ライフサイエンスコーパス: spontaneous discharge

1 istent with the trajectory computed from the spontaneous discharge.

2 be insufficient to totally account for their spontaneous discharge.

3 ating that intrinsic currents underlie their spontaneous discharge.

4 Responsive afferents had low spontaneous discharge (1.6 +/- 0.3 impulses s-1) and sho

5 ected INs) or absence (MNs and other INs) of spontaneous discharge, (2) a cluster analysis of selecte

6 acellular unit recordings revealed increased spontaneous discharge, afterdischarge, hyperresponsivene

7 LC spontaneous discharge and activation by intracerebrovent

8 nimals, both repair groups showed changes in spontaneous discharge and persistent reductions in condu

9 Spontaneous discharges and mechanical stimulation-evoked

10 4-AP-induced spontaneous discharges are blocked by 20 microM DNQX and

11 ffectively a stochastic renewal process, and spontaneous discharges are fully characterized by their

12 tamide (U50488) into the LC did not alter LC spontaneous discharge but attenuated phasic discharge ev

13 C abolished the morphine-induced decrease of spontaneous discharge but did not prevent the depression

14 0 suppresses the abnormal paclitaxel-induced spontaneous discharges by DRG neurons to promote recover

15 uning, disrupted tonotopic maps, and reduced spontaneous discharge correlation in the primary auditor

16 characterized by the presence or absence of spontaneous discharge following stimulation.

17 all diameter sensory neurones that may drive spontaneous discharge in nociceptive nerve fibres during

18 of 1.3 +/- 0.9 Hz and only totally abolished spontaneous discharge in one neurone.

19 a role in the initiation and maintenance of spontaneous discharge in Purkinje fibres was studied by

20 Thus, the initiation and maintenance of spontaneous discharge in Purkinje strands appear to invo

21 aluminal acid and bradykinin, as well as the spontaneous discharge in WT mice.

22 IL-10 suppressed abnormal paclitaxel-induced spontaneous discharges in DRG neurons.

23 VEGF reduced spontaneous discharges in slices from these rats but had

24 The duration and pattern of spontaneous discharge is seen to be critically dependent

25 viable for up to seven months and exhibited spontaneous discharges most likely originating from Purk

26 of 64 +/- 2 mmHg produced weak reductions in spontaneous discharge of 1.3 +/- 0.9 Hz and only totally

27 MnPO-PVH cells had an average spontaneous discharge of 2.1+/-0.4 Hz.

28 Spontaneous discharge of basal ganglia neurons is often

29 crine and bipolar cells, we suggest that the spontaneous discharge of DA cells is inhibited in the da

30 All EAA antagonists inhibited the spontaneous discharge of MSNs/PSNs and NENs (P < 0.01 fo

31 haracterization of the nonlinear features of spontaneous discharge of neurons in the primate basal ga

32 olesions of the inferior olive increased the spontaneous discharge of SSs in contralateral folia 8-10

33 tin (100 nM-1 microM) potently inhibited the spontaneous discharge of the majority (86%) of MVN neuro

34 Of the subpopulation of units with spontaneous discharges, only 3 of 20 cells responded to

35 id not observe any direct effects of PrRP on spontaneous discharge or postsynaptic excitability in ei

36 This study examined the nature of spontaneous discharge patterns in cochlear ganglion cell

37 The spontaneous discharge patterns of developing retinal gan

38 ctances can have differential effects on the spontaneous discharge patterns of retinal ganglion cells

39 n all striatal territories displayed similar spontaneous discharge properties and similar temporal mo

40 fibers differ in threshold sensitivity, and spontaneous discharge rate (SR), by more than a factor o

41 ed into three functional groups according to spontaneous discharge rate (SR): those with low SR have

42 These findings suggest that auditory cortex spontaneous discharge rate can be modulated transiently

43 rved bursting activity was abolished and the spontaneous discharge rate of infected cells was markedl

44 asic CRDs and intracisternal (ic) CRF on the spontaneous discharge rate of LC neurons in chloral hydr

45 thane-anesthetized adult male rats increased spontaneous discharge rate of LC neurons while producing

46 Locus coeruleus spontaneous discharge rate was recorded from halothane-a

47 line organ to displacement while increasing spontaneous discharge rate.

48 injection of alpha-hCRH into LC increased LC spontaneous discharge rate; consequently, CRH was microi

49 Spontaneous discharge rates (SRs) were lower than normal

50 In active cells, mean spontaneous discharge rates [9.4 +/- 10.4 spikes (Sp)/se

51 pressure (MAP) of 99.6+/-2.8 mmHg, the mean spontaneous discharge rates of EPI ADR SPNs and NE ADR S

52 Spontaneous discharge rates of individual LC neurons wer

53 The spontaneous discharge rates of WSNs and CSNs were record

54 C (the source of afferents with low and high spontaneous discharge rates, respectively).

55 bers with all characteristic frequencies and spontaneous discharge rates.

56 LC spontaneous discharge was higher in adrenalectomized ver

57 of electrotonically coupled SPNs to generate spontaneous discharges within the spinal cord provides a