ライフサイエンスコーパス: spontaneous firing

1 tion, induces a long-lasting increase in GoC spontaneous firing.

2 ted by dopamine to a greater extent than was spontaneous firing.

3 to suprathreshold stimulation and increased spontaneous firing.

4 shed from background inhibition arising from spontaneous firing.

5 zed resting membrane potential and increased spontaneous firing.

6 trains of synaptic inhibition that interrupt spontaneous firing.

7 s were suprathreshold, generating repetitive spontaneous firing.

8 l, which increased RS and the probability of spontaneous firing.

9 rmining the ionic conductances that underlie spontaneous firing.

10 (135/171 or 79%) of these MRF neurons lacked spontaneous firing.

11 mV, and this current is sufficient to drive spontaneous firing.

12 s with an intrinsic propensity for rhythmic, spontaneous firing.

13 y 18 spikes/sec, compared with 16 spikes/sec spontaneous firing.

14 zing afterpotential is sufficient to trigger spontaneous firing.

15 but had a scarce effect on the frequency of spontaneous firing.

16 fane eliminated evoked firing and suppressed spontaneous firing.

17 timulus-evoked firing was affected more than spontaneous firing.

18 neocortical pyramidal neurons and increases spontaneous firing.

19 rent plots at firing frequencies slower than spontaneous firing.

20 that SNr neurons lacking NALCN have impaired spontaneous firing.

21 enlarged mGluR1/5 responses and accelerated spontaneous firing.

22 nt-threshold, increased firing-frequency and spontaneous firing.

23 id not drive spike responses, but suppressed spontaneous firings.

24 ectively, resulted in significant changes in spontaneous firings.

25 During spontaneous firing, a rise in free cytoplasmic calcium w

26 nhibited LTSIs, reducing or abolishing their spontaneous firing activity and causing membrane hyperpo

27 ty genes, including these critical for their spontaneous firing activity and synaptic functions.

28 esponsiveness to peripheral stimuli, reduced spontaneous firing activity from WDR neurons, and improv

29 e the growth factor positively regulates the spontaneous firing activity of both NAc- and PFC-project

30 The overall spontaneous firing activity of Purkinje cells was increa

31 Reducing spontaneous firing activity with 10 nM tetrodotoxin (TTX

32 NC) and ventral tegmental area (VTA) exhibit spontaneous firing activity.

33 in animals with tinnitus exhibited enhanced spontaneous firing, altered burst properties and increas

34 onist, WIN 55,212-2, significantly increased spontaneous firing and bursting rates of VTA DA neurons,

35 NE iontophoresis inhibited spontaneous firing and decreased the responsiveness of B

36 Both spontaneous firing and evoked bursts of spikes were dimi

37 M) cells, noradrenergic activation decreases spontaneous firing and focuses receptive fields.

38 in adult Fgf14(-/-) Purkinje neurons rescues spontaneous firing and improves motor performance.

39 These results held both for spontaneous firing and in the presence of independent vi

40 p recordings showed that riluzole suppressed spontaneous firing and increased the action potential fi

41 f neural populations, including decreases in spontaneous firing and neural habituation.

42 Ephedrine (100-1000 microM) slowed spontaneous firing and produced a modest concentration-d

43 Arousal suppressed spontaneous firing and strongly altered the temporal pat

44 and proximal dendrites of STN neurons during spontaneous firing and their accumulation during driven

45 ivates the superior colliculus by increasing spontaneous firing and, in some cells, whisker-evoked re

46 Hyperpolarization to -85 mV prevented spontaneous firing, and brief depolarization then induce

47 ial of dorsal root ganglion neurons, enhance spontaneous firing, and increase evoked firing of these

48 tured on MEAs displayed a rich repertoire of spontaneous firing, and Shank3 deletion led to reduced f

49 t modulation of membrane potential dynamics, spontaneous firing, and tone-evoked synaptic potentials.

50 but the ionic mechanisms responsible for the spontaneous firing are apparently different.

51 zing shift in resting potential and enhanced spontaneous firing are due to persistent activity of var

52 ls, in the absence of glucose, sustained SNr spontaneous firing at basal rates, but glycolysis may st

53 e of applied odors, piriform neurons exhibit spontaneous firing at mean rates that vary systematicall

54 aneous VP neuronal activity; DAMGO inhibited spontaneous firing but potentiated AMG-evoked glutamater

55 cific PDE3 inhibitor, milrinone, accelerated spontaneous firing by approximately 47% (effects of othe

56 ity and trigger action potentials or inhibit spontaneous firing by depolarization block.

57 uce a large range of the naturally occurring spontaneous firing characteristics of SNc DAs.

58 nin effect on resting membrane potential and spontaneous firing; co-activation of GABA(B) receptors i

59 n the PFC caused a simultaneous reduction in spontaneous firing (consistent with extracellular in viv

60 Both evoked and spontaneous firing could be inhibited by iontophoresis o

61 ld while profoundly suppressing 4-AP-induced spontaneous firing, demonstrating a functional synergy b

62 l of DA subthreshold oscillations (STOs) and spontaneous firing emerges.

63 During quiet wakefulness, the brain produces spontaneous firing events that can spread over large are

64 marked differences between the two types in spontaneous firing, excitability and electrical coupling

65 onductance, may contribute to the changes in spontaneous firings exhibited by retinal ganglion cells

66 ngs reveal that EPG neurons exhibit elevated spontaneous firing following sleep deprivation, which li

67 Similarly, isoprenaline increased the spontaneous firing frequency by an effect exclusively on

68 Circadian changes in membrane potential and spontaneous firing frequency have been observed in micro

69 The spontaneous firing frequency lay in the middle of the dy

70 mp recordings revealed a twofold increase in spontaneous firing frequency of MA-GnRH neurons.

71 luster of differentiation 4 (CD4)), enhanced spontaneous firing frequency.

72 The ongoing synaptic barrage from spontaneous firing, frequency-dependent short-term depre

73 We find that spontaneous firing generates tonic Ca signals in both so

74 During spontaneous firing, glycine release was decreased due to

75 Such spontaneous firing has a structure that reflects the coo

76 d sensory neuron excitability, manifested as spontaneous firing, hyper-responsiveness to stimulation,

77 Increased spontaneous firing (hyperactivity) is induced in fusifor

78 roduced a small depolarization and increased spontaneous firing in 10 of 30 retrogradely labelled gas

79 y and indiscriminately increased the rate of spontaneous firing in all MS/DB neurons.

80 citatory postsynaptic potentials (EPSPs) and spontaneous firing in both types of PGN.

81 strate that SDF-1 alpha dramatically reduces spontaneous firing in Cajal-Retzius cells via hyerpolari

82 of NGF to individual MS/DB neurons increased spontaneous firing in cholinergic, but not in the noncho

83 activation to produce hyperexcitability and spontaneous firing in DRG neurons.

84 n was mainly attributable to the increase of spontaneous firing in DTX.

85 of Ih in the excitability and generation of spontaneous firing in hippocampal stratum oriens-alveus

86 To determine whether SFL is caused by spontaneous firing in nociceptive neurons, we studied th

87 Here, we study spontaneous firing in pyramidal neurons (PNs) from rat s

88 of WDR neurons in OA rats but did not alter spontaneous firing in sham rats.

89 potentials during inspiration, but also have spontaneous firing in the absence of synaptic input.

90 esting membrane potential and suppressed the spontaneous firing in the Arc neurons in slice preparati

91 a role of persistent sodium channels in the spontaneous firing in these cardiorespiratory GABAergic

92 The spontaneous firing in these GABAergic neurons was not al

93 ansient on-chip THC treatment also decreased spontaneous firing in these organoids.

94 Spontaneous firing in TM cells was suppressed by glutama

95 induction of sensitization (i.e., increased spontaneous firing; increased neuronal sensitivity to in

96 rent-clamp recordings demonstrated increased spontaneous firing, lower current threshold, and enhance

97 e found that hCSF increased the frequency of spontaneous firing more than twofold in the two groups o

98 During spontaneous firing, net ionic current flowing between sp

99 Whereas cholinergic activation increases the spontaneous firing (noise) and enlarges the receptive fi

100 serotonergic neuroarchitecture and increased spontaneous firing of 5-HT neurons.

101 Spontaneous firing of a modified Hodgkin-Huxley model ax

102 ed an immediate and dramatic increase in the spontaneous firing of BLA neurons that persisted (and in

103 ndogenous acetylcholine (ACh) release to the spontaneous firing of both regular (probably fusiform ce

104 c neurons in brain slice, including rhythmic spontaneous firing of broad action potentials and, in so

105 tro, with human CSF (hCSF) powerfully boosts spontaneous firing of CA1, CA3 and layer 5 pyramidal neu

106 ill describe the chemokinergic modulation of spontaneous firing of Cajal-Retzius cells, mediated by t

107 Spontaneous firing of cartwheel cells led to activity-de

108 Here we show that changes in spontaneous firing of cartwheel interneurons in the mous

109 uces a profound and reliable increase in the spontaneous firing of CINs in both dorsal striatum and n

110 The effects of different EEG brain states on spontaneous firing of cortical populations are not well

111 lular amphetamine and methamphetamine on the spontaneous firing of cultured midbrain dopaminergic neu

112 rficial DCN, and support the hypothesis that spontaneous firing of DCN neurons is sustained in part b

113 was shown to induce a transient pause in the spontaneous firing of dopamine neurons.

114 evented the dopamine-induced increase in the spontaneous firing of dopaminergic neurons and the corre

115 ry neurons resulted in hyperexcitability and spontaneous firing of dorsal root ganglia (DRG) neurons,

116 Na(V)1.7 that increase firing frequency and spontaneous firing of dorsal root ganglion (DRG) neurons

117 r beta-hydroxybutyrate, while monitoring the spontaneous firing of GABAergic neurons in mouse substan

118 Local CGP55845 application increased the spontaneous firing of GPe and GPi neurons, suggesting th

119 iquely required for determining the inherent spontaneous firing of hippocampal CA1 pyramids, independ

120 Spontaneous firing of injured nerves is believed to play

121 tion produced a compensatory increase in the spontaneous firing of layer 2/3 pyramidal neurons in acu

122 alamocortical synapse, caused by significant spontaneous firing of LGNd cells (approximately 8 Hz).

123 ted that the tongue tumor produced increased spontaneous firing of lingual fibers compared to control

124 Electrotonic coupling synchronizes the spontaneous firing of locus ceruleus (LC) neurons in the

125 same slices, naloxone increased the average spontaneous firing of locus coeruleus cells to 0.96 Hz (

126 er-responsiveness to D-amphetamine, elevated spontaneous firing of midbrain dopamine neurons, and dis

127 ide channel in skeletal muscle, which causes spontaneous firing of muscle action potentials (myotonia

128 r goal was to identify currents that trigger spontaneous firing of muscle in the setting of reduced C

129 rimary striatal cultures, caffeine increased spontaneous firing of neurons between 12 and 80 min afte

130 activation, to produce hyperexcitability and spontaneous firing of nociceptive neurons that underlie

131 e TRESK activator, cloxyquin, can reduce the spontaneous firing of nociceptors in an in vitro human p

132 ion of DRN 5-HT neurons rapidly inhibits the spontaneous firing of olfactory cortical neurons, acting

133 mulation of astrocytes in vivo increases the spontaneous firing of parvalbumin-positive (PV(+)) inhib

134 CUS exposure increased spontaneous firing of POMC neurons in both male and fema

135 sibility, we measured the effects of 5-HT on spontaneous firing of projection neurons in the premotor

136 maintaining the frequency and regularity of spontaneous firing of Purkinje cells.

137 We conclude that the spontaneous firing of Purkinje neuron cell bodies depend

138 We tested for modulation of spontaneous firing of Purkinje neurons in cerebellar sli

139 We have examined the spontaneous firing of Purkinje neurons in isolation from

140 y of interneurons, but did suppress aberrant spontaneous firing of pyramidal neurons and was associat

141 Spontaneous firing of SL-S (20.6 +/- 2.2 impulses s(-1))

142 n grip force behavior, and on the evoked and spontaneous firing of spinal wide dynamic range (WDR) an

143 of (1) flinches induced by formalin and (2) spontaneous firing of spinal wide dynamic range cells.

144 They are believed to be initiated by the spontaneous firing of Starburst Amacrine Cells (SACs), w

145 After DA-depletion, the spontaneous firing of Str-GPe neurons increases, and MC

146 s to quantify the ionic currents driving the spontaneous firing of substantia nigra pars compacta neu

147 rast, WIN55,212,2 hyperpolarized and reduced spontaneous firing of the neighboring hypocretin cells,

148 elatively larger diameter and higher rate of spontaneous firing of the off-centre cells were maintain

149 Excitability and spontaneous firing of the presynaptic VIP+ neurons were

150 onous EPSCs were observed that resulted from spontaneous firing of the same presynaptic fiber.

151 Although superfused 5HT inhibits the spontaneous firing of these cells, the persistence of au

152 Spontaneous firing of ventral tegmental area (VTA) dopam

153 echanical stimulation of the knee and on the spontaneous firing of WDR neurons adds to the growing ap

154 inistration of A-889425 reduced the elevated spontaneous firing of WDR neurons in OA rats but did not

155 Spontaneous firing of WDR neurons was elevated in the OA

156 Spontaneous firings of ectopic foci, coupled with sinus

157 nhibitory postsynaptic currents (sIPSCs) and spontaneous firings of rat ventrolateral periaqueductal

158 s and subsequent recovery and enhancement of spontaneous firings of somatosensory cortical pyramidal

159 e other receptive field led to a decrease of spontaneous firings of the same neuron.

160 neurons reduced GABA release and accelerated spontaneous firings of VTA dopamine neurons.

161 When basal intracellular Ca is raised by spontaneous firing or reduced by voltage clamping at sub

162 tanding still to running, without changes in spontaneous firing or stimulus selectivity.

163 ith p.Asn1768Asp channels revealed increased spontaneous firing, paroxysmal-depolarizing-shift-like c

164 Golgi cells were identified by both spontaneous firing pattern and response properties, and

165 Current clamp studies reveal complex spontaneous firing patterns in a subset of neurons, incl

166 The spontaneous firing patterns of striatal cholinergic inte

167 ereby creating mechanisms for control of the spontaneous firing patterns of these neurons.

168 brainstem demonstrate distinct, synchronized spontaneous firing patterns only in animals that develop

169 variable interspike intervals, and different spontaneous firing patterns than did type II ventral pal

170 xtrasynaptic GABA(A) receptors may influence spontaneous firing patterns that are critical for the es

171 Spontaneous firing patterns with bursts of action potent

172 ed by glutamatergic antagonists, even though spontaneous firing persists in many "autonomously active

173 AS mice as shown by synaptic plasticity and spontaneous firing properties that resembled those of co

174 d low-dimensional controllers for regulating spontaneous firing properties, and gain insight into how

175 During the dark period, the mean spontaneous firing rate (5.00 +/- 0.88 spikes s-1; mean

176 ion than on GSNs and only a 200% increase in spontaneous firing rate (P < 0.05 vs. GSN).

177 The SCN exhibits a daily oscillation in spontaneous firing rate (SFR), but the ionic conductance

178 Synchrony and bursting, as well as spontaneous firing rate (SFR), correlated with behaviora

179 al single action potentials, but the average spontaneous firing rate (spikes/s) was almost 10-fold gr

180 d ocular pressure resulted in differences in spontaneous firing rate and action potential threshold c

181 Furthermore, we show that spontaneous firing rate and burst activity are modulated

182 plasticity depended on the baseline level of spontaneous firing rate and cell excitability.

183 eurons (ChNs) in the mHb exhibited increased spontaneous firing rate and enhanced firing regularity i

184 R agonists were all inhibitory, reducing the spontaneous firing rate and hyperpolarizing vGluT2 neuro

185 wer daytime irradiance, daytime peaks in SCN spontaneous firing rate and membrane depolarization were

186 erse other aspects of central sensitization: spontaneous firing rate and neuronal response magnitude

187 l, a beta-receptor antagonist, decreased the spontaneous firing rate and potentiated the NE-evoked in

188 omol/l) caused a 500% increase (P < 0.01) in spontaneous firing rate and rapid and lasting depolariza

189 bility of cultured neurons by increasing the spontaneous firing rate and reducing the threshold for r

190 ses of SGNs have been characterized by their spontaneous firing rate and responses to sound and those

191 wed significant circadian variation in their spontaneous firing rate and resting membrane potential.

192 e arcopallium (RA), show increased intrinsic spontaneous firing rate and soma size when birds are in

193 2C/D-containing receptors decreases both the spontaneous firing rate and the overall firing rate elic

194 An increase in whole cell I(Na) changes the spontaneous firing rate and this may be the underlying c

195 dor stimulation, ORNs and PNs display a high spontaneous firing rate but KCs are nearly silent.

196 n 55212-2 (WIN2) and CP 55940 increased SNpr spontaneous firing rate by 13-46%, similar to the effect

197 ow that sustained (>40 min) increases in the spontaneous firing rate can be triggered by activation o

198 ation and skin stimulation did not decrease; spontaneous firing rate did not increase.

199 ed mouse SCN expressed a circadian rhythm in spontaneous firing rate for weeks in culture.

200 The spontaneous firing rate in CA3 neurons transiently decre

201 nduced tinnitus is associated with increased spontaneous firing rate in dorsal cochlear nucleus princ

202 nnel blocker (XE991)-induced increase in the spontaneous firing rate in LHb neurons was smaller.

203 or stromatoxin-1 significantly increased the spontaneous firing rate in NPY neurons from lean mice.

204 ) significantly and reversibly increased the spontaneous firing rate of 37/45 cholinergic interneuron

205 e enzyme, in the patch pipette increased the spontaneous firing rate of all dopamine neurons tested i

206 We find that dopamine lesion decreases the spontaneous firing rate of ChIs, whereas chronic treatme

207 ns of bicuculline or picrotoxin enhanced the spontaneous firing rate of cortical neurons, indicating

208 ization of Tmod2 KO neurons showed increased spontaneous firing rate of early postnatal and adult cor

209 Here we report that histamine reduced the spontaneous firing rate of GABAergic preoptic neurons by

210 m of long-term plasticity that regulates the spontaneous firing rate of GoCs in the rat cerebellar co

211 tonic inhibition significantly increases the spontaneous firing rate of granule cells while only mode

212 th agents produced significant reductions in spontaneous firing rate of hippocampal pyramidal neurons

213 However, the spontaneous firing rate of individual retinal ganglion c

214 Ang II (0.3 to 1 mumol/L) increased the spontaneous firing rate of most bulbospinal neurons (+25

215 hydroxybutyrate or acetoacetate) reduced the spontaneous firing rate of neurons in slices from rat or

216 many painful conditions, an increase in the spontaneous firing rate of neurons is often observed in

217 are mediated by increasing or decreasing the spontaneous firing rate of pacemaker cells in the sinoat

218 e reveal a tinnitus-specific increase in the spontaneous firing rate of principal neurons (hyperactiv

219 IPSCs evoked at the mean spontaneous firing rate of Purkinje cells (50 Hz) depres

220 onto cerebellar nuclear somata and the high spontaneous firing rate of Purkinje neurons.

221 The rhythmic spontaneous firing rate of RMTg neurons was decreased an

222 Activation of M5 also increased the spontaneous firing rate of SNc neurons, suggesting that

223 of ion channels that is crucial for the high spontaneous firing rate of SNr neurons.

224 athing nigral slices caused increases in the spontaneous firing rate of some dopamine neurons.

225 Spontaneous firing rate of the basket cells is unaltered

226 We show that high salt intake increases the spontaneous firing rate of VP neurons in vivo and that c

227 Hb neurons in brain slices and increased the spontaneous firing rate of VTA dopaminergic neurons in v

228 cadian pacemaker, show a circadian rhythm in spontaneous firing rate that can be recorded in vitro.

229 Our results show that part of spontaneous firing rate variability in regions best know

230 In dopaminergic neurons the spontaneous firing rate was enhanced by extracellular ap

231 er high spinal transaction demonstrated that spontaneous firing rate was intrinsic to the EMNs and wa

232 afterhyperpolarization, which increases the spontaneous firing rate without affecting the resting me

233 In sensitized rats LC neurons had a higher spontaneous firing rate, and clonidine-an alpha2A-adrene

234 esponse probability correlated strongly with spontaneous firing rate, but weakly with tuning properti

235 arized resting membrane potential, decreased spontaneous firing rate, increased current-induced firin

236 Finally, spontaneous firing rate, interspike interval variance, a

237 the cells underlying these events have a low spontaneous firing rate, unlike the cells giving rise to

238 n electrophysiological properties other than spontaneous firing rate.

239 size, shape, input resistance, I(h) size, or spontaneous firing rate.

240 ptin neurons, which also exhibited increased spontaneous firing rate.

241 nsmitter release, and, consequently, reduced spontaneous firing rate.

242 function of pulse rate, pulse amplitude, and spontaneous firing rate.

243 nd that endogenous 5-HT could roughly double spontaneous firing rate.

244 % of neurons that immediately elevated their spontaneous firing rates (FRs) and developed firing resp

245 ons with very fast conducting axons and high spontaneous firing rates (largely "Cx" type) receives mo

246 itory nerve fibers (ANFs) exhibit a range of spontaneous firing rates (SRs) that are inversely correl

247 e sole partner of 10-30 ANFs with a range of spontaneous firing rates (SRs).

248 cochlear damage, bushy cells show increased spontaneous firing rates across a wide-frequency range,

249 t stress significantly increased the in vivo spontaneous firing rates and bursting events in suscepti

250 s were identified: silent neurones having no spontaneous firing rates and EPSP-driven neurones having

251 aining NMDA receptors in vivo decreased both spontaneous firing rates and firing evoked by amplitude-

252 rization triggered long-lasting increases in spontaneous firing rates and firing responses to intrace

253 rats with SCI show significant increases in spontaneous firing rates and in the magnitude and durati

254 Spontaneous firing rates and mechanical responses to dur

255 Spontaneous firing rates and patterns of cell discharge

256 Densely innervated FTNs had high spontaneous firing rates and pronounced postinhibitory r

257 itory thalamus, however, engagement enhanced spontaneous firing rates but did not affect evoked respo

258 Mean spontaneous firing rates decreased by 58% in the CM/CL n

259 Some neurons increased their spontaneous firing rates during flight, though their inc

260 stimulus reduced positive stimulus bias and spontaneous firing rates in SC but not S1, suggesting th

261 mechanisms, most of which invoke changes in spontaneous firing rates of central auditory neurons res

262 y prevented the morphine-induced increase in spontaneous firing rates of LC neurons in brain slices.

263 These results show that spontaneous firing rates of midlayer spiny populations a

264 Indeed, the spontaneous firing rates of neurons in the amygdala are

265 Similarly, the spontaneous firing rates of SC but not S1 neurons predic

266 Spontaneous firing rates of TC neurons were higher, and

267 Thresholds and spontaneous firing rates of VCN and MNTB neurons were no

268 and tended to have smaller somata and lower spontaneous firing rates than did type II ventral pallid

269 e time constant, capacitance, and evoked and spontaneous firing rates were all increased in the breed

270 Finally, we found that spontaneous firing rates were shifted up or down by dnCa

271 lative CO activity correlate with changes in spontaneous firing rates within RA and that patterns of

272 s, slower Purkinje-mediated IPSCs, and lower spontaneous firing rates, but rotarod performances were

273 ss, an animal model of depression, decreases spontaneous firing rates, increases firing irregularity

274 Substantia innominata neurons had lower spontaneous firing rates, more variable interspike inter

275 They have lower spontaneous firing rates, narrower dynamic ranges, and m

276 reliable affinity for palatable tastes, low spontaneous firing rates, phasic responses, and relative

277 trongest modulation to aversive tastes, high spontaneous firing rates, protracted responses, and broa

278 The postsynaptic SGNs differ in their spontaneous firing rates, sound thresholds, and operatin

279 oca neurons while having no direct effect on spontaneous firing rates.

280 orthodromic activation latencies and higher spontaneous firing rates.

281 se two subtypes upregulated or downregulated spontaneous firing, respectively.

282 ous pain behavior is associated with ongoing/spontaneous firing (SF) in adult DRG C-fiber nociceptors

283 ty of the neuronal firing decreases from the spontaneous firing state value when the attractor networ

284 tials in SCN neurons during a period of slow spontaneous firing such as occurs during nighttime.

285 perpolarization current (IAHP) and increased spontaneous firing through SK channel suppression, indic

286 ma, and control the frequency and pattern of spontaneous firing through their close association with

287 GnRH release increased with higher frequency spontaneous firing to a point; release reached a plateau

288 ing somatic hyperpolarizations that silenced spontaneous firing to approximately 150 Hz during sponta

289 amus, a cell type where BK currents regulate spontaneous firing under distinct day and night conditio

290 In slice preparations, spontaneous firing was detected in CA1 pyramidal neurons

291 urons and voltage-gated Ca(2+) currents, but spontaneous firing was diminished by riluzole, demonstra

292 Spontaneous firing was driven by the combined action of

293 Spontaneous firing was observed in subsets of neurons in

294 Spontaneous firing was significantly elevated in 3D moto

295 Spontaneous firing was significantly reduced by blockers

296 By simulating synaptic release during spontaneous firing, we found that recruitment of low-Pr

297 ased synchrony and bursting of fusiform cell spontaneous firing, which correlate with frequency-speci

298 suggest that strong somatic stimuli decrease spontaneous firing while increasing depolarization-evoke

299 rea by comparing voltage trajectories during spontaneous firing with ramp-evoked currents in voltage

300 SCN neurons exhibit 24 h oscillations in spontaneous firing, with higher firing during day compar