ライフサイエンスコーパス: glutamatergic

1 afferent pathway for MGF-mediated escape is glutamatergic.

2 cating a subpopulation of RXFP3+ neurons are glutamatergic.

3 ent pathways, the vast majority of which are glutamatergic.

4 precursor of glucagon-like peptide 1 and are glutamatergic; able to modulate the firing pattern of th

5 pectroscopy ((1)H-MRS) studies have examined glutamatergic abnormalities in schizophrenia, mostly in

6 ents with attenuated psychotic symptoms have glutamatergic abnormalities, although only CHR patients

7 G) endocannabinoid signaling reduced BLA-NAc glutamatergic activity and that pharmacological 2-AG aug

8 ffect of prophylactic drug administration on glutamatergic activity in CA3.

9 Hence, in the absence of TRESK, glutamatergic activity is unregulated leading to membran

10 ng these neurons we identify a population of glutamatergic Adcyap1-positive cells, the activity of wh

11 However, the relationship between striatal glutamatergic afferents and behavioral reinforcement is

12 we show, using mouse behavioral models, that glutamatergic afferents from the ventral tegmental area

13 how that optogenetic stimulation of cortical glutamatergic afferents to the striatum triggers dopamin

14 restricted the therapeutic effects of these glutamatergic agents.

15 n NO released by local microinjection of the glutamatergic agonist N-methyl-d-aspartate (NMDA).

16 increased levels and altered organization of glutamatergic AMPA receptors in LRRK2 mutants.

17 ctly modulate the activity of interconnected glutamatergic and cholinergic mushroom body output neuro

18 Unlike previous studies of BF glutamatergic and cholinergic neurons, arousals induced

19 ponses, does not allow the relative roles of glutamatergic and cholinergic synapses in the induction

20 cal to striatal connectivity consistent with glutamatergic and cortical-limbic related theories of de

21 underpinned by how the relationship between glutamatergic and dopaminergic dysfunction in schizophre

22 atergic neurons only (Glu-CB1-KO) or in both glutamatergic and forebrain GABAergic neurons (Glu/GABA-

23 on changes in inflammatory-related genes and glutamatergic and GABAergic (gamma-aminobutyric acidergi

24 We conclude that the glutamatergic and GABAergic deficits in the frontal lobe

25 in and propose that its localization in both glutamatergic and GABAergic neurons could be compatible

26 These two groups of neurons coincide with glutamatergic and GABAergic neurons identified by optota

27 d metabolic rate of cortical and hippocampal glutamatergic and GABAergic neurons.

28 forms puncta that are frequently apposed to glutamatergic and GABAergic synapses.

29 nduced by lipopolysaccharides on hippocampal glutamatergic and GABAergic synaptic transmission.

30 s electrophysiological perturbations of both glutamatergic and GABAergic transmission, as observed by

31 We identified and profiled both neuronal (glutamatergic and GABAergic) and nonneuronal (oligodendr

32 ytes also led to decreased expression of the glutamatergic and increased expression of the GABA-ergic

33 orly understood interplay between excitatory glutamatergic and inhibitory GABAergic receptor effects.

34 l that AT1aR neurons in the area are largely glutamatergic and send projections to the paraventricula

35 Y(1) receptor (Y(1)R)-expressing neurons are glutamatergic and were broadly distributed throughout th

36 Dopaminergic, glutamatergic, and neuroendocrine PRS showed evidence of

37 e-sets comprised serotonergic, dopaminergic, glutamatergic, and neuroendocrine signaling pathways.

38 he co-activation of dopaminergic, GABAergic, glutamatergic, and serotoninergic neurotransmitters in f

39 These findings suggest that glutamatergic AON projections to the OB impede early olf

40 Likewise, activation of glutamatergic AON projections to the olfactory bulb (OB)

41 ings revealed that optogenetic activation of glutamatergic AON terminals in the OB transiently decrea

42 aluated whether acute 5-HT(4)R activation in glutamatergic axon terminals arising from the medial pre

43 ntiation (LTP), does not exclusively recruit glutamatergic axons.

44 as reflected by alteration in GABAergic and glutamatergic balance (i.e., GABA/Glu), may underlie tha

45 demonstrate that deletion of beta-klotho in glutamatergic, but not GABAergic, neurons abrogated the

46 hronic stimulation with lipopolysaccharides, glutamatergic, but not GABAergic, neurons exhibit an enh

47 iated with circadian rhythm and entrainment, glutamatergic/cholinergic/dopaminergic synaptic function

48 lateral amygdala-nucleus accumbens (BLA-NAc) glutamatergic circuit reduced SI and increased social av

49 ogical mechanism regulating formation of the glutamatergic circuitry in the amygdala.

50 ghly palatable food, demonstrating that this glutamatergic circuitry regulates aspects of feeding.

51 efine critical windows during which specific glutamatergic circuits may be vulnerable to disruption b

52 nergic transmission shapes the maturation of glutamatergic circuits, yet the developmental sources of

53 We demonstrate that in rodents the glutamatergic connection from basolateral to central amy

54 ulatory systems are essential for remodeling glutamatergic connectivity during experience-dependent c

55 f regulatory synaptic mechanism for specific glutamatergic cortical circuits in which MET is enriched

56 3 contributes to the generation of ultrafast glutamatergic currents at these synapses, which is impor

57 s the ultrafast kinetics of endbulb synapses glutamatergic currents by promoting the insertion of pos

58 Gene-set PRS confirmed involvement of shared glutamatergic, dopaminergic, and neuroendocrine genetic

59 of zinc plasticity observed at the zinc-rich glutamatergic dorsal cochlear nucleus (DCN) parallel fib

60 ased the strength of primary afferent-evoked glutamatergic drive onto DYN neurons within the adult mo

61 midal neurons underscoring the importance of glutamatergic drive onto MGE-derived interneurons for hi

62 These discoveries relative to the glutamatergic drive to BAT sympathoexcitatory neurons in

63 ween GluN and mGluR5 pathways as integral to glutamatergic dysregulation and suggest protein-protein

64 anism preventing inappropriate post-synaptic glutamatergic effects is unexplored and unknown.

65 gated the electrophysiological properties of glutamatergic ENs labeled by the transcription factor ol

66 itory markers, but some of them also express glutamatergic excitatory markers and a subpopulation eve

67 We confirm that the AON forms glutamatergic excitatory synapses onto piriform pyramida

68 ng role for chronic environmental stress and glutamatergic excitotoxicity in AD, suggesting that targ

69 PVH afferents are glutamatergic (express Slc17a6/Vglut2) and are distinct

70 On-demand optogenetic excitation of glutamatergic fastigial neurons either ipsilateral or co

71 ition was greater when selectively targeting glutamatergic fastigial neurons than when an approach th

72 lut2(Flp) to show that these neurons adopt a glutamatergic fate in the adult brain.

73 Within the medulla, retrogradely-labeled, glutamatergic, glycinergic and GABAergic neurons were fo

74 activated mTORC1 or mTORC2 in cultured mouse glutamatergic hippocampal neurons.

75 pathways with attention given to the role of glutamatergic hippocampal outputs onto nucleus accumbens

76 Glutamatergic innervation of the striatum by the cortex

77 uron, an amacrine cell, receiving excitatory glutamatergic input exclusively from S-ON bipolar cells.

78 D1-MSNs receive glutamatergic input from several brain regions; however,

79 utamate neurons receive a major monosynaptic glutamatergic input from the lateral hypothalamic area (

80 y in the newborn LA perturbed development of glutamatergic input to CeA, identifying KARs as a physio

81 lation of both receptors enhanced excitatory glutamatergic input to mouse prefrontal cortex pyramidal

82 elta(9)-THC had no effect on net strength of glutamatergic input to NAc shell arising from midbrain d

83 We found that glutamatergic inputs arose from a variety of sources and

84 from the internal globus pallidus (GPi) and glutamatergic inputs from motor cortices.

85 esocortical circuits and their corresponding glutamatergic inputs gives rise to clinical and cognitiv

86 term synaptic depression (LTD) plasticity at glutamatergic inputs to dorsal striatum mediates many do

87 We then expand on the role of glutamatergic inputs to these dopamine circuits and dopa

88 interneuron (cha-lOLP) and hyperpolarizes a glutamatergic interneuron (glu-lOLP).

89 The glutamatergic-like neurons fire at high rate and respond

90 activation of Purkinje cells can entrain the glutamatergic-like, but not the GABAergic-like, cells ov

91 one or more neuropeptides, and two expressed glutamatergic markers.

92 sting that G-CSF influences drug seeking via glutamatergic mechanisms.

93 dings suggest a positive association between glutamatergic metabolites and cognitive function that do

94 ion between cognitive function and levels of glutamatergic metabolites and GABA has not been investig

95 s with CUD would be associated with abnormal glutamatergic metabolites in the putamen.

96 otential structural changes in GABAergic and glutamatergic microcircuits in the VApc and CM of MPTP-t

97 y bulb the smooth dendrites of the principal glutamatergic mitral cells (MCs) form reciprocal dendrod

98 ort that, indeed, the connexin-36-containing glutamatergic mossy fiber synapses of the rat hippocampu

99 owing manipulations of tonic Ib or phasic Is glutamatergic motoneurons that coinnervate postsynaptic

100 , limbic structures, and auditory brainstem, glutamatergic nerve terminals corelease zinc to modulate

101 naptic site of action that is independent of glutamatergic network disinhibition.

102 orhabditis elegans results in stress-induced glutamatergic neurodegeneration; this neurodegeneration

103 enriched in the postsynaptic regions of the glutamatergic neuromuscular junctions.

104 models of psychosis propose that hippocampal glutamatergic neuron hyperactivity drives increased stri

105 Constitutive Ahnak KO mice or forebrain glutamatergic neuron-selective Ahnak KO mice display a d

106 code reward, recent studies revealed a novel glutamatergic neuronal population in the VP [VP neurons

107 ntact-mediated signaling, reminiscent of the glutamatergic neuronal synapse, inducing spatial self-or

108 lia-specific pathogenic Trem2 variant boosts glutamatergic neuronal transmission and suppresses LTP b

109 Both types of glutamatergic neurons (mEC LVa and LVb) as well as fast-

110 Selective deletion of IL-1R1 in glutamatergic neurons (nIL-1R1(-/-)) abrogated the stres

111 he L-type calcium influx is observed in both glutamatergic neurons and parvalbumin (PV) GABAergic int

112 We find that open chromatin regions in glutamatergic neurons are enriched for neuropsychiatric

113 ncreases statistical power and confirms that glutamatergic neurons are most affected.

114 , recent work suggests that POA GABAergic or glutamatergic neurons capable of regulating endogenous s

115 t the novel finding that stimulation of VLPO glutamatergic neurons causes a strong increase in wakefu

116 ion-specific activity of ventral hippocampus glutamatergic neurons causing behaviorally diverse respo

117 show that activating MnPO/VLPO GABAergic or glutamatergic neurons does not alter anesthetic inductio

118 astroglia and rarely in microglia; instead, glutamatergic neurons express LepR, some of which projec

119 tudy, we compared the projection patterns of glutamatergic neurons here with a subpopulation expressi

120 irectly enhances NMDAR activity on principal glutamatergic neurons in medial prefrontal cortex (mPFC)

121 We previously found that glutamatergic neurons in the external lateral parabrachi

122 On-demand optogenetic inhibition of glutamatergic neurons in the fastigial nucleus of the ce

123 ontrast, on-demand optogenetic excitation of glutamatergic neurons in the fastigial nucleus successfu

124 ibition of either cholinergic, GABAergic, or glutamatergic neurons in the medial septum/diagonal band

125 Overall, glutamatergic neurons in the PB region project to a wide

126 We identify glutamatergic neurons in the peri-locus coeruleus (periL

127 te that CB1 signaling especially in cortical glutamatergic neurons is essential for the development o

128 Specifically, FGF21 signaling in glutamatergic neurons is necessary for protection agains

129 Conditional deletion of HIF-1alpha in glutamatergic neurons of the nucleus tractus solitarius

130 ns within the lamina terminalis-particularly glutamatergic neurons of the subfornical organ expressin

131 feelings after withdrawal that involves the glutamatergic neurons of the ventral pallidum.

132 pecific CB1 deletion in dorsal telencephalic glutamatergic neurons only (Glu-CB1-KO) or in both gluta

133 and, more moderately, by brain region, with glutamatergic neurons showing the largest regional varia

134 The transient cholinergic phenotype of these glutamatergic neurons suggests a homosynaptic source of

135 ude that activation of preoptic GABAergic or glutamatergic neurons that increase sleep or wakefulness

136 on, as well as efferent sympathetic premotor glutamatergic neurons that regulate gastrointestinal tra

137 IL-17a receptor was expressed in cortical glutamatergic neurons under steady state and its genetic

138 However, beta-klotho expression in glutamatergic neurons was dispensable for the effects of

139 thermore, selective restoration of IL-1R1 on glutamatergic neurons was sufficient to reestablish the

140 Cortical OTR cells are largely glutamatergic neurons with the exception of cells in lay

141 inside-out radial migration of post-mitotic glutamatergic neurons, and axonal tract projections.

142 cture in four distinct populations of cells (glutamatergic neurons, GABAergic neurons, oligodendrocyt

143 tripartite synapses between cancer cells and glutamatergic neurons, presenting a rationale for brain

144 SCZ cINs, but not SCZ glutamatergic neurons, show dysregulated Oxidative Phosp

145 t miR-383 expression is enriched in cortical glutamatergic neurons, suggesting a unique role in these

146 in is evenly expressed in both GABAergic and glutamatergic neurons, suggesting the GABAergic neuron-p

147 mine the impact of aberrant FGFR function on glutamatergic neurons, we generated a FGFR gain-of-funct

148 from mice expressing GCaMP6, leptin excites glutamatergic neurons.

149 he hippocampus, where it was co-expressed in glutamatergic neurons.

150 not in iPSCs from individuals with SCZ or in glutamatergic neurons.

151 so encloses a subgroup of aversion-promoting glutamatergic neurons.

152 f Elavl4 translation dictates development of glutamatergic neurons.

153 OS decrease calcium transients in C. elegans glutamatergic neurons.

154 ulate the inhibitory drive on the "aversive" glutamatergic neurons.

155 nterrogation of a subpopulation of claustral glutamatergic neurons.

156 ctivated FGFR3 (FGFR3(K650E)) in postmitotic glutamatergic neurons.

157 distant brain areas derive by and large from glutamatergic neurons.

158 ion in NTS-HIF-1alpha(-/-) was restricted to glutamatergic neurons.

159 f its own receptor and synergizes with local glutamatergic neurons.

160 ated a variety of known relationships (e.g., glutamatergic neurotransmission and inflammation with de

161 velopment, alpha2delta1 subunits promote the glutamatergic neurotransmission and synaptogenesis, as w

162 accumulation and deposition of Abeta altered glutamatergic neurotransmission in a temporally and spat

163 tamate transporters are essential players in glutamatergic neurotransmission in the brain, where they

164 lutamate clearance and altered modulation of glutamatergic neurotransmission in the lateral part of t

165 H and the previously described plasticity in glutamatergic neurotransmission in the NTS with CH.

166 d VGLUT3-mGluR5 signaling influences overall glutamatergic neurotransmission is warranted.

167 een both pre- and postsynaptic components of glutamatergic neurotransmission plays a crucial role in

168 chanisms are disrupted in T1D, which affects glutamatergic neurotransmission related to emotional or

169 Here we tested the hypothesis that glutamatergic neurotransmission specifically contributes

170 europharmacological evidence linking reduced glutamatergic neurotransmission to impaired information

171 Glutamatergic neurotransmission via alpha-amino-3-hydrox

172 pression, a paradigm shift from monoamine to glutamatergic neurotransmission, thus making it a unique

173 mised probabilistic reasoning due to reduced glutamatergic neurotransmission.

174 luence both physiologic and pathophysiologic glutamatergic neurotransmission.

175 disorders characterized by dysregulation of glutamatergic neurotransmission.

176 their effects on NMDA receptor signaling and glutamatergic neurotransmission.

177 Surprisingly, the blockade of both glutamatergic NMDA and GABA(A) receptors improved neuron

178 rons that express EP3R and mediate fever are glutamatergic, not GABAergic.

179 Selective excitation of glutamatergic nuclear neurons provides greater seizure i

180 We used optogenetic stimulation of either glutamatergic or cholinergic afferents to probe the rela

181 and inhibition of excitation globally, or in glutamatergic or cholinergic neurons, increases longevit

182 ransporters (VGLUTs) that ultimately dictate glutamatergic output.

183 al modulation of GABA input to GABAergic and glutamatergic pallidal neurons and may therefore affect

184 cannabinoid CB(1) receptor localizes to the glutamatergic parallel fiber (PF) terminals of the cereb

185 In addition to glutamatergic pathways, AAV1 also spreads through GABAer

186 h different patterns of co-expression of the glutamatergic phenotype along the rostrocaudal brain axi

187 served, suggesting that co-expression of the glutamatergic phenotype in DA cells influences their sur

188 We hypothesized that, as in zebrafish, the glutamatergic phenotype is present preferentially in the

189 However, in contexts where the glutamatergic phenotype of CCK(+)VGluT3(+)INTs is amplif

190 The first circuit is characterized by glutamatergic photoreceptors and responds to the directi

191 Furthermore, effects of junk-foods on glutamatergic plasticity in females are unknown.

192 to determine effects of diet manipulation on glutamatergic plasticity within the NAc of males and fem

193 Glutamatergic plumes overlapped anatomically with a redu

194 RNAscope technique identified a glutamatergic population of MnPO neurons that projects t

195 Purkinje cell stimulation entrains glutamatergic projection cells at their firing frequency

196 of the two main cortical neuronal subtypes, glutamatergic projection neurons and GABAergic interneur

197 ) nucleus, we identify five major classes of glutamatergic projection neurons distinguished by gene e

198 Optogenetic inhibition of glutamatergic projection neurons in the MD also resulted

199 at it mirrored the establishment of relevant glutamatergic projection pathways.

200 we tested whether optogenetic activation of glutamatergic projections from the IL to the nucleus acc

201 Reduced effect of glutamatergic projections from the prefrontal cortex to

202 sively studied and the former has excitatory glutamatergic projections to the latter.

203 spontaneously with wide dynamic ranges, send glutamatergic projections to the ventrolateral periaqued

204 n, G-CSF leads to downregulation of synaptic glutamatergic proteins in medial prefrontal cortex (mPFC

205 reduced membrane excitability and decreased glutamatergic receptor activity, consistent with increas

206 At excitatory synapses, glutamatergic receptors activated by spontaneous and evo

207 xia was blunted after blockade of ionotropic glutamatergic receptors at the level of the pFRG; and c)

208 eurons in the thalamic reticular nucleus and glutamatergic relay neurons in the ventrobasal thalamus

209 Rather, their loss reduces sites of glutamatergic sensory neurotransmission that normally en

210 nt of dopaminergic as well as noradrenergic, glutamatergic, serotonergic and adenosine pathways provi

211 um spiny neuron responses to corticostriatal glutamatergic signaling acutely, and we hypothesize that

212 tion dominates CCK(+)VGluT3(+)INT signaling, glutamatergic signaling becomes predominant when glutama

213 f NSCs through a dominant astrocyte-mediated glutamatergic signaling cascade.

214 Evidence is presented that glutamatergic signaling contributes to plasticity at the

215 These data identify glutamatergic signaling dysfunction and nitric oxide def

216 high-density lipoproteins in the heart, and glutamatergic signaling in the brain.

217 Multiple lines of evidence point to glutamatergic signaling in the postsynaptic density (PSD

218 Integral to PSD glutamatergic signaling is reciprocal interplay between

219 larming rate, novel therapeutic targeting of glutamatergic signaling should be further explored again

220 e here focus on an alternative way to modify glutamatergic signaling through positive allosteric modu

221 N -> NAc neurons express VGLUT1, a marker of glutamatergic signaling.

222 females and paralleled by sex differences in glutamatergic signaling.

223 Serine-modulated glutamatergic signalling and changes in bioenergetics ma

224 nt to trigger heterosynaptic potentiation of glutamatergic signalling to oriens interneurons in the h

225 ficient to trigger a lasting potentiation of glutamatergic signalling.

226 GABAergic external globus pallidus (GPe) and glutamatergic subthalamic nucleus (STN) neurons form a k

227 GABAergic external globus pallidus (GPe) and glutamatergic subthalamic nucleus (STN) neurons form a k

228 This study suggested that glutamatergic synapse and axon guidance pathways were sp

229 a transsynaptic adhesion protein regulating glutamatergic synapse assembly on dendrites of central n

230 To unravel the roles of CAST/ELKS in glutamatergic synapse development and in presynaptic fun

231 xcitatory synapse size diversity, we studied glutamatergic synapse size dynamics and diversification

232 atic plasticity rules are well described for glutamatergic synapses but less clear for GABAergic syna

233 ipal cells where the nodes are interregional glutamatergic synapses containing silent but ready-to-us

234 sting of principal cells where the nodes are glutamatergic synapses containing silent but ready-to-us

235 s and the generation of AMPA receptor-silent glutamatergic synapses in the adult nucleus accumbens sh

236 ptic mechanisms recruited by HA signaling at glutamatergic synapses in the NAc.

237 of transient synaptic potentiation (t-SP) at glutamatergic synapses in the nucleus accumbens core (NA

238 DA receptor-dependent synaptic plasticity of glutamatergic synapses in the prelimbic prefrontal corte

239 napses coexisting in one of the best studied glutamatergic synapses of the brain, the mossy fiber syn

240 um and that their terminals form excitatory, glutamatergic synapses on host cortical neurons.

241 her acute stress engages these mechanisms at glutamatergic synapses onto D(1) receptor-expressing [D1

242 genous H(3) receptor signaling in the NAc at glutamatergic synapses onto D1(+)-MSNs.

243 t authentic and transmitted stress can prime glutamatergic synapses onto hippocampal CA1 neurons to u

244 een synapses.SIGNIFICANCE STATEMENT Sizes of glutamatergic synapses vary tremendously, even when form

245 the complex network of interacting sCAMs in glutamatergic synapses will be an important strategy for

246 oles in the nervous system, in particular at glutamatergic synapses, a potential role for Rh50 protei

247 ng at putative axo-dendritic and axo-spinous glutamatergic synapses, and intracellular labeling on th

248 nderstanding of GluD1 regulation of striatal glutamatergic synapses, but also suggest possible extras

249 o demonstrate that in addition to excitatory glutamatergic synapses, MOC neurons receive inhibitory G

250 key roles in the use-dependent adaptation of glutamatergic synapses-along the dendritic arbor.

251 neuromuscular junctions, representing large glutamatergic synapses.

252 ng proteins that are expressed in excitatory glutamatergic synapses.

253 g of the functional diversity of hippocampal glutamatergic synapses.

254 etylcholine for the maturation of developing glutamatergic synapses.

255 f the potent vasodilator nitric oxide during glutamatergic synaptic activity.

256 bers of inhibitory synapses without altering glutamatergic synaptic density.

257 uctuations are sufficient to fully diversify glutamatergic synaptic sizes, with activity-dependent pr

258 extracellular application of Abetaos reduced glutamatergic synaptic transmission and long-term potent

259 f the GluA1 subunit prevented enhancement of glutamatergic synaptic transmission associated with stat

260 ates the slow, Ca(2+)-permeable component of glutamatergic synaptic transmission in the central nervo

261 such as APP, PSEN1/PSEN2, are implicated in glutamatergic synaptic transmission, a function that is

262 as also found to stimulate axonal branching, glutamatergic synaptic transmission, and neuronal excita

263 siveness and presynaptic release to optimize glutamatergic synaptic transmission.

264 ulation of group III mGluRs and dysregulated glutamatergic synaptic transmission.

265 ibe the physiological role of cholesterol in glutamatergic synaptic transmission.

266 d neurite outgrowth and dominantly inhibited glutamatergic synaptogenesis in hippocampal neurons.

267 Dysregulation of the glutamatergic system and its receptors in medial prefron

268 Glutamatergic system dysregulation that is observed in A

269 relapse demonstrate an important role of the glutamatergic system, in particular, cerebral metabotrop

270 Imbalances in the glutamatergic system, leading to excessive, toxic stimul

271 We first show that optogenetic activation of glutamatergic terminals from the PeF to the basolateral

272 ed after optogenetically inhibiting cortical glutamatergic terminals in the DRN.

273 ty in TRN neurons, which were driven by fast glutamatergic thalamoreticular inputs but did not requir

274 The observed lower levels of multiple glutamatergic transcripts across both medial and lateral

275 ynthesis and degradation is found to disrupt glutamatergic transmission and excitability in networks

276 antibody occludes the boost in amplitude of glutamatergic transmission and LTP suppression observed

277 its and anxiety-like behaviors with enhanced glutamatergic transmission and neuronal excitability.

278 Glutamatergic transmission carrying reward-associated si

279 Furthermore, HA asymmetrically regulates glutamatergic transmission from the prefrontal cortex an

280 ncing prophylactics may alter AMPAR-mediated glutamatergic transmission in CA3.

281 Dopamine receptor D1 modulates glutamatergic transmission in cortico-basal ganglia circ

282 se physiological BRI2 functions, we analyzed glutamatergic transmission in FDD and FBD knock-in mice,

283 mbic circuit function.SIGNIFICANCE STATEMENT Glutamatergic transmission in the nucleus accumbens (NAc

284 it a form of long-term potentiation (LTP) of glutamatergic transmission that does not depend on NMDA

285 Long-term potentiation of glutamatergic transmission to hippocampal interneurons i

286 brain concentrations of TNF-alpha, augmented glutamatergic transmission, suppression of Long-term-Pot

287 KO) mice to assess the effects of Abetaos on glutamatergic transmission, synaptic plasticity, and den

288 We propose a model where PICALM modulates glutamatergic transmission, together with BIN1, to ameli

289 mor necrosis factor-alpha (TNF-alpha) boosts glutamatergic transmission, which is excitatory, and sup

290 rol levels, suggesting that lap may modulate glutamatergic transmission.

291 tion of larger dendritic spines and stronger glutamatergic transmission.

292 the tonic control of the eCB signaling over glutamatergic transmission.

293 nction at synapses, which results in reduced glutamatergic transmission.

294 First, immunocytochemistry for glutamatergic (VGlut1 and VGlut2) and GABAergic (VGAT) s

295 Further, a decrease in the number of DRv glutamatergic (VGLUT3+) neurons was observed in all stre

296 ely moving mice, optogenetically stimulating glutamatergic vlPAG neurons that express Chx10 reliably

297 In contrast, glutamatergic VP neurons are essential for movements to

298 Our results indicate that GABAergic and glutamatergic VP neurons encode the drive for approach a

299 Here, we show that GABAergic and glutamatergic VP neurons selectively control behavior in

300 We show that Opn5 is expressed in glutamatergic warm-sensing POA neurons that receive syna