ライフサイエンスコーパス: inhibitory postsynaptic potential

1 to reduce membrane potential during the slow inhibitory postsynaptic potential.

2 ten the AP afterdepolarization, and generate inhibitory postsynaptic potentials.

3 y inputs were often followed by long-latency inhibitory postsynaptic potentials.

4 cells was no longer balanced by synchronous inhibitory postsynaptic potentials.

5 excitability and the reversal potential for inhibitory postsynaptic potentials.

6 o significant change in evoked excitatory or inhibitory postsynaptic potentials, and intrinsic cellul

7 aled that the activation of h-currents by an inhibitory postsynaptic potential can cause a short-term

8 Thus, GABAB inhibitory postsynaptic potentials can elicit low-thresh

9 iunit spikes increased with age, whereas the inhibitory postsynaptic potential caused by Purkinje cel

10 The threshold inhibitory postsynaptic potential conductance for reboun

11 d that ethanol had little effect on compound inhibitory postsynaptic potentials/currents (IPSP/Cs) co

12 ss nuclear cell spiking, whereas synchronous inhibitory postsynaptic potentials entrain nuclear cell

13 evoked an excitatory postsynaptic potential/inhibitory postsynaptic potential (EPSP/IPSP) sequence,

14 ionotropic receptors to cause excitatory or inhibitory postsynaptic potentials (EPSPs or IPSPs), res

15 Lateral inhibition, inhibitory postsynaptic potentials evoked by intrabulbar

16 tic transmission, DHPG induces depression of inhibitory postsynaptic potentials evoked by primary aff

17 This inhibitory postsynaptic potential-excitatory postsynapti

18 otein, induces a long-term transformation of inhibitory postsynaptic potentials from basket interneur

19 Synthetic GABAB inhibitory postsynaptic potentials, generated by a hybri

20 calcium spikes in both cell types when peak inhibitory postsynaptic potential hyperpolarization was

21 of GABAergic interneurons produces a strong inhibitory postsynaptic potential in spiny neurons, the

22 comitantly, as the reversal potential of the inhibitory postsynaptic potential in VPN neurons became

23 (NE) causes an increase in the frequency of inhibitory postsynaptic potentials in CA1 pyramidal neur

24 yperpolarizations in relay cells and unitary inhibitory postsynaptic potentials in interneurons.

25 N density, which was associated with reduced inhibitory postsynaptic potentials in layer 2/3 pyramida

26 lation of the brachium produced monosynaptic inhibitory postsynaptic potentials in morphologically id

27 it hyperpolarizes the reversal potential for inhibitory postsynaptic potentials in motoneurons.

28 LTS activity was closely correlated with inhibitory postsynaptic potentials in neighboring FS int

29 ular stimulation of an OC interneuron evokes inhibitory postsynaptic potentials in the B3 motoneurons

30 rectifying K+ channels (GIRK) generate slow inhibitory postsynaptic potentials in the brain via G(i/

31 n betagamma subunits, thereby mediating slow inhibitory postsynaptic potentials in the brain.

32 hed the NO-induced potentiation of GABAergic inhibitory postsynaptic potentials in the NTS.

33 ddition, nicotine reduced field monosynaptic inhibitory postsynaptic potentials in the presence of ML

34 precision and reliability of excitatory and inhibitory postsynaptic potentials, in contrast to Media

35 ions and reversed the basket interneuron-CA1 inhibitory postsynaptic potential into an excitatory pos

36 silent cells, TS stimulation evoked an EPSP-inhibitory postsynaptic potential (IPSP) complex.

37 otentials in response to single stimuli, the inhibitory postsynaptic potential (IPSP) conductance and

38 ISS evokes an inhibitory postsynaptic potential (IPSP) followed by an

39 nerator potentials, but had no affect on the inhibitory postsynaptic potential (IPSP) in the B cell t

40 It has been reported that the inhibitory postsynaptic potential (IPSP) is abolished be

41 The noradrenergic slow inhibitory postsynaptic potential (IPSP) was abolished b

42 f a gamma-aminobutyric acid type B (GABA(B)) inhibitory postsynaptic potential (IPSP), but in drug-ex

43 and GABAB receptor-mediated hyperpolarizing inhibitory postsynaptic potentials (IPSPAs and IPSPBs, r

44 The frequency of inhibitory postsynaptic potentials (IPSPs) ("responses p

45 synaptic perforant path-evoked fast and slow inhibitory postsynaptic potentials (IPSPs) (53% and 66%,

46 y hyperpolarizing the reversal potential for inhibitory postsynaptic potentials (IPSPs) after SCI.

47 ased GABA type A (GABA(A)) receptor-mediated inhibitory postsynaptic potentials (IPSPs) and currents

48 Spontaneous inhibitory postsynaptic potentials (IPSPs) and currents

49 of ghrelin increased the amplitude of evoked inhibitory postsynaptic potentials (IPSPs) and the frequ

50 he amplitude of stimulus-evoked monosynaptic inhibitory postsynaptic potentials (IPSPs) between acute

51 cular thalamic (RE) neurons in vivo revealed inhibitory postsynaptic potentials (IPSPs) between RE ce

52 ished basal-evoked GABA(A) receptor-mediated inhibitory postsynaptic potentials (IPSPs) by decreasing

53 t mitral cell synchrony was mainly driven by inhibitory postsynaptic potentials (IPSPs) imposed by GA

54 and cLF, respectively) revealed monosynaptic inhibitory postsynaptic potentials (IPSPs) in 75% and 65

55 rneurons in the hippocampus, eliciting giant inhibitory postsynaptic potentials (IPSPs) in CA3 pyrami

56 s (NRGc) evoked large amplitude, glycinergic inhibitory postsynaptic potentials (IPSPs) in cat motone

57 Inhibitory postsynaptic potentials (IPSPs) in ICd neuron

58 cells at the central canal elicits GABAergic inhibitory postsynaptic potentials (IPSPs) in intraspina

59 and stimulation evokes bicuculline-sensitive inhibitory postsynaptic potentials (IPSPs) in motorneuro

60 this system is the amplitude and duration of inhibitory postsynaptic potentials (IPSPs) in thalamocor

61 ly inhibited 5-HT(1A) receptor-mediated slow inhibitory postsynaptic potentials (IPSPs) in the dorsal

62 amplitude, whereas basket cells evoke slower inhibitory postsynaptic potentials (IPSPs) in their post

63 These findings indicate that they were inhibitory postsynaptic potentials (IPSPs) mediated by g

64 sent report, we studied the arrival times of inhibitory postsynaptic potentials (IPSPs) observed in i

65 s exhibited large amplitude monophasic GABAB inhibitory postsynaptic potentials (IPSPs) synchronous w

66 Recordings in DP revealed presumed inhibitory postsynaptic potentials (IPSPs) that were lar

67 equency of spontaneous bicuculline-sensitive inhibitory postsynaptic potentials (IPSPs) when recorded

68 n of sympathetic postganglionic axons evoked inhibitory postsynaptic potentials (IPSPs), and stimulat

69 nin hyperpolarizes the reversal potential of inhibitory postsynaptic potentials (IPSPs), E(IPSP), in

70 issues and play key roles in generating late inhibitory postsynaptic potentials (IPSPs), slowing hear

71 Interneurone-to-interneurone inhibitory postsynaptic potentials (IPSPs), studied with

72 elicited by short, high-frequency trains of inhibitory postsynaptic potentials (IPSPs), which reliab

73 cludes large amplitude active sleep-specific inhibitory postsynaptic potentials (IPSPs).

74 synaptic B photoreceptors where they mediate inhibitory postsynaptic potentials (IPSPs).

75 citatory postsynaptic potentials (EPSPs) and inhibitory postsynaptic potentials (IPSPs).

76 in the amplitude of intracellularly recorded inhibitory postsynaptic potentials (IPSPs).

77 Ps), followed by disynaptic, hyperpolarizing inhibitory postsynaptic potentials (IPSPs).

78 stimulation produced bilateral, long latency inhibitory postsynaptic potentials (IPSPs).

79 ver, is that LTD in layer IV is modulated by inhibitory postsynaptic potentials (IPSPs); postsynaptic

80 Monosynaptic inhibitory postsynaptic potentials mediated by gamma-ami

81 Cl- levels required for the hyperpolarizing inhibitory postsynaptic potentials mediated by ionotropi

82 In vitro, dynamically clamped asynchronous inhibitory postsynaptic potentials mimicking Purkinje af

83 Inhibitory postsynaptic potentials of the granular and a

84 vectors increased the amplitude of cortical inhibitory postsynaptic potentials, only viral expressio

85 e lateral rectus muscle completely abolishes inhibitory postsynaptic potentials onto abducens motoneu

86 ogical blockers reduced the amplitude of the inhibitory postsynaptic potential recorded from CA1 PNs

87 technique did not affect the GABAA-mediated inhibitory postsynaptic potentials, the membrane resista

88 of the gamma gamma-aminobutyric acid (GABA) inhibitory postsynaptic potentials was markedly decrease

89 Inhibitory postsynaptic potentials were evoked in mechan

90 ceive strong barrages of both excitatory and inhibitory postsynaptic potentials, with the inhibitory