ライフサイエンスコーパス: tetanic stimulation

1 ty (assessed during re-lengthening following tetanic stimulation).

2 m a persistent presynaptic [Ca2+]i following tetanic stimulation.

3 sticity, or LTP induced by several trains of tetanic stimulation.

4 ppocampus by enhancing synaptic responses to tetanic stimulation.

5 ressions could not be reversed by subsequent tetanic stimulation.

6 of synaptic depression during high-frequency tetanic stimulation.

7 ike endocytosis, depended on the duration of tetanic stimulation.

8 synapses that is dependent on the pattern of tetanic stimulation.

9 ts' appearing in repeatable locations during tetanic stimulation.

10 ose at specific, repeatable locations during tetanic stimulation.

11 TR) function-blocking antiserum, or previous tetanic stimulation.

12 profiles of ARGs in response to LTP-inducing tetanic stimulation.

13 ablished LTP when applied 1, 3, or 5 h after tetanic stimulation.

14 ion from internalized membrane objects after tetanic stimulation.

15 aving synaptic inhibition more intact during tetanic stimulation.

16 omuscular transmission, during and following tetanic stimulation.

17 s containing polyribosomes were larger after tetanic stimulation.

18 thening of the ILCx-BNST synapses after ILCx tetanic stimulation.

19 expressing long-term potentiation induced by tetanic stimulation.

20 air mobilization of synaptic vesicles during tetanic stimulation.

21 gnificantly reduced the effectiveness of the tetanic stimulation.

22 ow-frequency control stimulation or repeated tetanic stimulation.

23 naptic depression after different amounts of tetanic stimulation.

24 h prior to and following 100 or 200 Hz (1 s) tetanic stimulation.

25 ion and endocytosis were slowed by prolonged tetanic stimulation.

26 l, synaptic potentiation induced by a single tetanic stimulation (100 Hz for 1 s) was enhanced after

27 However, under high-frequency tetanic stimulation (100 Hz; > 100 ms) typically used to

28 CA1 pyramidal neurons after weak and strong tetanic stimulations (100 Hz, 400 and 1000 msec, respect

29 was significantly increased following brief tetanic stimulation (18.1 +/- 1.6 to 22.3 +/- 2.0 flashe

30 ynaptic potentiation produced by rather mild tetanic stimulation (20 Hz, 2 sec) at Aplysia sensory-mo

31 n (n=11) and paired-pulse enhancement (n=4); tetanic stimulation (25 Hz, 1.0 s) produced sustained (>

32 A submaximal tetanic stimulation (2x50 Hz/1 s) in control slices elic

33 ashes/1000 mum(2).100 s) following prolonged tetanic stimulation (40 tetani).

34 Tetanic stimulation (50 Hz, 1 s) increases PKA and PKC a

35 Nerves sustained repeated tetanic stimulations (50 Hz or 100 Hz for 1 min) alterna

36 n adult zebra finch brain slices reveal that tetanic stimulation alone does not produce LTP.

37 Following tetanic stimulation an outside-out patch was excised fro

38 We investigated whether tetanic-stimulation and activation of metabotropic gluta

39 measure the rate of membrane retrieval after tetanic stimulation, and the amount of membrane transfer

40 be reliably induced by specific patterns of tetanic stimulation, and the level of LTD depends on bot

41 In neuronal somas, however, tetanic stimulation appears to result in long-lasting in

42 Tetanic stimulation at 50 Hz elicited long-term potentia

43 scillations were evoked in the CA1 region by tetanic stimulation at one or two sites simultaneously,

44 on CA1 and that LTD was found in response to tetanic stimulation at the trough of the local theta wav

45 Thirty minutes after tetanic stimulation, autophosphorylated CaM kinase II (P

46 ce TrkB was regulated only by high frequency tetanic stimulation, but not by low frequency stimulatio

47 L-LTP is typically induced by homosynaptic tetanic stimulation; but associative forms of learning a

48 actin/G-actin equilibrium, we show here that tetanic stimulation causes a rapid, persistent shift of

49 Tetanic stimulation causes an initial enhancement follow

50 A weak tetanic stimulation consisting of 20 pulses at 100 Hz in

51 Local tetanic stimulation decreased the Zn(2+) signal observed

52 Tetanic stimulation decreases a bicuculline-sensitive fi

53 hypothesis for the mechanism of PTP is that tetanic stimulation elevates presynaptic calcium that in

54 Tetanic stimulation elicited distinct increases in fluor

55 ed from preganglionic nerve terminals during tetanic stimulation enhanced neuronal excitability and e

56 ts (PBs) stimulation are among the effective tetanic stimulations for induction of long-term potentia

57 At a maximal tetanic stimulation frequency, intact KO extensor digito

58 Tetanic stimulation in Ca(2+)-free medium elicited an in

59 were compared after low-frequency control or tetanic stimulation in hippocampal slices from postnatal

60 ed vesicle depletion near active zones after tetanic stimulation in staurosporine-treated preparation

61 ation (L-LTP) induced by either forskolin or tetanic stimulation in the hippocampal mossy fiber and S

62 rical activity in response to high-frequency tetanic stimulation in the hippocampus after head injury

63 ed in induction of long-term potentiation by tetanic stimulation in the hippocampus.

64 genous BDNF promoted the induction of LTP by tetanic stimulation in young (postnatal day 12-13) hippo

65 ous alphaCaMKII and MAP2 proteins induced by tetanic stimulations in hippocampal slices.

66 In both pathways, tetanic stimulation induce significant long-term synapti

67 Tetanic stimulations induce N-methyl-d-aspartate recepto

68 Tetanic stimulation induced diverse forms of excitatory

69 nist or an endogenous ligand released during tetanic stimulation induced robust rhythms of the subthr

70 nse to theta-burst stimulation and to 100-Hz tetanic stimulation is much reduced.

71 ng presynaptic calcium increases produced by tetanic stimulation may activate these isoforms to produ

72 Here we show that, upon tetanic stimulation of afferents to lateral amygdala, pr

73 Tetanic stimulation of axons terminating in the CA1 regi

74 permeable AMPA receptors exhibited LTD after tetanic stimulation of CA3 excitatory inputs.

75 Here, we report that tetanic stimulation of cerebellar climbing fiber-Purkinj

76 Brief tetanic stimulation of granule cell parallel fibers acti

77 ns on single CA3 pyramidal neurons following tetanic stimulation of individual dentate gyrus granule

78 Tetanic stimulation of local circuitry induced effects s

79 Tetanic stimulation of monoamine-depleted ganglia (from

80 Tetanic stimulation of monoamine-depleted ganglia in the

81 Tetanic stimulation of mossy fibers induced long-term po

82 Tetanic stimulation of parallel fibres (PFs) produces a

83 tion takes place in hippocampal slices after tetanic stimulation of Schaffer collateral synapses.

84 was an attenuation of LTP elicited by either tetanic stimulation of Schaffer collaterals or a pairing

85 tic Ca(2+) signaling were also evident after tetanic stimulation of Schaffer collaterals.

86 rge and the contractile tension generated by tetanic stimulation of single motor units.

87 Moreover, tetanic stimulation of the MD caused a longer-lasting (a

88 Brief tetanic stimulation of the muscle nerve (25 Hz, 90 s) de

89 tion of EPSP and population spike, following tetanic stimulation of the perforant path, was observed

90 icity, homosynaptic potentiation produced by tetanic stimulation of the presynaptic neuron in Aplysia

91 blocked long-lasting potentiation induced by tetanic stimulation of the presynaptic neuron.

92 mporoammonic afferents to CA1 neurons, brief tetanic stimulation of the residual excitatory synapses

93 Here we show that tetanic stimulation of the Schaffer collateral pathway c

94 We suggest that tetanic stimulation of the Schaffer collateral pathway m

95 otential (fEPSP) slope in area CA1 following tetanic stimulation of the Schaffer collaterals.

96 ssed at Aplysia sensorimotor synapses when a tetanic stimulation of the sensory neurons was paired wi

97 Oscillations induced in CA1 in vitro by tetanic stimulation of the stratum radiatum or oriens we

98 In Ca(2+)-free medium, tetanic stimulation of Xenopus motoneurons induced a str

99 receptors (mGluRs), either by high-frequency tetanic stimulation or an agonist, induced eCB-LTD.

100 DNF was of the same order as that induced by tetanic stimulation or substitution of the bathing mediu

101 s PKC isozymes in slices subjected to low or tetanic stimulation, or perfused with phorbol esters (PD

102 halogram recording before and after auditory tetanic stimulation (Pre/Post Blocks).

103 hat LTP induced by a theta-burst pairing and tetanic stimulation protocols causes the rapid delivery

104 S or TBS gave similar levels of LTP and post tetanic stimulation (PTP), suggesting that the response

105 bility of hippocampal synapses to respond to tetanic stimulation, rather than to a direct modulation

106 r superfusion of CO in the presence of ZnPP, tetanic stimulation readily evoked LTP.

107 riple KO mice, calcium transients induced by tetanic stimulation rely on calcium entry via La(3+)- an

108 During high-frequency (tetanic) stimulation, somatic synaptic inhibition is sup

109 stable platelet-activating factor analogue, tetanic stimulation that normally induces long-term syna

110 ot on NMDARs, but, when induced by a form of tetanic stimulation that produced prolonged postsynaptic

111 synaptic function and reduces the ability of tetanic stimulation to induce LTP.

112 howed that PBs could be used as an effective tetanic stimulation to study the synaptic plasticity in

113 m potentiation (LTP) induced by one train of tetanic stimulation (TS) in the CA1 region of hippocampa

114 To induce synaptic plasticity, tetanic stimulation was applied to either continuous or

115 LTP and conventional L-LTP induced by strong tetanic stimulation were completely normal in BDNF-KIV m

116 The effects of tetanic stimulation were examined in each pathway.

117 LTD could be reversed by subsequent tetanic stimulation whereas E-S dissociation remained un

118 Brief tetanic stimulation, which normally generated LTP, could

119 In contrast, LTP induced by 100 Hz tetanic stimulation, which requires Ca(2+) influx throug

120 terminals during and for some minutes after tetanic stimulation, while at the same time the plasma m

121 fter control stimulation to 39% +/- 4% after tetanic stimulation, with a commensurate loss of polyrib