ライフサイエンスコーパス: optogenetic stimulation

1 ic acid and chronic activation of the ACC by optogenetic stimulation.

2 physiological recordings with electrical and optogenetic stimulation.

3 prediction, we aligned periodic tactile and optogenetic stimulation.

4 nce was achieved through subnetwork-specific optogenetic stimulation.

5 o be restored in a controllable manner using optogenetic stimulation.

6 s area reflects their choosing to experience optogenetic stimulation.

7 re-entrant AT (induced via rapid pacing) via optogenetic stimulation.

8 ng the intensity, duration, and frequency of optogenetic stimulation.

9 s temporal resolution by MRI with sensory or optogenetic stimulation.

10 ustic, and electrical stimuli indicated that optogenetic stimulation achieves better frequency resolu

11 as been reported on the response kinetics of optogenetic stimulation across different neuronal subtyp

12 del thus offers a theoretical account of how optogenetic stimulation alters the excitability of corti

13 Using a combination of optogenetic stimulation and 2-photon imaging in mice, we

14 avioural assays, volumetric calcium imaging, optogenetic stimulation and circuit modelling to reveal

15 Using optogenetic stimulation and in vivo two-photon imaging i

16 By combining optogenetic stimulation and intracellular recordings in

17 ictable chronic mild stress and repeated ACC optogenetic stimulation and is reversed by fluoxetine.

18 Finally, we use optogenetic stimulation and multicircuit recording techn

19 Moreover, using concurrent optogenetic stimulation and opto-fMRI), we observed opto

20 This was obtained through optogenetic stimulation and subsequent confocal imaging

21 using optical imaging of intrinsic signals, optogenetic stimulation, and multi-unit recording.

22 hronic multielectrode recording, closed-loop optogenetic stimulation, and pharmacology to show that r

23 value of sucrose relative to sucralose plus optogenetic stimulation, and that leptin decreased it.

24 iode (LED)-based fluorescence microscopy and optogenetic stimulation as well as a Peltier-based tempe

25 We show that targeted optogenetic stimulation based on analysis of AT morpholo

26 We show that targeted optogenetic stimulation based on automated, non-invasive

27 locked the dopamine release induced by local optogenetic stimulation but only partially antagonized d

28 tonic currents, and that both electrical and optogenetic stimulation can evoke NMDA-mediated synaptic

29 Responses to sinusoidally modulated optogenetic stimulation confirmed that the CA3 network o

30 Finally, optogenetic stimulation confirmed the functional role of

31 ptors to their axon terminals in the EB, and optogenetic stimulation coupled with electrophysiologica

32 Surprisingly, we find the effects of optogenetic stimulation depend primarily on distance and

33 Optogenetic stimulation designed to saturate LTD produce

34 Long-term in vivo recordings, optogenetic stimulation, drug perturbation and analysis

35 fire immediately before slow waves and their optogenetic stimulation during ON periods of NREM sleep

36 ynaptic to specific populations targeted for optogenetic stimulation, giving rise to all-optical func

37 ltaneous patch-clamp recordings and targeted optogenetic stimulation in acute mouse hippocampal slice

38 strong neural modulations can be evoked with optogenetic stimulation in macaque motor cortex without

39 Optogenetic stimulation in pgant mutants alters presynap

40 ion-making tasks [9-13], previous studies of optogenetic stimulation in primates have not demonstrate

41 Optogenetic stimulation in the caudate-putamen and neoco

42 Optogenetic stimulation, in contrast, initiated and main

43 Increasing neuronal activity by sensory or optogenetic stimulation increased neuronal DSBs in relev

44 In vivo optogenetic stimulation-induced downregulation of CP-AMP

45 Importantly, we also show that LDT-VTA optogenetic stimulation is reinforcing, and that iuGC an

46 his spatiotemporal dynamic using closed-loop optogenetic stimulation is sufficient to increase moveme

47 ption of a direct path, using electrical and optogenetic stimulation methods that selectively activat

48 s from layer V pyramidal neurons showed that optogenetic stimulation normalized cortical hyperexcitab

49 for the anxiolytic effect observed following optogenetic stimulation of 5-HT inputs into the dBNST.

50 on, Lee et al. (2014) show that subthreshold optogenetic stimulation of a brainstem locomotion area c

51 Here, we show that selective optogenetic stimulation of a molecularly defined subset

52 Conversely, optogenetic stimulation of adult-born neurons has been s

53 Here we combined optogenetic stimulation of afferents from the visual tha

54 e resolve this paradox by showing that brief optogenetic stimulation of AgRP neurons before food avai

55 Despite these observations, optogenetic stimulation of AgRP neurons reliably produce

56 Furthermore, we find that constant optogenetic stimulation of anesthetized cat area 21a pro

57 to the hypothalamic paraventricular nucleus; optogenetic stimulation of ARC TH axons inhibited parave

58 Optogenetic stimulation of ARC TH cells inhibited pro-op

59 micking pH-evoked Ca2+ responses by means of optogenetic stimulation of astrocytes expressing channel

60 ing an animal to associate a foot shock with optogenetic stimulation of auditory inputs targeting the

61 Responses to self-generated optogenetic stimulation of auditory thalamocortical term

62 ts by increasing germline proliferation, and optogenetic stimulation of AWB neurons is sufficient to

63 Moreover, optogenetic stimulation of axon collaterals of double-pr

64 ing cholinergic levels in the cortex through optogenetic stimulation of basal forebrain cholinergic n

65 n cells, we observed that temporally precise optogenetic stimulation of basolateral amygdala (BLA) te

66 us, the wake-promoting effect of "selective" optogenetic stimulation of BF cholinergic neurons could

67 d by C3 neurons is less than that induced by optogenetic stimulation of C1 neurons; however, combined

68 Here we demonstrate in rats that optogenetic stimulation of C3 neurons induces sympathoex

69 Optogenetic stimulation of CA3 pyramidal cells at 1 Hz l

70 Specifically, we used 1 Hz optogenetic stimulation of calcium/calmodulin-dependent

71 Optogenetic stimulation of CANE-captured social-fear neu

72 express ChR2 solely in Tac2 neurons, in vivo optogenetic stimulation of CeA Tac2-expressing neurons d

73 Dentate hyperactivity was abolished by optogenetic stimulation of cholinergic fibers.

74 , we now provide physiological evidence that optogenetic stimulation of cholinergic interneurons trig

75 Using optogenetic stimulation of cholinergic neurons in ChAT-C

76 Furthermore, optogenetic stimulation of cholinergic neurons/fibers ca

77 Furthermore, optogenetic stimulation of ChR2 expressing DRGs induces

78 Optogenetic stimulation of ChR2-expressing FS interneuro

79 A single short-lasting (30-300 milliseconds) optogenetic stimulation of CN neuron activity abruptly s

80 Here, we show that optogenetic stimulation of cortical neurons within rhesu

81 They also suggest that optogenetic stimulation of cortical projection systems m

82 Therefore, we hypothesized that optogenetic stimulation of cortical projections would re

83 Unilateral optogenetic stimulation of cortical pyramidal neurons bo

84 Mice preferred optogenetic stimulation of DA neurons to sucralose, but

85 Electrical and optogenetic stimulation of dopamine terminals evoked rob

86 ts of choice behavior, we employed selective optogenetic stimulation of dopamine terminals in the NAc

87 Conversely, optogenetic stimulation of dopamine-excitable cells in d

88 We found that transient optogenetic stimulation of dorsal striatal dopamine D1 a

89 Optogenetic stimulation of DRN Pet-1 neurons reinforces

90 Although optogenetic stimulation of either cell type significantl

91 is specific to vHIP afferents to the NAc, as optogenetic stimulation of either mPFC or AMY afferents

92 tion channels that have been widely used for optogenetic stimulation of electrically excitable cells.

93 aventricular hypothalamic nucleus (PVH), and optogenetic stimulation of GABAergic LH --> PVH fibers i

94 drives voracious water consumption, and that optogenetic stimulation of GABAergic neurons in the same

95 Pathway-specific, optogenetic stimulation of glutamatergic LHA-LHb circuit

96 In mice, we show that optogenetic stimulation of glutamatergic neurons in MnPO

97 Responses to optogenetic stimulation of glutamatergic premotor neuron

98 Here, we applied optogenetic stimulation of HS cells to evaluate their be

99 Here, we combine optogenetic stimulation of identified Schaffer collatera

100 sults demonstrate that ketamine infusions or optogenetic stimulation of IL-PFC are sufficient to prod

101 n vivo reversal of this pathophysiology with optogenetic stimulation of infralimbic cortex-accumbens

102 her, our findings indicate that the targeted optogenetic stimulation of intracellular Ca(2+) signal a

103 In the mouse whisker system, we found that optogenetic stimulation of L6 in vivo results in a mixtu

104 oduced a real-time place preference, whereas optogenetic stimulation of LHA-LHb glutamatergic fibers

105 e show, using sniff-triggered, dynamic, 2-D, optogenetic stimulation of mitral/tufted cells, that vir

106 Consistently, optogenetic stimulation of MnR neurons suppressed ripple

107 Optogenetic stimulation of mouse ARC TH neurons increase

108 We find that optogenetic stimulation of mouse zona incerta (ZI) gamma

109 e-like phenotype, i.e., susceptible animals, optogenetic stimulation of mPFC exerted potent antidepre

110 We previously found that optogenetic stimulation of mPFC neurons in susceptible m

111 inhibited EPSCs evoked at -70 mV in vitro by optogenetic stimulation of mPFC-NAcore terminals in alco

112 Furthermore, optogenetic stimulation of mPOA(Nts)-VTA circuitry promo

113 Optogenetic stimulation of NAc cell bodies induced a pos

114 Optogenetic stimulation of neurons in the left or right

115 -aspartate microinjection in the SNpc and/or optogenetic stimulation of nigro-vagal terminals in the

116 To explore this directly, we paired optogenetic stimulation of OH cells (at rates that promo

117 Finally, selective optogenetic stimulation of olfactory cortical projection

118 al that both the application of oxytocin and optogenetic stimulation of oxytocinergic terminals suffi

119 Optogenetic stimulation of P2ry1 neurons acutely silence

120 In agreement, selective optogenetic stimulation of parvalbumin-expressing, FS in

121 Optogenetic stimulation of parvalbumin-positive cells ev

122 ated chloride channel abolishes pumping, and optogenetic stimulation of pharyngeal muscle in these an

123 Indeed, optogenetic stimulation of PPN axons reliably evoked spi

124 Here we show that direct optogenetic stimulation of prefrontal cortex (PFC) desce

125 eptor-mediated IPSCs evoked by electrical or optogenetic stimulation of Purkinje cells were more than

126 tent with their central role in NVC, in vivo optogenetic stimulation of pyramidal cells evoked COX-2-

127 IL-17 deficiency can be bypassed by optogenetic stimulation of RMG.

128 Optogenetic stimulation of RTN with channelrhodopsin-2,

129 Furthermore, optogenetic stimulation of S1 in expert mice was suffici

130 adults rescued the transport defects, while optogenetic stimulation of select synapses revealed CaMK

131 Serotonin release elicited by direct optogenetic stimulation of serotonergic neurons activate

132 Optogenetic stimulation of serotonin neurons in the dors

133 Furthermore, optogenetic stimulation of SGNs restored auditory activi

134 Selective optogenetic stimulation of somatostatin-expressing, PLTS

135 lectrical stimulation of dmPFC layer I or by optogenetic stimulation of specific interneurons ex vivo

136 l neurons in combination with mechanical and optogenetic stimulation of specific mechanoreceptor type

137 Optogenetic stimulation of spiral ganglion neurons (SGNs

138 ized step function opsin (SSFO) in the mPFC; optogenetic stimulation of SSFO at mPFC-to-NAc projectio

139 Intra-NAc optogenetic stimulation of SSFO selectively at mPFC-to-N

140 Our results show that optogenetic stimulation of Sst-GABA neurons results in a

141 triatal neurons combined with electrical and optogenetic stimulation of striatal afferents in mouse b

142 at/vglut2) neurons produces minimal wake and optogenetic stimulation of SuM(vgat/vglut2) terminals el

143 Local optogenetic stimulation of sympathetic inputs induces a

144 pproach, our results indicate that selective optogenetic stimulation of TH(VTA) neurons enhanced cere

145 ns of the facial vibrissae and electrical or optogenetic stimulation of thalamic neurons that project

146 Finally, delta-frequency optogenetic stimulation of thalamic synaptic terminals o

147 Furthermore, optogenetic stimulation of the ACC was sufficient to ind

148 Our study demonstrates a strategy for optogenetic stimulation of the auditory pathway in roden

149 Optogenetic stimulation of the circuitry can drive behav

150 ivo and disrupted locomotor activation after optogenetic stimulation of the direct pathway.

151 Random optogenetic stimulation of the DOG thermosensory neurons

152 We also found that optogenetic stimulation of the IL-PFC produced rapid and

153 Focused optogenetic stimulation of the lateral orbitofrontal cor

154 Here, we find that optogenetic stimulation of the MLR in awake, head-fixed

155 In this work, we use optogenetic stimulation of the premotor cortex in awake,

156 Optogenetic stimulation of the RIA interneurons has a mo

157 We first demonstrated that optogenetic stimulation of the STN excited its major pro

158 ed locomotion could be reversed in adults by optogenetic stimulation of the touch receptor (mechanose

159 reduced aggression-seeking behavior, whereas optogenetic stimulation of the VMHvl accelerated moment-

160 Furthermore, optogenetic stimulation of these GABAergic projections f

161 Optogenetic stimulation of these neurons inhibited a sub

162 lls, in flies that are blind, we reveal that optogenetic stimulation of these neurons is typically su

163 Simultaneous optogenetic stimulation of these neurons produces vigoro

164 Functionally, optogenetic stimulation of these neurons promotes the ac

165 Next, we studied how optogenetic stimulation of these projections affects beh

166 g reward with fear extinction training or by optogenetic stimulation of this circuit during fear exti

167 Optogenetic stimulation of this circuit has net excitato

168 We also demonstrate that optogenetic stimulation of this population of TRP-expres

169 in the host hippocampal network via targeted optogenetic stimulation of transplanted hESC-derived neu

170 We find that optogenetic stimulation of TRN neurons and their axons e

171 Optogenetic stimulation of tVTA neurons inhibited VTA DA

172 e activated during theta network activity or optogenetic stimulation of ventral CA1 pyramidal cell ax

173 Optogenetic stimulation of VMHvl in male mice evokes att

174 Furthermore, optogenetic stimulation of VTA GABA neurons directly sup

175 We report that optogenetic stimulation of VTA glutamate neurons or term

176 Optogenetic stimulation of wM1 evokes rhythmic whisker p

177 Optogenetic stimulation of wS1 drove activity in wM1 wit

178 Brief optogenetic stimulations of CN interneurons, through sel

179 osing the loop optogenetically (i.e., basing optogenetic stimulation on simultaneously observed dynam

180 circumvent this limitation, we used in vivo optogenetic stimulation or inhibition of glutamatergic f

181 that endogenous NPY, released in response to optogenetic stimulation or synaptically evoked spiking o

182 ity to manic behaviors, we developed a novel optogenetic stimulation paradigm that produces a sustain

183 Cortical electrical and local optogenetic stimulation produced significant increases i

184 esponses and memory formation, whereas their optogenetic stimulation produces defensive responses and

185 Optogenetic stimulation provides a powerful tool for ana

186 0-45 min, and in vivo electrophysiology with optogenetic stimulation requires 1-4 h.

187 Network analysis based on optogenetic stimulation revealed a symmetrical sham netw

188 Optogenetic stimulation revealed that this population wa

189 Previous optogenetic stimulation studies have confirmed that rein

190 t was ipsilateral, but not contralateral, to optogenetic stimulation, suggesting involvement of inter

191 After local optogenetic stimulation, SWA and cortical synchrony decr

192 Constant optogenetic stimulation targeting both pyramidal cells a

193 tested this hypothesis using electrical and optogenetic stimulation to determine if brain slices cou

194 glutamatergic terminals (lower frequency of optogenetic stimulation to induce glutamate release).

195 functional effect of such networks, we used optogenetic stimulation to trigger antidromic spikes in

196 croscopy, functional imaging, and electrical/optogenetic stimulation tools, super-resolution fluoresc

197 ists even under the artificial conditions of optogenetic stimulation, underscoring the canonical natu

198 Optogenetic stimulation using cre recombinase-dependent

199 in glucose metabolism (BGluM) in response to optogenetic stimulation (using the excitatory channelrho

200 However, the mice preferred sucralose plus optogenetic stimulation versus sucrose.

201 rtex as a Wilson-Cowan neural field in which optogenetic stimulation was represented by an external c

202 a wide range of variation in both visual and optogenetic stimulation we find linear addition of the t

203 Using optogenetic stimulation, we determined that these neuron

204 Using optogenetic stimulation, we find that these subtypes rec

205 Using optogenetic stimulation, we show that GLP-1 excites medi

206 Electrical and optogenetic stimulations were used to analyze amygdala-d

207 locally transformed into a type II medium by optogenetic stimulation which predominantly targets inhi

208 Here, we used animal models to characterize optogenetic stimulation, which is the optical stimulatio

209 nts, e.g., when combining Ca(2+) uncaging or optogenetic stimulation with Ca(2+) imaging in cells exp

210 implant produces sufficient light power for optogenetic stimulation with minimal tissue heating (<1

211 at pairing central nucleus of amygdala (CeA) optogenetic stimulation with one option for earning intr

212 ted in increasingly powerful ways, combining optogenetic stimulation with simultaneous multichannel e

213 The consequences of optogenetic stimulation would optimally be recorded by n