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 Thus, GABAB inhibitory postsynaptic potentials can elicit low-thresh

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

9 The threshold inhibitory postsynaptic potential conductance for reboun

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

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

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

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

14 Lateral inhibition, inhibitory postsynaptic potentials evoked by intrabulbar

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

16 This inhibitory postsynaptic potential-excitatory postsynapti

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

18 Synthetic GABAB inhibitory postsynaptic potentials, generated by a hybri

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

43 Spontaneous inhibitory postsynaptic potentials (IPSPs) and currents

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

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

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

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

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

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

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

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

52 Inhibitory postsynaptic potentials (IPSPs) in ICd neuron

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

75 Monosynaptic inhibitory postsynaptic potentials mediated by gamma-ami

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

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

78 Inhibitory postsynaptic potentials of the granular and a

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

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

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

82 Inhibitory postsynaptic potentials were evoked in mechan

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