ライフサイエンスコーパス: GABAergic

1 ons; no forebrain subsystems are exclusively GABAergic.

2 nsmitter asynchronously, and are exclusively GABAergic.

3 P3R and mediate fever are glutamatergic, not GABAergic.

4 Among GABAergic AC subtypes, Rbfox2 was colocalized with choli

5 rent GABA(A) receptor blocker), suggesting a GABAergic activation induced by OTR.

6 ing the phasic control of eCB signaling over GABAergic activity and plasticity in the BLA.

7 Indeed, recruitment of GABAergic activity in RAIC promotes the disinhibition of

8 Such transient patterning of GABAergic activity is a functional scaffold that links t

9 ses questions about whether drugs increasing GABAergic activity may impair motor learning and rehabil

10 ence is necessary to sustain the increase in GABAergic activity observed in the PFC during this perio

11 lly reduces the presynaptic functionality of GABAergic activity over that of excitatory synapses.

12 e PAG as a source of highly opioid-sensitive GABAergic afferents and support the idea that different

13 concentrations of the transmitter and other GABAergic agents can modify tonically and phasically act

14 ovide optogenetic evidence for an inhibitory GABAergic Agrp->orexin hypothalamic neurocircuit, and fi

15 These are GABAergic amacrine cells with long, relatively straight

16 Although the majority of VP neurons are GABAergic and encode reward, recent studies revealed a n

17 itory control, as reflected by alteration in GABAergic and glutamatergic balance (i.e., GABA/Glu), ma

18 py to assess potential structural changes in GABAergic and glutamatergic microcircuits in the VApc an

19 al GPR56 protein is evenly expressed in both GABAergic and glutamatergic neurons, suggesting the GABA

20 ows differential modulation of GABA input to GABAergic and glutamatergic pallidal neurons and may the

21 Our results indicate that GABAergic and glutamatergic VP neurons encode the drive

22 in adult retinas, and it is present in both GABAergic and glycinergic amacrine cells.

23 This circuitry, mediated by GABAergic and glycinergic synapses, provides expiratory

24 gic synapses, MOC neurons receive inhibitory GABAergic and glycinergic synaptic inputs.

25 synchronously, and are mediated by combined GABAergic and glycinergic transmission.

26 these were Meis2 and Tcf4, expressed by most GABAergic and most glycinergic types, respectively.

27 grees of neuroinflammation and activation of GABAergic and neuronal activation in mice regardless of

28 rincipal neurons that are well poised to use GABAergic and NPY signaling to regulate the excitability

29 ecting cells are oxytocinergic and destinate GABAergic and OTR-expressing cells inside RAIC.

30 s to the rostral agranular insular cortex on GABAergic and oxytocin receptor-expressing neurons.

31 At least by normalizing the function of GABAergic and PV interneurons, EA may represent a promis

32 highly dependent on cell type (GABAergic/non-GABAergic) and location (module/matrix).

33 nd profiled both neuronal (glutamatergic and GABAergic) and nonneuronal (oligodendrocytes, microglia,

34 ed with significant changes of dopaminergic, GABAergic, and histaminergic systems in selective brain

35 s building blocks are anatomically clustered GABAergic assemblies mostly composed by prospective parv

36 onal collateral formation and hypertrophy of GABAergic basket cell axonal processes, could be compens

37 Mutations of Mecp2 that are restricted to GABAergic cell types largely replicate the behavioral ph

38 he NOS-1 AC: a multistratified, axon-bearing GABAergic cell, with dendrites in both ON and OFF synapt

39 Here, we found that staining for GABAergic cells and perineuronal nets differentiates the

40 und that the proportions of four subtypes of GABAergic cells differentiate intercollicular nuclei fro

41 Excitation of GABAergic cells in the substantia nigra pars reticulata

42 they differentially target dopaminergic and GABAergic cells in the ventral tegmental area (VTA).

43 Here, we study coordinated activity in GABAergic cells of the mouse barrel cortex using in vivo

44 GABAergic cells that did not contain GFP or PV were iden

45 (GABA) and parvalbumin (PV) to characterize GABAergic cells that project to the pretectum (PT), vent

46 e critically reliant on their local circuit, GABAergic cells.

47 llosal activities drive massive apoptosis of GABAergic chandelier cells (ChCs) in the binocular regio

48 re propensity and impairments in hippocampal GABAergic circuitry in Ophn1 mouse model of X-linked int

49 nderstand how ankyrin-G and GABARAP regulate GABAergic circuitry in vivo.

50 GABAergic circuits are critical for the synchronization

51 To begin to unravel the complexities of GABAergic circuits in the superior colliculus (SC), we u

52 s is due to specific alterations of distinct GABAergic circuits is unknown.

53 geneous in size and shape, including a small GABAergic component.

54 How a dysfunction of GABAergic cortical interneurons interacts with maturatio

55 e show an acute increase in O-GlcNAc dampens GABAergic currents onto principal cells in rodent hippoc

56 in the PFC that correlates linearly with the GABAergic deficit.

57 We conclude that the glutamatergic and GABAergic deficits in the frontal lobe are potential tar

58 We found a transition of the main GABAergic drug effects from auditory cortex in standard

59 ift toward cortical excitation likely due to GABAergic dysfunction.

60 he population level and is decreased through GABAergic enforcement.

61 CeA afferents are GABAergic (express Slc32a1/Vgat) and are distributed lar

62 Reciprocally connected GABAergic external globus pallidus (GPe) and glutamaterg

63 also suggest that the diminished prefrontal GABAergic function could arise from a deficit in the rec

64 Of particular interest is the gain of GABAergic function in the PFC during adolescence and its

65 ce is necessary for refinement of prefrontal GABAergic function, the absence of which results in imma

66 g adolescence enables the gain of prefrontal GABAergic function, which is required for maintaining pr

67 GABAergic (gamma-aminobutyric-acid-releasing) ovipositio

68 negatively correlated with inflammatory and GABAergic gene expression, respectively.

69 x-4 attenuates cocaine seeking and highlight GABAergic GLP-1R-expressing circuits in the midbrain as

70 By contrast, interneurons, such as GABAergic granule cells (GCs), integrate across multiple

71 The indirect GABAergic habenula pathway derives from neurons in the s

72 Here, we probe GABAergic influences in the networks using double-blind

73 Thus, altered GABAergic inhibition adds to a growing list of adaptatio

74 oride importer NKCC1 and timely emergence of GABAergic inhibition are modulated by proteasome distrib

75 Although under normal conditions, GABAergic inhibition dominates CCK(+)VGluT3(+)INT signal

76 GABAergic inhibition gates weak nociceptive encodings fr

77 Manipulations that enhance GABAergic inhibition have been associated with improved

78 Decreasing GABAergic inhibition is a key feature of motor learning

79 Selective enhancement of GABAergic inhibition is thought to impact many vital bra

80 parkinsonism, GATs are downregulated, tonic GABAergic inhibition of DA release augmented, and nigros

81 here were no overall changes to TMS measured GABAergic inhibition with this low dose of baclofen.

82 of mechanisms for gain modulation, including GABAergic inhibition, synaptically driven fluctuations i

83 l Cl(-) extrusion capacity, and thus impairs GABAergic inhibition.

84 tion of DAergic activity states, loss of PFC GABAergic inhibitory control and affective and cognitive

85 g interneurons, most VTA Sst neurons express GABAergic inhibitory markers, but some of them also expr

86 ty and spontaneous MFR failed in hippocampal GABAergic inhibitory neurons, which remained hyperexcita

87 by comparing mice lacking either protein in GABAergic inhibitory neurons.

88 This demonstrates that GABAergic innervation to abDGCs develops during a prolon

89 Voluntary wheel running in mice scaled the GABAergic input to abDGCs by increasing the number of sy

90 P neurons provide coordinated daily waves of GABAergic input to target cells across the paraventricul

91 gamma2 subunit, and dampening rhythmicity of GABAergic input to the PVH reduces diurnal rhythmicity i

92 tent with impaired post-synaptic response to GABAergic input, suggesting a potential mechanism for ne

93 ptogenetic manipulation of individual distal GABAergic inputs also revealed differential behavioral e

94 few GABAergic neurons, and that most of its GABAergic inputs arise from CeA.

95 of the stria terminalis (aBNST) make direct GABAergic inputs onto AgRP neurons.

96 optogenetically driving two opiate-sensitive GABAergic inputs to the VTA, the rostromedial tegmental

97 in animals showed a reduction in inhibitory, GABAergic inputs.

98 hese findings provide evidence that cortical GABAergic interneuron dysfunction plays a key role in se

99 hibitory networks by controlling the size of GABAergic interneuron populations in the developing brai

100 he clustered Protocadherins (cPCDHs) control GABAergic interneuron survival during developmentally-re

101 Chandelier cells (ChCs) are a type of GABAergic interneuron that control pyramidal cell output

102 Chandelier cells (ChCs) are a unique type of GABAergic interneuron that selectively innervate the axo

103 s represent a unified definition of cortical GABAergic interneuron types, providing a systematic fram

104 Cortical GABAergic interneurons (CINs) are implicated in NF1 path

105 cipal neurons (L5-6_Fezf2 and L2-3_Cux2) and GABAergic interneurons (Sst and Pvalb), whereas other su

106 However, it is largely unknown how GABAergic interneurons and astrocytes interact and contr

107 operties of over 4,200 mouse visual cortical GABAergic interneurons and reconstructed the local morph

108 While it is clear that spinal GABAergic interneurons are comprised of multiple subpopu

109 In the mouse neocortex, a third of GABAergic interneurons are eliminated by BAX-dependent a

110 Abnormalities of or reductions in GABAergic interneurons are implicated in the pathology o

111 ty-dependent rules that govern the wiring of GABAergic interneurons are not well understood.

112 Recent work has identified GABAergic interneurons as targets of neuromodulatory inp

113 population and mutual inhibition mediated by GABAergic interneurons between populations affect the ro

114 GABAergic interneurons can be subdivided into three subc

115 that human tau accumulation in dentate gyrus GABAergic interneurons disrupts AHN and strengthening GA

116 ed that intracellular accumulation of tau in GABAergic interneurons impairs AHN by suppressing GABAer

117 ivated in corticolimbic parvalbumin-positive GABAergic interneurons in Grin1 mutant mice.

118 Nonpyramidal GABAergic interneurons in the basolateral nuclear comple

119 are self-innervating synaptic connections in GABAergic interneurons in the brain.

120 minent accumulation of phosphorylated tau in GABAergic interneurons in the dentate gyrus (DG) of AD p

121 cular network are the natural substrates for GABAergic interneurons in the developing mouse forebrain

122 Two abundant populations of cortical GABAergic interneurons include the low-threshold, somato

123 However, GABAergic interneurons likewise receive excitatory input

124 h glutamatergic neurons and parvalbumin (PV) GABAergic interneurons of Ahnak KO mice.

125 GABAergic interneurons represent a heterogenous group of

126 igher resolution, vHPC input onto prefrontal GABAergic interneurons was specifically disrupted, where

127 However, the subpopulations of mature GABAergic interneurons which are compromised by early-li

128 has identified an unprecedented diversity of GABAergic interneurons with pronounced anatomical, molec

129 atal CINs, but not of parvalbumin-expressing GABAergic interneurons, and altered their electrophysiol

130 tic targets are the presynaptic dendrites of GABAergic interneurons, and GAD67-GFP interneurons are a

131 al for the wiring of specific populations of GABAergic interneurons, in which it paradoxically regula

132 rder (MDD) is associated with alterations of GABAergic interneurons, notably somatostatin (Sst) as we

133 ause of the expression of PV in fast-spiking GABAergic interneurons, we hypothesized that PV upregula

134 he production of proper numbers of forebrain GABAergic interneurons.

135 pends on synchronized inhibition provided by GABAergic interneurons.

136 rite-targeting somatostatin-expressing (SST) GABAergic interneurons.

137 with the apoptotic elimination of a third of GABAergic interneurons.

138 te and patterns precisely fine-tuned through GABAergic interneurons.

139 s, but autapses were rare in nonfast-spiking GABAergic interneurons.

140 Moreover, our data indicate that decreased GABAergic levels in dorsal ACC are involved in schizophr

141 of Purkinje cell population inputs, whereas GABAergic-like neurons only respond to the mean populati

142 GABAergic long-range axons that derive from, or project

143 hip, are inactive during copulation, whereas GABAergic mAL neurons remain active during copulation, s

144 erexcitability and the associated changes in GABAergic markers can be rescued at the adult stage in O

145 The intensity of immunostaining for GABAergic markers in VApc and CM did not differ between

146 to seizures, accompanied by an alteration of GABAergic markers were rescued by Rho-associated protein

147 rward circuitry, suggesting that a different GABAergic mechanism might control coincidence detection

148 In contrast with GABAergic-mediated feed-forward inhibition, the depolari

149 GABAergic medium spiny neurons are the main neuronal pop

150 ions, we identify the effect of tiagabine on GABAergic modulation of deep pyramidal and interneuronal

151 tion of [(3)H]muscimol binding by allosteric GABAergic modulators such as barbiturates and steroid an

152 We found in C. elegans that GABAergic motor neurons (D-MNs) bias toward the reward b

153 evelopment, as well as synaptic functions of GABAergic motor neurons.

154 herapeutic pathway to correct alterations in GABAergic networks and dampen pathological hyperexcitabi

155 by our finding that genetic manipulation of GABAergic networks that restores accurate retrieval beha

156 At GABAergic neuromuscular junctions, the short isoform MAD

157 PD, we find associations between SN DaNs and GABAergic neuron gene expression and multiple neuropsych

158 An enrichment of neuroligin-1 A1 in GABAergic neuron types suggests a role in synchrony of c

159 ic and glutamatergic neurons, suggesting the GABAergic neuron-preferential activity of the minimal e1

160 he midbrain, and this is required for proper GABAergic neuronal migration into the substantia nigra p

161 ockout mice with DORs deleted from forebrain GABAergic neurons (Dlx-DOR), and investigated the outcom

162 Likewise, deletion of Orai1 in GABAergic neurons abrogates the chemoconvulsant-induced

163 We discovered a distinct population of GABAergic neurons activated by GA in the mouse central a

164 Mice with selective deletion of Orai1 in GABAergic neurons alone also showed stronger seizures to

165 e mutation resulting in the loss of striatal GABAergic neurons and motor functional deficits.

166 ion cells at their firing frequency, whereas GABAergic neurons are only inhibited.

167 e early postnatal period in developing mice, GABAergic neurons are transient preferential recipients

168 y enhancing endogenous NMDAR activity on the GABAergic neurons can effectively enhance inhibitory act

169 t its localization in both glutamatergic and GABAergic neurons could be compatible with a role in inf

170 ortical networks, the collective dynamics of GABAergic neurons during that neonatal period remain unk

171 s of neurons coincide with glutamatergic and GABAergic neurons identified by optotagging after Chrims

172 nology to reprogram striatal astrocytes into GABAergic neurons in both R6/2 and YAC128 HD mouse model

173 amma-Protocadherins (Pcdhgs) from developing GABAergic neurons in mice of either sex causes a severe

174 nic eminence represent the largest cohort of GABAergic neurons in the hippocampus.

175 s, accounting for approximately one-third of GABAergic neurons in the IC.

176 ime, that GLP-1Rs are expressed primarily on GABAergic neurons in the LDTg and that the efficacy of E

177 atal asphyxia on different subpopulations of GABAergic neurons in the striatum and to assess the outc

178 We found that circuits formed by GABAergic neurons in the thalamic reticular nucleus and

179 Here, we identify a novel population of GABAergic neurons in the ventral brainstem, distinguishe

180 These GABAergic neurons integrate wide-ranging inputs and inne

181 Mice lacking ALK4 in GABAergic neurons of the medial ganglionic eminence (MGE

182 second largest subpopulation of neocortical GABAergic neurons that contain diverse subtypes, which p

183 We found that GABAergic neurons that project to the PBG are primarily

184 and horizontal dendritic morphologies, while GABAergic neurons that project to the PT and vLGN are pr

185 dely-labeled, glutamatergic, glycinergic and GABAergic neurons were found in the ventral respiratory

186 hat, in both rats and mice, LPB contains few GABAergic neurons, and that most of its GABAergic inputs

187 t regions, GLP-1R primarily colocalized with GABAergic neurons, except within some regions such as th

188 populations of cells (glutamatergic neurons, GABAergic neurons, oligodendrocytes, and microglia/astro

189 Of these GABAergic neurons, we identified three categories of pot

190 thermore, EGFP is predominantly expressed in GABAergic neurons, whereas the total GPR56 protein is ev

191 ng P2Y2 purinoceptor activation matured into GABAergic neurons.

192 f cortical and hippocampal glutamatergic and GABAergic neurons.

193 x5/6 enhancer, which restricts expression to GABAergic neurons.

194 hanced yellow fluorescent protein to GAD1(+) GABAergic neurons.

195 ictal increase in firing of substantia nigra GABAergic neurons.

196 nists such as ketamine act preferentially on GABAergic neurons.

197 Nr gamma-aminobutyric acid (GABA)-releasing (GABAergic) neurons was preferentially active in states o

198 ion of beta-klotho in glutamatergic, but not GABAergic, neurons abrogated the effects of dietary prot

199 lipopolysaccharides, glutamatergic, but not GABAergic, neurons exhibit an enhanced synaptic strength

200 dynamic activity changes involving rhythmic GABAergic neurotransmission mediates diurnal rhythmicity

201 ety-like behaviors, and rescued ACE-impaired GABAergic neurotransmitter system and PV interneurons in

202 Therefore, aBNST GABAergic nociceptin neurons may act as a gateway to fee

203 patterns are highly dependent on cell type (GABAergic/non-GABAergic) and location (module/matrix).

204 We show that activating MnPO/VLPO GABAergic or glutamatergic neurons does not alter anesth

205 We conclude that activation of preoptic GABAergic or glutamatergic neurons that increase sleep o

206 er sex, we found that the main basal ganglia GABAergic output in the midbrain, the substantia nigra p

207 ic zones is eliminated without Purkinje cell GABAergic output.

208 Activation of the GABAergic PAG terminals in the VTA promotes immobility,

209 We investigated GABAergic parvalbumin-expressing basket cells (pvBCs) in

210 ojecting via a direct excitatory or indirect GABAergic pathway onto the catecholaminergic VTA/SNc hom

211 lepsy; response to medications targeting the GABAergic pathway was inconsistent.

212 fferents and support the idea that different GABAergic pathways to the VTA control distinct behaviors

213 ix protein, is required for the formation of GABAergic, perisomatic synapses by PV(+) cells.

214 egulation supports the acquisition of mature GABAergic phenotype necessary to sustain adult PFC funct

215 We uncover a transient structure in GABAergic population dynamics that disappears in a senso

216 neurons represent a previously unrecognized GABAergic population of ARC neurons distinct from well-d

217 hat HFOs are generated locally within the LS GABAergic population.

218 neurogenic niche, suggesting a potential of GABAergic potentiators for pro-neurogenic or cell therap

219 uctural data prove NMDAR presence within the GABAergic presynapse.

220 ide Y (NPY) expression identifies a class of GABAergic principal neurons that constitute one-third of

221 the past 10 years has revealed that cortical GABAergic projection neurons are highly diverse in terms

222 As GABAergic projection neurons connect many cortical areas

223 ct future research to examine how long-range GABAergic projections fine-tune activity in distinct dis

224 c) and the centromedian nucleus (CM) receive GABAergic projections from the internal globus pallidus

225 get of addictive drugs and receives multiple GABAergic projections originating outside the VTA.

226 These results demonstrate that GABAergic projections to the VTA are a major contributor

227 The sources of GABAergic projections were more widespread, displayed a

228 pends, in part, on activation of LDTg-to-VTA GABAergic projections.

229 ween excitatory glutamatergic and inhibitory GABAergic receptor effects.

230 at positively correlates with a delay in the GABAergic response switch.

231 Neuronal GABAergic responses switch from excitatory to inhibitory

232 MENT The ventral pallidum consists mainly of GABAergic reward-promoting neurons, but it also encloses

233 Activation of GABAergic RMTg terminals in the VTA in vivo is aversive,

234 GABAergic self-inhibition conductance was similar in hum

235 pharmacological modification of cholinergic, GABAergic, serotonergic or dopaminergic systems, or redu

236 ess to a better understanding of the role of GABAergic signaling between neurons and OLs.

237 BA(A)Rs in OLs may help to study the role of GABAergic signaling during myelination.

238 , we identify the functional determinants of GABAergic signaling in parasitized phagocytes and demons

239 plasma gondii and Neospora caninum activated GABAergic signaling in phagocytes.

240 The findings reveal a regulatory role for a GABAergic signaling machinery in the host-pathogen inter

241 interneurons disrupts AHN and strengthening GABAergic signaling restores AHN and improves cognition

242 GABAergic signaling through GABA(A) receptors (GABA(A)Rs

243 misinins also interfere presynaptically with GABAergic signaling.

244 We find that blocking GABAergic signalling strongly widens the coincidence det

245 analysis of the organoids revealed enhanced GABAergic specification and reduced cell proliferation f

246 for schizophrenia also confirmed the excess GABAergic specification of the patients' neural progenit

247 alian brain, we speculate that NO control of GABAergic synapse efficacy may be more widespread than h

248 th neurons and reveal how astrocytes control GABAergic synapse formation and function.

249 c synapses, indicating its essential role in GABAergic synapse formation and maintenance.

250 d loss of GABA(A) receptors, supporting that GABAergic synapse loss by S-SCAM overexpression is due t

251 with various domain deletions indicated that GABAergic synapse loss correlates with their ability to

252 BC terminals, where it regulates function of GABAergic synapses and assembly of RBC synaptic dyads.

253 fficient recruitment of GABA(A) receptors at GABAergic synapses in C. elegans The interaction of N-MA

254 onsequences of aberrant S-SCAM expression on GABAergic synapses is little studied.

255 ependent pathway that strengthens inhibitory GABAergic synapses of cerebellar molecular layer interne

256 e retina, we find that LRRTM4 is enriched at GABAergic synapses on axon terminals of rod bipolar cell

257 yrin-G plays a key role in the regulation of GABAergic synapses on the axon initial segment and somat

258 uantal events established that the number of GABAergic synapses onto abDGCs increased with maturation

259 matergic pathways, AAV1 also spreads through GABAergic synapses to both excitatory and inhibitory cel

260 ingly, S-SCAM overexpression also attenuated GABAergic synapses, but the effect is mediated by the lo

261 of both pre- and post-synaptic components of GABAergic synapses, indicating its essential role in GAB

262 potential-independent inhibitory currents at GABAergic synapses, using (+)-bilobalide as a negative c

263 are frequently apposed to glutamatergic and GABAergic synapses.

264 the interaction between MADD-4B and NLG-1 at GABAergic synapses.

265 or glutamatergic synapses but less clear for GABAergic synapses.

266 between inferior olive neurons by inhibitory GABAergic synapses.

267 rotein that localizes to both excitatory and GABAergic synapses.

268 ty and gene expression were decreased, while GABAergic synaptic gene expression was increased in male

269 by 2 weeks of abstinence, and then recorded GABAergic synaptic input evoked either electrically or o

270 tection fidelity is thought to depend on the GABAergic synaptic input through a feedforward inhibitor

271 nt abstinence, PTSD-like behavior responses, GABAergic synaptic transmission in the central amygdala

272 uced a concentration-dependent inhibition of GABAergic synaptic transmission onto medial OFC (mOFC),

273 eurons induces a long-lasting suppression of GABAergic synaptic transmission, which depends on subreg

274 saccharides on hippocampal glutamatergic and GABAergic synaptic transmission.

275 apse assembly and elevated expression of the GABAergic synthetic enzyme GAD67 also cooperate to decre

276 ABA-acting drug, we assessed the role of the GABAergic system on the behavioral stress response.

277 e related to the acute effects of alcohol on GABAergic systems that are associated with sleep regulat

278 signaling from postsynaptic cholinergic and GABAergic systems, among others.

279 y neurons or pharmacologically strengthening GABAergic tempos rescued the tau-induced AHN deficits an

280 compensatory responses to restore cerebellar GABAergic tone and cerebellar cortical inhibitory effica

281 s-unit response patterns to taste, enhancing GABAergic tone in rNTS reconfigures the neural activity

282 vels in the CeA may be responsible for hyper-GABAergic tone in the CeA that is observed in individual

283 Cells where enhanced GABAergic tone increased lick coherence conveyed more in

284 has acted as a selection pressure to reduce GABAergic tone, which in turn reduces energetic needs in

285 cortical insular level by favoring cortical GABAergic transmission and activating descending spinal

286 rgic interneurons impairs AHN by suppressing GABAergic transmission and disinhibiting neural circuits

287 in their adulthood, accompanied by increased GABAergic transmission and PV interneurons in PrL.

288 Voltage imaging of GABAergic transmission at the axon initial segment (AIS)

289 dicative of hyperarousal, with increased CeA GABAergic transmission in NOV females.

290 rgeneralization in novel contexts, increased GABAergic transmission in the CeA, and a profile of incr

291 arvalbumin positive (PV+) cells and impaired GABAergic transmission in the dentate gyrus (DG), accomp

292 We report that GABAergic transmission is decreased in Trem2(R47H/R47H)

293 GEE mice exhibit decreased GABAergic transmission onto DLS projection neurons, incl

294 ls in the PFC was sufficient to reduce local GABAergic transmission onto pyramidal neurons, disrupt p

295 ical perturbations of both glutamatergic and GABAergic transmission, as observed by altered frequency

296 e, we aim to further investigate the role of GABAergic transmission, especially parvalbumin (PV) inte

297 he cortical level, oxytocin can modulate the GABAergic transmission; consequently, an interaction mod

298 ry for glutamatergic (VGlut1 and VGlut2) and GABAergic (VGAT) synapses demonstrated that overall syna

299 Furthermore, GABAergic VP neurons are essential for movements toward

300 Lesioning or chemogenetically inhibiting VTA GABAergic (VTA(Vgat)) neurons generated persistent wakef