ライフサイエンスコーパス: neuronal firing

1 cal work (for example, muscle contraction or neuronal firing).

2 eas of the axon that are critical for proper neuronal firing.

3 scription coupling, synaptic plasticity, and neuronal firing.

4 tauopathy on hippocampal SWRs and associated neuronal firing.

5 no approach yet permits feedback control of neuronal firing.

6 tamatergic synaptic potentials with moderate neuronal firing.

7 ring with a resultant increase of excitatory neuronal firing.

8 ich are major determinants of high-frequency neuronal firing.

9 e monophosphate signaling, which reduces PFC neuronal firing.

10 ause they require artificial manipulation of neuronal firing.

11 tivity-regulated Arc gene affect patterns of neuronal firing.

12 of sleep-active VLPO neurons to promote TMN neuronal firing.

13 e channels are known to critically influence neuronal firing.

14 f distinctive slow potentials that accompany neuronal firing.

15 tauopathy on hippocampal SWRs and associated neuronal firing.

16 uently a blunted neurosteroid suppression of neuronal firing.

17 ight-activatable PIRK switch for suppressing neuronal firing.

18 s as important as functional mitochondria in neuronal firing.

19 ortex, where nAChR blockade had no effect on neuronal firing.

20 for counteracting MOR-mediated inhibition of neuronal firing.

21 pulation oscillations, and precise timing of neuronal firing.

22 k oscillations with a regularized pattern of neuronal firing.

23 ed the synergistic action of leptin/CCK-8 on neuronal firing.

24 nels, leading to membrane depolarization and neuronal firing.

25 nels, leading to membrane depolarization and neuronal firing.

26 5-HT(1A) receptor-mediated inhibition of DRN neuronal firing.

27 an oscillations of clock gene expression and neuronal firing.

28 -2beta results in significant alterations in neuronal firing.

29 (PKC) signaling, which diminishes prefrontal neuronal firing.

30 go-related K(+) channel KCNH2 that modulates neuronal firing.

31 control in order to avoid extreme limits of neuronal firing.

32 ency-independent phase shifts of oscillatory neuronal firing.

33 ducing neuronal sensitization or spontaneous neuronal firing.

34 neuroblastoma cells and expectedly decreased neuronal firing.

35 ization block in neurons with a reduction of neuronal firing.

36 arched this space for stimuli that maximized neuronal firing.

37 dent changes in pump activity also influence neuronal firing.

38 in the presence of blockers of VIP, GABA or neuronal firing.

39 -triggered signaling could elicit changes in neuronal firing.

40 gar food in an operant task and inhibited DA neuronal firing.

41 ich were found to synchronize the Kiss1(ARH) neuronal firing.

42 hat relate the sensory or motor streams with neuronal firing.

43 transcription and boosted Na(+) currents and neuronal firing.

44 89%), evoked synaptic activity (46%), evoked neuronal firing (200%) and increases expression of cellu

45 receptors on SNc neurons leads to increased neuronal firing, activation of M5 receptors in the stria

46 m-activated potassium channel that regulates neuronal firing activities and patterns.

47 y neurons, a variety of the observed dynamic neuronal firing activities can be replicated.

48 nously released ATP in the CN contributes to neuronal firing activity by facilitating AP generation a

49 Regulation of BNSTALG neuronal firing activity is tightly regulated by the opp

50 receded the inhibition of cortical pyramidal neuronal firing activity.

51 aracterized by a 60 degrees -wide correlated neuronal firing (activity packet), both within and acros

52 However, what happens to neuronal firing after a long period of being awake is no

53 on, under conditions known to suppress raphe neuronal firing, also reduced VCMs.

54 s with halorhodopsin (NpHR3.0) increases lHb neuronal firing and abolishes CPP to the intruder-paired

55 ly studied because they play a major role in neuronal firing and bursting.

56 Repeated restraint stress increased BLA neuronal firing and caused hypertrophy of BLA neurons in

57 rons in males, while it decreased LAT and BA neuronal firing and caused hypotrophy of neurons in the

58 oly-spike activity associated with increased neuronal firing and CBF, whereas frontal cortex showed s

59 rtex showed slow oscillations with decreased neuronal firing and CBF.

60 activity provides a link between patterns of neuronal firing and changes in protein translation.

61 hibition of this channel leads to changes in neuronal firing and chemical message transmission.

62 roduces an inverted-U dose response on dlPFC neuronal firing and cognitive performance during working

63 focal epilepsy correlates with reduction of neuronal firing and enhanced interneuronal network activ

64 of alpha4beta2-nAChR agonists increased the neuronal firing and enhanced the spatial tuning of delay

65 ctivations involve a stereotyped sequence of neuronal firing and have been behaviourally linked to me

66 n assumptions about the relationship between neuronal firing and hemodynamic response that are not fi

67 v1.2 gating-changes alter cell excitability, neuronal firing and hormone release on a molecular basis

68 hat these abnormal networks promote abnormal neuronal firing and hyperexcitability, it has yet to be

69 eases catecholamine release in PFC, reducing neuronal firing and impairing cognitive abilities.

70 ic adenosine monophosphate signaling reduces neuronal firing and impairs working memory by increasing

71 ortical rhythm characterized by synchronized neuronal firing and important for sleep and memory.

72 maphos oxon, cause a depolarization-block of neuronal firing and inhibit nicotinic responses.

73 show that marked changes in both cue-induced neuronal firing and input-specific synaptic strength occ

74 h of which can involve nonclassical modes of neuronal firing and integration.

75 This current shapes neuronal firing and is inhibited by neuromodulators, sug

76 array that enables simultaneous recording of neuronal firing and local dopamine receptor antagonist i

77 tum showed increased synchronization between neuronal firing and local field potential activity durin

78 Here, we recorded neuronal firing and local field potentials from the medi

79 tional role of CB(2)R activation, we induced neuronal firing and observed a CB(2)R-mediated reduction

80 s with channelrhodopsin (ChR2) decreases lHb neuronal firing and promotes CPP to the intruder-paired

81 BOLD) signal provides an indirect measure of neuronal firing and reflects slow-evolving hemodynamic a

82 changes in pump activity can also influence neuronal firing and regulate rhythmic network output.

83 een striatal projection cells in controlling neuronal firing and shaping the output of this circuit.

84 al diseases that are associated with altered neuronal firing and signaling.

85 ion was observed to exert complex actions on neuronal firing and synaptic neurotransmission that were

86 In view of their critical role in neuronal firing and their strong sequence conservation d

87 BA 5-HT pathway amplifies fear-associated BA neuronal firing and theta power and phase-locking.

88 for blood pressure regulation and control of neuronal firing, and MthK, a prokaryotic Ca(2+)-gated K(

89 nnels to weaken synaptic efficacy and reduce neuronal firing, and over a longer timeframe, driving ca

90 ing-triggered elevated NPY/AgRP and low POMC neuronal firing, and resulted in decreased feeding of DI

91 energy-related visual information encoded by neuronal firing; and (2) a substantial increase in the a

92 Intra-Acb NPY reduced neuronal firing, as well as preproenkephalin messenger R

93 is unknown whether this compound stops local neuronal firing at concentrations that prevent seizures.

94 Oscillatory septal neuronal firing at delta, theta, and gamma frequencies m

95 and partially opposite effects in regulating neuronal firing at frequencies typical of bursting.

96 analgesia to heat in vivo and a decrease in neuronal firing at the single-cell level.

97 timulation can lead to persistent changes in neuronal firing behavior including switching between fir

98 ing glutamatergic neurons leads to decreased neuronal firing, brainstem inflammation, motor and respi

99 entropy) have been explored to characterize neuronal firings, but only analyze temporal information

100 her AGS kindling results in changes in vlPAG neuronal firing by chronically implanting microwire elec

101 The genes influence neuronal firing by modulating calcium and sodium channel

102 between gene expression, ionic currents, and neuronal firing capacity.

103 iring exclusively during PTC, and this vlPAG neuronal firing change was seen only in kindled GEPR-9s.

104 mine release can be observed under different neuronal firing conditions.

105 Neuronal firing data was obtained from 110 PMv neurons i

106 or for the trial-to-trial variability of the neuronal firing decreases from the spontaneous firing st

107 raic connectivity metric) caused by abnormal neuronal firing during a seizure onset.

108 The dynamics of neuronal firing during natural vision are poorly underst

109 We observed a significant change in neuronal firing during presentation of the cue.

110 ynapses, thereby contributing to a decreased neuronal firing during sleep.

111 Electrophysiologists report on-going neuronal firing during stimulation or task in regions be

112 Neuronal firing during the retrieval of each memory was

113 d sensory and motor timing task suggest that neuronal firing during the sensory and motor phases are

114 When we interfere with the pattern of neuronal firing during this period, coordination is also

115 cortex in awake behaving mice, we found that neuronal firing early in the olfactory pathway simultane

116 Current theories hypothesize that dopamine neuronal firing encodes reward prediction errors.

117 The neuronal firing entropies and oscillations in both nucle

118 ts, Ro25-6981 (500 micromol/L) inhibited ACC neuronal firing, evoked by 30 and 50 mm Hg CRD, by 98% a

119 ffect, which correlates an MRI observable to neuronal firing, evolves over a period that is 2 orders

120 pocampal slice cultures, a 3-5-d blockade of neuronal firing facilitated uptake and degradation of an

121 irole (50-200 nM), resulted in inhibition of neuronal firing followed by DIR.

122 working memory representation, with enhanced neuronal firing following low doses of mGluR2/3 agonists

123 unction biophysical changes and increases in neuronal firing for the two epilepsy-causing mutations a

124 In turn, the Na(+) current can control neuronal firing frequency in a negative feedback loop.

125 cally modified in dyskinetic monkeys and its neuronal firing frequency significantly increased in ON

126 rhythm of activation that correlates with LC neuronal firing frequency.

127 We analyzed the relationship between the neuronal firing from intraoperative microrecordings from

128 antagonist, DNQX, which might suppress local neuronal firing, generate either appetitive or defensive

129 he temporal pattern of astrocyte response to neuronal firing has not been fully characterized.

130 BK) channels, important in vasodilation and neuronal firing, have been suggested to be directly stim

131 es with discontinuous theta oscillations and neuronal firing in both lateral entorhinal cortex and ve

132 o neurons produced a 42% greater increase in neuronal firing in cells from the SHR than the WKY rat.

133 we investigated to what extent modulation of neuronal firing in cerebellar nuclei (CN), which are ana

134 e proposed a functional role for synchronous neuronal firing in generating the neural code of a senso

135 not downregulation, of alpha2delta3 enhances neuronal firing in immature cultures, whereas later in d

136 Accordingly, 5-HT abolished spontaneous neuronal firing in naive and dependent rats but had bidi

137 Finally, CO2-evoked neuronal firing in patch-clamped subfornical organ neuro

138 However, both mutations increased neuronal firing in primary neuronal cultures.

139 We investigated the quality and strength of neuronal firing in primate visual area V2 by analyzing c

140 rm of homeostatic plasticity that stabilizes neuronal firing in response to changes in synapse number

141 Neuronal firing in response to current injection was pro

142 ssociated with a more pronounced increase in neuronal firing in response to D2 agonist, compared to t

143 ng to increased reliability or regularity of neuronal firing in single neurons and across populations

144 tatory networks that can maintain persistent neuronal firing in the absence of external stimulation.

145 NPY reduces neuronal firing in the Acb resulting in increased palata

146 To investigate the relationship between neuronal firing in the basal ganglia and cortical gamma

147 channels and contribute to the inhibition of neuronal firing in the central nervous system or to faci

148 lay an important role in the coordination of neuronal firing in the entorhinal (EC)-hippocampal syste

149 te) receptor mediates two dynamic changes in neuronal firing in the hippocampal CA1 area during novel

150 Neuronal firing in the hippocampal formation (HF) of fre

151 Here we report that neuronal firing in the locus coeruleus is especially sen

152 We investigated whether dynorphinergic neuronal firing in the NAc is sufficient to induce avers

153 em, clofibrate blocked nicotine's effects on neuronal firing in the ventral tegmental area and on dop

154 7 had no effect on basal and CRD-induced ACC neuronal firing in VH and control groups.

155 short latency and intensity-dependent vlPAG neuronal firing increases.

156 temporal sequence of pre- and post-synaptic neuronal firing into corresponding synaptic weights.

157 Increased neuronal firing irregularity was seen in the PCL and, to

158 Neuronal firing is a fundamental element of cerebral fun

159 Organized neuronal firing is crucial for cortical processing and i

160 Massed synchronised neuronal firing is detrimental to information processing

161 When neuronal firing is facilitated by depolarizing juxtasoma

162 ch here indicate that increased or decreased neuronal firing is responsible for distinct clinical phe

163 this study it was tested whether periods of neuronal firing lead to a rapid change of membrane prope

164 ophysiological studies whereby reduced AcbSh neuronal firing leads to food intake.

165 e-an alpha2A-adrenergic agonist-inhibited LC neuronal firing less efficiently than in control animals

166 rate how this system can be used to decouple neuronal firing levels from ongoing changes in network e

167 ynamic LFOs correlated both with Ca(2+)i and neuronal firing (local field potentials), indicating tha

168 chemical inputs to the LC with changes in LC neuronal firing, making it a highly coordinated event.

169 trolateral clock neurons, and suppression of neuronal firing may be the general response to sNPF rece

170 Correspondingly, DA neuronal firing measured 24 h after nicotine exposure us

171 The claustral neuronal firings mostly correlated with cortical SW acti

172 irectly demonstrate, for the first time, how neuronal firing of dopamine neurons originating in the V

173 d function, CREB-mediated transcription, and neuronal firing of relay neurons during injury-induced c

174 To explore the potential effects of neuronal firing on ECoG, we developed a model to estimat

175 low these cells to exacerbate or synchronize neuronal firing on shorter time scales of milliseconds t

176 laps during model tuning, we show that, from neuronal firing, one can accurately estimate log-concent

177 uption of neural communication by inhibiting neuronal firing or by physical cutting suppresses both S

178 ion within these vulnerable sLNvs depends on neuronal firing or light.

179 In contrast, neuronal firing order during interictal bursts appeared

180 ic voltage fluctuations and strongly impacts neuronal firing output.

181 hypothesized that 1) the temporal pattern of neuronal firing, particularly co-firing, is key to decod

182 s is sensitive to noise and stochasticity in neuronal firing patterns and assembly heterogeneity.

183 cuits, the extent to which it will determine neuronal firing patterns and network activity remains po

184 Since alterations in axonal signaling affect neuronal firing patterns and neurotransmitter release, t

185 Behaviorally adequate neuronal firing patterns are critically dependent on the

186 Neuronal firing patterns are established by the collecti

187 n "informational lesion," whereby pathologic neuronal firing patterns are replaced by low-entropy, st

188 Here, we examined hippocampal neuronal firing patterns as rats ran in place on a tread

189 ring patterns are distinctive: whereas multi-neuronal firing patterns at larger distances can be pred

190 ject associations represented by hippocampal neuronal firing patterns but did not affect spatial firi

191 Abnormal neuronal firing patterns characteristic of the fast deac

192 Acoustic responses and neuronal firing patterns during AGS were compared in non

193 c appearance of the LFP, the organization of neuronal firing patterns during spindles bears little re

194 Computational modeling based on neuronal firing patterns in animals suggests that one pu

195 Moreover, InSyn1 null mice exhibit elevated neuronal firing patterns in the hippocampus and deficits

196 associated with increased synchronization of neuronal firing patterns in the hippocampus and the conn

197 work level, on the replay of spatially tuned neuronal firing patterns representing discrete places an

198 navigation and episodic memory, but how its neuronal firing patterns underlie those functions is not

199 Neuronal firing patterns were analysed by constructing h

200 Neuronal firing patterns, neuromodulators, and cerebral

201 ed with a reorganization of the postsaccadic neuronal firing patterns, which follow a similar retinot

202 ing calcium and potassium channels) to shape neuronal firing patterns.

203 tectal cells could be distinguished based on neuronal firing patterns.

204 Ventral striatal neuronal firing phase-locked not only to hippocampal the

205 Temporally precise neuronal firing phase-locked to gamma oscillations is th

206 oamine transporters has been shown to impact neuronal firing potentials and could play a role in path

207 As information flows through the brain, neuronal firing progresses from encoding the world as se

208 nized to play important roles in determining neuronal firing properties and regulating neuronal excit

209 t, "ramping" activity, a monotonic change in neuronal firing rate across time, is observed throughout

210 tational approaches, we identified decreased neuronal firing rate and deficits in gamma frequency in

211 ese tuning changes occurred rapidly, as both neuronal firing rate and Fano factor showed no evidence

212 When a sensory stimulus repeats, neuronal firing rate and functional MRI blood oxygen lev

213 We found that scopolamine reduced overall neuronal firing rate and impaired rule discriminability

214 However, to date, inconsistent changes in neuronal firing rate and pattern have been reported in p

215 In the belt areas, changes in neuronal firing rate and response dynamics greatly enhan

216 nase pathway can control both neuroendocrine neuronal firing rate and the state of CREB phosphorylati

217 We found that task difficulty modulates neuronal firing rate at the earliest stages of cortical

218 ific: increasing task difficulty enhanced V1 neuronal firing rate at the focus of attention and suppr

219 he LC elicited a significant, dose-dependent neuronal firing rate change in a subset of adrenergic ne

220 de novo sequential experience and increased neuronal firing rate correlations can explain the differ

221 r time despite a persistent reduction in the neuronal firing rate during the task.

222 blue and violet light so as to modulate the neuronal firing rate in a bidirectional way.

223 ptic plasticity which functions to reset the neuronal firing rate in response to chronic neuronal act

224 In parallel, attentional modulation of neuronal firing rate is not uniform but depends upon the

225 We find that, although basal neuronal firing rate is unaffected, there is a dose-depe

226 l regions revealed statistically significant neuronal firing rate modulations during all task phases

227 y, may reflect the effect of fluctuations in neuronal firing rate on the animal's decision, but it ca

228 ing of place fields in CA2 with no effect on neuronal firing rate or immediate early gene expression.

229 es in excitation and inhibition that restore neuronal firing rate to an optimal range.

230 observed progressive increase or decrease in neuronal firing rate, particularly in the supplementary

231 tributed to the homeostatic stabilization of neuronal firing rate.

232 ariability and topographical organization of neuronal firing-rate persistence can provide information

233 quilibrium: synaptic strengths wax and wane, neuronal firing rates adjust up and down, and neural cir

234 nstrate that the mRNA 3'UTR of ppk29 affects neuronal firing rates and associated heat-induced seizur

235 usion in their neurites, and increasing POMC neuronal firing rates and excitability.

236 Alcohol increases CeA activity (neuronal firing rates and GABA release) in naive rats by

237 t relationships could be established between neuronal firing rates and the percentage of CRs or the e

238 Analytical forms for neuronal firing rates are important theoretical tools fo

239 Finally, during spindles neuronal firing rates are not consistently modulated, al

240 onstrated that alternative splicing controls neuronal firing rates by regulating the polarized target

241 Process S as a function of the deviation of neuronal firing rates from a locally defined set-point,

242 Hand stimulation evoked similar neuronal firing rates in lesion and control monkeys.

243 We analyzed neuronal firing rates in relation to a large number of b

244 nisms within the intact CNS act to stabilize neuronal firing rates in the face of sustained sensory p

245 In cortex that is recruited to the seizure, neuronal firing rates increase and waveforms become long

246 Homeostatic adjustment of neuronal firing rates is considered a vital mechanism to

247 Sun et al. discover that neuronal firing rates of hippocampal place cells code fo

248 can produce modulations of cortical area V4 neuronal firing rates that resemble spatial attention-li

249 When neuronal firing rates were perturbed by visual deprivati

250 Neuronal firing rates were threefold higher in Fmr1(-/-)

251 vibrations, up to 800 Hz, is not encoded in neuronal firing rates, but rather in the phase-locked re

252 ot alter the running speed-dependent gain in neuronal firing rates.

253 , we obtain a new spectral representation of neuronal firing rates.

254 to their postsynaptic targets independent of neuronal firing rates.

255 ng-term potentiation or depression driven by neuronal firing rates.

256 d by intrinsic plasticity that downregulates neuronal firing rates.

257 late metabolic signals into an alteration in neuronal firing rates.

258 temporal structure of shared variability in neuronal firing relates to perceptual choices.

259 HP induced by supra-threshold pulses reduced neuronal firing reliability during swimming.

260 construct concentration ratios from observed neuronal firing, representing a powerful mechanism to se

261 ojection to the NAc core, contributes to NAc neuronal firing responses to reward-predictive cues.

262 hanism to prevent excessive and uncontrolled neuronal firing resulting from the lack of inhibition or

263 ve to the presence of contextual cues: shell neuronal firing reveals a significant shift from a predo

264 Although CA2 neuronal firing showed only weak spatial selectivity, it

265 Neuronal firing, synaptic transmission, and its plastici

266 t regulators of cellular processes including neuronal firing, synaptic transmission, cochlear hair ce

267 e inferior colliculus (IC) exhibits enhanced neuronal firing that is critical in the initiation of re

268 odulator, integrating spontaneous and evoked neuronal firing, thereby providing an index of global ac

269 itory cells that exert a powerful control of neuronal firing through proximal synapses on their posts

270 Synaptic scaling stabilizes neuronal firing through the homeostatic regulation of po

271 We observed robust, phasic changes in neuronal firing time locked to the onset of methamphetam

272 ion of gain-modulated firing rates, allowing neuronal firing to be efficiently read out by downstream

273 hannel-FMRP interactions may link changes in neuronal firing to changes in protein translation.

274 n mice enhanced opioid-induced inhibition of neuronal firing to modulate morphine-induced analgesia,

275 Multiple aspects of neural activity, from neuronal firing to neuromodulator release and signaling,

276 a natural consequence of adaptive coding of neuronal firing to optimise sensitivity across large ran

277 Hippocampal theta oscillations coordinate neuronal firing to support memory and spatial navigation

278 ring distinct behavioral states can regulate neuronal firing, transmitter release at glutamatergic an

279 Experiments and theory indicate that neuronal firing typically represents the sum of synaptic

280 The TH loss depends on reduced dopaminergic neuronal firing under aberrant tonic inhibition, which i

281 K currents generate bidirectional effects on neuronal firing under distinct conditions.

282 ulate the hippocampal activity by timing the neuronal firing via monosynaptic afferents, thalamic nuc

283 coordinate in regulating mesolimbic dopamine neuronal firing via presynaptic regulation.

284 Neuronal firing was associated with high rates of inform

285 relative disparity could not predict whether neuronal firing was related to the monkeys' perceptual r

286 Thalamic neuronal firing was studied in a cerebellar relay nucleu

287 Unexpectedly, this resetting of neuronal firing was suppressed during sleep.

288 Using a novel method to track neuronal firing, we analyzed microelectrode array record

289 ates, we demonstrate a robust enhancement of neuronal firing when the figure, as opposed to the groun

290 owever, in low-calcium ACSF, MT-II decreased neuronal firing, whereas alpha-MSH increased it.

291 on process and an initial disfacilitation of neuronal firing (which was later recovered), together wi

292 decreased broadband EEG power and decreased neuronal firing, which demonstrate a steep decline in ne

293 nduce the two GluR1-dependent changes of CA1 neuronal firing, which in turn determine information flo

294 g by AgRP neurons are mediated by changes in neuronal firing, while the control of glucose balance by

295 urons, resulting in a decrease of inhibitory neuronal firing with a resultant increase of excitatory

296 s emerged on P8 as evoked spindle-bursts and neuronal firing with a signal-to-noise ratio higher than

297 However, inhibition of neuronal firing with infrared light was only observed in

298 ht-gated ion channels widely used to control neuronal firing with light (optogenetics).

299 These new analyses showed continued neuronal firing with widespread intense activation and s

300 maintain stable circuit function by keeping neuronal firing within a set point range, but such firin