Afferent axons and their relations with neurons in the nucleus lateralis of the cerebellum: A light microscopic study

Summary The axons of Purkinje cells are the sole corticonuclear afferents to the lateral nucleus. The terminal arborizations of these axons consist of many (30–50) varicose branchlets, which issue from a thick, myelinated parent axon. Each terminal plexus fills a conical field which penetrates the lateral nucleus radially encompassing the cell bodies and parts of the dendritic trees of approximately 40 neurons. The fields of neighboring Purkinje axons overlap considerably. The non-cortical axons are simple, usally unbranched varicose fibers of three sizes: (1) thick, with large varicosities, (2) medium sized with smaller varicosities, or (3) fine, delicate threads with beadlike varicosities. These axons cross the dendritic trees of successive neurons as they penetrate into the nucleus in a radial fashion.The configuration of the dendritic trees of neurons in the various parts of the nucleus—the multipolar neurons and the columnar neurons—can be related to the conical shape of the Purkinje axonal plexus. It is suggested that the organization of converging Purkinje cell axonal fields determines the pattern of input to the cells of the lateral nucleus, rather than the topographical arrangement of Purkinje cells in the cortex. The terminal arborizations of Purkinje cell axons adjacent to one another in the lateral nucleus need not necessarily arise from neighboring Purkinje cells in the cerebellar cortex.The relationships between neurons in the central columnar zone and in the swirled zones of the lateral nucleus with the two classes of afferents are discussed. It is suggested that by virtue of their slender profiles, each of the large columnar neurons falls into the field of one Purkinje cell axonal cone whereas elsewhere, the multipolar neurons tend to share their well spread dendrites with neighboring Purkinje axonal fields. The small neurons that span columns in the central zone are oriented to sample larger numbers of axonal inputs than are adjacent columnar neurons.Supported in part by U.S. Public Health Service Research Grants NS10536, NS03659, Training Grant NS 05591 from the National Institute of Neurological Diseases and Stroke, and a William F. Milton Fund Award from Harvard University.     

The Orienting Response as Novelty and Significance Detector: Reply to O''Gorman

O'Goiman's (1979) criticisms of the orienting response (OR) significance hypothesis are not well-founded. The hypothesis is not based solely on electrodermal data—studies reporting significance effects for heart rate and pupillary OR are cited. The hypothesis does not discard novelty but suggests that an interaction between uncertainty and significance triggers OR. Differential reactivity across OR components reflects stimulus- and individual-response factors, and does not require separate “significance registers.” Since the hypothesis specifically maintains that appraisals of stimulus significance affect the OR, not the mere fact of cognitive appraisal per se, no general “cognitive appraisal effect” was ever expected. O'Gorman confuses the difficulty of estimating the subject's spontaneous judgments of significance with the relative ease of manipulating significance in the laboratory. He considers classic OR theory more “objective” only because he fails to look closely enough at the complex judgmental processes involved in stimulus intake, model building, and matching functions. O'Gorman's contentions of different initial- and test-ORs, and of a simple additive relationship between significance and OR, lack supportive data and are challenged by available evidence. Literature is cited suggesting that: a) scanning is continuously biased toward the detection of significant stimuli; b) detection of a sgnificant stimulus feature triggers increased information scanning, increasing the possibility that previously unrecognized uncertainty will be detected, and c) lowers the criterion level of the OR “threshold,” increasing the likelihood of OR if uncertainty is detected. Evidence is cited suggesting that the significance-OR, and perhaps attention in general, is mediated by neocortical-limbic interaction, the limbic' “motivational” evaluator of stimulus input steering and switching neocortical “intellectual” analyzers of stimulus pattern.     

Development and testing of a simple algorithm for a glucose clamp

The glucose clamp technique is widely used in clinical research studies to maintain a constant blood glucose (BG) level during metabolic perturbation. An algorithm is used to set the rate of an intravenous glucose infusion according to measured BG concentrations. Currently used clamp algorithms are unnecessarily complex. This paper describes the development and use of a new algorithm which is simpler to implement. The algorithm employs proportional and differential feedback control. Discrete BG sampling with a sampling period of 5 min is used. Computer simulation with a two-compartment model of glucose dynamics was used to refine the algorithm. A Monte Carlo approach was adopted to examine the effects of random variations in measured BG concentrations and the elapsed time between blood sampling and adjustment of the glucose infusion rate. A coefficient of variation in BG concentration of less than 4 per cent was predicted for a euglycemic clamp. This was confirmed when the algorithm was applied in clinical research studies. This degree of BG control compares well with other published algorithms.     

Ultrastructural features of the myocardium of newborn mini-pigs after chronic parental alcoholization

Department of Mini-Pig Models, Research Laboratory of Experimental Biological Models, Academy of Medical Sciences of the USSR, Krasnogorsk, Moscow Region. (Presented by Academician of the Academy of Medical Sciences of the USSR A. P. Avtsyn.) Translated from Byulleten' Éksperimental'noi Biologii i Meditsiny, Vol. 109, No. 4, pp. 398–400, April, 1990.     

Silicon neuron simulation with SPICE: tool for neurobiology and neural networks

The paper deals with computer simulations of ‘silicon neurons’, which are assemblies of CMOS circuits that generate the equivalents of the ionic currents and of the action potentials of real (biological) neurons. The circuit simulation program SPICE is used to simulate the generation of action potentials by a silicon neuron. Moreover, the equivalent circuits of silicon synapses are described and the behaviours of simple two- and three-neuron networks are analysed. Implications for the areas of neurobiology and formal neural networks are briefly considered.     

Summary of a National Institute of Mental Health workshop: developing animal models of anxiety disorders

RATIONALE: There exists a wide range of animal models and measures designed to assess anxiety or fearfulness. However, the relationship between these models and clinical anxiety symptoms and syndromes is unclear. The National Institute of Mental Health convened a workshop to discuss the relationship between existing behavioral models of anxiety and the clinical profile of anxiety disorders. A second goal of this workshop was to outline various approaches towards modeling components of anxiety disorders. OBJECTIVES: To briefly describe epidemiological and behavioral manifestations of clinical anxiety syndromes and how they relate to commonly employed animal models of anxiety. To describe approaches and considerations for developing, improving, and adapting anxiety models to better understand the neurobiology of anxiety. METHODS: Clinicians, psychiatrists and clinical and basic neuroscientists presented data exemplifying different approaches towards understanding anxiety and the role of animal models. Panel members outlined what they considered to be critical issues in developing and employing animal models of anxiety. RESULTS: This review summarizes the discussions and conclusions of the workshop including recommendations for improving upon existing models and strategies for developing novel models. CONCLUSIONS: The probability of developing comprehensive animal models that accurately reflect the relative influences of factors contributing to anxiety disorder syndromes is quite low. However, ample opportunity remains to better define and extend existing models and behavioral measures related to specific processes that may be disrupted in anxiety disorders and to develop new models that consider the impact of combined factors in determining anxious behaviors.     

不同温度处理肌桥修复周围神经效果的比较

用变性骨骼肌桥修复周围神经缺损。为比较不同温度处理骨骼肌桥的优劣，用热变性和冷变性的方法处理大鼠的骨骼肌桥。桥接１～３个月后对大鼠桥接神经作大体观察、神经电生理检测及组织学检查。结果表明，冷变性－１９６℃组在自主运动恢复，再生神经传导速度及再生神经纤维的数量、质量诸方面均明显优于热变性６０℃组和４５℃组。     

Anxiety-like behaviour in mice exposed to tannery wastewater: The effect of photoelectrooxidation treatment

The leather industry is a major producer of wastewaters and releases large quantities of many different chemical agents used in hide processing into the environment. Since the central nervous system is sensitive to many different contaminants, our aim was to investigate the neurobehavioral effects of exposure of mice to tannery effluents using animal models of depression and anxiety, namely forced swim and elevated plus-maze. In order to propose a clean technology for the treatment of this effluent, we also investigated the exposure of mice to effluents treated by photoelectrooxidation process (PEO). Adult male Swiss albino mice (CF1 strain) were given free access to water bottles containing an effluent treated by a tannery (non-PEO) or PEO-treated tannery wastewater (0.1 and 1% in drinking water). Exposure to tannery wastewater induced behavioural changes in the mice in elevated plus-maze. Exposure to non-PEO 1% decreased the percentage of time spent in the open arms, indicating anxiety-like behaviour. Exposure to tannery wastewater did not alter immobility time in the forced swim test, suggesting that tannery effluents did not induce depression-like behaviour in the mice. These behavioural data suggest that non-PEO tannery effluent has an anxiogenic effect, whereas PEO-treated tannery effluents do not alter anxiety levels.