<?xml version="1.0" encoding="UTF-8" standalone="no" ?>
<rss version="2.0">
  <channel>
    <title>Ruigrok, T.J.H.</title>
    <link>http://repub.eur.nl/res/aut/7536/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>The cerebellar nuclei take center stage (Article)</title>
      <link>http://repub.eur.nl/res/pub/34334/</link>
      <pubDate>2011-12-01T00:00:00Z</pubDate>
      <description></description>
    </item> <item>
      <title>Spontaneous activity signatures of morphologically identified interneurons in the vestibulocerebellum (Article)</title>
      <link>http://repub.eur.nl/res/pub/23603/</link>
      <pubDate>2011-01-12T00:00:00Z</pubDate>
      <description>Cerebellar cortical interneurons such as Golgi cells, basket cells, stellate cells, unipolar brush cells, and granule cells play an essential role in the operations of the cerebellum. However, detailed functional studies of the activity of these cells in both anesthetized and behaving animals have been hampered by problems in recognizing their physiological signatures. We have extracellularly recorded the spontaneous activity of vestibulocerebellar interneurons in ketamine/xylazine-anesthetized rats and subsequently labeled them with Neurobiotin using the juxtacellular technique. After recovery and morphological identification of these cells, they were related to statistical measures of their spontaneous activity. Golgi cells display a somewhat irregular firing pattern with relatively low average frequencies. Unipolar brush cells are characterized by more regular firing at higher rates. Basket and stellate cells are alike in their firing characteristics, which mainly stand out by their irregularity; some of them are set apart by their very slow average rate. The spontaneous activity of interneurons examined in the ketamine/xylazine rabbit fit within this general pattern. In the rabbit, granule cells were identified by the spontaneous occurrence of extremely high-frequency bursts of action potentials, which were also recognized in the rat. On the basis of these observations, we devised an algorithm that reliably determined the identity of 75% of the cells with only 2% incorrect classifications. The remaining cells were placed into border categories within which no classification was attempted. We propose that this algorithm can be used to help classify vestibulocerebellar interneurons recorded in awake, behaving animals.</description>
    </item> <item>
      <title>Encoding of whisker input by cerebellar Purkinje cells (Article)</title>
      <link>http://repub.eur.nl/res/pub/27666/</link>
      <pubDate>2010-10-01T00:00:00Z</pubDate>
      <description>The cerebellar cortex is crucial for sensorimotor integration. Sensorimotor inputs converge on cerebellar Purkinje cells via two afferent pathways: the climbing fibre pathway triggering complex spikes, and the mossy fibre-parallel fibre pathway, modulating the simple spike activities of Purkinje cells. We used, for the first time, the mouse whisker system as a model system to study the encoding of somatosensory input by Purkinje cells. We show that most Purkinje cells in ipsilateral crus 1 and crus 2 of awake mice respond to whisker stimulation with complex spike and/or simple spike responses. Single-whisker stimulation in anaesthetised mice revealed that the receptive fields of complex spike and simple spike responses were strikingly different. Complex spike responses, which proved to be sensitive to the amplitude, speed and direction of whisker movement, were evoked by only one or a few whiskers. Simple spike responses, which were not affected by the direction of movement, could be evoked by many individual whiskers. The receptive fields of Purkinje cells were largely intermingled, and we suggest that this facilitates the rapid integration of sensory inputs from different sources. Furthermore, we describe that individual Purkinje cells, at least under anaesthesia, may be bound in two functional ensembles based on the receptive fields and the synchrony of the complex spike and simple spike responses. The 'complex spike ensembles' were oriented in the sagittal plane, following the anatomical organization of the climbing fibres, while the 'simple spike ensembles' were oriented in the transversal plane, as are the beams of parallel fibres. © 2010 The Authors. Journal compilation </description>
    </item> <item>
      <title>Differential olivo-cerebellar cortical control of rebound activity in the cerebellar nuclei (Article)</title>
      <link>http://repub.eur.nl/res/pub/27279/</link>
      <pubDate>2010-05-04T00:00:00Z</pubDate>
      <description>The output of the cerebellar cortex is controlled by two main inputs, (i.e., the climbing fiber and mossy fiber-parallel fiber pathway) and activations of these inputs elicit characteristic effects in its Purkinje cells: that is, the so-called complex spikes and simple spikes. Target neurons of the Purkinje cells in the cerebellar nuclei show rebound firing, which has been implicated in the processing and storage of motor coordination signals. Yet, it is not known to what extent these rebound phenomena depend on different modes of Purkinje cell activation. Using extracellular as well as patch-clamp recordings, we show here in both anesthetized and awake rodents that simple and complex spike-like train stimuli to the cerebellar cortex, as well as direct activation of the inferior olive, all result in rebound increases of the firing frequencies of cerebellar nuclei neurons for up to 250 ms, whereas single-pulse stimuli to the cerebellar cortex predominantly elicit well-timed spiking activity without changing the firing frequency of cerebellar nuclei neurons. We conclude that the rebound phenomenon offers a rich and powerful mechanism for cerebellar nuclei neurons, which should allow them to differentially process the climbingfiber andmossyfiber inputs in a physiologically operating cerebellum.</description>
    </item> <item>
      <title>Ins and Outs of Cerebellar Modules (Article)</title>
      <link>http://repub.eur.nl/res/pub/28505/</link>
      <pubDate>2010-03-16T00:00:00Z</pubDate>
      <description>The modular concept of cerebellar connections has been advocated in the lifetime work of Jan Voogd. In this concept, a cerebellar module is defined as the conglomerate of one or multiple and non-adjacent, parasagittally arranged zones of Purkinje cells, their specific projection to a well-defined region of the cerebellar nuclei, and the climbing fiber input to these zones by a well-defined region of the inferior olivary complex. The modular organization of these olivo-cortico-nuclear connections is further exemplified by matching reciprocal connections between inferior olive and cerebellar nuclei. Because the different regions of the cerebellar nuclei show highly specific output patterns, cerebellar modules have been suggested to constitute functional entities. This idea is strengthened by the observation that anatomically defined modules adhere to the distribution of chemical markers in the cerebellar cortex suggesting that modules not only differ in their input and output relations but also may differ in operational capabilities. Here, I will briefly review some recent data on the establishment of cerebellar modules in rats. Furthermore, some evidence will be shown suggesting that the other main afferent system (i.e., mossy fibers), at least to some extent, also adheres to the modular organization. Finally, using retrograde transneuronal tracing with rabies virus, some evidence will be provided that several cerebellar modules may be involved in the control of individual muscles. </description>
    </item> <item>
      <title>Multiple cerebellar zones are involved in the control of individual muscles: A retrograde transneuronal tracing study with rabies virus in the rat (Article)</title>
      <link>http://repub.eur.nl/res/pub/29868/</link>
      <pubDate>2008-07-01T00:00:00Z</pubDate>
      <description>To identify cerebellar regions that are involved in the control of limb muscles, rabies virus was injected into the tibialis anterior (TA), the gastrocnemius (GC) or, for comparison, into the flexor digitorum (FD) muscles of the rat. Progression of retrograde transneuronal infection at supraspinal levels was assessed after variable time spans and was divided into three groups. Initially, infected neurons were observed in the reticular formation, lateral vestibular nucleus, red nucleus and motor cortex (group 1). Group 2 was characterized by labelling within the cerebellar nuclei as well as of two vermal strips of Purkinje cells (PCs). Double-labelling with zebrin enabled identification of these strips as the lateral part of the A1- and B-zone. For TA both zones were ipsilateral, whereas for GC the A1 strip predominated contralaterally. Group 3 infections showed additional labelling of multiple, in part bilateral, identifiable strips of PCs in vermis, paravermis and hemisphere. FD injections resulted in less robust labelling of vermal strips and more pronounced labelling within paravermal and hemispheral zonal regions. Only sporadic labelling in corresponding regions of the inferior olive and no labelling of cortical interneurons or granule cells was observed. Prolonged infection was seen to result in degeneration of PCs and possibly of motoneurons. We conclude that vermal, paravermal as well as hemispheral zones of the cerebellar cortex converge upon motoneurons that innervate a particular muscle. In addition, individual zones may control motorpools of different muscles and thus contribute to muscle synergies. </description>
    </item> <item>
      <title>Selective impairment of the cerebellar C1 module involved in rat hind limb control reduces step-dependent modulation of cutaneous reflexes (Article)</title>
      <link>http://repub.eur.nl/res/pub/29552/</link>
      <pubDate>2008-02-27T00:00:00Z</pubDate>
      <description>The cerebellum is divided into multiple parasagittally organized modules, which are thought to represent functional entities. How individual modules participate in cerebellar control of complex movements such as locomotion remains largely unknown. To a large extent, this is caused by the inability to study the contribution of individual modules during locomotion. Because of the architecture of modules, based on narrow, elongated cortical strips that may be discontinuous in the rostrocaudal direction, lesion of a complete module, without affecting neighboring modules, has not been possible. Here, we report on a new method for inducing a selective dysfunction of spatially separated parts of a single module using a small cortical injection of a retrogradely transported neurotoxin, cholera toxin b-subunit-saporin. We show that such a local injection into the C1 module results in climbing fiber and partial mossy fiber deafferentation of functionally related areas of this module, thereby resulting in a severe impairment of the whole module without affecting neighboring modules. A subsequent functional analysis indicates that such an impairment of the hindlimb part of the C1 module did not have a significant impact on skilled walking or overall stepping pattern. However, the modulation of cutaneously induced reflexes during stepping was severely diminished. We propose that the C1 module is specifically involved in the adaptive control of reflexes. Copyright </description>
    </item> <item>
      <title>Deformation of network connectivity in the inferior olive of connexin 36-deficient mice is compensated by morphological and electrophysiological changes at the single neuron level (Article)</title>
      <link>http://repub.eur.nl/res/pub/8440/</link>
      <pubDate>2003-01-01T00:00:00Z</pubDate>
      <description>Compensatory mechanisms after genetic manipulations have been documented
      extensively for the nervous system. In many cases, these mechanisms
      involve genetic regulation at the transcription or expression level of
      existing isoforms. We report a novel mechanism by which single neurons
      compensate for changes in network connectivity by retuning their intrinsic
      electrical properties. We demonstrate this mechanism in the inferior
      olive, in which widespread electrical coupling is mediated by abundant gap
      junctions formed by connexin 36 (Cx36). It has been shown in various
      mammals that this electrical coupling supports the generation of
      subthreshold oscillations, but recent work revealed that rhythmic activity
      is sustained in knock-outs of Cx36. Thus, these results raise the question
      of whether the olivary oscillations in Cx36 knock-outs simply reflect the
      status of wild-type neurons without gap junctions or the outcome of
      compensatory mechanisms. Here, we demonstrate that the absence of Cx36
      results in thicker dendrites with gap-junction-like structures with an
      abnormally wide interneuronal gap that prevents electrotonic coupling. The
      mutant olivary neurons show unusual voltage-dependent oscillations and an
      increased excitability that is attributable to a combined decrease in leak
      conductance and an increase in voltage-dependent calcium conductance.
      Using dynamic-clamp techniques, we demonstrated that these changes are
      sufficient to transform a wild-type neuron into a knock-out-like neuron.
      We conclude that the absence of Cx36 in the inferior olive is not
      compensated by the formation of other gap-junction channels but instead by
      changes in the cytological and electroresponsive properties of its
      neurons, such that the capability to produce rhythmic activity is
      maintained.</description>
    </item>
  </channel>
</rss>