ライフサイエンスコーパス: excitatory response

1 -induced inhibition but had no effect on the excitatory response.

2 acid (ACPD) produced a robust, long-lasting excitatory response.

3 ily during the first few milliseconds of the excitatory response.

4 IN8, in contrast, shows a delayed inhibitory/excitatory response.

5 se properties is compensated by an increased excitatory response.

6 ere was no evidence of abnormal heteronymous excitatory responses.

7 Simulated microsaccades generate solely excitatory responses.

8 in the LPO or LH evoked both inhibitory and excitatory responses.

9 natively, to short-term enhancements of both excitatory responses.

10 e on EAAT3 internalization and its action on excitatory responses.

11 pinch versus brush was not as great as with excitatory responses.

12 n a blunting of 5-HT- and hypocretin-induced excitatory responses.

13 EM sleep, exhibited exclusively or initially excitatory responses.

14 sia that is capable of modifying the central excitatory responses.

15 iments revealed an unexpected enhancement of excitatory responses and dendritic calcium signals in th

16 sing (SOM) neurons principally subtract from excitatory responses and sharpen selectivity.

17 gan with an increase in firing probability ('excitatory' responses) and others with a decrease in fir

18 gonist AP-5 attenuated 67% of the STN-evoked excitatory responses, and the AMPA-selective antagonist

19 It is assumed that ganglion cell excitatory responses are driven by these bipolar cell sy

20 The evoked respiratory excitatory responses are probably mediated by glutamate

21 coclaustral afferents generated monosynaptic excitatory responses as well as disynaptic inhibitory re

22 Glutamate receptor ion channels mediate excitatory responses at the majority of CNS synapses.

23 of the monaural EPSCs predicted the binaural excitatory response but less well than the summation of

24 te and butyrate homologs of c3HA could evoke excitatory responses but only at moderate-to-high concen

25 The duration of long-lasting excitatory responses, but not short-lasting responses of

26 n (POMC) cells, coupled with a robust direct excitatory response by POMC neurons (n > 200) to kisspep

27 We discovered that altering the magnitude of excitatory responses by dopamine neurons in response to

28 but not females, had significantly increased excitatory responses compared to Controls (p<0.05, n=10

29 Some excitatory responses continue beyond the end of odor del

30 rhythmical discharges following the initial excitatory response (conventional reflex) result from a

31 ebellar nuclear cells, which then produce an excitatory response corresponding to the learned movemen

32 ore, many CS-CN correlograms show an initial excitatory response, demonstrating the ability of climbi

33 mAChR activation generates inhibitory and/or excitatory responses, depending on neuron subtype.

34 , and relative proportions of inhibitory and excitatory responses differed in an event-specific manne

35 stimulation and during STN-BHFS, the STN-GPe excitatory response dominates over the STN-GPe-GPe recur

36 uring the day as well as reduced NMDA-evoked excitatory responses during the night.

37 nhibitory synaptic activity and/or decreased excitatory responses during the train at 40 Hz, but not

38 recordings in anaesthetised rats showed that excitatory responses evoked by physiological vibrissa af

39 The remaining excitatory responses evoked by stimulation of the LPO an

40 The first inhibitory and excitatory responses evoked by tap stimuli had latencies

41 The excitatory response field for each class was spatially d

42 Following RaN stimulation we observed an excitatory response followed by a period of reduced disc

43 To this end, we recorded excitatory responses from the bitter-sensitive taste cel

44 of the segmental dorsal root evoked a prompt excitatory response in almost every neurone sampled (161

45 imarily comprised of anions and result in an excitatory response in DA neurons at lower DA concentrat

46 , followed by DA-D(1)-like receptor-mediated excitatory response in ETCs.

47 put to the BNST, preferentially reducing the excitatory response in ex vivo mouse brain slices.

48 mechanisms and call for re-evaluation of the excitatory response in primate research.

49 ibuted a major portion of the proton-induced excitatory response in SG neurons, and (3) ASIC2 null mi

50 hibitory response dominates over the STN-GPi excitatory response in the GPi.

51 oned animal evoked a robust and long-lasting excitatory response in the STN and, concurrently, a long

52 projecting vCA1 neurons induced monosynaptic excitatory responses in both the mPFC and basal amygdala

53 Here we describe excitatory responses in CNS myelin that are gated by a g

54 Entorhinal stimulation produced excitatory responses in four bursting cells and it was t

55 00 Hz) of the STN (STN-BHFS) evoked powerful excitatory responses in GPe neurons.

56 Extracellular ATP evoked two excitatory responses in hippocampal neuroblastoma cells

57 In contrast to the consistent excitatory responses in LN activity following fast appli

58 We find that odor-evoked excitatory responses in M/T cells typically consist of b

59 ned blockade of AMPARs and NMDARs eliminated excitatory responses in nearly all neurons, whereas sepa

60 ly produced inhibitory responses in mPFC and excitatory responses in OFC.

61 and early monosynaptic and late polysynaptic excitatory responses in postsynaptic nucleus accumbens n

62 n to show that six putative pheromones evoke excitatory responses in single vomeronasal neurons, lead

63 w that intracellular acidification generates excitatory responses in sour taste cells, which can be a

64 Stimulation of this region evokes excitatory responses in the CA1 region of the hippocampu

65 pharmacological agents, we found that the MC excitatory responses in the MOB were mediated by 5-HT2A

66 xydopamine (6-OHDA) affected differently the excitatory responses in the STN evoked by amphetamine an

67 ction shifted balance between inhibitory and excitatory responses in the TeA-LA pathway toward excita

68 was persistence of short onset heteronymous excitatory responses in triceps brachii, while a normal

69 callosal inputs evokes progressively smaller excitatory responses in type B but not type A neurons.

70 ponses and potentiate NMDA receptor-mediated excitatory responses in vitro.

71 vix evoked significantly more inhibitory (vs excitatory) responses in P than in E and M, and the resp

72 These excitatory responses increase as the reward value increa

73 had no direct effects on synaptically evoked excitatory responses, long-term potentiation, or synapti

74 al stimuli that would otherwise yield strong excitatory responses, luminance transients produce signi

75 ignificantly less than the threshold for the excitatory response (median: 0.75 N).

76 One subtype had a striking biphasic excitatory response mediated by AMPAR and mGluR1alpha.

77 neural correlate of behavioral vigor in the excitatory response of accumbens neurons to reward-predi

78 he central neural system that mediate a fast excitatory response of neurons.

79 nduced a previously unreported depolarizing, excitatory response of these cells, which was often asso

80 of lumbosacral dorsal roots facilitated the excitatory response of thoracolumbar dorsal horn neurons

81 cally localized to modulate the postsynaptic excitatory responses of catecholamine-containing neurons

82 or presentation (2-4 sec); in contrast, both excitatory responses of granule cells and M/T cell later

83 Acute estradiol (E2) can potentiate the excitatory responses of hypothalamic ventromedial nucleu

84 LC activation increased excitatory responses of mitral cells evoked by weak (i.e

85 ther inhibit the release of SP or reduce the excitatory responses of second-order neurons to SP.

86 tinspiratory firing patterns associated with excitatory responses on pattern or inhibitory responses

87 Maximal short-latency excitatory responses originated from stimulation sites i

88 In 1% halothane, the excitatory responses produced by FMRFamide were substant

89 Non-cholinergic excitatory responses remained after loss of ICC-DMP.

90 mast cell tryptase evoked slowly activating excitatory responses reminiscent of slow synaptic excita

91 Differences in the dynamics of excitatory responses seem to reflect differences in pres

92 ngly, injection of tx3a into mice elicits an excitatory response similar to that of the m-2 branch pe

93 tive RPEs became unreliable, yet significant excitatory responses still remained.

94 ) inhibit the transient after-discharge, the excitatory response that occurs just after the disappear

95 n GABA is depolarizing, may allow the robust excitatory responses that are critical for normal synaps

96 ergic neurons in TRN exhibited large initial excitatory responses that quickly plateaued during repet

97 ensors to directly convert local acidosis to excitatory responses, therefore offering a cellular mech

98 (5-hydroxytryptamine or 5-HT) mediates rapid excitatory responses through ligand-gated channels (5-HT

99 inhibition and the direction of the shift in excitatory response time course correlated with the cell

100 This excitatory response to 5-HT3 receptor activation may be

101 After the GP lesions, the excitatory response to amphetamine in the STN was not di

102 In contrast, the GP lesions altered the excitatory response to apomorphine, 3 mg/kg.

103 Among the latter, 16.4% exhibited an excitatory response to CRD and were labelled 'CRD-excite

104 A higher incidence of excitatory response to glucose occurred in gastric- than

105 ium but had no effect on the photoreceptor's excitatory response to intracellular injection of InsP(3

106 nes were identified antidromically and by an excitatory response to intravenously injected cholecysto

107 bition by dynorphin-A, whereas at -70 mV the excitatory response to orexin-A prevails.

108 bition by dynorphin-A, whereas at -70 mV the excitatory response to orexin-A prevails.

109 c cell exhibits a significantly nonmonotonic excitatory response to premature monophasic and, to a mu

110 Application of KYN blocked the excitatory response to stimulation of the MPO in 8/16 ce

111 The latency to onset of the excitatory response to stimulation of the MPO was longer

112 tivity, AA either enhanced or attenuated the excitatory response to test pulses of GLU.

113 SPL was increased, despite the fact that the excitatory response to the masker was often saturating o

114 ifts were not usually caused by a persistent excitatory response to the masker; instead we propose a

115 om neighboring neurons rather than increased excitatory response to the stimulus.

116 es of CT cells: those having a short-latency excitatory response to whisker deflection, those having

117 The excitatory responses to 100 nM NMC were accompanied by s

118 1 receptor signalling whereby inhibitory and excitatory responses to ACh in pyramidal neurons represe

119 s showed wide receptive fields, representing excitatory responses to almost the entire range of frequ

120 enoceptor-mediated excitation was unchanged, excitatory responses to AMPA were enhanced and the 5-HT1

121 an electrophysiological assay, we find that excitatory responses to both cAMP- and IP3-producing odo

122 The excitatory responses to both glucose and alpha-MDG are a

123 Dorsal horn neurons showing excitatory responses to colorectal distention (80 mm Hg,

124 1 mg/kg I.V.) attenuated MD and Sm neuronal excitatory responses to CRD in a dose-dependent fashion,

125 n of responsive neurons and the magnitude of excitatory responses to CRF in the ventral portion of th

126 urones (11 of 20) showing clear reproducible excitatory responses to CRH applications.

127 Excitatory responses to decrements were slightly larger

128 s to enhanced basal firing rate and stronger excitatory responses to dopamine in striatal cholinergic

129 itive interneurons (SOMs) selectively reduce excitatory responses to frequent tones: suppression of S

130 g alters homeostatic mechanisms to eliminate excitatory responses to GABA but rejected this hypothesi

131 The stimulus-response curves of excitatory responses to graded urinary bladder distentio

132 age in sound-guided behavior, pyramidal cell excitatory responses to habituated sounds are enhanced,

133 It potentiated excitatory responses to HAs (20 out of 48 cells tested)

134 Morphine pretreatment attenuated subsequent excitatory responses to hypocretin, suggesting a long-la

135 erneurons tested also exhibited long latency excitatory responses to lumbar dorsal root stimulation s

136 baseline activity and augmented or revealed excitatory responses to mPFC stimulation independent of

137 The duration of excitatory responses to noxious UBD during acute colonic

138 In conclusion, exaggerated excitatory responses to primary muscle afferent input we

139 eteromeric 5-HT(3AB) receptors mediate rapid excitatory responses to serotonin in the central and per

140 form of spectrotemporal integration in which excitatory responses to sounds at one frequency are faci

141 ith slices of rat brain, all LC cells showed excitatory responses to the hypocretin-2 peptide.

142 Excitatory responses to the serine proteases are mediate

143 tor blocker) greatly diminished or abolished excitatory responses to the STN stimulation.

144 The threshold volume for excitatory responses to urinary bladder distention in ra

145 In addition, bicuculline enhanced excitatory responses to vagal stimulation and increased

146 ion, and had biphasic inhibitory followed by excitatory, responses to phasic ACh application.

147 cts of 10 Hz stimulation of the ILCx on BNST excitatory responses, under different conditions of expo

148 oupled to Galphaq/11 proteins and display an excitatory response upon activation, whereas the cannabi

149 recordings from principal cells showed only excitatory responses upon POR stimulation.

150 Certain cell types generate excitatory responses using primarily AMPA receptors or d

151 (+) channels in PDGFRalpha(+) cells, and the excitatory response was mediated by activation of a Cl(-

152 The difference in the proportion of excitatory responses was also significant (P < 0.01).

153 The amplitude of putative unitary excitatory responses was approximately 1.5 times larger

154 ty of superficial neurons with short-lasting excitatory responses was significantly lower than that o

155 While excitatory responses were apparent at postnatal day 10,

156 onses evoked from MD were unchanged, whereas excitatory responses were enhanced.

157 ocol, strength-interval maps of the cellular excitatory responses were generated for rectangular mono

158 Long-lasting excitatory responses were more frequently encountered (P

159 latency (< 50 ms) and long-latency (> 50 ms) excitatory responses were seen.

160 urons that was attenuated after DBS, whereas excitatory responses were unchanged.

161 cells show highly selective and reproducible excitatory responses when presented with a familiar obje

162 vity reverts to a more gradual transition of excitatory responses with respect to stimulus prematurit

163 ain using crossover inhibition and enhancing excitatory responses within the RF center.