ライフサイエンスコーパス: nucleus basalis

1 ic immunotoxin, anti-p75NTR-saporin into the nucleus basalis.

2 ppocampus (CA 2/3), and neuronal loss in the nucleus basalis.

3 l septal nucleus, the diagonal band, and the nucleus basalis.

4 reciprocal cortical projections back to the nucleus basalis.

5 th activation of cholinergic inputs from the nucleus basalis.

6 th activation of cholinergic inputs from the nucleus basalis.

7 bulb, striatum, globus pallidus, septum, and nucleus basalis.

8 Lhx8 mutants lack the nucleus basalis, a major source of the cholinergic input

9 However, the effect of nucleus basalis activation on sensory processing remains

10 Pairing sensory stimulation with nucleus basalis activation shifted the preferred stimuli

11 ameters of the acoustic stimulus paired with nucleus basalis activation.

12 neurons in the neocortex, limbic system, and nucleus basalis, among others.

13 including the hippocampus, caudate nucleus, nucleus basalis and cortex.

14 Rats received unilateral lesions of the nucleus basalis and were infused intracerebroventricular

15 ive cells were detected in the contralateral nucleus basalis, and in the ipsilateral and contralatera

16 storically identified as an extension of the nucleus basalis, as well as ChAT(-) cells, release the i

17 Within the nucleus basalis, choline acetyltransferase was found in

18 ces in parietal cholinergic fiber density or nucleus basalis cholinergic neuron number or volume were

19 umber ofm2-immunoreactive neurons within the nucleus basalis complex from aged controls and AD patien

20 hether pairing a tone with activation of the nucleus basalis could induce RF plasticity in the waking

21 yltransferase (ChAT)-containing cells in the nucleus basalis following a unilateral injection of ibot

22 cholinergic neurons in the medial septum and nucleus basalis from the effects of excitotoxic or mecha

23 These results strengthen the hypothesis that nucleus basalis gates neural plasticity necessary for in

24 ilateral injection of ibotenic acid into the nucleus basalis; however, these effects were not related

25 ies can also be found in the locus ceruleus, nucleus basalis, hypothalamus, cerebral cortex, cranial

26 limbic affiliation explains the role of the nucleus basalis in modulating the impact and memorabilit

27 distributed neural circuits, as evidenced by nucleus basalis-induced changes in thalamic responses.

28 omodulatory systems, such as the cholinergic nucleus basalis, interact with and refine cortical circu

29 Bilateral ibotenic acid lesions of the nucleus basalis interfered with passive avoidance and sp

30 understood, the cholinergic circuitry of the nucleus basalis is emerging as one of the most strategic

31 The nucleus basalis is located at the confluence of the limb

32 m, and cholinergic projection neurons in the nucleus basalis is observed and is ascribed to an early

33 Thus paired activation of the nucleus basalis is sufficient to induce receptive field

34 ecamylamine-sensitive manners in bilaterally nucleus basalis lesioned rats; and (3) elevate high-affi

35 New results indicate that nucleus basalis lesions prevent motor cortex map plastic

36 ocortical atrophy and degeneration following nucleus basalis lesions.

37 o detected in the striatum (4.2%) and in the nucleus basalis magnocellularis (19.2%) 3-12 h following

38 Since the Nucleus Basalis Magnocellularis (Meynert in humans and p

39 es of evidence have supported a role for the nucleus basalis magnocellularis (NB) in attentional mech

40 Rats with quisqualic acid lesions of the nucleus basalis magnocellularis (nBM) and control rats w

41 Rats with 192 IgG-saporin lesions of the nucleus basalis magnocellularis (NBM) and sham-operated

42 Previous research has demonstrated that nucleus basalis magnocellularis (nbm) corticopetal choli

43 termine if a selective cholinergic lesion of nucleus basalis magnocellularis (Nbm) could affect the n

44 s tested the hypothesis that the cholinergic nucleus basalis magnocellularis (NBM) is involved in sol

45 ic lesions of the medial septum area (MS) or nucleus basalis magnocellularis (NBM) on amplitude and p

46 ed in aging rats: cholinergic lesions of the nucleus basalis magnocellularis (NBM) produce larger dec

47 LS, animals were lesioned bilaterally in the nucleus basalis magnocellularis (nBM) using either quisq

48 of the diagonal band of Broca (HDB) and the nucleus basalis magnocellularis (NBM) were counted.

49 Fluctuations in the nucleus basalis magnocellularis (NBM) were highly variab

50 ith bilateral 192 IgG-saporin lesions to the nucleus basalis magnocellularis (nBM) were tested on olf

51 c immunotoxic- or sham-lesion surgery of the nucleus basalis magnocellularis (NBM), the basal forebra

52 F receptor immunoreactive neurons within the nucleus basalis magnocellularis (NBM), the horizontal li

53 The BLA projects to the nucleus basalis magnocellularis (NBM), which sends broad

54 ith a 2-week-old right-sided ablation of the nucleus basalis magnocellularis (NBM).

55 ormation and its release is regulated by the nucleus basalis magnocellularis (NBM).

56 A) and the cholinergic substantia innominata/nucleus basalis magnocellularis (SI/nBM) is important fo

57 A from the cholinergic substantia innominata/nucleus basalis magnocellularis (SI/nBM) on performance

58 s in the sublenticular substantia innominata/nucleus basalis magnocellularis (SI/nBM), as well as cer

59 no marked loss of cholinergic neurons in the nucleus basalis magnocellularis after intracerebroventri

60 Results demonstrated that lesions of the nucleus basalis magnocellularis and frontal cortex selec

61 ticopetal cholinergic lesions applied to the nucleus basalis magnocellularis and substantia innominat

62 as suggested that cholinergic neurons in the nucleus basalis magnocellularis and substantia innominat

63 Injection of lidocaine into the nucleus basalis magnocellularis produced a profile of be

64 Lesions of the nucleus basalis magnocellularis were without effect on t

65 nt changes in trkA mRNA were detected in the nucleus basalis magnocellularis, and no significant chan

66 rizontal limb of the diagonal band of Broca, nucleus basalis magnocellularis, and striatum of gonadec

67 h the medial septum, diagonal band of Broca, nucleus basalis magnocellularis, and striatum were proce

68 ilateral injection of ibotenic acid into the nucleus basalis magnocellularis, or unilateral transecti

69 ell bodies in the medial septal area and the nucleus basalis magnocellularis, radiofrequency lesions

70 nfusions of colchicine or vehicle in the rat nucleus basalis magnocellularis, the time course of chan

71 ved bilateral quisqualic acid lesions of the nucleus basalis magnocellularis.

72 ow-affinity p75 neurotrophin receptor in the nucleus basalis Meynert failed to reveal differences bet

73 mygdala; nucleus accumbens; ventral pallium; nucleus basalis Meynert; bed nucleus of the stria termin

74 re paired with electrical stimulation of the nucleus basalis (NB) 300 to 400 times per day for 20-25

75 cy paired with electrical stimulation of the nucleus basalis (NB) at tone offset.

76 ubstance P (SP) excites large neurons of the nucleus basalis (NB) by inhibiting an inward rectifier K

77 Degeneration of cholinergic nucleus basalis (NB) cortical projection neurons is asso

78 The nucleus basalis (NB) has been implicated in memory forma

79 The nucleus basalis (NB) in the basal forebrain provides mos

80 cholinergic innervation of the cortex by the nucleus basalis (NB) is known to modulate cortical neuro

81 The nucleus basalis (NB) mediates cortical electroencephalog

82 Cholinergic basal forebrain (CBF) nucleus basalis (NB) neurons display neurofibrillary tan

83 Electrical activation of the nucleus basalis (NB) of Meynert, the source of neocortic

84 Pairing pulsed noises with nucleus basalis (NB) stimulation in awake rats for 4 wee

85 NFT evolution within the CBF neurons of the nucleus basalis (NB) using tissue from subjects with no

86 ring acoustic stimuli with activation of the nucleus basalis neuromodulatory system.

87 on of ACh release from cortical afferents of nucleus basalis neurones in vivo.

88 Both markers were expressed robustly in nucleus basalis neurons and across all three groups.

89 a indicate that alterations in the number of nucleus basalis neurons containing trkA immunoreactivity

90 T8 (or Alz-50) immunostaining in cholinergic nucleus basalis neurons existed even in the cognitively

91 ere is a marked reduction in trkA-containing nucleus basalis neurons in end-stage Alzheimer's disease

92 The percentage of tauopathy-containing nucleus basalis neurons was greater in the cognitively i

93 The number of p75(NTR)-immunoreactive nucleus basalis neurons was significantly correlated wit

94 Seventy-five days later, cholinergic nucleus basalis neurons were atrophic ipsilateral to the

95 , nucleus of the diagonal band (DB), and the nucleus basalis of Meynert (NB).

96 the medial septal/diagonal band (MS/DB) and nucleus basalis of Meynert (NBM) also reveal a selective

97 creases in ChAT and trkA are observed in the nucleus basalis of Meynert (nBM) of both age groups.

98 In the nucleus basalis of Meynert (NBM) of middle-aged monkeys,

99 bution of these receptor subunits within the nucleus basalis of Meynert (NBM) of non-demented elderly

100 Acetylcholine neurons in nucleus basalis of Meynert (NBM) were selectively lesion

101 mine total cholinergic neuron numbers in the nucleus basalis of Meynert (nbM), stereologic methods we

102 of Broca (MS) and the substantia innominata/nucleus basalis of Meynert (SI).

103 tantia nigra, raphe nuclei, locus coeruleus, nucleus basalis of Meynert and dorsal motor nucleus of v

104 therapy (ERT) on cholinergic neurons in the nucleus basalis of Meynert and on cholinergic fibers in

105 Although cholinergic neurons in the nucleus basalis of Meynert are a major source of choline

106 counterpart in budgerigars of the mammalian nucleus basalis of Meynert consists of a field of cholin

107 o difference in orexinergic fiber density in nucleus basalis of Meynert or locus ceruleus compared to

108 aphe, locus coeruleus, ventral tegmentum and nucleus basalis of Meynert, and efferent projections to

109 ntal limb of the diagonal band of Broca, the nucleus basalis of Meynert, and the inferior olivary nuc

110 l and medial septum, diagonal band of Broca, nucleus basalis of Meynert, bed nucleus of stria termina

111 limbs of the diagonal band of Broca, and the nucleus basalis of Meynert, medial habenular nucleus, zo

112 were no differences in ChAT activity in the nucleus basalis of Meynert, nor any of several neocortic

113 l motor nucleus of the vagus, but not in the nucleus basalis of Meynert, raphe nucleus, or other brai

114 as (pedunculopontine/laterodorsal tegmentum, nucleus basalis of Meynert, thalamus, and locus ceruleus

115 re most pronounced in posterior parts of the nucleus basalis of Meynert, whereas in AD, atrophy was m

116 ic fibers that originate from neurons in the nucleus basalis of Meynert.

117 l limb of the diagonal band of Broca and the nucleus basalis of Meynert.

118 ca, the magnocellular preoptic area, and the nucleus basalis of Meynert.

119 al motor nucleus of the X cranial nerve, and nucleus basalis of Meynert.

120 ei, such as the pedunculopontine nucleus and nucleus basalis of Meynert.

121 , dorsal motor nucleus of the vagus, and the nucleus basalis of Meynert.

122 tion is located in the Ch4 cell group of the nucleus basalis of Meynert.

123 The nucleus basalis of the basal forebrain is an essential c

124 For example, the nucleus basalis of the forebrain plays a critical role i

125 diagonal band, but not in the medial septum, nucleus basalis, or striatum of females vs. males.

126 icant and similar reduction in the number of nucleus basalis p75(NTR)-immunoreactive neurons was seen

127 that episodic electrical stimulation of the nucleus basalis, paired with an auditory stimulus, resul

128 the OX-26-NGF conjugate restored the size of nucleus basalis perikarya to within normal limits relati

129 memory, area 46, and in the component of the nucleus basalis projecting to this region.

130 vealed long-range connections from thalamus, nucleus basalis, raphe, and distant cortical areas, incl

131 inergic neurons of the substantia innominata/nucleus basalis region, and their innervation of the pos

132 iagonal band (HDB) and substantia innominata/nucleus basalis (SI/NB) following ovariectomy.

133 s in the contralateral substantia innominata/nucleus basalis (SI/nBM) failed to show the enhanced att

134 ROSAB or EHD2-scTNFR2 into the magnocellular nucleus basalis significantly protected cholinergic neur

135 ecording in rat visual cortex, we found that nucleus basalis stimulation caused prominent decorrelati

136 Nucleus basalis stimulation produced electroencephalogra

137 Paired tone/nucleus basalis stimulation, but not unpaired stimulatio

138 2) located primarily outside the cholinergic nucleus basalis subfields.

139 its vehicle was infused into the area of the nucleus basalis/substantia innominata of the basal foreb

140 ty, we paired a tone with stimulation of the nucleus basalis, the main subcortical source of cortical

141 to identify pre-tangle cytopathology in the nucleus basalis, the source of cortical cholinergic inne

142 ng tones with stimulation of the cholinergic nucleus basalis to induce auditory cortex map plasticity

143 dles of cholinergic fibres extended from the nucleus basalis to the cerebral cortex and amygdala and

144 ys which link the cholinergic neurons of the nucleus basalis to the human cerebral cortex.

145 Large neurons of the cholinergic nucleus basalis together with CA1 and CA3 pyramidal neur

146 d in the olfactory bulbs, frontal cortex, or nucleus basalis/ventral pallidum following hormone treat

147 yriform cortex, olfactory bulbs, septum, and nucleus basalis/ventral pallidum were dissected.

148 projecting to this region of cortex from the nucleus basalis was also reduced by 50 +/- 6%.

149 Although nucleus basalis was stimulated only for a few minutes, r

150 Cholinergic neurons in the medial septum and nucleus basalis were detected and quantified using immun

151 to nucleus basorostralis (previously called nucleus basalis), whereas input from the rest of the bod

152 agonal band and in the posterior half of the nucleus basalis, which is where there was the greatest o

153 The anatomical continuity of the nucleus basalis with other basomedial limbic structures