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<pubDate>Sun, 27 Jul 2008 06:16:41 BST</pubDate>


	<title>CiteULike: awooga's Abbott</title>
	<description>CiteULike: awooga's Abbott</description>


	<link>http://www.citeulike.org/user/awooga/author/Abbott</link>
	<dc:publisher>CiteULike.org</dc:publisher>
	<dc:language>en-gb</dc:language>
	<dc:rights>Copyright &#169; 2004-2008 citeulike.org</dc:rights>
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        <rdf:li rdf:resource="http://www.citeulike.org/user/awooga/article/2605796"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/awooga/article/781429"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/awooga/article/1207953"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/awooga/article/233773"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/awooga/article/1268001"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/awooga/article/952053"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/awooga/article/419795"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/awooga/article/1002092"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/awooga/article/552756"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/awooga/article/554572"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/awooga/article/918558"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/awooga/article/915388"/>
        <rdf:li rdf:resource="http://www.citeulike.org/user/awooga/article/894205"/>

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<item rdf:about="http://www.citeulike.org/user/awooga/article/2605796">
    <title>Functional Significance of Long-Term Potentiation for Sequence Learning and Prediction</title>
    <link>http://www.citeulike.org/user/awooga/article/2605796</link>
    <description>&lt;i&gt;Cereb. Cortex, Vol. 6, No. 3. (1 May 1996), pp. 406-416.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Population coding, where neurons with broad and overlapping firing rate tuning curves collectively encode information about a stimulus, is a common feature of sensory systems. We use decoding methods and measured properties of NMDA-mediated LTP induction to study the impact of long-term potentiation of synapses between the neurons of such a coding array. We find that, due to a temporal asymmetry in the induction of NMDA-mediated LTP, firing patterns in a neuronal array that initially represent the current value of a sensory input will, after training, provide an experienced-based prediction of that input instead. We compute how this prediction arises from and depends on the training experience. We also show how the encoded prediction can be used to generate learned motor sequences, such as the movement of a limb. This involves a novel form of memory recall that is driven by the motor response so that it automatically generates new information at a rate appropriate for the task being performed. 10.1093/cercor/6.3.406</description>
    <dc:title>Functional Significance of Long-Term Potentiation for Sequence Learning and Prediction</dc:title>

    <dc:creator>Abbott</dc:creator>
    <dc:creator>Kenneth Blum</dc:creator>
    <dc:identifier>doi:10.1093/cercor/6.3.406</dc:identifier>
    <dc:source>Cereb. Cortex, Vol. 6, No. 3. (1 May 1996), pp. 406-416.</dc:source>
    <dc:date>2008-03-28T10:43:33-00:00</dc:date>
    <prism:publicationYear>1996</prism:publicationYear>
    <prism:publicationName>Cereb. Cortex</prism:publicationName>
    <prism:volume>6</prism:volume>
    <prism:number>3</prism:number>
    <prism:startingPage>406</prism:startingPage>
    <prism:endingPage>416</prism:endingPage>
    <prism:category>calcium</prism:category>
    <prism:category>line-attractor</prism:category>
    <prism:category>ltp</prism:category>
    <prism:category>nmda</prism:category>
    <prism:category>plasticity</prism:category>
    <prism:category>stdp</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/awooga/article/781429">
    <title>Extending the effects of spike-timing-dependent plasticity to behavioral timescales.</title>
    <link>http://www.citeulike.org/user/awooga/article/781429</link>
    <description>&lt;i&gt;Proc Natl Acad Sci U S A, Vol. 103, No. 23. (6 June 2006), pp. 8876-8881.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Activity-dependent modification of synaptic strengths due to spike-timing-dependent plasticity (STDP) is sensitive to correlations between pre- and postsynaptic firing over timescales of tens of milliseconds. Temporal associations typically encountered in behavioral tasks involve times on the order of seconds. To relate the learning of such temporal associations to STDP, we must account for this large discrepancy in timescales. We show that the gap between synaptic and behavioral timescales can be bridged if the stimuli being associated generate sustained responses that vary appropriately in time. Synapses between neurons that fire this way can be modified by STDP in a manner that depends on the temporal ordering of events separated by several seconds even though the underlying plasticity has a much smaller temporal window.</description>
    <dc:title>Extending the effects of spike-timing-dependent plasticity to behavioral timescales.</dc:title>

    <dc:creator>PJ Drew</dc:creator>
    <dc:creator>LF Abbott</dc:creator>
    <dc:identifier>doi:10.1073/pnas.0600676103</dc:identifier>
    <dc:source>Proc Natl Acad Sci U S A, Vol. 103, No. 23. (6 June 2006), pp. 8876-8881.</dc:source>
    <dc:date>2006-08-01T06:40:05-00:00</dc:date>
    <prism:publicationYear>2006</prism:publicationYear>
    <prism:publicationName>Proc Natl Acad Sci U S A</prism:publicationName>
    <prism:issn>0027-8424</prism:issn>
    <prism:volume>103</prism:volume>
    <prism:number>23</prism:number>
    <prism:startingPage>8876</prism:startingPage>
    <prism:endingPage>8881</prism:endingPage>
    <prism:category>reinforcement-learning</prism:category>
    <prism:category>stdp</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/awooga/article/1207953">
    <title>Drivers and modulators from push-pull and balanced synaptic input.</title>
    <link>http://www.citeulike.org/user/awooga/article/1207953</link>
    <description>&lt;i&gt;Prog Brain Res, Vol. 149 (2005), pp. 147-155.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;In 1998, Sherman and Guillery proposed that there are two types of inputs to cortical neurons; drivers and modulators. These two forms of input are required to explain how, for example, sensory driven responses are controlled and modified by attention and other internally generated gating signals. One might imagine that driver signals are carried by fast ionotropic receptors, whereas modulators correspond to slower metabotropic receptors. Instead, we have proposed a novel mechanism by which both driver and modulator inputs could be carried by transmission through the same types of ionotropic receptors. In this scheme, the distinction between driver and modulator inputs is functional and changeable rather than anatomical and fixed. Driver inputs are carried by excitation and inhibition acting in a push-pull manner. This means that increases in excitation are accompanied by decreases in inhibition and vice versa. Modulators correspond to excitation and inhibition that covary so that they increase or decrease together. Theoretical and experimental work has shown that such an arrangement modulates the gain of a neuron, rather than driving it to respond. Constructing drivers and modulators in this manner allows individual excitatory synaptic inputs to play either role, and indeed to switch between roles, depending on how they are linked with inhibition.</description>
    <dc:title>Drivers and modulators from push-pull and balanced synaptic input.</dc:title>

    <dc:creator>LF Abbott</dc:creator>
    <dc:creator>FS Chance</dc:creator>
    <dc:identifier>doi:10.1016/S0079-6123(05)49011-1</dc:identifier>
    <dc:source>Prog Brain Res, Vol. 149 (2005), pp. 147-155.</dc:source>
    <dc:date>2007-04-05T08:37:32-00:00</dc:date>
    <prism:publicationYear>2005</prism:publicationYear>
    <prism:publicationName>Prog Brain Res</prism:publicationName>
    <prism:issn>0079-6123</prism:issn>
    <prism:volume>149</prism:volume>
    <prism:startingPage>147</prism:startingPage>
    <prism:endingPage>155</prism:endingPage>
    <prism:category>drivers-and-modulators</prism:category>
    <prism:category>neuromodulation</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/awooga/article/233773">
    <title>Theoretical Neuroscience: Computational and Mathematical Modeling of Neural Systems</title>
    <link>http://www.citeulike.org/user/awooga/article/233773</link>
    <description>&lt;i&gt;(01 December 2001)&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Theoretical neuroscience provides a quantitative basis for describing what nervous systems do, determining how they function, and uncovering the general principles by which they operate. This text introduces the basic mathematical and computational methods of theoretical neuroscience and presents applications in a variety of areas including vision, sensory-motor integration, development, learning, and memory.&#60;br /&#62; &#60;br /&#62; The book is divided into three parts. Part I discusses the relationship between sensory stimuli and neural responses, focusing on the representation of information by the spiking activity of neurons. Part II discusses the modeling of neurons and neural circuits on the basis of cellular and synaptic biophysics. Part III analyzes the role of plasticity in development and learning. An appendix covers the mathematical methods used, and exercises are available on the book's Web site.</description>
    <dc:title>Theoretical Neuroscience: Computational and Mathematical Modeling of Neural Systems</dc:title>

    <dc:creator>Peter Dayan</dc:creator>
    <dc:creator>LF Abbott</dc:creator>
    <dc:source>(01 December 2001)</dc:source>
    <dc:date>2005-06-21T16:12:00-00:00</dc:date>
    <prism:publicationYear>2001</prism:publicationYear>
    <prism:publisher>The MIT Press</prism:publisher>
    <prism:category>no-tag</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/awooga/article/1268001">
    <title>A quantitative description of short-term plasticity at excitatory synapses in layer 2/3 of rat primary visual cortex.</title>
    <link>http://www.citeulike.org/user/awooga/article/1268001</link>
    <description>&lt;i&gt;J Neurosci, Vol. 17, No. 20. (15 October 1997), pp. 7926-7940.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Cortical synapses exhibit several forms of short-term plasticity, but the contribution of this plasticity to visual response dynamics is unknown. In part, this is because the simple patterns of stimulation used to probe plasticity in vitro do not correspond to patterns of activity that occur in vivo. We have developed a method of quantitatively characterizing short-term plasticity at cortical synapses that permits prediction of responses to arbitrary patterns of stimulation. Synaptic responses were recorded intracellularly as EPSCs and extracellularly as local field potentials in layer 2/3 of rat primary visual cortical slices during stimulation of layer 4 with trains of electrical stimuli containing random mixtures of frequencies. Responses exhibited complex dynamics that were well described by a simple three-component model consisting of facilitation and two forms of depression, a stronger form that decayed exponentially with a time constant of several hundred milliseconds and a weaker, but more persistent, form that decayed with a time constant of several seconds. Parameters obtained from fits to one train were used to predict accurately responses to other random and constant frequency trains. Control experiments revealed that depression was not caused by a decrease in the effectiveness of extracellular stimulation or by a buildup of inhibition. Pharmacological manipulations of transmitter release and postsynaptic sensitivity suggested that both forms of depression are mediated presynaptically. These results indicate that firing evoked by visual stimuli is likely to cause significant depression at cortical synapses. Hence synaptic depression may be an important determinant of the temporal features of visual cortical responses.</description>
    <dc:title>A quantitative description of short-term plasticity at excitatory synapses in layer 2/3 of rat primary visual cortex.</dc:title>

    <dc:creator>JA Varela</dc:creator>
    <dc:creator>K Sen</dc:creator>
    <dc:creator>J Gibson</dc:creator>
    <dc:creator>J Fost</dc:creator>
    <dc:creator>LF Abbott</dc:creator>
    <dc:creator>SB Nelson</dc:creator>
    <dc:source>J Neurosci, Vol. 17, No. 20. (15 October 1997), pp. 7926-7940.</dc:source>
    <dc:date>2007-04-30T14:00:39-00:00</dc:date>
    <prism:publicationYear>1997</prism:publicationYear>
    <prism:publicationName>J Neurosci</prism:publicationName>
    <prism:issn>0270-6474</prism:issn>
    <prism:volume>17</prism:volume>
    <prism:number>20</prism:number>
    <prism:startingPage>7926</prism:startingPage>
    <prism:endingPage>7940</prism:endingPage>
    <prism:category>model</prism:category>
    <prism:category>plasticity</prism:category>
    <prism:category>short-term-depression</prism:category>
    <prism:category>short-term-facilitation</prism:category>
    <prism:category>visual-cortex</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/awooga/article/952053">
    <title>Models and properties of power-law adaptation in neural systems.</title>
    <link>http://www.citeulike.org/user/awooga/article/952053</link>
    <description>&lt;i&gt;J Neurophysiol, Vol. 96, No. 2. (August 2006), pp. 826-833.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Many biological systems exhibit complex temporal behavior that cannot be adequately characterized by a single time constant. This dynamics, observed from single channels up to the level of human psychophysics, is often better described by power-law rather than exponential dependences on time. We develop and study the properties of neural models with scale-invariant, power-law adaptation and contrast them with the more commonly studied exponential case. Responses of an adapting firing-rate model to constant, pulsed, and oscillating inputs in both the power-law and exponential cases are considered. We construct a spiking model with power-law adaptation based on a nested cascade of processes and show that it can be &#34;programmed&#34; to produce a wide range of time delays. Finally, within a network model, we use power-law adaptation to reproduce long-term features of the tilt aftereffect.</description>
    <dc:title>Models and properties of power-law adaptation in neural systems.</dc:title>

    <dc:creator>PJ Drew</dc:creator>
    <dc:creator>LF Abbott</dc:creator>
    <dc:identifier>doi:10.1152/jn.00134.2006</dc:identifier>
    <dc:source>J Neurophysiol, Vol. 96, No. 2. (August 2006), pp. 826-833.</dc:source>
    <dc:date>2006-11-19T20:42:12-00:00</dc:date>
    <prism:publicationYear>2006</prism:publicationYear>
    <prism:publicationName>J Neurophysiol</prism:publicationName>
    <prism:issn>0022-3077</prism:issn>
    <prism:volume>96</prism:volume>
    <prism:number>2</prism:number>
    <prism:startingPage>826</prism:startingPage>
    <prism:endingPage>833</prism:endingPage>
    <prism:category>adaptation</prism:category>
    <prism:category>power-law</prism:category>
    <prism:category>scale-invariance</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/awooga/article/419795">
    <title>Gain modulation from background synaptic input.</title>
    <link>http://www.citeulike.org/user/awooga/article/419795</link>
    <description>&lt;i&gt;Neuron, Vol. 35, No. 4. (15 August 2002), pp. 773-782.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Gain modulation is a prominent feature of neuronal activity recorded in behaving animals, but the mechanism by which it occurs is unknown. By introducing a barrage of excitatory and inhibitory synaptic conductances that mimics conditions encountered in vivo into pyramidal neurons in slices of rat somatosensory cortex, we show that the gain of a neuronal response to excitatory drive can be modulated by varying the level of &#34;background&#34; synaptic input. Simultaneously increasing both excitatory and inhibitory background firing rates in a balanced manner results in a divisive gain modulation of the neuronal response without appreciable signal-independent increases in firing rate or spike-train variability. These results suggest that, within active cortical circuits, the overall level of synaptic input to a neuron acts as a gain control signal that modulates responsiveness to excitatory drive.</description>
    <dc:title>Gain modulation from background synaptic input.</dc:title>

    <dc:creator>FS Chance</dc:creator>
    <dc:creator>LF Abbott</dc:creator>
    <dc:creator>AD Reyes</dc:creator>
    <dc:source>Neuron, Vol. 35, No. 4. (15 August 2002), pp. 773-782.</dc:source>
    <dc:date>2005-12-02T15:41:17-00:00</dc:date>
    <prism:publicationYear>2002</prism:publicationYear>
    <prism:publicationName>Neuron</prism:publicationName>
    <prism:issn>0896-6273</prism:issn>
    <prism:volume>35</prism:volume>
    <prism:number>4</prism:number>
    <prism:startingPage>773</prism:startingPage>
    <prism:endingPage>782</prism:endingPage>
    <prism:category>dynamic-clamp</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/awooga/article/1002092">
    <title>The dynamic clamp: artificial conductances in biological neurons.</title>
    <link>http://www.citeulike.org/user/awooga/article/1002092</link>
    <description>&lt;i&gt;Trends Neurosci, Vol. 16, No. 10. (October 1993), pp. 389-394.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The dynamic clamp is a novel method that uses computer simulation to introduce conductances into biological neurons. This method can be used to study the role of various conductances in shaping the activity of single neurons, or neurons within networks. The dynamic clamp can also be used to form circuits from previously unconnected neurons. This approach makes computer simulation an interactive experimental tool, and will be useful in many applications where the role of synaptic strengths and intrinsic properties in neuronal and network dynamics is of interest.</description>
    <dc:title>The dynamic clamp: artificial conductances in biological neurons.</dc:title>

    <dc:creator>AA Sharp</dc:creator>
    <dc:creator>MB O'Neil</dc:creator>
    <dc:creator>LF Abbott</dc:creator>
    <dc:creator>E Marder</dc:creator>
    <dc:source>Trends Neurosci, Vol. 16, No. 10. (October 1993), pp. 389-394.</dc:source>
    <dc:date>2006-12-19T16:27:40-00:00</dc:date>
    <prism:publicationYear>1993</prism:publicationYear>
    <prism:publicationName>Trends Neurosci</prism:publicationName>
    <prism:issn>0166-2236</prism:issn>
    <prism:volume>16</prism:volume>
    <prism:number>10</prism:number>
    <prism:startingPage>389</prism:startingPage>
    <prism:endingPage>394</prism:endingPage>
    <prism:category>dynamic-clamp</prism:category>
    <prism:category>review</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/awooga/article/552756">
    <title>Dynamic clamp: computer-generated conductances in real neurons.</title>
    <link>http://www.citeulike.org/user/awooga/article/552756</link>
    <description>&lt;i&gt;J Neurophysiol, Vol. 69, No. 3. (March 1993), pp. 992-995.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;1. We describe a new method, the dynamic clamp, that uses a computer as an interactive tool to introduce simulated voltage and ligand mediated conductances into real neurons. 2. We simulate a gamma-aminobutyric acid (GABA) response of a cultured stomatogastric ganglion neuron to illustrate that the dynamic clamp effectively introduces a conductance into the target neuron. 3. To demonstrate an artificial voltage-dependent conductance, we simulate the action of a voltage-dependent proctolin response on a neuron in the intact stomatogastric ganglion. We show that shifts in the activation curve and the maximal conductance of the response produce different effects on the target neuron. 4. The dynamic clamp is used to construct reciprocal inhibitory synapses between two stomatogastric ganglion neurons that are not coupled naturally, illustrating that this method can be used to form new networks at will.</description>
    <dc:title>Dynamic clamp: computer-generated conductances in real neurons.</dc:title>

    <dc:creator>AA Sharp</dc:creator>
    <dc:creator>MB O'Neil</dc:creator>
    <dc:creator>LF Abbott</dc:creator>
    <dc:creator>E Marder</dc:creator>
    <dc:source>J Neurophysiol, Vol. 69, No. 3. (March 1993), pp. 992-995.</dc:source>
    <dc:date>2006-03-15T11:16:14-00:00</dc:date>
    <prism:publicationYear>1993</prism:publicationYear>
    <prism:publicationName>J Neurophysiol</prism:publicationName>
    <prism:issn>0022-3077</prism:issn>
    <prism:volume>69</prism:volume>
    <prism:number>3</prism:number>
    <prism:startingPage>992</prism:startingPage>
    <prism:endingPage>995</prism:endingPage>
    <prism:category>dynamic-clamp</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/awooga/article/554572">
    <title>The dynamic clamp comes of age.</title>
    <link>http://www.citeulike.org/user/awooga/article/554572</link>
    <description>&lt;i&gt;Trends Neurosci, Vol. 27, No. 4. (April 2004), pp. 218-224.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The dynamic clamp uses computer simulation to introduce artificial membrane or synaptic conductances into biological neurons and to create hybrid circuits of real and model neurons. In the ten years since it was first developed, the dynamic clamp has become a widely used tool for the study of neural systems at the cellular and circuit levels. This review describes recent state-of-the-art implementations of the dynamic clamp and summarizes insights gained through its use, ranging from the role of voltage-dependent conductances in shaping neuronal activity to the effects of synaptic dynamics on network behavior and the impact of in vivo-like input on neuronal information processing.</description>
    <dc:title>The dynamic clamp comes of age.</dc:title>

    <dc:creator>AA Prinz</dc:creator>
    <dc:creator>LF Abbott</dc:creator>
    <dc:creator>E Marder</dc:creator>
    <dc:identifier>doi:10.1016/j.tins.2004.02.004</dc:identifier>
    <dc:source>Trends Neurosci, Vol. 27, No. 4. (April 2004), pp. 218-224.</dc:source>
    <dc:date>2006-03-16T18:07:22-00:00</dc:date>
    <prism:publicationYear>2004</prism:publicationYear>
    <prism:publicationName>Trends Neurosci</prism:publicationName>
    <prism:issn>0166-2236</prism:issn>
    <prism:volume>27</prism:volume>
    <prism:number>4</prism:number>
    <prism:startingPage>218</prism:startingPage>
    <prism:endingPage>224</prism:endingPage>
    <prism:category>dynamic-clamp</prism:category>
    <prism:category>review</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/awooga/article/918558">
    <title>Memory from the dynamics of intrinsic membrane currents</title>
    <link>http://www.citeulike.org/user/awooga/article/918558</link>
    <description>&lt;i&gt;PNAS, Vol. 93, No. 24. (26 November 1996), pp. 13481-13486.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;Almost all theoretical and experimental studies of the mechanisms underlying learning and memory focus on synaptic efficacy and make the implicit assumption that changes in synaptic efficacy are both necessary and sufficient to account for learning and memory. However, network dynamics depends on the complex interaction between intrinsic membrane properties and synaptic strengths and time courses. Furthermore, neuronal activity itself modifies not only synaptic efficacy but also the intrinsic membrane properties of neurons. This paper presents examples demonstrating that neurons with complex temporal dynamics can provide short-term &#34;memory&#34; mechanisms that rely solely on intrinsic neuronal properties. Additionally, we discuss the potential role that activity may play in long-term modification of intrinsic neuronal properties. While not replacing synaptic plasticity as a powerful learning mechanism, these examples suggest that memory in networks results from an ongoing interplay between changes in synaptic efficacy and intrinsic membrane properties. 10.1073/pnas.93.24.13481</description>
    <dc:title>Memory from the dynamics of intrinsic membrane currents</dc:title>

    <dc:creator>Eve Marder</dc:creator>
    <dc:creator>L F Abbott</dc:creator>
    <dc:creator>Gina g Turrigiano</dc:creator>
    <dc:creator>Zheng Liu</dc:creator>
    <dc:creator>Jorge Golowasch</dc:creator>
    <dc:source>PNAS, Vol. 93, No. 24. (26 November 1996), pp. 13481-13486.</dc:source>
    <dc:date>2006-10-30T15:42:56-00:00</dc:date>
    <prism:publicationYear>1996</prism:publicationYear>
    <prism:publicationName>PNAS</prism:publicationName>
    <prism:volume>93</prism:volume>
    <prism:number>24</prism:number>
    <prism:startingPage>13481</prism:startingPage>
    <prism:endingPage>13486</prism:endingPage>
    <prism:category>memory</prism:category>
    <prism:category>neuromodulators</prism:category>
    <prism:category>target-activity-level</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/awooga/article/915388">
    <title>Neuromodulation of spike-timing precision in sensory neurons.</title>
    <link>http://www.citeulike.org/user/awooga/article/915388</link>
    <description>&lt;i&gt;J Neurosci, Vol. 26, No. 22. (31 May 2006), pp. 5910-5919.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The neuropeptide allatostatin decreases the spike rate in response to time-varying stretches of two different crustacean mechanoreceptors, the gastropyloric receptor 2 in the crab Cancer borealis and the coxobasal chordotonal organ (CBCTO) in the crab Carcinus maenas. In each system, the decrease in firing rate is accompanied by an increase in the timing precision of spikes triggered by discrete temporal features in the stimulus. This was quantified by calculating the standard deviation or &#34;jitter&#34; in the times of individual identified spikes elicited in response to repeated presentations of the stimulus. Conversely, serotonin increases the firing rate but decreases the timing precision of the CBCTO response. Intracellular recordings from the afferents of this receptor demonstrate that allatostatin increases the conductance of the neurons, consistent with its inhibitory action on spike rate, whereas serotonin decreases the overall membrane conductance. We conclude that spike-timing precision of mechanoreceptor afferents in response to dynamic stimulation can be altered by neuromodulators acting directly on the afferent neurons.</description>
    <dc:title>Neuromodulation of spike-timing precision in sensory neurons.</dc:title>

    <dc:creator>CP Billimoria</dc:creator>
    <dc:creator>RA DiCaprio</dc:creator>
    <dc:creator>JT Birmingham</dc:creator>
    <dc:creator>LF Abbott</dc:creator>
    <dc:creator>E Marder</dc:creator>
    <dc:identifier>doi:10.1523/JNEUROSCI.4659-05.2006</dc:identifier>
    <dc:source>J Neurosci, Vol. 26, No. 22. (31 May 2006), pp. 5910-5919.</dc:source>
    <dc:date>2006-10-27T15:49:41-00:00</dc:date>
    <prism:publicationYear>2006</prism:publicationYear>
    <prism:publicationName>J Neurosci</prism:publicationName>
    <prism:issn>1529-2401</prism:issn>
    <prism:volume>26</prism:volume>
    <prism:number>22</prism:number>
    <prism:startingPage>5910</prism:startingPage>
    <prism:endingPage>5919</prism:endingPage>
    <prism:category>neuromodulation</prism:category>
    <prism:category>spike-timing</prism:category>
</item>



<item rdf:about="http://www.citeulike.org/user/awooga/article/894205">
    <title>Global Structure, Robustness, and Modulation of Neuronal Models</title>
    <link>http://www.citeulike.org/user/awooga/article/894205</link>
    <description>&lt;i&gt;J. Neurosci., Vol. 21, No. 14. (15 July 2001), pp. 5229-5238.&lt;/i&gt;&lt;br /&gt;&lt;br /&gt;The electrical characteristics of many neurons are remarkably robust in the face of changing internal and external conditions. At the same time, neurons can be highly sensitive to neuromodulators. We find correlates of this dual robustness and sensitivity in a global analysis of the structure of a conductance-based model neuron. We vary the maximal conductance parameters of the model neuron and, for each set of parameters tested, characterize the activity pattern generated by the cell as silent, tonically firing, or bursting. Within the parameter space of the five maximal conductances of the model, we find directions, representing concerted changes in multiple conductances, along which the basic pattern of neural activity does not change. In other directions, relatively small concurrent changes in a few conductances can induce transitions between these activity patterns. The global structure of the conductance-space maps implies that neuromodulators that alter a sensitive set of conductances will have powerful, and possibly state-dependent, effects. Other modulators that may have no direct impact on the activity of the neuron may nevertheless change the effects of such direct modulators via this state dependence. Some of the results and predictions arising from the model studies are replicated and verified in recordings of stomatogastric ganglion neurons using the dynamic clamp.</description>
    <dc:title>Global Structure, Robustness, and Modulation of Neuronal Models</dc:title>

    <dc:creator>Mark Goldman</dc:creator>
    <dc:creator>Jorge Golowasch</dc:creator>
    <dc:creator>Eve Marder</dc:creator>
    <dc:creator>LF Abbott</dc:creator>
    <dc:source>J. Neurosci., Vol. 21, No. 14. (15 July 2001), pp. 5229-5238.</dc:source>
    <dc:date>2006-10-12T12:20:07-00:00</dc:date>
    <prism:publicationYear>2001</prism:publicationYear>
    <prism:publicationName>J. Neurosci.</prism:publicationName>
    <prism:volume>21</prism:volume>
    <prism:number>14</prism:number>
    <prism:startingPage>5229</prism:startingPage>
    <prism:endingPage>5238</prism:endingPage>
    <prism:category>computational</prism:category>
    <prism:category>model</prism:category>
    <prism:category>neuromodulators</prism:category>
</item>



</rdf:RDF>

