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The characteristic features of guinea pig amygdala (CA), as shown by volumetric comparisons of the individual nuclei, are the poor development of the basolateral (BL) and lateral olfactory tract (NLOT) nuclei as well as the strong formation of the lateral (LA) and basomedial (BM) nuclei. The central (CE), cortical (CO) and medial (ME) nuclei also appear to be well represented in this species. All these features are even more pronounced when the total number of neurons in the nuclei referred to was taken into consideration. A comparison of the densities of neurons in the individual nuclei with the mean numerical density of cells in the guinea pig CA indicates that the densities of neurons in LA, BL, BM, CE and CO are significantly lower than the mean (p < 0.05), whereas in the ME and NLOT these values are significantly higher than the mean (p < 0.05). It is noteworthy, that the densities of the neurons in CE and CO do not differ statistically from each other (p > 0.05) and are significantly higher than the respective values in LA, BL and BM (p < 0.05). Furthermore, a similar division of the guinea pig CA may to some extent be made using the size parameters of the amygdaloid neurons as a marker. Interestingly, the large neurons populate organised CA areas like LA, BL and BM less densely, whereas the small cells create ME and NLOT, where the neurons are densely arranged. CE and CO occupy intermediate positions, with the neurons similar in size to the mean for the guinea pig CA.
Over the past decade we used genetic manipulations to study the contribution of GABAergic interneurones for rhythmic synchronous activity. We focused on the hippocampus on the medial entorhinal cortex, two brain structures that are crucially involved in spatial coding and spatial memory. Genetic manipulations included ablations of glutamate receptors or electrical coupling in GABAergic interneurones in the whole forebrain, or locally in the hippocampal‑entorhinal formation. Our studies underline the functional role of local GABAergic interneurones for spatial or temporal coding in the hippocampus. The genetic manipulations were always associated with distinct spatial memory deficits. These results will be summarized and discussed in the context of current models of memory formation and storage. In addition, I will present data demonstrating the presence of long-range GABAergic cells that connect the hippocampus and entorhinal cortex reciprocally. Also these data will be discussed in a larger context, since there is good reason to believe that long-range GABAergic neurones are more abundant in the forebrain as previously thought. Most recent studies in the lab focus on long-range GABA that connect several cortical areas involved in pain perception. By virtue of their connectivity – the target cells are most often local interneurones – this class of cells is ideally suited to synchronize brain regions over long distance.
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The role of arginine vasopressin (AVP) dialyzed into the hippocampus or caudate nucleus as the reference structure in the acquisition and extinction of the conditioned eyelid reflex in rabbit was investigated. Phonopneumatic stimulator was used for the generation of conditioned and unconditioned stimuli, and for control of the recorder. Opto-electronic sensor transduced the behavioral responses. Microdialysis probes were chronically implanted into the brain structures. AVP was dialyzed into the brain structures during the extinction procedure. Restraining of the process of extinction was shown during AVP dialysis through the hippocampus and caudate nucleus but the effect in hippocampus was stronger and longer lasting than in caudate nucleus. The influence of AVP dialyzed through the hippocampus on the course of acquisition was biphasic. Some insignificant improvement of learning was observed at the beginning of training and then compensatory, significant restraining of learning. After AVP dialysis through the caudate nucleus only the late, insignificant tendency to improve learning was shown. The effects of AVP were dose-dependent in inversely proportional manner and long-term in nature, especially the effects in hippocampus.
Intracranial physiological calcifications are unaccompanied by any evidence of disease and have no demonstrable pathological cause. They are often due to calcium and sometimes iron deposition in the blood vessels of different structures of the brain. Computed tomography (CT) is the most sensitive means of detection of these calcifications. The aim of this study was the assessment of intracranial physiological calcifications in adults. We studied 1569 cases ranging in age from 15 to 85 in Tabriz Imam Khomeini Hospital, Iran. These patients had a history of head trauma and their CT scan did not show any evidence of pathological findings. The structures evaluated consisted of (A) the pineal gland, (B) the choroid plexus, (C) the habenula, (D) the basal ganglia, (E) the tentorium cerebelli, sagittal sinus and falx cerebri, (F) vessels and (G) lens and other structures which could be calcified. Of the 1569 subjects, 71.0% had pineal calcification, 66.2% had choroid plexus calcification, 20.1% had habenular calcification, 7.3% had tentorium cerebelli, sagittal sinus or falx cerebri calcifications, 6.6% had vascular calcification, 0.8% had basal ganglia calcification and 0.9% had lens and other non-defined calcifications. In general, the frequency of intracranial physiological calcifications was greater in men than in women. All types of calcification increased at older ages except for lens and other non-defined calcifications. We evaluated all the cranial structures and determined percentages for all types of intracranial physiological calcification. These statistics can be used for comparing physiological and pathological intracranial calcifications. Moreover, these statistics may be of interest from the clinical perspective and are potentially of clinical use.
1,2,3,4-Tetrahydroisoquinolines, among them the most interesting neuroprotective substance, an inhibitor of MAO, 1-methyl-1,2,3,4-tetrahydroisoquinoline (1MeTIQ), are endogenous compounds present in the central nervous system of mammals and humans. In this study, we investigated the effect of 1MeTIQ on morphine-induced analgesia, tolerance and abstinence syndrome as well as its effect on morphine-induced changes in dopamine metabolism in rat brain structures (nucleus accumbens, striatum, substantia nigra) using HPLC methodology. The experiments were carried out on male Wistar rats. Morphine analgesia was measured in the “hot-plate” test. To induce tolerance, morphine was given chronically (20 mg/kg i.p.) alone or following 1MeTIQ (50 mg/kg i.p.) injection. The development of dependence was assessed in the naloxone (2 mg/kg i.p.) precipitation test, after 10 days of morphine administration. The behavioral studies have shown that an endogenous compound, 1MeTIQ produced strong potentiation of morphine analgesia, prevented the development of morphine tolerance and inhibited expression of morphine abstinence syndrome in morphine-dependent rats. In neurochemical studies, we have demonstrated that 1MeTIQ antagonized morphine-induced changes in dopamine metabolism observed in rat brain structures. The main finding of this study was demonstration for the first time of an anti-abuse effect of an endogenous compound, 1MeTIQ, and its efficiency in counteracting morphine-induced addiction in the way useful from clinical point of view. The obtained results suggested a possibility of clinical application of 1MeTIQ in morphine addiction.
The shape of the inferior horn of the lateral ventricle has been investigated in 100 (50right and 50 left) human brain hemispheres which were fixed in 40% formaldehyde solution and cut frontally. It has been found that the shape of the inferior horn depends on the course and depth of the collateral and occipitotemporal sulci. In most cases a part from two main ventricular surfaces: The hippocampal and superolateral, there is one surface more, either the inferior - collateral eminence (Type I - 97% of cases in the posterior part of the inferior horn, 49%- in the middle and 42%- in the anterior part) or the inferolateral, adjacent to the occipitotemporal sulcus ( Type II- 0%, 26% and 35%, respectively). In a few cases both collateral eminence and inferolateral surfaces were present (Type III- 3% , 2% and 6% respectively). In type IV neither collateral eminence nor the inferolateral surface appeared (0%, 23%, 17% respectively). The authors suggest to designate the inferolateral surface, not mentioned in the literature, as the occipitotemporal eminence (of the inferior horn).
Insulin insufficiency and increased glucose levels are the major features of diabetes type 1 leading to cognitive dysfunctions and neurodegeneration. A reason why different brain structures are characterized by diverse response to increased glucose level is not known. Our previous study showed increased ceramide levels in the brains of rats with diabetes induced by streptozotocin (STZ) injection, which was abolished by myriocin, the inhibitor of serine palmitylotransferase. Ceramides may be important mediators of neuropathological changes and its elevation was found in many brain disorders. The main goal of our present study was to verify if hippocampus, prefrontal cortex and cerebellum response differently to hyperglycemia/hypoinsulinemia in terms of changes in sphingolipids concentrations. We attempted to identify potential source of ceramides by measuring the sphingomyelinase concentrations and by blocking the ceramide de novo synthesis pathway. We found that in cerebellum and hippocampus of hyperglycemic animals sphingolipids concentrations underwent subtle modifications while prefrontal cortex exhibited massive changes in ceramides and SMs content. Total ceramide levels was significantly elevated in prefrontal cortex of diabetic rats, which was reduced by myriocin, while rats exposed to STZ showed only small increase of total SM in this brain structure. The increased content of ceramides containing SAFAs (saturated fatty acids) in prefrontal cortex was diminished by myriocin. SAFA-contained SMs did not present changes. Elevation of MUFA- (monounsaturated fatty acids), and PUFA-ceramides (polyunsaturated fatty acids) in prefrontal cortex of STZ-treated rats was reduced by myriocin, similarly as MUFA-SMs augmentation. PUFA-ceramides and PUFA-SMs experienced only slight modifications. Both – ceramides and omega-6 – SMs increased dramatically and were downregulated by myriocin. We conclude that the prefrontal cortex may be particularly sensitive to hyperglycemic conditions and hypoinsulinemia. Moreover, the novo synthesis seems to be an important pathway of ceramide generation since usage of myriocin strongly reduced ceramide levels enhanced by STZ injection. Augmentation in ceramide content was correlated with enhancement of SMs production. These unexpected results may be explained by the incorporation of redundant ceramides into SMs, a mechanism by which the toxic level of ceramides is reduced in the brain. Supported by grant 123-27575 P from the State Committee for Scientific Research, Warsaw, Poland
Multituberculate and eutriconodontan endocasts differ from those of primitive therian mammals in their lack of visible midbrain exposure on the dorsal side and in having a vermis−like triangular bulge (recognized herein as the cast of a large sinus—the superior cistern) inserted between the cerebral hemispheres. As the shape and proportions of multituberculate, eutriconodontan, and Cretaceous eutherian endocasts are otherwise similar, one might speculate that the multituberculate and eutriconodontan brains did not differ essentially from those of primitive eutherian and marsupial mammals, in which the midbrain is exposed dorsally. This conclusion might have important phylogenetic implications, as multituberculates and eutriconodontans may lay closer to the therians sensu strico, than hitherto believed. We describe an endocast of the Late Cretaceous multituberculate Kryptobaatar, which differs from those of other multituberculates (Ptilodus, Chulsanbaatar, and Nemegtbaatar) in having unusually long olfactory bulbs and the paraflocculi elongated transversely, rather than ball−shaped. We estimate the encephalization quotient (EQ) of Kryptobaatar, using: 1) Jerison’s classical equation (1) based on estimation of endocranial volume and body mass; 2) McDermott et al.’s derived body mass estimation equation (2) using upper molar lengths; and 3) estimation of body mass based on new equations (3a, 3b, 3c, and 3d₁₋₉), which we propose, using measurements of the humerus, radius, ulna, femur and tibia. In both Jerison’s method and a mean of our series of derived formulae, the EQ varies around 0.71, which is higher than estimated for other multituberculate mammals. It remains an open question whether the evolutionary success of Kryptobaatar(which was a dominant mammal during the ?early Campanian on the Gobi Desert and survived until the ?late Campanian) might have been related to its relatively high EQ and well developed sensorimotor adaptations, in particular olfaction and coordinated movements.
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