Az első hazai bázisközösségek : a Bulányi-jelenség és a Katolikus Egyház az 50-es évek elején

The activities of György Bulányi piarist priest in the 1970s and 1980s and the so-called “Bokor” (Bush) basic community that he founded have been explored in scholarly literature. However, research has not paid enough attention to the period of 1945-1952 when Bulányi was involved in establishing and organising fellowship groups. This paper is an attempt to fill this gap by examining so for neglected, mainly state security papers (trial minutes) that have been barred from researchers before. The aforementioned period saw the development of the first Hungarian youth basic communities, in which almost all Catholic teaching orders and the leaders of the earlier Catholic youth movements played important roles. The youth work was coordinated via the regular meetings of the leaders of the Catholic youth movements and the Actio Catholica. In 1952 the imprisonment and conviction of Bulányi and his fellow leaders resulted in the termination of the nationally organised activities of the basic communities

Tanulással összefüggő előagyi rendszerek madarakban = Learning-associated forebrain systems in birds

A kutatóprogram a viselkedés motivációjának idegi alapjait vizsgálja multidiszciplináris megközelítéssel, madár idegrendszeri modell felhasználásával. A vizsgálatból extrapolálható eredmények felhasználhatók az emlős viszonyok leírására és értelmezésére is. A kutatócsoport korábbi nemzetközi tapasztalataira épülő program megvalósításával a következő területeken értünk el eredményeket: (1) A tanulással és motivációval összefüggő agyterületek (thalamus, septum, nucl. accumbens, ventralis tegmentalis area) funkciós morfológiai jellemzése. Ezen belül a jutalmazásban és addikcióban kulcsszerepet játszó nucleus accumbens pontos lokalizációja, szubdiviziói és kapcsolatrendszerének feltárása madarakon, valamint az amygdalo-accumbens pályarendszer elhárító tanulásban játszott szerepének igazolása; (2) Dopaminerg és dopaminoceptív neuronrendszerek szerepe háziszárnyas tanulási és motivációs folyamataiban. Dopamin receptor antagonisták hatása a memória retenciójára. Striato-tegmentalis pályarendszerek és szelektív projekciókkal rendelkező neuronjaik jellemzése. (3) A serkentő neurotranszmitterek és a dopamin striatalis kölcsönhatása, motivációban, döntéshozatalban és tanulásban játszott szerepe. Az aszpartát sajátos magatartásfüggő szerepének kimutatása a striatum és a törzsdúcok neurális hálózatában. (4) Cannabinoid receptorok megoszlása és a tanulási folyamatra gyakorolt hatása. | In the research program we investigated the neural foundations of motivation, using multidisciplinary approach and the avian nervous system as a model. The results extrapolated from the study may be adapted also for the description and interpretation of mammalian systems. Based upon international experience of the group, progress has been made primarily in the following areas: (1) Functional morphological characterisation of learning and behaviour associated brain regions (thalamus, septum, nucl. accumbens, ventral tegmental area). In particular, precise localization of the nucleus accumbens, its subdivisions and connectivity, and evidence for the role of amygdalo-accumbens pathway in avoidance learning. (2) The role of dopaminergic and dopaminoceptive neuronal systems in learning and motivation of domestic chicks. Effect of dopamine receptor antagonists on memory retention. Characterisation of striato-tegmental pathways and neurons with selective projections. (3) Striatal interaction between excitatory transmitter amino acids and dopamine, its role in motivation, decision-making and learning. Verification of specific behaviour-linked effect of the excitatory transmitter aspartate in the neural circuits of striatum and basal ganglia. (4) Tissue distribution of cannabinoid receptors and their effect on the learning process

Human keratinocytes are vanilloid resistant

BACKGROUND: Use of capsaicin or resiniferatoxin (RTX) as analgesics is an attractive therapeutic option. RTX opens the cation channel inflammatory pain/vanilloid receptor type 1 (TRPV1) permanently and selectively removes nociceptive neurons by Ca(2+)-cytotoxicity. Paradoxically, not only nociceptors, but non-neuronal cells, including keratinocytes express full length TRPV1 mRNA, while patient dogs and experimental animals that underwent topical treatment or anatomically targeted molecular surgery have shown neither obvious behavioral, nor pathological side effects. METHODS: To address this paradox, we assessed the vanilloid sensitivity of the HaCaT human keratinocyte cell line and primary keratinocytes from skin biopsies. RESULTS: Although both cell types express TRPV1 mRNA, neither responded to vanilloids with Ca(2+)-cytotoxicity. Only ectopic overproduction of TRPV1 rendered HaCaT cells sensitive to low doses (1-50 nM) of vanilloids. The TRPV1-mediated and non-receptor specific Ca(2+)-cytotoxicity ([RTX]>15 microM) could clearly be distinguished, thus keratinocytes were indeed resistant to vanilloid-induced, TRPV1-mediated Ca(2+)-entry. Having a wider therapeutic window than capsaicin, RTX was effective in subnanomolar range, but even micromolar concentrations could not kill human keratinocytes. Keratinocytes showed orders of magnitudes lower TRPV1 mRNA level than sensory ganglions, the bona fide therapeutic targets in human pain management. In addition to TRPV1, TRPV1b, a dominant negative splice variant was also noted in keratinocytes. CONCLUSION: TRPV1B expression, together with low TRPV1 expression, may explain the vanilloid paradox: even genuinely TRPV1 mRNA positive cells can be spared with therapeutic (up to micromolar) doses of RTX. This additional safety information might be useful for planning future human clinical trials