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<title>Cerebral Cortex - current issue</title>
<link>http://cercor.oxfordjournals.org</link>
<description>Cerebral Cortex - RSS feed of current issue</description>
<prism:eIssn>1460-2199</prism:eIssn>
<prism:coverDisplayDate>July 2009</prism:coverDisplayDate>
<prism:publicationName>Cerebral Cortex</prism:publicationName>
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<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1487?rss=1">
<title><![CDATA[Krieg Cortical Kudos 2008]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1487?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Swanson, L. W.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhp104</dc:identifier>
<dc:title><![CDATA[Krieg Cortical Kudos 2008]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1489</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1487</prism:startingPage>
<prism:section>News</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1490?rss=1">
<title><![CDATA[Fragile X Mental Retardation Protein in the Driver's Seat]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1490?rss=1</link>
<description><![CDATA[]]></description>
<dc:creator><![CDATA[Brenman, J. E.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhp089</dc:identifier>
<dc:title><![CDATA[Fragile X Mental Retardation Protein in the Driver's Seat]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1492</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1490</prism:startingPage>
<prism:section>Commentary</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1493?rss=1">
<title><![CDATA[Retrieval and Unification of Syntactic Structure in Sentence Comprehension: an fMRI Study Using Word-Category Ambiguity]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1493?rss=1</link>
<description><![CDATA[
<p>Sentence comprehension requires the retrieval of single word information from long-term memory, and the integration of this information into multiword representations. The current functional magnetic resonance imaging study explored the hypothesis that the left posterior temporal gyrus supports the retrieval of lexical-syntactic information, whereas left inferior frontal gyrus (LIFG) contributes to syntactic unification. Twenty-eight subjects read sentences and word sequences containing word-category (noun&ndash;verb) ambiguous words at critical positions. Regions contributing to the syntactic unification process should show enhanced activation for sentences compared to words, and only within sentences display a larger signal for ambiguous than unambiguous conditions. The posterior LIFG showed exactly this predicted pattern, confirming our hypothesis that LIFG contributes to syntactic unification. The left posterior middle temporal gyrus was activated more for ambiguous than unambiguous conditions (main effect over both sentences and word sequences), as predicted for regions subserving the retrieval of lexical-syntactic information from memory. We conclude that understanding language involves the dynamic interplay between left inferior frontal and left posterior temporal regions.</p>
]]></description>
<dc:creator><![CDATA[Snijders, T. M., Vosse, T., Kempen, G., Van Berkum, J. J.A., Petersson, K. M., Hagoort, P.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn187</dc:identifier>
<dc:title><![CDATA[Retrieval and Unification of Syntactic Structure in Sentence Comprehension: an fMRI Study Using Word-Category Ambiguity]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1503</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1493</prism:startingPage>
<prism:section>Feature Article</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1504?rss=1">
<title><![CDATA[Limbic Epileptogenesis in a Mouse Model of Fragile X Syndrome]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1504?rss=1</link>
<description><![CDATA[
<p>Fragile X syndrome (FXS), caused by silencing of the <I>Fmr1</I> gene, is the most common form of inherited mental retardation. Epilepsy is reported to occur in 20&ndash;25% of individuals with FXS. However, no overall increased excitability has been reported in <I>Fmr1</I> knockout (KO) mice, except for increased sensitivity to auditory stimulation. Here, we report that kindling increased the expressions of <I>Fmr1</I> mRNA and protein in the forebrain of wild-type (WT) mice. Kindling development was dramatically accelerated in <I>Fmr1</I> KO mice, and <I>Fmr1</I> KO mice also displayed prolonged electrographic seizures during kindling and more severe mossy fiber sprouting after kindling. The accelerated rate of kindling was partially repressed by inhibiting N-methyl-D-aspartic acid receptor (NMDAR) with MK-801 or mGluR5 receptor with 2-methyl-6-(phenylethynyl)-pyridine (MPEP). The rate of kindling development in WT was not effected by MPEP, however, suggesting that FMRP normally suppresses epileptogenic signaling downstream of metabolic glutamate receptors. Our findings reveal that FMRP plays a critical role in suppressing limbic epileptogenesis and predict that the enhanced susceptibility of patients with FXS to epilepsy is a direct consequence of the loss of an important homeostatic factor that mitigates vulnerability to excessive neuronal excitation.</p>
]]></description>
<dc:creator><![CDATA[Qiu, L.-F., Lu, T.-J., Hu, X.-L., Yi, Y.-H., Liao, W.-P., Xiong, Z.-Q.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn163</dc:identifier>
<dc:title><![CDATA[Limbic Epileptogenesis in a Mouse Model of Fragile X Syndrome]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1514</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1504</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1515?rss=1">
<title><![CDATA[Downregulation of Tonic GABAergic Inhibition in a Mouse Model of Fragile X Syndrome]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1515?rss=1</link>
<description><![CDATA[
<p>The absence of fragile X mental retardation protein results in the fragile X syndrome (FXS), a common form of mental retardation associated with attention deficit, autistic behavior, and epileptic seizures. The phenotype of FXS is reproduced in fragile X mental retardation 1 (<I>fmr1</I>) knockout (KO) mice that have region-specific altered expression of some -aminobutyric acid (GABA<SUB>A</SUB>) receptor subunits. However, little is known about the characteristics of GABAergic inhibition in the subiculum of these animals. We employed patch-clamp recordings from subicular pyramidal cells in an in vitro slice preparation. In addition, semiquantitative polymerase chain reaction and western blot experiments were performed on subiculum obtained from wild-type (WT) and KO mice. We found that tonic GABA<SUB>A</SUB> currents were downregulated in <I>fmr1</I> KO compared with WT neurons, whereas no significant differences were observed in phasic GABA<SUB>A</SUB> currents. Molecular biology analysis revealed that the tonic GABA<SUB>A</SUB> receptor subunits 5 and  were underexpressed in the <I>fmr1</I> KO mouse subiculum compared with WT. Because the subiculum plays a role in both cognitive functions and epileptic disorders, we propose that altered tonic inhibition in this structure contributes to the behavioral deficits and epileptic activity seen in FXS patients. This conclusion is in line with evidence implicating tonic GABA<SUB>A</SUB> inhibition in learning and memory.</p>
]]></description>
<dc:creator><![CDATA[Curia, G., Papouin, T., Seguela, P., Avoli, M.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn159</dc:identifier>
<dc:title><![CDATA[Downregulation of Tonic GABAergic Inhibition in a Mouse Model of Fragile X Syndrome]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1520</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1515</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1521?rss=1">
<title><![CDATA[Emotional Context Enhances Auditory Novelty Processing in Superior Temporal Gyrus]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1521?rss=1</link>
<description><![CDATA[
<p>Visualizing emotionally loaded pictures intensifies peripheral reflexes toward sudden auditory stimuli, suggesting that the emotional context may potentiate responses elicited by novel events in the acoustic environment. However, psychophysiological results have reported that attentional resources available to sounds become depleted, as attention allocation to emotional pictures increases. These findings have raised the challenging question of whether an emotional context actually enhances or attenuates auditory novelty processing at a central level in the brain. To solve this issue, we used functional magnetic resonance imaging to first identify brain activations induced by novel sounds (NOV) when participants made a color decision on visual stimuli containing both negative (NEG) and neutral (NEU) facial expressions. We then measured modulation of these auditory responses by the emotional load of the task. Contrary to what was assumed, activation induced by NOV in superior temporal gyrus (STG) was enhanced when subjects responded to faces with a NEG emotional expression compared with NEU ones. Accordingly, NOV yielded stronger behavioral disruption on subjects&rsquo; performance in the NEG context. These results demonstrate that the emotional context modulates the excitability of auditory and possibly multimodal novelty cerebral regions, enhancing acoustic novelty processing in a potentially harming environment.</p>
]]></description>
<dc:creator><![CDATA[Dominguez-Borras, J., Trautmann, S.-A., Erhard, P., Fehr, T., Herrmann, M., Escera, C.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn188</dc:identifier>
<dc:title><![CDATA[Emotional Context Enhances Auditory Novelty Processing in Superior Temporal Gyrus]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1529</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1521</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1530?rss=1">
<title><![CDATA[Impaired Tactile Acuity in Old Age Is Accompanied by Enlarged Hand Representations in Somatosensory Cortex]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1530?rss=1</link>
<description><![CDATA[
<p>The representations of the human hand in primary somatosensory cortex (SI) undergo continuous adaptational plastic processes, which arise from learning, altered use, or injury. The resulting reorganization affects size, extent, and position of the cortical maps, which parallels alterations of tactile behavior indicating a close relationship between map changes and perception. Here we investigate the influence of healthy aging on the cortical hand representation and on age-related changes of tactile performance. Using somatosensory evoked potential mapping in combination with electric source localization, we found that in elderly subjects aged 60&ndash;85 years the distance between the dipoles of the index and the little fingers increased indicating an expansion of the representations within SI by approximately 40%. Assessment of tactile spatial 2-point discrimination thresholds in the same subjects showed a strong decline with age. These results indicate that healthy aging strongly affects the homuncular structures of the hand representations within SI. Map expansion typically observed in young and adult subjects during learning is associated with a gain in performance. Whereas learning-related map changes are assumed to result from specific strengthening of synaptic connections, we suggest that the age-related map changes are related to the reduction of intracortical inhibition developing with age.</p>
]]></description>
<dc:creator><![CDATA[Kalisch, T., Ragert, P., Schwenkreis, P., Dinse, H. R., Tegenthoff, M.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn190</dc:identifier>
<dc:title><![CDATA[Impaired Tactile Acuity in Old Age Is Accompanied by Enlarged Hand Representations in Somatosensory Cortex]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1538</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1530</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1539?rss=1">
<title><![CDATA[Contextual Processing in Episodic Future Thought]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1539?rss=1</link>
<description><![CDATA[
<p>Remembering events from one's past (i.e., episodic memory) and envisioning specific events that could occur in one's future (i.e., episodic future thought) invoke highly overlapping sets of brain regions. The present study employed functional magnetic resonance imaging to test the hypothesis that one source of this shared architecture is that episodic future thought&mdash;much like episodic memory&mdash;tends to invoke memory for known visual&ndash;spatial contexts. That is, regions of posterior cortex (within posterior cingulate cortex [PCC], parahippocampal cortex [PHC], and superior occipital gyrus [SOG]) elicit indistinguishable activity during remembering and episodic future thought, and similar regions have been identified as important for establishing visual&ndash;spatial contextual associations. In the present study, these regions were similarly engaged when participants thought about personal events in familiar contexts, irrespective of temporal direction (past or future). The same regions, however, exhibited very little activity when participants envisioned personal future events in unfamiliar contextual settings. These findings suggest that regions within PCC, PHC, and SOG support the activation of well-known contextual settings that people tend to imagine when thinking about personal events, whether in the past or future. Hence, this study pinpoints an important similarity between episodic future thought and episodic memory.</p>
]]></description>
<dc:creator><![CDATA[Szpunar, K. K., Chan, J. C. K., McDermott, K. B.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn191</dc:identifier>
<dc:title><![CDATA[Contextual Processing in Episodic Future Thought]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1548</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1539</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1549?rss=1">
<title><![CDATA[Regionally Specific Cortical Thinning in Children with Sickle Cell Disease]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1549?rss=1</link>
<description><![CDATA[
<p>Sickle cell disease (SCD) is a chronic disease with a significant rate of neurological complications in the first decade of life. In this retrospective study, cortical thickness was examined in children with SCD who had no detectable abnormalities on conventional magnetic resonance imaging/magnetic resonance angiography. Regional differences in cortical thickness from SCD were explored using age-matched healthy controls as comparison. A comparison analysis was done for SCD (<I>n</I> = 28) and controls (<I>n</I> = 29) based on age (5&ndash;11; 12&ndash;21 years), due to the age-dependent variation in cortex maturation. Distinct regions of thinning were found in SCD patients in both age groups. The number, spatial extent, and significance (<I>P</I> &lt; 0.001) of these areas of thinning were increased in the older SCD group. Regions of interest (ROIs) were defined on the areas of highly significant thinning in the older group and then mapped onto the younger cohort; a multiparametric linear regression analysis of the ROI data demonstrated significant (<I>P</I> &lt; 0.001) cortical thinning in SCD subjects, with the largest regions of thinning in the precuneus and the posterior cingulate. The regionally specific differences suggest that cortical thickness may serve as a marker for silent insults in SCD and hence may be a useful tool for identifying SCD patients at risk for neurological sequelae.</p>
]]></description>
<dc:creator><![CDATA[Kirk, G. R., Haynes, M. R., Palasis, S., Brown, C., Burns, T. G., McCormick, M., Jones, R. A.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn193</dc:identifier>
<dc:title><![CDATA[Regionally Specific Cortical Thinning in Children with Sickle Cell Disease]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1556</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1549</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1557?rss=1">
<title><![CDATA[The Contributions of Prefrontal Cortex and Executive Control to Deception: Evidence from Activation Likelihood Estimate Meta-analyses]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1557?rss=1</link>
<description><![CDATA[
<p>Previous neuroimaging studies have implicated the prefrontal cortex (PFC) and nearby brain regions in deception. This is consistent with the hypothesis that lying involves the executive control system. To date, the nature of the contribution of different aspects of executive control to deception, however, remains unclear. In the present study, we utilized an activation likelihood estimate (ALE) method of meta-analysis to quantitatively identify brain regions that are consistently more active for deceptive responses relative to truthful responses across past studies. We then contrasted the results with additional ALE maps generated for 3 different aspects of executive control: working memory, inhibitory control, and task switching. Deception-related regions in dorsolateral PFC and posterior parietal cortex were selectively associated with working memory. Additional deception regions in ventrolateral PFC, anterior insula, and anterior cingulate cortex were associated with multiple aspects of executive control. In contrast, deception-related regions in bilateral inferior parietal lobule were not associated with any of the 3 executive control constructs. Our findings support the notion that executive control processes, particularly working memory, and their associated neural substrates play an integral role in deception. This work provides a foundation for future research on the neurocognitive basis of deception.</p>
]]></description>
<dc:creator><![CDATA[Christ, S. E., Van Essen, D. C., Watson, J. M., Brubaker, L. E., McDermott, K. B.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn189</dc:identifier>
<dc:title><![CDATA[The Contributions of Prefrontal Cortex and Executive Control to Deception: Evidence from Activation Likelihood Estimate Meta-analyses]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1566</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1557</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1567?rss=1">
<title><![CDATA[The Timing of Feedback to Early Visual Cortex in the Perception of Long-Range Apparent Motion]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1567?rss=1</link>
<description><![CDATA[
<p>When 2 visual stimuli are presented one after another in different locations, they are often perceived as one, but moving object. Feedback from area human motion complex hMT/V5+ to V1 has been hypothesized to play an important role in this illusory perception of motion. We measured event-related responses to illusory motion stimuli of varying apparent motion (AM) content and retinal location using Electroencephalography. Detectable cortical stimulus processing started around 60-ms poststimulus in area V1. This component was insensitive to AM content and sequential stimulus presentation. Sensitivity to AM content was observed starting around 90 ms post the second stimulus of a sequence and most likely originated in area hMT/V5+. This AM sensitive response was insensitive to retinal stimulus position. The stimulus sequence related response started to be sensitive to retinal stimulus position at a longer latency of 110 ms. We interpret our findings as evidence for feedback from area hMT/V5+ or a related motion processing area to early visual cortices (V1, V2, V3).</p>
]]></description>
<dc:creator><![CDATA[Wibral, M., Bledowski, C., Kohler, A., Singer, W., Muckli, L.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn192</dc:identifier>
<dc:title><![CDATA[The Timing of Feedback to Early Visual Cortex in the Perception of Long-Range Apparent Motion]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1582</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1567</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1583?rss=1">
<title><![CDATA[Neuroanatomical Correlates of Musicianship as Revealed by Cortical Thickness and Voxel-Based Morphometry]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1583?rss=1</link>
<description><![CDATA[
<p>We used a multimethod approach to investigate the neuroanatomical correlates of musicianship and absolute pitch (AP). Cortical thickness measures, interregional correlations applied to these thicknesses, and voxel-based morphometry (VBM) were applied to the same magnetic resonance imaging data set of 71 musicians (27 with AP) and 64 nonmusicians. Cortical thickness was greater in musicians with peaks in superior temporal and dorsolateral frontal regions. Correlations between 2 seed points, centered on peaks of thickness difference within the right frontal cortex, and all other points across the cortex showed greater specificity of significant correlations among musicians, with fewer and more discrete areas correlating with the frontal seeds, including the superior temporal cortex. VBM of gray matter (GM)&ndash;classified voxels yielded a strongly right-lateralized focus of greater GM concentration in musicians centered on the posterolateral aspect of Heschl's gyrus. Together, these results are consistent with functional evidence emphasizing the importance of a frontotemporal network of areas heavily relied upon in the performance of musical tasks. Among musicians, contrasts of AP possessors and nonpossessors showed significantly thinner cortex among possessors in a number of areas, including the posterior dorsal frontal cortices that have been previously implicated in the performance of AP tasks.</p>
]]></description>
<dc:creator><![CDATA[Bermudez, P., Lerch, J. P., Evans, A. C., Zatorre, R. J.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn196</dc:identifier>
<dc:title><![CDATA[Neuroanatomical Correlates of Musicianship as Revealed by Cortical Thickness and Voxel-Based Morphometry]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1596</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1583</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1597?rss=1">
<title><![CDATA[Interneuron Diversity in Layers 2-3 of Monkey Prefrontal Cortex]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1597?rss=1</link>
<description><![CDATA[
<p>The heterogeneity of -aminobutyric acid interneurons in the rodent neocortex is well-established, but their classification into distinct subtypes remains a matter of debate. The classification of interneurons in the primate neocortex is further complicated by a less extensive database of the features of these neurons and by reported interspecies differences. Consequently, in this study we characterized 8 different morphological types of interneurons from monkey prefrontal cortex, 4 of which have not been previously classified. These interneuron types differed in their expression of molecular markers and clustered into 3 different electrophysiological classes. The first class consisted of fast-spiking parvalbumin-positive chandelier and linear arbor cells. The second class comprised 5 different morphological types of continuous-adapting calretinin- or calbindin-positive interneurons that had the lowest level of firing threshold. However, 2 of these morphological types had short spike duration, which is not typical for rodent adapting cells. Neurogliaform cells (NGFCs), which coexpressed calbindin and neuropeptide Y, formed the third class, characterized by strong initial adaptation. They did not exhibit the delayed spikes seen in rodent NGFCs. These results indicate that primate interneurons have some specific properties; consequently, direct translation of classification schemes developed from studies in rodents to primates might be inappropriate.</p>
]]></description>
<dc:creator><![CDATA[Zaitsev, A. V., Povysheva, N. V., Gonzalez-Burgos, G., Rotaru, D., Fish, K. N., Krimer, L. S., Lewis, D. A.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn198</dc:identifier>
<dc:title><![CDATA[Interneuron Diversity in Layers 2-3 of Monkey Prefrontal Cortex]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1615</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1597</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1616?rss=1">
<title><![CDATA[Chronic but not Acute Dopaminergic Transmission Interruption Promotes a Progressive Increase in Cortical Beta Frequency Synchronization: Relationships to Vigilance State and Akinesia]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1616?rss=1</link>
<description><![CDATA[
<p>Dopaminergic (DA) denervation results in the appearance of an excessive cortical beta frequency synchronization in parkinsonian patients and animal models of the disease. The present study analyzed electrocorticogram signals in awake rats to further characterize this excessive synchronization in terms of time course, relation to motor activity and state of vigilance. Using substantia nigra <I>pars compacta</I> lesions and both acute and chronic pharmacological interruptions of DA transmission, the present data demonstrated that the appearance of excessive beta synchronization requires a prolonged interruption in DA transmission and builds up progressively. This synchronization was vigilance-state dependent and observed solely during awake-like activity. Furthermore, these data demonstrated for the first time that the appearance of akinesia preceded the excessive cortical beta synchronization. In addition, this synchronization was stronger in the motor than in the somato-sensory cortex and in unilaterally compared with bilaterally lesioned animals. Finally, excessive beta synchronization was accompanied by an increased coherence between motor and somato-sensory cortical activities. These data suggest that excessive beta synchronization is associated with plastic processes whose time course is delayed with respect to the akinesia. Moreover, the expression of this phenomenon, which likely reflects functional changes in the cortico-basal ganglia circuits, requires a specific brain state.</p>
]]></description>
<dc:creator><![CDATA[Degos, B., Deniau, J.-M., Chavez, M., Maurice, N.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn199</dc:identifier>
<dc:title><![CDATA[Chronic but not Acute Dopaminergic Transmission Interruption Promotes a Progressive Increase in Cortical Beta Frequency Synchronization: Relationships to Vigilance State and Akinesia]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1630</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1616</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1631?rss=1">
<title><![CDATA[Brain Oscillations Dissociate between Semantic and Nonsemantic Encoding of Episodic Memories]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1631?rss=1</link>
<description><![CDATA[
<p>Prior studies, mostly using intentional learning, suggest that power increases in theta and gamma oscillations and power decreases in alpha and beta oscillations are positively related to later remembering. Using incidental learning, this study investigated whether these brain oscillatory subsequent memory effects can be differentiated by encoding task. One group of subjects studied material performing a semantic (deep) encoding task, whereas the other group studied the same material performing a nonsemantic (shallow) encoding task. Successful encoding in the semantic task was related to power decreases in the alpha (8&ndash;12 Hz) and beta (12&ndash;20 Hz) frequency band, and a power increase in the gamma band (55&ndash;70 Hz). In the shallow task, successful encoding was related to a power decrease in the alpha band and a power increase in the theta frequency band (4&ndash;7 Hz). A direct comparison of results between the 2 encoding tasks revealed that semantic subsequent memory effects were specifically reflected by power decreases in the beta (0.5&ndash;1.5 s) and the alpha frequency band (0.5&ndash;1.0 s), whereas nonsemantic subsequent memory effects were specifically reflected by a power increase in the theta frequency band (0.5&ndash;1.0 s).</p>
]]></description>
<dc:creator><![CDATA[Hanslmayr, S., Spitzer, B., Bauml, K.-H.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn197</dc:identifier>
<dc:title><![CDATA[Brain Oscillations Dissociate between Semantic and Nonsemantic Encoding of Episodic Memories]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1640</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1631</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1641?rss=1">
<title><![CDATA[Cortical Plasticity of Audio-Visual Object Representations]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1641?rss=1</link>
<description><![CDATA[
<p>Several regions in human temporal and frontal cortex are known to integrate visual and auditory object features. The processing of audio&ndash;visual (AV) associations in these regions has been found to be modulated by object familiarity. The aim of the present study was to explore training-induced plasticity in human cortical AV integration. We used functional magnetic resonance imaging to analyze the neural correlates of AV integration for unfamiliar artificial object sounds and images in na&iuml;ve subjects (PRE training) and after a behavioral training session in which subjects acquired associations between some of these sounds and images (POST-training). In the PRE-training session, unfamiliar artificial object sounds and images were mainly integrated in right inferior frontal cortex (IFC). The POST-training results showed extended integration-related IFC activations bilaterally, and a recruitment of additional regions in bilateral superior temporal gyrus/sulcus and intraparietal sulcus. Furthermore, training-induced differential response patterns to mismatching compared with matching (i.e., associated) artificial AV stimuli were most pronounced in left IFC. These effects were accompanied by complementary training-induced congruency effects in right posterior middle temporal gyrus and fusiform gyrus. Together, these findings demonstrate that short-term cross-modal association learning was sufficient to induce plastic changes of both AV integration of object stimuli and mechanisms of AV congruency processing.</p>
]]></description>
<dc:creator><![CDATA[Naumer, M. J., Doehrmann, O., Muller, N. G., Muckli, L., Kaiser, J., Hein, G.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn200</dc:identifier>
<dc:title><![CDATA[Cortical Plasticity of Audio-Visual Object Representations]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1653</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1641</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1654?rss=1">
<title><![CDATA[Two Phases of Interhemispheric Inhibition between Motor Related Cortical Areas and the Primary Motor Cortex in Human]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1654?rss=1</link>
<description><![CDATA[
<p>Interhemispheric inhibition (IHI) refers to the neurophysiological mechanism in which one hemisphere of the brain inhibits the opposite hemisphere. IHI can be studied by transcranial magnetic stimulation using a conditioning-test paradigm. We investigated IHI from 5 motor related cortical areas in the right hemisphere to the left primary motor cortex (M1). These areas are hand and face representations of M1, dorsal premotor cortex, somatosensory cortex, and dorsolateral prefrontal cortex. Test stimulus was delivered to the left M1 and conditioning stimulus (CS) was delivered to one of 5 motor related cortical areas in the right hemisphere. The time course of IHI, effects of different CS intensities and current directions on IHI were tested. Maximum IHI was found at interstimulus intervals of ~10 ms (short latency IHI, SIHI) and ~50 ms (long latency IHI, LIHI) for the motor related areas tested. LIHI could be elicited over a wide range of CS intensities, whereas SIHI required higher CS intensities. We conclude that there are 2 distinct phases of IHI from motor related cortical areas to the opposite M1 through the corpus callosum, and they are mediated by different neuronal populations.</p>
]]></description>
<dc:creator><![CDATA[Ni, Z., Gunraj, C., Nelson, A. J., Yeh, I-J., Castillo, G., Hoque, T., Chen, R.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn201</dc:identifier>
<dc:title><![CDATA[Two Phases of Interhemispheric Inhibition between Motor Related Cortical Areas and the Primary Motor Cortex in Human]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1665</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1654</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1666?rss=1">
<title><![CDATA[Major Vault Protein is Expressed along the Nucleus-Neurite Axis and Associates with mRNAs in Cortical Neurons]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1666?rss=1</link>
<description><![CDATA[
<p>Major Vault Protein (MVP), the main constituent of the vault ribonucleoprotein particle, is highly conserved in eukaryotic cells and upregulated in a variety of tumors. Vaults have been speculated to function as cargo transporters in several cell lines, yet no work to date has characterized the protein in neurons. Here we first describe the cellular and subcellular expression of MVP in primate and rodent cerebral cortex, and in cortical neurons in vitro. In prefrontal, somatosensory and hippocampal cortices, MVP was predominantly expressed in pyramidal neurons. Immunogold labeled free and attached ribosomes, and structures reminiscent of vaults on the rough endoplasmic reticulum and the nuclear envelope. The nucleus was immunoreactive in association with nucleopores. Axons and particularly principal dendrites expressed MVP along individual microtubules, and in pre- and postsynaptic structures. Synapses were not labeled. Colocalization with microtubule-associated protein-2, tubulin, tau, and phalloidin was observed in neurites and growth cones in culture. Immunoprecipitation coupled with reverse transcription PCR showed that MVP associates with mRNAs that are known to be translated in response to synaptic activity. Taken together, our findings provide the first characterization of neuronal MVP along the nucleus&ndash;neurite axis and may offer new insights into its possible function(s) in the brain.</p>
]]></description>
<dc:creator><![CDATA[Paspalas, C. D., Perley, C. C., Venkitaramani, D. V., Goebel-Goody, S. M., Zhang, Y., Kurup, P., Mattis, J. H., Lombroso, P. J.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn203</dc:identifier>
<dc:title><![CDATA[Major Vault Protein is Expressed along the Nucleus-Neurite Axis and Associates with mRNAs in Cortical Neurons]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1677</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1666</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1678?rss=1">
<title><![CDATA[Pyramidal Neurons in Rat Prefrontal Cortex Projecting to Ventral Tegmental Area and Dorsal Raphe Nucleus Express 5-HT2A Receptors]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1678?rss=1</link>
<description><![CDATA[
<p>The prefrontal cortex (PFC) is involved in higher brain functions altered in schizophrenia. Classical antipsychotics modulate cortico-limbic circuits mainly through subcortical D2 receptor blockade, whereas second generation (atypical) antipsychotics preferentially target cortical 5-HT receptors. Anatomical and functional evidence supports a PFC-based control of the brainstem monoaminergic nuclei. Using a combination of retrograde tracing experiments and in situ hybridization we report that a substantial proportion of PFC pyramidal neurons projecting to the dorsal raphe (DR) and/or ventral tegmental area (VTA) express 5-HT<SUB>2A</SUB> receptors. Cholera-toxin B application into the DR and the VTA retrogradely labeled projection neurons in the medial PFC (mPFC) and in orbitofrontal cortex (OFC). In situ hybridization of 5-HT<SUB>2A</SUB> receptor mRNA in the same tissue sections labeled a large neuronal population in mPFC and OFC. The percentage of DR-projecting neurons expressing 5-HT<SUB>2A</SUB> receptor mRNA was ~60% in mPFC and ~75% in OFC (<I>n</I> = 3). Equivalent values for VTA-projecting neurons were ~55% in both mPFC and ventral OFC. Thus, 5-HT<SUB>2A</SUB> receptor activation/blockade in PFC may have downstream effects on dopaminergic and serotonergic systems via direct descending pathways. Atypical antipsychotics may distally modulate monoaminergic cells through PFC 5-HT<SUB>2A</SUB> receptor blockade, presumably decreasing the activity of neurons receiving direct cortical inputs<b>.</b></p>
]]></description>
<dc:creator><![CDATA[Vazquez-Borsetti, P., Cortes, R., Artigas, F.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn204</dc:identifier>
<dc:title><![CDATA[Pyramidal Neurons in Rat Prefrontal Cortex Projecting to Ventral Tegmental Area and Dorsal Raphe Nucleus Express 5-HT2A Receptors]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1686</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1678</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://cercor.oxfordjournals.org/cgi/content/short/19/7/1687?rss=1">
<title><![CDATA[Seeing with Profoundly Deactivated Mid-level Visual Areas: Non-hierarchical Functioning in the Human Visual Cortex]]></title>
<link>http://cercor.oxfordjournals.org/cgi/content/short/19/7/1687?rss=1</link>
<description><![CDATA[
<p>A fundamental concept in visual processing is that activity in high-order object-category distinctive regions (e.g., lateral occipital complex, fusiform face area, middle temporal+) is dependent on bottom-up flow of activity in earlier retinotopic areas (V2, V3, V4) whose main input originates from primary visual cortex (V1). Thus, activity in down stream areas should reflect lower-level inputs. Here we qualify this notion reporting case LG, a rare case of developmental object agnosia and prosopagnosia. In this person, V1 was robustly activated by visual stimuli, yet intermediate areas (V2&ndash;V4) were strongly deactivated. Despite this intermediate deactivation, activity in down stream visual areas remained robust, showing selectivity for houses and places, while selectivity for faces and objects was impaired. The extent of impairment evident in functional magnetic resonance imaging and electroencephalography activations was somewhat larger in the left hemisphere. This pattern of brain activity, coupled with fairly adequate everyday visual performance is compatible with models emphasizing the role of nonlinear local "amplification" of neuronal inputs in eliciting activity in ventral and dorsal visual pathways as well as perceptual experience in the human brain. Thus, while the proper functioning of intermediate areas appears essential for specialization in the cortex, daily visual behavior and reading are maintained even with deactivated intermediate visual areas.</p>
]]></description>
<dc:creator><![CDATA[Gilaie-Dotan, S., Perry, A., Bonneh, Y., Malach, R., Bentin, S.]]></dc:creator>
<dc:date>2009-06-08</dc:date>
<dc:identifier>info:doi/10.1093/cercor/bhn205</dc:identifier>
<dc:title><![CDATA[Seeing with Profoundly Deactivated Mid-level Visual Areas: Non-hierarchical Functioning in the Human Visual Cortex]]></dc:title>
<dc:publisher>Oxford University Press</dc:publisher>
<prism:number>7</prism:number>
<prism:volume>19</prism:volume>
<prism:endingPage>1703</prism:endingPage>
<prism:publicationDate>2009-07-01</prism:publicationDate>
<prism:startingPage>1687</prism:startingPage>
<prism:section>Articles</prism:section>
</item>

</rdf:RDF>