ライフサイエンスコーパス: ventral pallidum

1 halin immunoreactivity, both markers for the ventral pallidum.

2 l but not into the core, dorsal striatum, or ventral pallidum.

3 ced reinstatement of cocaine seeking via the ventral pallidum.

4 men, bed nucleus of the stria terminalis, or ventral pallidum.

5 orsal-lateral BF, in regions occupied by the ventral pallidum.

6 t projections from the nucleus accumbens and ventral pallidum.

7 blocking the motor response by DAMGO in the ventral pallidum.

8 us accumbens, globus pallidus and the medial ventral pallidum.

9 als from iMSNs than their projections to the ventral pallidum.

10 the dorsolateral part of the subcommissural ventral pallidum.

11 tate identification of subterritories in the ventral pallidum.

12 the mid-insula and the ventral striatum and ventral pallidum.

13 o mouse nucleus accumbens projections to the ventral pallidum.

14 spot circuits in nucleus accumbens (NAc) and ventral pallidum.

15 on the dorsal striatum, prelimbic cortex, or ventral pallidum.

16 his manner, with both cell types innervating ventral pallidum.

17 ther vector functioned when infused into the ventral pallidum.

18 ctively lost in D2, but not D1 inputs to the ventral pallidum.

19 circuits involving the nucleus accumbens and ventral pallidum.

20 coded in neural signals coursing through the ventral pallidum.

21 0 increased extracellular GABA levels in the ventral pallidum.

22 ), rostromedial lateral globus pallidus, and ventral pallidum.

23 days withdrawal in the nucleus accumbens and ventral pallidum.

24 mbic projections of the NAcc, such as to the ventral pallidum.

25 and in the globus pallidus (+9%; p=0.06) and ventral pallidum (+11%; p=0.1), whereas binding was slig

26 ll (77 and 83% of control, respectively) and ventral pallidum (82% of control) as well as in the caud

27 A ventral pallidum, a basal cholinergic cell group, and me

28 ver pressing by cocaine was blocked by intra-ventral pallidum administration of the mu receptor antag

29 he stimulation of mu-opioid receptors in the ventral pallidum also elicits motor activation, and this

30 nsmission in the rostral anterior cingulate, ventral pallidum, amygdala, and inferior temporal cortex

31 teral cluster spanning the ventral striatum, ventral pallidum, amygdala, midbrain, and orbitofrontal

32 left dlPFC functional connectivity with the ventral pallidum, an AVP receptor-rich region previously

33 al band nuclei), lateral VTA and medial SNC (ventral pallidum and anterior half of substantia innomin

34 in other brain regions studied (hippocampus, ventral pallidum and cerebellum), or of the effects of c

35 By contrast, damage to sites in the ventral pallidum and globus pallidus impaired grooming a

36 and monosynaptic inhibitory currents in the ventral pallidum and lateral habenula, though the net ef

37 the ventromedial part of the subcommissural ventral pallidum and pallidal parts of the olfactory tub

38 d PHA-L-labeled presynaptic terminals in the ventral pallidum and substantia innominata were found to

39 Neurons in the ventral pallidum and substantia innominata were recorded

40 ced response in the DRD3-rich regions of the ventral pallidum and substantia nigra.

41 xtrapyramidal nuclei, such as the globus and ventral pallidum and the substantia nigra, pars reticula

42 ic projections from the nucleus accumbens to ventral pallidum and ventral tegmental area (VTA) are in

43 ampus, nucleus accumbens, prefrontal cortex, ventral pallidum and ventral tegmentum, and more intense

44 cell types send GABAergic projections to the ventral pallidum and were found to differentially promot

45 in a number of limbic (nucleus accumbens and ventral pallidum) and cortical (medial/ventral orbital a

46 nsmission in the rostral anterior cingulate, ventral pallidum, and amygdala was correlated with the i

47 ide substantial GABAergic innervation to the ventral pallidum, and chemogenetic inhibition of ventral

48 en specific neurons in nucleus accumbens and ventral pallidum, and how these changes are associated w

49 ntal cortex, including the ventral striatum, ventral pallidum, and mediodorsal thalamus, the amygdala

50 conditioning (through the ventral striatum, ventral pallidum, and PPTN) and the other to adaptively

51 ioral function for D1-MSN innervation of the ventral pallidum, and suggest that losing LTDGABA in D2-

52 ion in ventral tegmentum, nucleus accumbens, ventral pallidum, and the orbitofrontal prefrontal corte

53 iated with reduced extracellular GABA in the ventral pallidum, and the reduction in GABA was also pre

54 een in both pallidal segments, including the ventral pallidum, and the subthalamic nucleus, consisten

55 minata, bed nucleus of the stria terminalis, ventral pallidum, and ventrolateral globus pallidus.

56 Also, compound 13 injected into the rat ventral pallidum antagonized the locomotor activity elic

57 the dorsolateral part of the subcommissural ventral pallidum, anterograde labeling was weak in the m

58 In addition, following injections into the ventral pallidum, anterogradely transported biotinylated

59 bed nucleus of the stria terminalis, medial ventral pallidum, arcuate nucleus, and ventral tegmental

60 brain particularly the nucleus accumbens and ventral pallidum as well as actions within the ascending

61 o sadness-induced mu-opioid activation (left ventral pallidum, bilateral anterior cingulate cortices,

62 g pairing in the right nucleus accumbens and ventral pallidum but not in other areas.

63 VTA (by baclofen) or GABAA receptors in the ventral pallidum (by muscimol) inhibit the motor respons

64 rminals in the pallidum (globus pallidus and ventral pallidum) can be modulated by locally applied op

65 umbens, bed nucleus of the stria terminalis, ventral pallidum, central nucleus of the amygdala, and c

66 D1- versus D2-MSN GABAergic synapses in the ventral pallidum could explain the differential regulati

67 l ventral pallidum (RVP), but not the caudal ventral pallidum (CVP), were robustly Fos activated duri

68 ay to the dorsolateral subcompartment of the ventral pallidum (dlVP) and through the direct pathway t

69 ons in subregions of medial accumbens shell, ventral pallidum, elements of extended amygdala, and lat

70 s from these, including the globus pallidus, ventral pallidum, entopeduncular nucleus and substantia

71 ry bulbs, frontal cortex, or nucleus basalis/ventral pallidum following hormone treatment; however, a

72 nsory cortex, and in contralateral amygdala, ventral pallidum, globus pallidus, and hippocampus, as w

73 al and lateral septum, diagnoal band nuclei, ventral pallidum, globus pallidus, substantia innominata

74 circuitry in both the nucleus accumbens and ventral pallidum has been reported to mediate taste-reac

75 sion of opto-MOR in GABAergic neurons of the ventral pallidum hedonic cold spot led to real-time plac

76 umbens and the GABA(A) agonist muscimol into ventral pallidum (i.e., "disconnection" methods) also im

77 tside the nucleus accumbens (such as rostral ventral pallidum), immediately medial and adjacent to th

78 posing a role for mu-opioid receptors in the ventral pallidum in mediating the reinstatement of cocai

79 0 nl) into the tubercle but not the shell or ventral pallidum induced conditioned place preference.

80 However, the ventral pallidum is a heterogeneous structure, and how t

81 The ventral pallidum is centrally positioned within mesocort

82 Because the ventral pallidum is involved in reinforcement and addict

83 rebrain and brainstem targets, including the ventral pallidum, lateral and magnocellular preoptic nuc

84 connections with the hippocampus, amygdala, ventral pallidum, lateral hypothalamus, and ventral tegm

85 r cingulate, left orbitofrontal cortex, left ventral pallidum, left amygdala, and left inferior tempo

86 acity of morphine (0.01-10 microm) to reduce ventral pallidum levels of extracellular GABA was augmen

87 g LTDGABA in D2-MSN, but not D1-MSN input to ventral pallidum may promote cue-induced reinstatement o

88 uronal activity in the nucleus accumbens and ventral pallidum may underlie the augmented behavioral r

89 es in areas including the nucleus accumbens, ventral pallidum, medial preoptic area, medial amygdala,

90 The ability of intra-ventral pallidum morphine to reinstate lever pressing wa

91 Ventral pallidum neurons do not ordinarily fire vigorous

92 of sucrose in behavior and firing signals of ventral pallidum neurons, and likewise, they increased i

93 ons (caudate putamen, nucleus accumbens, and ventral pallidum) of mice that were given either water (

94 eral, or ventromedial neostriatum, or in the ventral pallidum or globus pallidus of rats.

95 lockade of kappa-opioid receptors within the ventral pallidum or mu-opioid receptors with the specifi

96 Naloxone infused into either the ventral pallidum or nucleus accumbens shell blocked the

97 n the caudate putamen, nucleus accumbens and ventral pallidum (p<0.001).

98 ager outputs to the forebrain, mainly to the ventral pallidum, preoptic-lateral hypothalamic continuu

99 projection from the nucleus accumbens to the ventral pallidum regulates the reinstatement of cocaine

100 receptors with morphine (1-30 microg) in the ventral pallidum reinstated cocaine seeking.

101 restricted within the nucleus accumbens and ventral pallidum, respectively.

102 the ventromedial part of the subcommissural ventral pallidum resulted in robust anterograde labeling

103 ounted in series of sections cut through the ventral pallidum, rostral globus pallidus, nucleus of th

104 und that projections to VTA from the rostral ventral pallidum (RVP), but not the caudal ventral palli

105 same reward within the nucleus accumbens to ventral pallidum segment of mesocorticolimbic circuitry.

106 d that accumbens neurons that project to the ventral pallidum showed adenosine A(2A) receptors immuno

107 Thus, only the ventral pallidum showed changes in molecular processes t

108 We further show that, in hippocampus and ventral pallidum, spinophilin is occasionally present in

109 This double dissociation in ventral pallidum subregional roles in drug seeking is li

110 tional significant changes were noted in the ventral pallidum, superior colliculus, dentate gyrus (in

111 the density was 346+/-27 fmol/g, and in the ventral pallidum the density was 317+/-27 fmol/g.

112 dial septum, the diagonal band of Broca, the ventral pallidum, the globus pallidus, the bed nucleus o

113 ata in the ventromedial globus pallidus, the ventral pallidum, the internal capsule, and the substant

114 ibution pattern, with high expression in the ventral pallidum, the islands of Calleja and pars compac

115 nveyed through the subiculum, accumbens, and ventral pallidum to the VTA where it contributes (along

116 ent dedicated neuronal subpopulations in the ventral pallidum tracked signal enhancements for hedonic

117 a1 siRNA vector (pHSVsiLA1) infused into the ventral pallidum, unrelated to TLR4.

118 bited a pattern of nucleus accumbens OTR and ventral pallidum V1aR binding different from that associ

119 In parallel with nucleus accumbens (NAS), ventral pallidum (VP) also receives a dopaminergic proje

120 her the nucleus accumbens shell (NAc) or the ventral pallidum (VP) amplifies hedonic "liking" reactio

121 t, Area X and surrounding MSt project to the ventral pallidum (VP) and dorsal thalamus via pallidal-l

122 Here, we identify the ventral pallidum (VP) as a site of convergence of medium

123 Neural activity in the ventral pallidum (VP) has been shown to encode changes i

124 The role of the nucleus accumbens (NAC) and ventral pallidum (VP) in food reward modulation was inve

125 of ionotropic glutamate receptors within the ventral pallidum (VP) in the expression of conditioned p

126 e amygdala (AMG), nucleus accumbens (NA) and ventral pallidum (VP) influence goal-oriented behaviors.

127 The ventral pallidum (VP) is a major intermediary in the pre

128 The ventral pallidum (VP) is a target of dense nucleus accum

129 Ventral pallidum (VP) is a well-established locus for th

130 Ventral pallidum (VP) is an important source of limbic i

131 The ventral pallidum (VP) is necessary for drug-seeking beha

132 The ventral pallidum (VP) is often viewed as an output struc

133 The ventral pallidum (VP) is posited to contribute to reward

134 ere, we present evidence suggesting that the ventral pallidum (VP) may participate in this process.

135 of parvalbumin-positive (PV) neurons in the ventral pallidum (VP) projecting to either the lateral h

136 GABAergic neurons in the ventral pallidum (VP) provide a major input to VTA neuro

137 The ventral pallidum (VP) receives orexin projections from l

138 e found that cue-evoked neural firing in the ventral pallidum (VP) reflected the strength of incentiv

139 Ventral pallidum (VP) serves important roles in reward a

140 We recorded neural activity in the ventral pallidum (VP) while rats learned a pavlovian rew

141 mino acid (EAA)-containing projection to the ventral pallidum (VP), a major limbic system output regi

142 o block alcohol-maintained responding in the ventral pallidum (VP), a novel alcohol reward substrate,

143 e to show that optogenetic inhibition of the ventral pallidum (VP), a region known for processing rew

144 e nucleus accumbens (NAc), lateral habenula, ventral pallidum (VP), and amygdala.

145 The NAc-S projects prominently to the ventral pallidum (VP), and in the current experiments, w

146 The medial preoptic area (MPOA), ventral pallidum (VP), and nucleus accumbens (NA) receiv

147 lized in the nucleus accumbens (NAC) and the ventral pallidum (VP), areas known to be important compo

148 rophic factor (BDNF) immunoreactivity in the ventral pallidum (VP), as determined by optical density

149 The dorsal-lateral BF, including the ventral pallidum (VP), contains reward-sensitive neurons

150 ons involves a projection from area X to the ventral pallidum (VP), which in turn projects to dopamin

151 amic nucleus (MD) via its projections to the ventral pallidum (VP), with the core and shell regions o

152 l segment (GPe), internal segment (GPi), and ventral pallidum (VP)-in 8 HD cases compared with 7 matc

153 tput structure of the mesolimbic system, the ventral pallidum (VP).

154 lateral nucleus of the amygdala (BLA) or the ventral pallidum (VP).

155 ctivation of a downstream target of BLA, the ventral pallidum (VP).

156 dopaminergic neurons via a connection in the ventral pallidum (VP).

157 d the motivation to eat generated within the ventral pallidum (VP)?

158 (PFCd), nucleus accumbens core (NAcore), and ventral pallidum (VP)] blocked the ability of footshock

159 core of the nucleus accumbens (NAcore), and ventral pallidum (VP)] prevented cocaine-induced reinsta

160 rly through its output to the rostral medial ventral pallidum (VP-m).

161 y was associated with V1aR expression in the ventral pallidum (VPall) or lateral septum, areas causal

162 umbens shell (AcbSh) terminate in the medial ventral pallidum (VPm) and neurons in the VPm project to

163 he membrane insertion of mu receptors in the ventral pallidum was altered by withdrawal from cocaine,

164 olfactory bulbs, septum, and nucleus basalis/ventral pallidum were dissected.

165 bic structures such as nucleus accumbens and ventral pallidum (where opioid/endocannabinoid/orexin si

166 and vasopressin-immunoreactive fibers in the ventral pallidum, with males showing a greater density o