ライフサイエンスコーパス: post-tetanic

1 e depolarizing GABA component underlying the post-tetanic depolarization.

2 d under control conditions was replaced by a post-tetanic depression with a slow time course of recov

3 The influence of latrunculin on post-tetanic EPPs depended on its concentration in the b

4 that a fast Na(+)/K(+)-ATPase (NKA)-mediated post-tetanic hyperpolarization (PTH) controls the probab

5 The HCNCs are activated by the post-tetanic hyperpolarization occurring during this tim

6 (SynI) phosphorylation in the expression of post-tetanic potentiation (PTP) and in its modulation by

7 However, like post-tetanic potentiation (PTP) and long-term potentiati

8 Moreover, transmission augmentation and post-tetanic potentiation (PTP) are disrupted in the mut

9 entration ([Ca(2+)](i)) in the generation of post-tetanic potentiation (PTP) at crayfish neuromuscula

10 BSTRACT: High-frequency stimulation leads to post-tetanic potentiation (PTP) at many types of synapse

11 High-frequency stimulation leads to post-tetanic potentiation (PTP) at many types of synapse

12 irement for a form of short-term plasticity, post-tetanic potentiation (PTP) at sensory neuron (SN)-m

13 d by high-frequency stimulation and mediates post-tetanic potentiation (PTP) in the rat hippocampus.

14 Post-tetanic potentiation (PTP) is a widespread form of

15 Post-tetanic potentiation (PTP) is a widespread form of

16 KEY POINTS: Post-tetanic potentiation (PTP) is attributed mainly to

17 Post-tetanic potentiation (PTP) is attributed mainly to

18 igh-frequency action potential train induces post-tetanic potentiation (PTP) of transmission at many

19 The mechanism of the post-tetanic potentiation (PTP) or edrophonium-induced f

20 Here, we identify a Ca(2+) sensor for post-tetanic potentiation (PTP), a form of plasticity th

21 se to short-term enhancement of release like post-tetanic potentiation (PTP).

22 e amplitude or the time-constant of decay of post-tetanic potentiation (PTP).

23 es exhibit a form of intrinsic facilitation: post-tetanic potentiation (PTP).

24 ng facilitation (F2), augmentation (AUG) and post-tetanic potentiation (PTP).

25 d the magnitude of LTP without affecting the post-tetanic potentiation (PTP).

26 d short-term facilitation and uniquely large post-tetanic potentiation (PTP).

27 aired-pulse facilitation (PPF) and increased post-tetanic potentiation (PTP); mice lacking synapsin I

28 homosynaptic plasticity induced by tetanus [post-tetanic potentiation (PTP)] or low-frequency stimul

29 st that exogenous adenosine can inhibit both post-tetanic potentiation and long-term potentiation in

30 yloid fragment augmented theta burst-induced post-tetanic potentiation and LTP in mouse hippocampal s

31 STE) such as facilitation, augmentation, and post-tetanic potentiation at central synapses in the sea

32 imately 3 min, with a time course similar to post-tetanic potentiation at chemical synapses.

33 nt in the periphery (perhaps attributable to post-tetanic potentiation at the neuromuscular junction)

34 red-pulse inhibition and increased GABAergic post-tetanic potentiation in both striatal and hippocamp

35 Peptidergic vesicle mobilization and post-tetanic potentiation of neuropeptide release are su

36 dependent capture of transiting vesicles and post-tetanic potentiation of neuropeptide release.

37 RyR and CaMKII are essential for post-tetanic potentiation of neuropeptide secretion.

38 During mitochondrial depolarization, the post-tetanic potentiation of the EPP observed under cont

39 ssion of short-term homosynaptic plasticity [post-tetanic potentiation or homosynaptic depression (HS

40 al ganglionic transmission without affecting post-tetanic potentiation or long-term potentiation.

41 ansmission, had no significant effect on the post-tetanic potentiation or long-term potentiation.

42 Mutant mice showed less post-tetanic potentiation than wild-type animals, and al

43 a small concentration (2 microM) blocked the post-tetanic potentiation without affecting long-term po

44 ter presynaptic activation (augmentation and post-tetanic potentiation), while leaving intact its cap

45 ity-induced synapse maturation and abolishes post-tetanic potentiation, a form of synaptic plasticity

46 rib mutants exhibit loss of facilitation and post-tetanic potentiation, and faster synaptic depressio

47 ent, such as facilitation, augmentation, and post-tetanic potentiation, are usually attributed to eff

48 thus, shares components of the mechanisms of post-tetanic potentiation, NMDA- and mGluR-dependent lon

49 aralleled by calcium/synaptotagmin-dependent post-tetanic potentiation.

50 trength and contributes to the generation of post-tetanic potentiation.

51 ity: short-term depression, facilitation and post-tetanic potentiation.

52 playing pronounced synaptic augmentation and post-tetanic potentiation.

53 paired-pulse facilitation, LTP induction, or post-tetanic potentiation.

54 ical manipulations implicate mitochondria in post-tetanic potentiation.

55 ission as well as long-term potentiation and post-tetanic potentiation.

56 ion in Sca1 null mice, whereas long-term and post-tetanic potentiations are normal.

57 By day 15, post-tetanic, short-term, and long-term potentiation wer

58 er HFS or TBS gave similar levels of LTP and post tetanic stimulation (PTP), suggesting that the resp

59 ntiation of excitatory transmission, and the post-tetanic time courses of decay of elevated [Ca(2+)](

60 rial Na+-Ca2+ exchanger and helps to sustain post-tetanic transmitter release at mouse neuromuscular