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B Schürmann

Publications and source records attributed to B Schürmann.

15 recordsLinked to original sources

A hierarchical neural system with attentional top-down enhancement of the spatial resolution for object recognition.

We present a hierarchical neurodynamical system for object recognition based on attentional control of the spatial resolution with which an object is analyzed during an iterative hypothesis testing cycle. Psychophysical evidence strongly suggests that attentional processing results in the enhancement of the spatial resolution in the input region corresponding to the focus of attention. We adopt a computational neuroscience approach in order to analyze this attentional enhancement of the spatial resolution for object recognition. The system consists of a where- and a what-module which include networks with feedforward and feedback interconnections describing the mutual links between different areas of the visual cortex.

Attention↗

A neuro-cognitive visual system for object recognition based on testing of interactive attentional top-down hypotheses.

We propose an extension of a systemic model for object recognition formulated by Rybak et al (1998 Vision Research 38 2387-2400) which is based on the functional organisation of the visual systems in primate brains. In contrast to the learning and recognition scheme of Rybak et al we do not assume a behavioural paradigm, i.e. a visuomotor programmed scanpath that determines the sequence of foveation on the different parts of the object. As in the basis architecture of Rybak et al, the system modules are separated into 'what'-like subsystems corresponding to the ventral occipito-inferotemporal visual path and 'where'-like complexes analogous to the dorsal occipito-parietal visual path. The 'what' system analyses local features in the actual foveation as in Rybak et al. But, in our case, the 'where' memory, instead of programming a behavioural scanpath, scores the spatial relationship between successive fixation and the spatial relationship between the associated main edges. The recognition is based on the identification of parts and their spatial relationship. This gives the learning and recognition mechanisms more flexibility in the sense that, for recognising an object, several different fixation sequences may be accepted.

Cognition↗

Spatiotemporal coding in the cortex: information flow-based learning in spiking neural networks.

We introduce a learning paradigm for networks of integrate-and-fire spiking neurons that is based on an information-theoretic criterion. This criterion can be viewed as a first principle that demonstrates the experimentally observed fact that cortical neurons display synchronous firing for some stimuli and not for others. The principle can be regarded as the postulation of a nonparametric reconstruction method as optimization criteria for learning the required functional connectivity that justifies and explains synchronous firing for binding of features as a mechanism for spatiotemporal coding. This can be expressed in an information-theoretic way by maximizing the discrimination ability between different sensory inputs in minimal time.

Action Potentials↗

The coding of information by spiking neurons: an analytical study.

We analyse analytically the coding of information by a spiking neuron. The emphasis is on the question of how many spikes are necessary for the reliable discrimination of two different input signals. The discrimination ability is measured by the second-order Rényi mutual information between the random variable describing the name of the signal and a sequence of n output spikes. Analysing this measure as a function of n, we study the coding strategy of a single spiking neuron, with the following main results. A small number of output spikes is required for efficient discrimination of input signals, i.e. for encoding them, if the separation is easy; a large number of output spikes is required in the difficult case of separation of very similar input signals. Three different versions of the spike response model of a single neuron are studied. The approach presented can be regarded as a non-parametric version of the reconstruction method of Bialek.

Action Potentials↗

Differential modulation of AMPA receptor mediated currents by evans blue in postnatal rat hippocampal neurones.

1. The modulation of non-N-methyl-D-aspartate (NMDA) receptor-mediated whole cell currents and of glutamatergic synaptic transmission by purified Evans Blue (EB) was investigated in rat cultured postnatal hippocampal neurones by use of patch clamp recordings and a fast drug application system. 2. Three different groups of neurones could be distinguished with respect to the type of modulation obtained with 10 microM EB: EB was either a predominant inhibitor of desensitization (13% of the neurones), a predominant inhibitor of current amplitudes (42%) or a mixed inhibitor of both properties (45%). Both effects were not use-dependent and reached maximal levels after 30 s of pre-equilibration with the diazo dye. 3. Dose-response curves obtained from glutamate activated whole cell currents yielded an IC50 value for EB of 13.3 microM (Hill coefficient: 1.3) for the inhibition of desensitization, and an IC50 value of 10.7 microM (Hill coefficient: 1.2) for the inhibition of current amplitudes. 4. Chicago acid SS (100 microM) which is one of the synthesis precursors of EB had no effect on current amplitudes of glutamate activated whole cell currents but was a weak inhibitor of desensitization in all hippocampal neurones investigated, irrespective of the type of modulation obtained with EB in the same neurone. 5. Oxidatively modified EB (the so-called VIMP (10 microM)) had no effect on the kinetics but was a partial inhibitor of glutamate-activated whole cell currents in all hippocampal neurones investigated. 6. EB (10 microM) inhibited the amplitudes of non-NMDA receptor mediated autaptic currents to the same extent (to 39 +/- 19% of control) as observed for glutamate activated whole cell currents (to 41 +/- 17% and 56 +/- 20%). However, the decay of the autaptic responses remained uninfluenced upon EB application, indicating that either receptor desensitization does not dominate the time course of the synaptic response or that the non-NMDA receptors sensitive to modulation of desensitization by EB are not present in the postsynaptic membrane. 7. In conclusion, EB differentially modulates alpha-amino-3-hydroxy-5-methyl -4-isoxazole propionic acid (AMPA) receptor gating in different subsets of neurones. Upon identification of the cellular determinants for the differential modulation (e.g. AMPA receptor subunit composition) EB could become a useful tool to investigate receptor subtypes during electrophysiological recordings.

Animals↗

[Immunohistochemical demonstration of extracerebral toxoplasmosis in AIDS].

Tissue slides obtained at autopsy from 80 cases with AIDS were studied immunhistochemically for infection with Toxoplasma gondii. In 35 cases (43.75%) toxoplasmosis could be found: in 22 cases (27.5%) only cerebral, in 9 cases (11.25%) cerebral and extracerebral and in 4 cases (5%) only extracerebral. Necrotizing lesions, due to the parasite could be seen in brain, heart, lungs, pancreas, adrenal glands and testis, only intracellular trophozoites without tissue damage in GIT, liver, lymphnodes, spleen, prostate, kidney and gl. parotis. The trophozoites and pseudocysts could be clearly demonstrated by immunohistochemistry.

Acquired Immunodeficiency Syndrome↗

[Clinical significance of the short-term incubation test for the therapy of metastatic breast cancer].

Between January 1978 and October 1980 97 tissue samples of histologically verified carcinoma of the breast were received for performance of the short-term incubation test. 25 tumour samples could not be prepared as cell suspension sufficient for testing. Among the 72 performed tests there were 9 with stimulation of 3H-uridine uptake by doxorubicin. Thus only 63 tests could be evaluated. Results were correlated with clinical data of the patients. No significant correlations could be established between tumour stage at time of diagnosis, age, menopausal state, receptor state, and the test result. There was also no differentiation between favourable and unfavourable prognoses as regards free interval and rate of survival. A correlation between results of tests and success or failure of cytostatic treatment could not be ascertained.

Adult↗