ライフサイエンスコーパス: electrosensory

1 oorly understood high-pass filtering seen in electrosensory afferents and downstream neurons.

2 Retinal and electrosensory afferents elicit local monosynaptic excit

3 y electric fish, probability coding (P-type) electrosensory afferents encode amplitude modulations of

4 nges in the frequency response properties of electrosensory afferents enhance mate detection by male

5 sed a lateral line placode-derived system of electrosensory ampullary organs and mechanosensory neuro

6 em, comprising mechanosensory neuromasts and electrosensory ampullary organs, is a useful model for i

7 se temporal coding is a hallmark of both the electrosensory and auditory systems.

8 in-like immunoreactivity was examined in the electrosensory and electromotor systems of the two famil

9 Recordings were made from fish electrosensory and monkey vestibular sensory neurons.

10 sory and electromotor command system, or the electrosensory and trigeminal motor command.

11 are many anastomoses between the peripheral electrosensory and trigeminal nerves, but these senses r

12 Auditory, electrosensory, and mechanosensory responses are dominat

13 field potentials evoked by auditory, visual, electrosensory, and water displacement stimuli in this w

14 ss the implications of preglomerular/pallial electrosensory-associated afferents with respect to a ma

15 Thus, electrosensory behavior may be used as a model system fo

16 tion of amphid sensory neurons also disrupts electrosensory behavior.

17 this circuit in relation to newly described electrosensory behaviors, including prey capture, social

18 we call this dominance of the electric sense electrosensory capture.

19 erinacea) and functionally couple to mediate electrosensory cell membrane voltage oscillations, which

20 (BK) channel are preferentially expressed by electrosensory cells in little skate (Leucoraja erinacea

21 ltaneous single unit recordings of principal electrosensory cells show that an increase in the spatia

22 Electrosensory cells within these ampullae can discrimin

23 ment and evolution of the mechanosensory and electrosensory components of the lateral line must be di

24 We provide evidence that the electrosensory consequences of tail bending are opposed

25 y processing generate negative images of the electrosensory consequences of the animal's own behavior

26 rmed into negative images of the predictable electrosensory consequences of the fish's motor commands

27 lus motion triggers paradoxical responses to electrosensory contrast.

28 t 'sensory conflict' when mechanosensory and electrosensory cues are separated, striking first toward

29 ronotus leptorhynchus can capture prey using electrosensory cues that are dominated by low temporal f

30 ates, but the effect of gonadal androgens on electrosensory encoding during the reproductive season i

31 location shows, for the first time, that the electrosensory flow contains behaviorally relevant infor

32 reconstruction of sensory input, we show how electrosensory flow is actively created during highly pa

33 ith their mammalian orthologues that support electrosensory functions: structural adaptations in CaV1

34 se neurons also showed low-pass filtering of electrosensory information but with larger maximum decli

35 Adaptive processing of electrosensory information occurs in the cerebellum-like

36 iform cells are efferent neurons that convey electrosensory information to higher stages of the syste

37 The responses of cells in ELL to electrosensory input are strongly affected by corollary

38 ry system, the statistical properties of the electrosensory input evoked by natural swimming movement

39 L) receives diencephalic inputs representing electrosensory input utilized for communication and navi

40 " that act to cancel predictable patterns of electrosensory input.

41 tectal neurons receive converging visual and electrosensory inputs, as investigated in the lamprey -

42 ectroreceptor pathway; in the nucleus of the electrosensory lateral line lobe (ELL) and the big cells

43 comparison mechanisms was identified in the electrosensory lateral line lobe (ELL) in the hindbrain

44 Phase-locking neurons in the electrosensory lateral line lobe (ELL) of a weakly elect

45 Differential-phase-sensitive neurons in the electrosensory lateral line lobe (ELL) of the African el

46 odulation of information transmission in the electrosensory lateral line lobe (ELL) of the hindbrain.

47 this report, we describe correlations among electrosensory lateral line lobe (ELL) pyramidal cells'

48 nts and E- and I-type pyramidal cells in the electrosensory lateral line lobe (ELL) to random distort

49 omatotopically ordered hindbrain maps of the electrosensory lateral line lobe (ELL), the dorsolateral

50 st brain station for central processing, the electrosensory lateral line lobe (ELL), were investigate

51 isparity thresholds of output neurons of the electrosensory lateral line lobe (ELL), where the repres

52 eakly labeled inhibitory interneurons in the electrosensory lateral line lobe (ELL).

53 ondary sensory neurons in the nucleus of the electrosensory lateral line lobe (NELL) act as relays of

54 Pyramidal cells in the electrosensory lateral line lobe burst in response to lo

55 electrosensory nucleus in electric fish, the electrosensory lateral line lobe, resulted in markedly d

56 nd their targets, the pyramidal cells in the electrosensory lateral-line lobe.

57 The electrosensory lobe (ELL) of mormyrid electric fish is a

58 The electrosensory lobe (ELL) of mormyrid electric fish is o

59 The electrosensory lobe (ELL) of mormyrid electric fish is t

60 In the electrosensory lobe (ELL) of mormyrid fish, a main cellu

61 Here we demonstrate that neurons in the electrosensory lobe (ELL) of weakly electric mormyrid fi

62 ere we use an advantageous model system--the electrosensory lobe (ELL) of weakly electric mormyrid fi

63 tests the adaptive filter hypothesis in the electrosensory lobe (ELL) of weakly electric mormyrid fi

64 Medium ganglion cells in the electrosensory lobe create negative images that predict

65 show here that such plasticity exists in the electrosensory lobe of mormyrid electric fish and that i

66 The electrosensory lobes (ELLs) of mormyrid and gymnotid fis

67 We recorded the responses of midbrain electrosensory neurons in the weakly electric fish Apter

68 properties to the temporal selectivities of electrosensory neurons in vivo.

69 tional role of serotonergic innervation onto electrosensory neurons in weakly electric fish by elicit

70 he temporal filtering properties of midbrain electrosensory neurons.

71 to the presence of mAChR3 in the ELL region, electrosensory nuclei including the nucleus praeeminenti

72 vations of different maps of the first-order electrosensory nucleus in electric fish, the electrosens

73 apture, social signaling and the tracking of electrosensory objects.

74 ng sharks, rays, and skates, use specialized electrosensory organs called ampullae of Lorenzini to de

75 In the active electrosensory pathway of mormyrids afferent input is pr

76 sensory trigeminal components as well as an electrosensory pathway.

77 omotor pathways and early in the time-coding electrosensory pathways do not follow this hypothesis, a

78 We reexamined the electrosensory pathways from the periphery to the midbra

79 teins in mormyrid and gymnarchid time-coding electrosensory pathways is consistent with the hypothesi

80 own jamming avoidance response as a probe of electrosensory perception, we show that the ambiguity at

81 primary androgen increase in wild males, the electrosensory primary afferent neurons show an increase

82 In the little skate, Raja erinacea, the electrosensory primary afferents are responsive to elect

83 pike latency is decoded at central stages of electrosensory processing are discussed.

84 Neurons at the first stage of electrosensory processing generate negative images of th

85 n cerebellum-like structures associated with electrosensory processing in fish.

86 ing network model of the first two stages of electrosensory processing replicates this correlation sh

87 the mediolateral axis of the DON, the first electrosensory processing station.

88 eurons of the first central nervous stage of electrosensory processing.

89 e fields of neurons within the first central electrosensory-processing region have an antagonistic ce

90 nomyrus brachyistius during stimulation with electrosensory pulse trains.

91 formance by pairs of simultaneously recorded electrosensory pyramidal cells in the hindbrain of weakl

92 that the function of serotonergic input onto electrosensory pyramidal neurons is to render them more

93 The paddlefish is a passive electrosensory ray-finned fish with a special rostral ap

94 in response to each cycle of the sinusoidal electrosensory signal (350-500 Hz) created by the fish's

95 n the presence and absence of self-generated electrosensory signals caused by tail movements.

96 arities on the order of microseconds between electrosensory signals received by electroreceptors in d

97 Two distinct sensory cues in electrosensory signals, amplitude modulation and differe

98 ization of sudden turns and reversals during electrosensory steering.

99 cellular responses to time-varying (2-30 Hz) electrosensory stimulation and current injection of 27 n

100 We found that electrosensory stimulation elicited evoked potentials in

101 f the large ganglion cells were inhibited by electrosensory stimuli in the center of their receptive

102 depression was similar to that observed for electrosensory stimuli of the same temporal frequency.

103 t study, sensitivity to temporal patterns of electrosensory stimuli was found to arise within the mid

104 weakly electric fish (Mormyridae) respond to electrosensory stimuli with a phase reset that results i

105 For electrosensory stimuli, however, these neurons showed lo

106 in response to continuous and discontinuous electrosensory stimuli.

107 ng the amplitude and phase, respectively, of electrosensory stimuli.

108 misperception of the amplitude and phase of electrosensory stimuli.

109 r sex differences in chirp responsiveness to electrosensory stimuli; males consistently chirp, wherea

110 surface determine responses to second-order electrosensory stimulus features in the weakly electric

111 der did not affect responses to second-order electrosensory stimulus features, other sources of heter

112 decreased in concert with the period of the electrosensory stimulus, whereas in the other four neuro

113 anges after a few minutes of pairing with an electrosensory stimulus.

114 Here, we asked whether the central electrosensory system actually detects the occurrence of

115 using both the natural heterogeneity of the electrosensory system and pharmacological blockade of de

116 Given the independent loss of the electrosensory system in multiple lineages, the developm

117 ns across multiple sensory maps by using the electrosensory system in weakly electric fish as a model

118 The elasmobranch electrosensory system is the most thoroughly understood

119 havior on a spike latency code in the active electrosensory system of mormyrid fish.

120 Here we use the electrosensory system of mormyrid weakly electric fish t

121 We use the well characterized electrosensory system of weakly electric fish to address

122 within the initial processing station of the electrosensory system of weakly electric fish to shift t

123 In the electrosensory system of weakly electric fish, single P-

124 of pairwise spike train correlations in the electrosensory system of weakly electric fish.

125 on in sharks is not solely performed via the electrosensory system, and that putative magnetoreceptor

126 sults from current lesion experiments in the electrosensory system, however, suggest an alternative p

127 ge about the circuitry and physiology of the electrosensory system, the statistical properties of the

128 esence evident in specialized regions of the electrosensory system, which suggests an important modul

129 ost thoroughly understood of the non-teleost electrosensory systems and is useful for studying centra

130 Progress in the study of electrosensory systems has been facilitated by the syste

131 ined experimental and theoretical studies of electrosensory systems have led to detailed accounts of

132 Recent work on electrosensory systems in fish has combined traditional

133 g this process have come from studies of the electrosensory systems of fish.

134 The electrosensory systems of weakly electric fish are recog

135 A is expressed in deep layers of the dorsal (electrosensory) torus semicircularis (TSd).

136 the diencephalic and mesencephalic nuclei in electrosensory, visual, and acousticolateral functions.

137 ore) project to midbrain regions involved in electrosensory/visual function.