ライフサイエンスコーパス: inhibitory interneuron

1 ive fast-spike inhibitory neurons (suspected inhibitory interneurons).

2 tes, postsynaptic dendrites, and networks of inhibitory interneurons.

3 t these effects have never been described in inhibitory interneurons.

4 cortical deficit in out-migrating GABAergic inhibitory interneurons.

5 d diverse group of GABAergic and glycinergic inhibitory interneurons.

6 inhibition from cool thermoreceptors through inhibitory interneurons.

7 eurons, coordinated by the diverse family of inhibitory interneurons.

8 excitatory neurons and the fast-spiking (FS) inhibitory interneurons.

9 bit class 2 excitability than other types of inhibitory interneurons.

10 ative sites different from the PWM originate inhibitory interneurons.

11 ted in the same compartments of fast-spiking inhibitory interneurons.

12 includes distinct classes of excitatory and inhibitory interneurons.

13 lved a previously unidentified population of inhibitory interneurons.

14 ilarity of their inputs, interacting through inhibitory interneurons.

15 lized to cortical parvalbumin (PV)-positive, inhibitory interneurons.

16 tatin-expressing subtype of GABAergic GAD67+ inhibitory interneurons.

17 of projection neurons and inhibition of the inhibitory interneurons.

18 TNF activates TNFR2 in cortical inhibitory interneurons.

19 to decreased postsynaptic GABAR currents on inhibitory interneurons.

20 sociates with excitatory synapses located on inhibitory interneurons.

21 rplay between excitatory pyramidal cells and inhibitory interneurons.

22 llations shaped by the activity of GABAergic inhibitory interneurons.

23 markers for specific subsets of dorsal horn inhibitory interneurons.

24 te that grid cells communicate primarily via inhibitory interneurons.

25 other principal cells via the recruitment of inhibitory interneurons.

26 to spread into the dendrites of neighboring inhibitory interneurons.

27 characteristics of individual fast-spiking, inhibitory interneurons.

28 xcitatory projection (pyramidal) neurons and inhibitory interneurons.

29 before it is conveyed to Purkinje cells and inhibitory interneurons.

30 ed spiking of a specific subtype of cortical inhibitory interneurons.

31 interneurons, and slow inhibition from local inhibitory interneurons.

32 on by contacting both excitatory neurons and inhibitory interneurons.

33 TNFalpha-TNFR1-p38 pathway within GABAergic inhibitory interneurons.

34 e production and organization of neocortical inhibitory interneurons.

35 e and increased activity in local fast-spike inhibitory interneurons.

36 he neocortex contains excitatory neurons and inhibitory interneurons.

37 d in somata and dendrites, but not axons, of inhibitory interneurons.

38 that project to cortical targets as well as inhibitory interneurons.

39 ynaptic inhibitory control of excitatory and inhibitory interneurons.

40 overns the tangential or radial migration of inhibitory interneurons.

41 lective marker for glutamatergic synapses on inhibitory interneurons.

42 equently displays loss of neurons, including inhibitory interneurons.

43 ng a subset of aromatase neurons as putative inhibitory interneurons.

44 f subpopulations of cortical and spinal cord inhibitory interneurons.

45 ity in the retina depends on the activity of inhibitory interneurons.

46 ural circuits contain diverse populations of inhibitory interneurons.

47 y regions is modulated by a diverse range of inhibitory interneurons.

48 little is known about NMDAR maturation onto inhibitory interneurons.

49 ch provide glutamatergic excitation of hilar inhibitory interneurons.

50 rons and gamma-aminobutyric acid (GABA)ergic inhibitory interneurons.

51 espects these biophysical observations about inhibitory interneurons.

52 (Up state), particularly among fast-spiking inhibitory interneurons.

53 here are two large populations of glomerular inhibitory interneurons: (1) GABAergic periglomerular (P

54 Inhibitory interneurons across diverse brain regions com

55 in the startle pathway caused by identified inhibitory interneurons activated by the prepulse.

56 tex (S1) may be the result of an increase in inhibitory interneuron activity and is mediated by the t

57 tartle behaviors; local sensory inputs drive inhibitory interneuron activity, which inhibits caudal m

58 ble with an influence of circadian timing on inhibitory interneuron activity.

59 d by fear conditioning are silenced by local inhibitory interneurons after extinction.

60 ablated ~30% of dendrite-targeting cortical inhibitory interneurons after the critical period by stu

61 show that, in addition to pyramidal neurons, inhibitory interneurons also grow cilia of comparable le

62 However, local thalamic inhibitory interneurons also play a role, and as we exam

63 that produces all postnatally born GABAergic inhibitory interneurons and astrocytes.

64 tic connectivity between molecularly defined inhibitory interneurons and CA1 pyramidal cell dendrites

65 are selectively expressed, respectively, in inhibitory interneurons and excitatory mitral projection

66 Such distinct forms of AIS plasticity in inhibitory interneurons and excitatory projection neuron

67 re mature brain, we assessed the inputs onto inhibitory interneurons and excitatory projection neuron

68 We assessed the inputs onto inhibitory interneurons and excitatory projection neuron

69 ronal gap junction protein connexin-36 among inhibitory interneurons and found a reduction in the vHI

70 ed activity in populations of olfactory bulb inhibitory interneurons and of synaptic terminals of olf

71 ial functional connectivity between putative inhibitory interneurons and pyramidal cells in PFC and V

72 hat in hippocampus is highly concentrated in inhibitory interneurons and regulates parvalbumin transc

73 The broad connectivity of inhibitory interneurons and the capacity of inhibitory s

74 tical neurons including parvalbumin-positive inhibitory interneurons, and blockade of GABAA receptors

75 ncluding principal cells and two subtypes of inhibitory interneurons, and compared between cortical r

76 Through recordings of motoneurons, inhibitory interneurons, and sensory neurons, we uncover

77 pyramidal cells through inhibition of other inhibitory interneurons, and they have very focused, "na

78 Distinct subtypes of inhibitory interneuron are known to shape diverse rhythm

79 Inhibitory interneurons are a diverse group of cells tha

80 ermine if contact patterns on excitatory and inhibitory interneurons are different; (3) to determine

81 piking (FS) or somatostatin-containing (SOM) inhibitory interneurons are electrically coupled to same

82 GABAergic inhibitory interneurons are embedded in almost all centr

83 Inhibitory interneurons are essential components of the

84 growth and synaptic integration of GABAergic inhibitory interneurons are essential for functional neu

85 spinal cords showed that the Ascl1-dependent inhibitory interneurons are key players of nociceptive r

86 citatory and inhibitory synaptic inputs onto inhibitory interneurons are largely normal.

87 the dorsal horn, whereas only the late-born inhibitory interneurons are missing in Ascl1(-/-) mice.

88 In the simulation, slow-inhibitory interneurons are shown to resonate to the 20

89 Networks of inhibitory interneurons are thought to be essential for

90 In mammals, many of the local GABAergic inhibitory interneurons arise from a single subcortical

91 On the other hand, inhibitory interneurons arise in the ventral telencephal

92 dynamics of activity in populations of local inhibitory interneurons, as well as the mechanisms that

93 This would be consistent with activation of inhibitory interneurons at shorter ISIs by BLA stimulati

94 , which lack a specific population of spinal inhibitory interneurons (B5-I neurons), develop patholog

95 tical excitatory cells and fast-spiking (FS) inhibitory interneurons, but only weak responses in soma

96 ses synaptic transmission from the AOC to OB inhibitory interneurons, but spares direct excitation to

97 hat CN principal cells are also contacted by inhibitory interneurons, but the properties of this conn

98 ian retina, the approximately 30 subtypes of inhibitory interneurons called amacrine cells (ACs) are

99 These results illustrate how a population of inhibitory interneurons can collectively encode bidirect

100 2015) show that transplantation of embryonic inhibitory interneurons can reactivate critical period p

101 Electrical coupling of inhibitory interneurons can synchronize activity across

102 ggest new approaches to target the different inhibitory interneuron classes pharmacologically in vivo

103 ded from the two largest genetically defined inhibitory interneuron classes, the perisomatically targ

104 Inhibitory interneurons comprise a diverse subpopulation

105 heir soma, axons almost exclusively targeted inhibitory interneurons, consistent with what had been f

106 Inhibitory interneurons constitute an essential componen

107 Inhibitory interneurons constitute approximately 20% of

108 In cortical networks, different types of inhibitory interneurons control the activity of glutamat

109 It has been hypothesized that inhibitory interneurons corral principal neurons into tr

110 on and integration of precursors of cortical inhibitory interneurons derived from the embryonic media

111 this question, finding that clonally related inhibitory interneurons dispersed widely across the fore

112 We conclude that inhibitory interneurons do not have synchronous activity

113 Electrically coupled inhibitory interneurons dynamically control network exci

114 years, schizophrenia research has focused on inhibitory interneuron dysfunction at the level of neuro

115 Parvalbumin (Pv)-positive inhibitory interneurons effectively control network exci

116 Moreover, optogenetic inactivation of inhibitory interneurons elicits a paradoxical increase i

117 er effect is presumably due to inhibition of inhibitory interneurons embedded in the respiratory netw

118 Both pyramidal neurons and inhibitory interneurons exhibited evidence of increased

119 campal and neocortical Kv4.3/KChIP1/DPP10(+) inhibitory interneurons expressed parvalbumin or somatos

120 hippocampal cell layers, diminished loss of inhibitory interneurons expressing parvalbumin, somatost

121 to demonstrate that 1) a particular class of inhibitory interneurons expressing the calcium binding p

122 Focusing on spinal V1 inhibitory interneurons, for which the spatial expressio

123 Multiple excitatory and inhibitory interneurons form the motor circuit with moto

124 d relevant animal models suggest loss of PFC inhibitory interneuron function.

125 16) show that ensembles of specific types of inhibitory interneurons generate coordinated activity in

126 ct origins: excitatory pyramidal neurons and inhibitory interneurons, generated in dorsal and ventral

127 et of GABAergic interneurons (GFP-expressing inhibitory interneurons [GINs]) by means of immunocytoch

128 diverse population of neocortical GABAergic inhibitory interneurons has been implicated in multiple

129 imulation targeting both pyramidal cells and inhibitory interneurons has recently been shown to elici

130 Most inhibitory interneurons have axons restricted to a nearb

131 Synchronized oscillations and inhibitory interneurons have important and interconnecte

132 Inhibitory interneurons have particularly diverse intrin

133 nted in a separate subpopulation, with those inhibitory interneurons having a diversity of tuning pro

134 Inhibitory interneurons help transform the input of a ne

135 come tuned through specific connections with inhibitory interneurons: horizontal and amacrine cells.

136 Some Ia inhibitory interneurons (IaINs) and all Renshaw cells (R

137 ntiation of adult Renshaw cells (RCs) and Ia inhibitory interneurons (IaINs), two subclasses that res

138 r players in Alzheimer's disease (AD), cause inhibitory interneuron impairments and aberrant neuronal

139 sing, (1) reciprocally connected feedforward inhibitory interneurons implement behavioral choice, (2)

140 inhibitory at rest and possibly mediated by inhibitory interneurones in the motor cortex.

141 ory circuits are tightly controlled by local inhibitory interneurons in a spatially and temporally de

142 ron highlights the importance of spinal cord inhibitory interneurons in generating motor activity by

143 we estimate that NPY is expressed by 18% of inhibitory interneurons in laminae I-II and 9% of those

144 ons make up a considerable proportion of the inhibitory interneurons in laminae I-III, and that their

145 Furthermore, fast-spiking inhibitory interneurons in layer 4 exhibit a shorter win

146 long-term synaptic plasticity in hippocampal inhibitory interneurons in learning and memory.

147 strate that the expression of AMPARs divides inhibitory interneurons in macaque V1 into two categorie

148 et intersectionally specified populations of inhibitory interneurons in mammalian hippocampus and neu

149 e determining the number of postnatally born inhibitory interneurons in odor-activated glomeruli.

150 els suggesting discrete functional roles for inhibitory interneurons in song production.

151 Other forms of TBI affect inhibitory interneurons in subcortical areas but it is u

152 Inhibitory interneurons in the cerebral cortex include a

153 the issue of what regulates the activity of inhibitory interneurons in the dorsal horn under non-pat

154 Ptf1a(-/-) mice lack all inhibitory interneurons in the dorsal horn, whereas only

155 specific circuits are tonically regulated by inhibitory interneurons in the dorsal horn.

156 ants is due to selective loss of a subset of inhibitory interneurons in the dorsal horn.

157 hindbrain, AptCB1R RNA probe weakly labeled inhibitory interneurons in the electrosensory lateral li

158 ynamics of activity in a large population of inhibitory interneurons in the first brain relay of the

159 uts from deeper-layer excitatory neurons and inhibitory interneurons in the first postnatal week.

160 uts from deeper-layer excitatory neurons and inhibitory interneurons in the first postnatal week.

161 nship influences the spatial distribution of inhibitory interneurons in the forebrain.

162 describe the discovery of a group of local, inhibitory interneurons in the fruit fly Drosophila key

163 e patch recording to identify excitatory and inhibitory interneurons in the hindbrain network for esc

164 ated with restoration of the excitability of inhibitory interneurons in the hippocampal dentate gyrus

165 At least 6.4% of inhibitory interneurons in the hippocampus coexpressed K

166 contrast, amacrine cells, a diverse class of inhibitory interneurons in the inner retina, collect inp

167 rm plasticity of glutamateric recruitment of inhibitory interneurons in the mammalian forebrain.

168 that such stimulation recruits a network of inhibitory interneurons in the molecular layer.

169 The specificity of connections made by inhibitory interneurons in the neocortex is not well und

170 Inhibitory interneurons in the neocortex often connect i

171 plays a pivotal role in the organization of inhibitory interneurons in the neocortex.

172 ical synapses and represent a major class of inhibitory interneurons in the neocortex.

173 pse between excitatory principle neurons and inhibitory interneurons in the olfactory bulb (OB), ante

174 rogenesis of sensory neurons in the nose and inhibitory interneurons in the olfactory bulb.

175 in the firing activity of both pyramidal and inhibitory interneurons in the subiculum.

176 inal ganglion cell terminals and superficial inhibitory interneurons in the tectum during looming and

177 with the density of somatostatin-expressing inhibitory interneurons in the vicinity of the recording

178 ecific populations of excitatory neurons and inhibitory interneurons in vivo in combination with elec

179 presynaptic mechanism for STH as well as the inhibitory interneurons in which this mechanism is deplo

180 perineuronal nets (PNNs) around fast-spiking inhibitory interneurons, in a rat model of TBI as well a

181 ells) make reciprocal connections with local inhibitory interneurons, including granule cells (GCs) a

182 neurons exhibited properties consistent with inhibitory interneurons, including tonic firing or initi

183 model incorporating excitatory pyramidal and inhibitory interneurons indicated that tACS effects like

184 phasic stimulation of perisomatic projecting inhibitory interneurons induced a somatic polarization a

185 We discuss here how the operations of inhibitory interneurons influence the behavior of a circ

186 To test the hypothesis that inhibitory interneuron innervation of spinal motoneurons

187 Commissural inhibitory interneurons (INs) are integral components of

188 Cortical inhibitory interneurons (INs) are subdivided into a vari

189 Inhibitory interneurons (INs) comprise a small, heteroge

190 Here, we show that inhibitory interneurons (INs) expressing the RORbeta orp

191 tivity has been extensively studied, that of inhibitory interneurons (INs) has received little attent

192 GABAergic inhibitory interneurons (INs) in the DG comprise fast-sp

193 into excitatory projection neurons (PNs) and inhibitory interneurons (INs).

194 gration of excitatory projection neurons and inhibitory interneurons into balanced local circuitry ar

195 he integrate local cues, such as activity of inhibitory interneurons, into their homeostatic fate cho

196 e receptor-mediated recruitment of GABAergic inhibitory interneurons is a critical determinant of net

197 rtance, excitation-transcription coupling in inhibitory interneurons is poorly understood.

198 Abeta-induced dysfunction of inhibitory interneurons likely increases synchrony among

199 gamma-Aminobutyric acid (GABA) release from inhibitory interneurons located within the cerebellar co

200 ssion, upregulating numerous Ptf1a-dependent inhibitory interneuron markers and ultimately generating

201 e great majority of these cells also express inhibitory interneuron markers.

202 Studies in rodents suggest, however, that inhibitory interneurons may be particularly vulnerable i

203 ther cellular populations including cortical inhibitory interneurons may contribute to this phenotype

204 regulation of synaptic transmission between inhibitory interneurons may serve as an important mechan

205 Furthermore, local inhibitory interneuron networks shifted their activity i

206 ensive electron microscopy reconstruction of inhibitory interneuron networks, modeling, electrophysio

207 Proper maturation of these fast-spiking inhibitory interneurons normally defines critical period

208 sis that inappropriate migration of cortical inhibitory interneurons occurs in schizophrenia.

209 L1 TC projections preferentially drove inhibitory interneurons of L1, especially those of the l

210 We found that, in cartwheel inhibitory interneurons of the dorsal cochlear nucleus,

211 Inhibitory interneurons of the dorsal lateral geniculate

212 in 5-HT1B receptors in cholecystokinin (CCK) inhibitory interneurons of the mammalian dentate gyrus (

213 We found that inhibitory interneurons of the same subtype were similar

214 Inhibitory interneurons of the spinal dorsal horn play c

215 (LTD) occurring at synapses either made onto inhibitory interneurons, or at inhibitory synapses onto

216 y of somatostatin- or parvalbumin-expressing inhibitory interneurons, or CaMKII-expressing excitatory

217 rtical neurogenesis, migrating precursors of inhibitory interneurons originating in subcortical areas

218 aque V1 for three distinct subpopulations of inhibitory interneurons: parvalbumin-immunoreactive (PV-

219 n of glutamatergic synapses onto perisomatic inhibitory interneurons (PIIs), which provide powerful f

220 Inhibitory interneurons play a critical role in coordina

221 Inhibitory interneurons play critical roles in shaping t

222 suppressed odor-evoked activity in GABAergic inhibitory interneuron populations in the OB.

223 consistent with properties of excitatory and inhibitory interneuron populations in this region of the

224 es have shown that transplantation of rodent inhibitory interneuron precursors from the medial gangli

225 articular, the development of excitatory and inhibitory interneuron presynaptic input has been hard t

226 more, the activity of parvalbumin-expressing inhibitory interneurons (PV+ INs) decreases in the stres

227 Parvalbumin-expressing inhibitory interneurons (PV+ INs) have functional proper

228 Parvalbumin inhibitory interneurons (PVIs) are crucial for maintaini

229 d that both excitatory pyramidal neurons and inhibitory interneurons received broad inputs in the fir

230 ction from recent physiological experiments, inhibitory interneurons received convergent anatomical i

231 Inhibitory interneurons regulate the responses of cortic

232 ting that neuronal VGF, expressed in part in inhibitory interneurons, regulates depression-like behav

233 In particular, in many brain regions inhibitory interneurons represent a diverse class of cel

234 Thus, restricted hilar transplantation of inhibitory interneurons restores normal cognitive functi

235 zebrafish model involves neuronal stress in inhibitory interneurons, resulting from mutant Sod1 expr

236 expression of Fgf13 impairs excitability of inhibitory interneurons, resulting in enhanced excitabil

237 /DPP10 was also detected in at least 6.9% of inhibitory interneurons scattered throughout the neocort

238 ed human ESC-derived cells biased to produce inhibitory interneurons significantly improve pain and b

239 putative inhibitory interneurons [suspected inhibitory interneurons (SINs)] and putative excitatory

240 irst evidence that links a specific class of inhibitory interneurons-somatostatin-positive cells-to t

241 Using inhibitory interneuron-specific conditional knock-out an

242 09 unitary connections made by the two major inhibitory interneuron subtypes in layer 4 of mouse soma

243 rabbit primary visual cortex (V1): putative inhibitory interneurons [suspected inhibitory interneuro

244 -yet-unrecognized maintenance function of an inhibitory interneuron that is not required for the init

245 e we demonstrate that a population of spinal inhibitory interneurons that are defined by the expressi

246 d preoptic area (PoA) give rise to GABAergic inhibitory interneurons that are distributed in the fore

247 Furthermore, inhibitory interneurons that are generally implicated in

248 ergic INs forms a class of local commissural inhibitory interneurons that are integral component of t

249 ful to the original coding goals while using inhibitory interneurons that are much more biophysically

250 activity by a relatively small population of inhibitory interneurons that exhibit remarkable anatomic

251 We studied cortical inhibitory interneurons that express somatostatin (SOM),

252 fied a new population of deep layer DH (dDH) inhibitory interneurons that express the receptor tyrosi

253 neurons are distinct from the well-described inhibitory interneurons that express these proteins in t

254 erein excitatory principal neurons stimulate inhibitory interneurons that feedback on the same princi

255 cium-binding protein parvalbumin (PV): local inhibitory interneurons that form Type II synapses, and

256 atory projection neurons and local GABAergic inhibitory interneurons that gate signal flow and sculpt

257 Properly functional CNS circuits depend on inhibitory interneurons that in turn rely upon activity-

258 Golgi cells (GoCs) are inhibitory interneurons that influence the cerebellar co

259 Pyramidal cells also activate inhibitory interneurons that mediate strong, local feedb

260 d the responses of excitatory neurons and of inhibitory interneurons that preferentially target dendr

261 for the survival of a specific population of inhibitory interneurons that regulate pruritus, and prov

262 e Mauthner command neuron for escape and the inhibitory interneurons that regulate swimming provide a

263 ally interconnected network of local circuit inhibitory interneurons that resembled neurogliaform cel

264 in- and a fraction of parvalbumin-expressing inhibitory interneurons that specialize in the control o

265 the explicit identification of the groups of inhibitory interneurons that switch, during odor stimula

266 es of cholecystokinin-positive local circuit inhibitory interneuron, the so-called 'basket cells' and

267 P change was mediated by a specific class of inhibitory interneurons, the low-threshold spiking cells

268 directly depolarizing the axon terminals of inhibitory interneurons, thus bypassing their somatodend

269 However, optical activation of these inhibitory interneurons to cues associated with reward s

270 als in motor neurons to generate spasms, and inhibitory interneurons to curtail them.

271 aptic transmission from parvalbumin-positive inhibitory interneurons to principal neurons without cha

272 ally enhance the responses of two classes of inhibitory interneurons to sensory input, that this effe

273 ng loss of tangential migration of GABAergic inhibitory interneurons to the neocortex.

274 he loss of tangential migration of GABAergic inhibitory interneurons to the neocortex.

275 hitecture of cortex incorporates a myriad of inhibitory interneuron types.

276 n pyramidal neurons (PNs) and a menagerie of inhibitory interneuron types.

277 poral lobe epilepsy, but the extent to which inhibitory interneurons undergo similar axonal reorganiz

278 ted by two classes of genetically identified inhibitory interneurons, V1 and V2b.

279 olves two classes of genetically identified, inhibitory interneurons: V1 and V2b.

280 Dendrites of both excitatory and inhibitory interneurons were arborized asymmetrically, p

281 In contrast, parvalbumin-positive (PV) inhibitory interneurons were highly interconnected with

282 in the mouse model of tauopathy; conversely, inhibitory interneurons were less likely to fire phase-l

283 We found that neocortical inhibitory interneurons were produced as spatially organ

284 was a drop in the firing reliability in some inhibitory interneurons when fictive swimming slowed.

285 rates that Erbb4 is expressed exclusively on inhibitory interneurons, where its presence on parvalbum

286 e AMPARs expressed by the different types of inhibitory interneurons, which are crucial for network f

287 istent breakdown of PNNs around fast-spiking inhibitory interneurons, which was contingent on TGFbeta

288 cally identical but morphologically distinct inhibitory interneurons will allow us to understand the

289 nsists of an identifiable "giant" nonspiking inhibitory interneuron with ubiquitous connectivity and

290 tatory projection neurons, HVC also contains inhibitory interneurons with a role in premotor patterni

291 ction causes increased firing of hippocampal inhibitory interneurons with concomitantly decreased fir

292 icotropin-releasing hormone (CRH)-expressing inhibitory interneurons with extensive presynaptic input

293 Neuron, Hamilton et al. stimulate identified inhibitory interneurons with optogenetics, revealing pow

294 regions of the CNS contain many subtypes of inhibitory interneurons with specialized roles in circui

295 whereas amacrine cells are usually monopolar inhibitory interneurons with synapses almost exclusively

296 ated by synchronous activity of fast-spiking inhibitory interneurons, with the resulting rhythmic inh

297 mical and functional arrangement of multiple inhibitory interneurons within a single computational mo

298 The function of inhibitory interneurons within brain microcircuits depen

299 erties of identified rhythmic excitatory and inhibitory interneurons within respiratory microcircuits

300 he variations in the subtypes and origins of inhibitory interneurons within the pallial and subpallia