a functional point of view and with the references.

Animals

[Quantitative examinations of stellate cells in the region of the cingulate gyrus in the rat].

Brains of three months old male rats were handled by a modified Golgi-Kopsch method. Stellate cells of the gyrus cinguli were drawn, classified into four types and analyzed quantitatively. The values of the four types were compared by means of a varianz analysis. The four types are: isodendritic stellate cells without spines (I/OS), isodendritic stellate cells with spines (AI/OS), anisodendritic stellate cells without spines (AI/OS), anisodendritic stellate cells with spines (AI/MS). Type I/OS and type AI/MS are the most contrary one. Main results are: 1. The lengths of the dendritic branches show maximum values in the 3rd order. The dendritic lengths exhibit great deviations in all the four types. The alteration of the lengths values from one to the next order is similar the basal dendritic tree of primitive pyramidal neurons. The same analogy you can find for the dendritic numbers of corresponding orders: highest numbers are in the 2nd order, in the following orders the numbers decrease permanently. Isodendritic stellate cells without spines have significantly more dendrites of the 1st order compared with the other three types. 2. The branching pattern --- revealed in the number of free dendritic endings --- shows differences between isodendritic stellate cells without spines and anisodendritic stellate cells with spines. 3. The total lengths of the dendritic branches and the lengthes of the single dendritic fields are similar in significant differences: least lengths there are in anisodendritic stellate cells with spines, they are significantly different from isodendritic stellate cells with and without spines. 4. There are differences in the values of spines and varicosities between all types which causes the possibility of classifying stellate cells according to this parameter. This is valid for spines values of the orders, spines values of single dendritic fields and for the total number of spines for one neuron. 5. Localization and extending in the layers: most stellate cells extend through several layers. The isodendritic type is preferentially localizes in layer III, the anisodendritic one in layer V.

Animals

Electric brain potentials evoked by pictures of faces and non-faces: a search for "face-specific" EEG-potentials.

In three different experimental series, electroencephalographic responses evoked by changes in pictorial patterns were recorded in 29 adult human subjects (19 females, 10 males). Quantitative data evaluation for the evoked responses from electrodes T5, T6, Cz, Pz (10-20 system) was performed. The stimuli were projected to a 4 x 6 degree binocularly viewed field. The patterns changed within 6 ms every 2.5-4.5 s according to a random program. Paradigm (1): Identical line drawings of a face, a tree and a chair were used, either black on white (P-stimuli) or white on black (N-stimuli); in each set altogether 160 slides appeared in semi-random order. At Cz and Pz a prototypical EEG-response evoked by face stimuli was found exhibiting 3 prominent peaks, very similar for P-stimuli and N-stimuli. A P150 maximum was especially pronounced in the responses to face stimuli but absent in the evoked potentials aroused by chair or tree stimuli. The difference curves (face-chair, face-tree, chair-tree) supported the hypothesis of "face-responsive" components in these responses. Paradigm (2): 4 x 6 degree slides (black and white photographs) of 54 different human faces, 53 different vases and 53 different pairs of shoes were projected as in paradigm (1), but instruction to the subjects on a supposed post-test memory task raised their attention during the recordings. "Face-responsive" components (an early N 140-160, P 210-240, N 300) were more marked in female than in male subjects, and again most pronounced at electrode Cz. Paradigm (3): When a recognition task was included in paradigm (2)--9 out of 192 items were memorized 20 minutes before the recording session--essentially the same evoked potentials were obtained as in (2), but an additional late positive wave (450-600 ms) appeared in the responses to all stimuli. We assume that the "face-specific" components--a designation which is used cautiously considering the limited number of non-face stimuli--do not originate in the temporo-occipital cortical face region, but in limbic structures (amygdala, hippocampus) deep in the temporal lobe or in the gyrus cinguli. In the present study no significant hemispheric differences (T5, T6) in the evoked responses were found (all stimulus categories), but such differences are known to appear with highly schematic face stimuli.

Adult

Adult-type citrullinemia.

An autopsy case of adult-type citrullinemia in a 42-year-old male is reported. The patient neuropathologically presented mixed cerebral changes consisting of the pseudoulegyric and ischemic types of hepatocerebral disease. In common with previously reported cases of the pseudoulegyric type, the nature and localization of the cerebral changes in this case were characteristic, in that neuronal loss occurred most severely and symmetrically in the mediobasal part of the frontal and occipital lobes, gyrus cinguli, claustrum, insula and temporal lobe, and that the watershed area of the cerebral cortex, basal ganglia and Purkinje cells were only slightly affected. The importance of hypercitrullinemia was stressed in the pathogenesis of the cerebral changes evident in adult-type citrullinemia.

Adult

Petit mal and grand mal seizures produced by toluene or benzene intoxication in the cat.

Motor incoordination, euphoria and hallucinations are symptoms reported for humans voluntarily intoxicated by industrial solvents. An epileptic-like consciousness impairment has also been noted. The present paper describes a technique used for the experimental study of solvent intoxication in which toluene and benzene can be applied directly into the trachea of freely moving cats with chronically implanted electrodes. This technique permits the control of solvent dose and time of exposure. Results showed a 3 Hz spike-wave activity in the gyrus cinguli recording with both toluene or benzene intoxication. Furthermore, benzene inhalation produced generalized tonic-clonic seizures. These effects were dose-related. However, a sensitization period was essential for the development of such alterations, and effects showed a tendency to shortening through chronic exposures. These alterations were correlated with behavioral disturbances such as nodding, twitching and apparent hallucinations. Results are discussed regarding the sensitization period, the optimal peak of effects, and the period of tolerance development relevant to an earlier found amygdalar activation that could be correlated with other methods inducing experimental seizures, such as repetitive stimulation of the brain (kindling).

Amygdala

The neocortico to mesio-basal limbic propagation of focal epileptic activity during the spike-wave complex.

In order to localize epileptogenic electrophysiological sources, a multichannel MEG system was used in 3 patients with partial epilepsy during presurgical evaluation. MEG and EEG (including scalp, sphenoidal and intracranial foramen ovale electrodes) were recorded simultaneously during a period of intensive video-EEG monitoring in order to observe single spontaneous spikes. In addition to MRI, SPECT and PET investigations were performed. Electrical activity subsequent to the activity of the epileptic focus could be localized by the MEG after noise reduction using a temporal correlation technique. Simultaneous registration of the magnetic field and the electrical field showed that the source of the primary focal epileptic activity (first period during the total spike wave complex where a dipolar magnetic field pattern is found) is localized in neocortical lateral regions, whereas another focal epileptic activity in a later phase of propagation occurs in temporal mesial regions. In 1 patient (case 1) the primary focal epileptic activity was localized in the surrounding neocortical tissue of an angioma and the middle and inferior temporal gyrus. The second phase of propagation is localized in temporo-basal-mesial regions, including para- and hippocampal structures. The latest center of activity occurred in posterior parts of the gyrus cinguli. In 2 other patients, the primary focal epileptogenic activity was localized at the insula and also spread into temporal basal mesial regions. A multi-modal approach to research of focal epilepsy, combining metabolic, electrical potential, magnetoencephalographic and morphological data, recorded by non-invasive techniques, offers new perspectives for the detection of involved brain regions. The 3-D and time-resolved localization of focal epileptic activity, correlated with the individual anatomy of the human brain, may improve the determination of neuronal populations involved in the individual epileptogenic process, especially in the interaction between temporal or extratemporal neocortex and limbic system.

Adult

Changes in the brain catecholamines in patients with dementia of Alzheimer type.

Brain monoamine concentrations were determined post mortem in 19 patients with dementia of Alzheimer type. Samples were taken from 10 parts of the brain and compared with an age-matched control group. There were lower mean concentrations of dopamine in the demented group of patients in seven regions of the brain, and two of these were at a significant level. There were also significantly lower concentrations of homovanillic acid in the nucleus caudatus and in the putamen. The means of the concentrations of noradrenaline were also lower, and in the putamen and the cortex gyrus frontalis significant differnces were observed. The 5-hydroxytryptamine concentrations were slightly lower in the demented group but the differences did not reach significance. The degree of intellectual deterioration was negatively correlated with the noradrenaline concentrations in the hypothalamus and the cortex gyrus cinguli.

Aged