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  • 1
    Online Resource
    Online Resource
    Society for Neuroscience ; 2005
    In:  The Journal of Neuroscience Vol. 25, No. 21 ( 2005-05-25), p. 5225-5229
    In: The Journal of Neuroscience, Society for Neuroscience, Vol. 25, No. 21 ( 2005-05-25), p. 5225-5229
    Abstract: Thalamic projections to prefrontal cortex are important for executive aspects of attention. Using two-photon imaging in prefrontal brain slices, we show that nicotine and the wakefulness neuropeptide hypocretin (orexin) excite the same identified synapses of the thalamocortical arousal pathway within the prefrontal cortex. Although it is known that attention can be improved when nicotine is infused directly into the midlayer of the prefrontal cortex in the rat, the effects of hypocretin on attention are not known. The overlap in thalamocortical synapses excited by hypocretin and nicotine and the lack of direct postsynaptic effects prompted us to compare their effects on a sustained and divided attention task in the rat. Similar to nicotine, infusions of hypocretin-2 peptide into the prefrontal cortex significantly improved accuracy under high attentional demand without effects on other performance measures. We show for the first time that hypocretin can improve attentional processes relevant to executive functions of the prefrontal cortex.
    Type of Medium: Online Resource
    ISSN: 0270-6474 , 1529-2401
    Language: English
    Publisher: Society for Neuroscience
    Publication Date: 2005
    detail.hit.zdb_id: 1475274-8
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  • 2
    Online Resource
    Online Resource
    Wiley ; 2005
    In:  European Journal of Neuroscience Vol. 21, No. 4 ( 2005-02), p. 945-958
    In: European Journal of Neuroscience, Wiley, Vol. 21, No. 4 ( 2005-02), p. 945-958
    Abstract: The somatodendritic 5‐HT 1A autoreceptor has been considered a major determinant of the output of the serotonin (5‐HT) neuronal system. However, recent studies in brain slices from the dorsal raphe nucleus have questioned the relevance of 5‐HT autoinhibition under physiological conditions. In the present study, we found that the difficulty in demonstrating 5‐HT tonic autoinhibition in slice results from in vitro conditions that are unfavorable for sustaining 5‐HT synthesis. Robust, tonic 5‐HT 1A autoinhibition can be restored by reinstating in vivo 5‐HT synthesizing conditions with the initial 5‐HT precursor l ‐tryptophan and the tryptophan hydroxylase co‐factor tetrahydrobiopterin (BH 4 ). The presence of tonic autoinhibition under these conditions was revealed by the disinhibitory effect of a low concentration of the 5‐HT 1A antagonist WAY 100635. Neurons showing an autoinhibitory response to l ‐tryptophan were confirmed immunohistochemically to be serotonergic. Once conditions for tonic autoinhibition had been established in raphe slice, we were able to show that 5‐HT autoinhibition is critically regulated by the tryptophan hydroxylase‐activating kinases calcium/calmodulin protein kinase II (CaMKII) and protein kinase A (PKA). In addition, at physiological concentrations of l ‐tryptophan, there was an augmentation of 5‐HT 1A receptor‐mediated autoinhibition when the firing of 5‐HT cells activated with increasing concentrations of the α 1 adrenoceptor agonist phenylephrine. Increased calcium influx at higher firing rates, by activating tryptophan hydroxylase via CaMKII and PKA, can work together with tryptophan to enhance negative feedback control of the output of the serotonergic system.
    Type of Medium: Online Resource
    ISSN: 0953-816X , 1460-9568
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2005
    detail.hit.zdb_id: 2005178-5
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  • 3
    Online Resource
    Online Resource
    Elsevier BV ; 2003
    In:  Neuron Vol. 40, No. 1 ( 2003-09), p. 139-150
    In: Neuron, Elsevier BV, Vol. 40, No. 1 ( 2003-09), p. 139-150
    Type of Medium: Online Resource
    ISSN: 0896-6273
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2003
    detail.hit.zdb_id: 2001944-0
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  • 4
    In: Journal of Neurobiology, Wiley, Vol. 66, No. 4 ( 2006-03), p. 408-420
    Abstract: BDNF is thought to provide critical trophic support for serotonin neurons. In order to determine postnatal effects of BDNF on the serotonin system, we examined a line of conditional mutant mice that have normal brain content of BDNF during prenatal development but later depletion of this neurotrophin in the postnatal period. These mice show a behavioral phenotype that suggests serotonin dysregulation. However, as shown here, the presynaptic serotonin system in the adult conditional mutant mice appeared surprisingly normal from histological, biochemical, and electrophysiological perspectives. By contrast, a dramatic and unexpected postsynaptic 5‐HT 2A deficit in the mutant mice was found. Electrophysiologically, serotonin neurons appeared near normal except, most notably, for an almost complete absence of expected 5‐HT 2A ‐mediated glutamate and GABA postsynaptic potentials normally displayed by these neurons. Further analysis showed that BDNF mutants had much reduced 5‐HT 2A receptor protein in dorsal raphe nucleus and a similar deficit in prefrontal cortex, a region that normally shows a high level of 5‐HT 2A receptor expression. Recordings in prefrontal slice showed a marked deficit in 5‐HT 2A ‐mediated excitatory postsynaptic currents, similar to that seen in the dorsal raphe. These findings suggest that postnatal levels of BDNF play a relatively limited role in maintaining presynaptic aspects of the serotonin system and a much greater role in maintaining postsynaptic 5‐HT 2A and possibly other receptors than previously suspected. © 2006 Wiley Periodicals, Inc. J Neurobiol, 2006
    Type of Medium: Online Resource
    ISSN: 0022-3034 , 1097-4695
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2006
    detail.hit.zdb_id: 1474900-2
    detail.hit.zdb_id: 2266191-8
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  • 5
    In: The Journal of Physiology, Wiley, Vol. 541, No. 1 ( 2002-05), p. 169-185
    Abstract: The noradrenergic neurons of the locus coeruleus (LC) play an important role in modulating arousal and selective attention. A similar function has been attributed to the hypocretin neurons of the hypothalamus which maintain a strong synaptic projection to the LC. As the LC can be difficult to detect in the embryonic and neonatal mouse brain, we used a new transgenic mouse with strong GFP expression in the LC under the regulation of a mouse prion promoter. GFP colocalized with immunoreactive tyrosine hydroxylase in sections and dispersed cultures of the LC, allowing visualization and whole cell or single‐unit recording from the LC in early stages of cellular development. GFP expression in the LC had no apparent effect on cellular physiology, including resting membrane potential, input resistance, spike threshold, depolarization‐induced spike frequency increase, current‐voltage relations, or hypocretin responses. In slices of the mature mouse and rat LC, hypocretin‐1 and −2 increased spike frequency, with hypocretin‐1 being an order of magnitude more potent. In the postnatal day (P) 0‐2 developing mouse slice during a developmental period when spikes could be elicited in some cells, other developing LC neurons showed rhythmic, subthreshold oscillations (≈1 Hz) in membrane potential (2.9‐7.4 mV amplitude); others were arrhythmic. Hypocretin‐1 depolarized the membrane potential, resulting in the appearance of spikes in developing LC cells that showed no spikes under control conditions. In the presence of TTX and glutamate receptor antagonists, hypocretin‐1‐mediated inward currents were blocked by substitution of choline‐Cl for NaCl, suggesting an excitatory mechanism based on an inward cation current. Hypocretin‐1 initiated strong regular membrane voltage oscillations in arrhythmic immature neurons. Hypocretin increased the temporal synchrony of action potentials studied with dual‐cell recording in P1‐P5 mouse LC slices, consistent with the view that synchrony of LC output, associated with improved cognitive performance, may be increased by hypocretin. Together these data suggest that the hypothalamus, via hypocretin projections, may therefore be in a position to enhance arousal and modulate plasticity in higher brain centres through the developing LC.
    Type of Medium: Online Resource
    ISSN: 0022-3751 , 1469-7793
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2002
    detail.hit.zdb_id: 1475290-6
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  • 6
    Online Resource
    Online Resource
    Society for Neuroscience ; 2001
    In:  The Journal of Neuroscience Vol. 21, No. 24 ( 2001-12-15), p. 9955-9963
    In: The Journal of Neuroscience, Society for Neuroscience, Vol. 21, No. 24 ( 2001-12-15), p. 9955-9963
    Abstract: Serotonin 5-HT 2A receptors have been implicated in psychiatric illness and the psychotomimetic effects of hallucinogens. In brain slices, focal stimulation of 5-HT 2A receptors in rat prefrontal cortex results in dramatically increased glutamate release onto layer V pyramidal neurons, as measured by an increase in “spontaneous” (nonelectrically evoked) EPSCs. This glutamate release is blocked by tetrodotoxin (TTX) and is thought to involve local spiking in thalamocortical axon terminals; however, the detailed mechanism has remained unclear. Here, we investigate parallels in EPSCs induced by either serotonin or the potassium channel blockers 4-aminopyridine (4-AP) or α-dendrotoxin (DTX). DTX, a selective blocker of Kv1.1-, Kv1.2-, and Kv1.6-containing potassium channels, has been shown to release glutamate in cortical synaptosomes, presumably by inhibiting a subthreshold-activated, slowly inactivating potassium conductance. By comparing DTX with other potassium channel blockers, we found that the ability to induce EPSCs in cortical pyramidal neurons depends on affinity for Kv1.2 subunits. DTX-induced EPSCs are similar to 5-HT-induced EPSCs in terms of sensitivity to TTX and ω-agatoxin-IVA (a blocker of P-type calcium channels) and laminar selectivity. The involvement of thalamocortical terminals in DTX-induced EPSCs was confirmed by suppression of these EPSCs by μ-opiates and thalamic lesions. More directly, DTX-induced EPSCs substantially occlude those induced by 5-HT, suggesting a common mechanism of action. No occlusion by DTX was seen when EPSCs were induced by a nicotinic mechanism. These results indicate that blockade of Kv1.2-containing potassium channels is part of the mechanism underlying 5-HT-induced glutamate release from thalamocortical terminals.
    Type of Medium: Online Resource
    ISSN: 0270-6474 , 1529-2401
    Language: English
    Publisher: Society for Neuroscience
    Publication Date: 2001
    detail.hit.zdb_id: 1475274-8
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  • 7
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2003
    In:  Neuropsychopharmacology Vol. 28, No. 2 ( 2003-2), p. 216-225
    In: Neuropsychopharmacology, Springer Science and Business Media LLC, Vol. 28, No. 2 ( 2003-2), p. 216-225
    Type of Medium: Online Resource
    ISSN: 0893-133X , 1740-634X
    RVK:
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2003
    detail.hit.zdb_id: 2008300-2
    SSG: 15,3
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  • 8
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2006
    In:  Neuropsychopharmacology Vol. 31, No. 8 ( 2006-8), p. 1682-1689
    In: Neuropsychopharmacology, Springer Science and Business Media LLC, Vol. 31, No. 8 ( 2006-8), p. 1682-1689
    Type of Medium: Online Resource
    ISSN: 0893-133X , 1740-634X
    RVK:
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2006
    detail.hit.zdb_id: 2008300-2
    SSG: 15,3
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  • 9
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 1981
    In:  Naunyn-Schmiedeberg's Archives of Pharmacology Vol. 317, No. 3 ( 1981-11), p. 273-275
    In: Naunyn-Schmiedeberg's Archives of Pharmacology, Springer Science and Business Media LLC, Vol. 317, No. 3 ( 1981-11), p. 273-275
    Type of Medium: Online Resource
    ISSN: 0028-1298 , 1432-1912
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1981
    detail.hit.zdb_id: 1462940-9
    SSG: 15,3
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  • 10
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 1982
    In:  Naunyn-Schmiedeberg's Archives of Pharmacology Vol. 321, No. 1 ( 1982-10), p. 32-37
    In: Naunyn-Schmiedeberg's Archives of Pharmacology, Springer Science and Business Media LLC, Vol. 321, No. 1 ( 1982-10), p. 32-37
    Type of Medium: Online Resource
    ISSN: 0028-1298 , 1432-1912
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1982
    detail.hit.zdb_id: 1462940-9
    SSG: 15,3
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