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 ubstantial DCV fusion, albeit not as much as tetanic stimulation.

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

10 ts' appearing in repeatable locations during tetanic stimulation.

11 ose at specific, repeatable locations during tetanic stimulation.

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

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

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

15 ion from internalized membrane objects after tetanic stimulation.

16 omuscular transmission, during and following tetanic stimulation.

17 s containing polyribosomes were larger after tetanic stimulation.

18 expressing long-term potentiation induced by tetanic stimulation.

19 air mobilization of synaptic vesicles during tetanic stimulation.

20 aving synaptic inhibition more intact during tetanic stimulation.

21 gnificantly reduced the effectiveness of the tetanic stimulation.

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

23 ow-frequency control stimulation or repeated tetanic stimulation.

24 naptic depression after different amounts of tetanic stimulation.

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

26 ion and endocytosis were slowed by prolonged tetanic stimulation.

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

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

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

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

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

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

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

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

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

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

37 We propose a model where tetanic stimulation activates Syt1-independent mechanism

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

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

40 EPSPs show little depression in response to tetanic stimulation and, therefore, can be distinguished

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

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

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

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

45 Tetanic stimulation at 50 Hz elicited long-term potentia

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

47 E4A5 does not impair LTP induced by repeated tetanic stimulation at the CA3-CA1 synapses.

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

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

50 ulation (TBS) triggered less DCV fusion than tetanic stimulation, but a similar fusion efficiency per

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

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

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

54 Tetanic stimulation causes an initial enhancement follow

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

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

57 Tetanic stimulation decreases a bicuculline-sensitive fi

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

59 Tetanic stimulation elicited distinct increases in fluor

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

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

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

63 K (PIK3R3) in vivo in response to novelty or tetanic stimulation in acute slices.

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

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

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

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

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

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

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

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

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

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

74 Tetanic stimulation induced diverse forms of excitatory

75 We found that TBS induced more LTP, whereas tetanic stimulation induced more LTD, in mouse spinal la

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

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

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

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

80 Tetanic stimulation of axons terminating in the CA1 regi

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

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

83 Brief tetanic stimulation of granule cell parallel fibers acti

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

85 Tetanic stimulation of local circuitry induced effects s

86 Tetanic stimulation of monoamine-depleted ganglia (from

87 Tetanic stimulation of monoamine-depleted ganglia in the

88 Tetanic stimulation of mossy fibers induced long-term po

89 Tetanic stimulation of parallel fibres (PFs) produces a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

109 Both phorbol esters and tetanic stimulation potentiate synaptic strength, and lo

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

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

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

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

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

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

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

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

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

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

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

121 We show that tetanic stimulation trains of 50-Hz action potential (AP

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

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

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

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

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

127 Brief tetanic stimulation, which normally generated LTP, could

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

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

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